Section 1 - Diagnostics
Entries A–Z
Published online by Cambridge University Press: 30 May 2019
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- Publisher: Cambridge University PressPrint publication year: 2019
References
Fong, GC, Shah, PU, Gee, MN, et al. Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3–4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24. Am J Hum Genet. 1998; 63(4): 1117–29.CrossRefGoogle ScholarPubMed
Guerrini, R, Belmonte, A, Genton, P. Antiepileptic drug-induced worsening of seizures in children. Epilepsia. 1998; 39 Suppl 3: S2–10.Google Scholar
Pavon, P, Bianchini, R, Trifiletti, RR, et al. Neuropsychological assessment in children with absence epilepsy. Neurology. 2001; 56(8): 1047–51.Google Scholar
Schwartzkroin, PA. Brain development and epilepsy. New York: Oxford University Press; 1995. xii, 337 p.Google Scholar
Burkhard, PR, Delavelle, J, Du Pasquier, R, Spahr, L. Chronic parkinsonism associated with cirrhosis: a distinct subset of acquired hepatocerebral degeneration. Arch Neurol. 2003; 60(4): 521–8.Google Scholar
Fernández-Rodriguez, R, Contreras, A, De Villoria, JG, Grandas, F. Acquired hepatocerebral degeneration: clinical characteristics and MRI findings. Eur J Neurol. 2010; 17(12): 1463–70.CrossRefGoogle ScholarPubMed
Saporta, MA, Andre, C, Bahia, PR, et al. Acquired hepatocerebral degeneration without overt liver disease. Neurology. 2004; 63: 1981–2.Google Scholar
Victor, M, Adams, RD, Cole, M. The acquired (non-Wilsonian) type of chronic hepatocerebral degeneration. Medicine (Baltimore). 1965; 44: 345–96.CrossRefGoogle ScholarPubMed
Ham, H, Jung, S, Jung, T, Heo, S. Cerebral actinomycosis : unusual clinical and radiological findings of an abscess. J Korean Neurosurg Soc. 2011; 50(2): 147.Google Scholar
Bradley, W. Actinomycosis. Neurology in clinical practice. Philadelphia: Butterworth-Heinemann; 2004. p. 1505.Google Scholar
Dua, R, Bhat, D, Indira, D. Spinal actinomycosis: a rare disease. Neurol India. 2010; 58(2): 298.Google Scholar
Banwell, B, Kennedy, J, Sadovnick, D, et al. Incidence of acquired demyelination of the CNS in Canadian children. Neurology. 2009; 72(3): 232–9.Google Scholar
Leake, JA, Albani, S, Kao, AS, et al. Acute disseminated encephalomyelitis in childhood: epidemiologic, clinical and laboratory features. Pediatr Infect Dis J. 2004; 23(8): 756–64.Google Scholar
Murthy, SN, Faden, HS, Cohen, ME, Bakshi, R. Acute disseminated encephalomyelitis in children. Pediatrics. 2002; 110(2 Pt 1): e21.CrossRefGoogle ScholarPubMed
Pohl, D, Hennemuth, I, von Kries, R, Hanefeld, F. Paediatric multiple sclerosis and acute disseminated encephalomyelitis in Germany: results of a nationwide survey. Eur J Pediatr. 2007; 166(5): 405–12.Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. Multiple sclerosis and other inflammatory demyelinating diseases. In Adams & Victor's principles of neurology. 10th ed. New York: McGraw-Hill; 2014.Google Scholar
Torisu, H, Kira, R, Ishizaki, Y, et al. Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan. Brain Dev. 2010; 32(6): 454–62.Google Scholar
Chiba, A, Kusunoki, S, Obata, H, et al. Serum anti-GQ1b IgG antibody is associated with ophthalmoplegia in Miller Fisher syndrome and Guillain-Barré syndrome: clinical and immunohistochemical studies. Neurology. 1993; 43: 1911.CrossRefGoogle ScholarPubMed
Dimachkie, MM, Barohn, RJ. Guillain-Barré syndrome and variants. Neurol Clin. 2013; 31(2): 491–510.Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. Diseases of the peripheral nerves. In Adams & Victor's principles of neurology. 10th ed. New York: McGraw-Hill; 2014.Google Scholar
Willison, HJ, Veitch, J, Paterson, G, Kennedy, PG. Miller Fisher syndrome is associated with serum antibodies to GQ1b ganglioside. J Neurol Neurosurg Psychiatry. 1993; 56: 204.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Kessler, RC, Sonnega, A, Bromet, E, et al. Post-traumatic stress disorder in the national comorbidity survey. Arch Gen Psychiatry. 1995; 52(12): 1048–60.CrossRefGoogle ScholarPubMed
Flomenberg, P, Kojaoghlanian, T. Epidemiology and clinical manifestations of adenovirus infection. In Hirsch, M, ed. UpToDate. Waltham, MA: Wolters Kluwer.Google Scholar
Huang, Y, Huang, S, Chen, S, et al. Adenovirus infection associated with central nervous system dysfunction in children. J Clin Virol. 2013; 57(4): 300–4.Google Scholar
Centers for Disease Control and Prevention. Adenovirus. Atlanta, GA: CDC; 2015. Accessed Jan 20, 2016. Available from www.cdc.gov/adenovirus/hcp/clinical-overview.htmlGoogle Scholar
Ficicioglu, C, Mandell, R, Shih, VE. Argininosuccinate lyase deficiency: longterm outcome of 13 patients detected by newborn screening. Mol Genet Metab. 2009; 98: 273–7. DOI: 10.1016/j.ymgme.2009.06.011Google Scholar
Nagamani, SCS, Erez, A, Lee, B. Argininosuccinate lyase deficiency. Feb 3, 2011 [Updated Feb 2, 2012]. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993–2017. Available from https://www.ncbi.nlm.nih.gov/books/NBK51784/Google Scholar
Summar, ML, Koelker, S, Freedenberg, D, et al. The incidence of urea cycle disorders. Mol Genet Metab. 2013; 110: 179–80.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Fabrega, H Jr, Mezzich, JE, Mezzich, AC. Adjustment disorder as a marginal or transitional illness category in DSM-III. Arch Gen Psychiatry. 1987; 44(6): 567–72.Google Scholar
Foster, P, Oxman, T. A descriptive study of AD diagnoses in general hospital patients. Isr J Psychol Med. 1994; 11: 153–7.Google Scholar
Popkin, MK, Callies, AL, Colón, EA, Stiebel, V. Adjustment disorders in medically ill patients referred for consultation in a university hospital. Psychosomatics. 1990; 31(4): 410–4.Google Scholar
Portzky, G, Audenaert, K, van Heeringen, K. Adjustment disorder and the course of the suicidal process in adolescents. J Affect Disord. 2005; 87(2–3): 265–70.CrossRefGoogle ScholarPubMed
Charmandari, E, Nicolaides, NC, Chrousos, GP. Adrenal insufficiency. Lancet. 2014; 383(9935): 2152–67. DOI: 10.1016/S0140-6736(13)61684-0CrossRefGoogle ScholarPubMed
Leigh, H, Kramer, SI. The psychiatric manifestations of endocrine disease. Adv Intern Med. 1984; 29: 413.Google ScholarPubMed
Ebinger, G, Six, R, Bruyland, M, Somers, G. Flexion contractures: a forgotten symptom in Addison's disease and hypopituitarism. Lancet. 1986; 2(8511): 858.Google Scholar
Bezman, L, Moser, AB, Raymond, GV, et al. Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screening. Ann Neurol. 2001; 49: 512–7.Google Scholar
Engelen, M, Barbier, M, Dijkstra, IM, et al. X-linked adrenoleukodystrophy in women: a cross-sectional cohort study. Brain. 2014; 137: 693–706.Google Scholar
Moser, HW, Moser, AB, Steinberg, SJ. X-linked adrenoleukodystrophy. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle, WA: University of Washington; 1993–2018. Accessed Feb 6, 2015. Available from www.genetests.orgGoogle Scholar
Moser, HW, Raymond, GV, Dubey, P. Adrenoleukodystrophy: new approaches to a neurodegenerative disease. JAMA. 2005; 294: 3131–4.Google Scholar
Percy, AK, Rutledge, SL. Adrenoleukodystrophy and related disorders. Ment Retard Dev Disabil Res Rev. 2001; 7: 179–89.Google Scholar
van Geel, BM, Bezman, L, Loes, DJ, et al. Evolution of phenotypes in adult male patients with X-linked adrenoleukodystrophy. Ann Neurol. 2001; 49: 186–94.3.0.CO;2-R>CrossRefGoogle ScholarPubMed
Paine, SJ, Fink, J, Gander, PH. Identifying advanced and delayed sleep phase disorders in the general population: a national survey of New Zealand adults. Chronobiol Int. 2014; 31: 627–36.Google Scholar
Sateia, M, Berry, RB, Bornemann, MC, et al. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Auger, RR, Burgess, HJ, Emens, JS, et al. Clinical practice guideline for the treatment of intrinsic circadian rhythm sleep-wake disorders: advanced sleep-wake phase disorder (ASWPD), delayed sleep-wake phase disorder (DSWPD), non-24-hour sleep-wake rhythm disorder (N24SWD), and irregular sleep-wake rhythm disorder (ISWRD) an update for 2015. J Clin Sleep Med. 2015; 11: 1199–236.Google Scholar
Bjorvatn, B, Pallesen, S. A practical approach to circadian rhythm sleep disorders. Sleep Med Rev. 2009; 13: 47–60.Google Scholar
Sack, RL, Auckley, D, Auger, RR, et al. Circadian rhythm sleep disorders: part II, advanced sleep phase disorder, delayed sleep phase disorder, free-running disorder, and irregular sleep-wake rhythm. Sleep. 2007; 30: 1484–501.Google Scholar
Schrader, H, Bovim, G, Sand, T. The prevalence of delayed and advanced sleep phase disorders. J. Sleep Res. 1993; 2: 51–5.Google Scholar
Perry, H. Inhalant abuse in children and adolescents. In Burns, MM, ed. UpToDate. Waltham, MA: Wolters Kluwer; 2018. Available from www.uptodate.com/contents/inhalant-abuse-in-children-and-adolescents?source=search_result&search=aerosol%20inhalation%20abuse&selectedTitle=2∼133Google Scholar
Leavatin, P. Pupillary escape in diseases of the retina or optic nerve. Arch Ophthalmol. 1959; 62: 768–79.Google Scholar
Hartveit, F, Lystad, H, Minken, A. The pathology of venous air embolism. Br J Exp Pathol. 1968; 49: 81–6.Google Scholar
Heckmann, JG, Lang, CJ, Kindler, K, et al. Neurologic manifestations of cerebral air embolism as a complication of central venous catheterization. Crit Care Med. 2000; 28: 1621–5.Google Scholar
Mirski, MA, Lele, AV, Fitzsimmons, L, Toung, TJ. Diagnosis and treatment of vascular air embolism. Anesthesiology. 2007; 106(1): 164–77.Google Scholar
Driessen, M, Lange, W, Junghanns, K, Wetterling, T. Proposal of a comprehensive clinical typology of alcohol withdrawal – a cluster analysis approach. Alcohol Alcohol. 2005; 40(4): 308–13.Google Scholar
Jesse, S, Brathen, G, Ferra, M, et al. Alcohol withdrawal syndrome: mechanisms, manifestations, and management. Acta Neurol Scand. 2016; 135: 4–16.CrossRefGoogle ScholarPubMed
Becker, HC. Kindling in alcohol withdrawal. Alcohol Health Res World. 1998; 22(1): 25–33. Available from http://pubs.niaaa.nih.gov/publications/arh22-1/25-34.pdfGoogle ScholarPubMed
National Institute on Alcohol Abuse and Alcoholism. Alcohol Alert: Alcohol withdrawal syndrome. Alcohol Alert. Washington, DC: National Institute on Alcohol Abuse and Alcoholism No. 5 PH 270. August 1989. Available from http://pubs.niaaa.nih.gov/publications/aa05.htmGoogle Scholar
Cohen, BH, Chinnery, PF, Copeland, WC. POLG-related disorders. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle, WA: University of Washington; 1993–2017. Available from www.ncbi.nlm.nih.gov/books/NBK26471/Google Scholar
Gordon, N. Alpers syndrome: progressive neuronal degeneration of children with liver disease. DMCN. 2006; 48: 1001–3.Google ScholarPubMed
Saneto, RP, Cohen, BH, Copeland, WC, Naviaux, RK. Alpers-Huttenlocher syndrome: a review. Pediatr Neurol. 2013; 48(3): 167–78.CrossRefGoogle Scholar
Plassman, BL, Langa, KM, Fisher, GG, et al. Prevalence of dementia in the United States: the aging, demographics, and memory study. Neuroepidemiology. 2007; 29: 125–32.Google Scholar
Stern, Y, Gurland, B, Tatemichi, TK, et al. Influence of education and occupation on the incidence of Alzheimer's disease. JAMA. 1994; 271: 1004–10.CrossRefGoogle ScholarPubMed
Beeri, MS, Ravona-Springer, R, Silverman, JM, Haroutunian, V. The effects of cardiovascular risk factors on cognitive compromise. Dialogues Clin Neurosci. 2009; 11: 201–12.Google Scholar
American Academy of Neurology. Detection, diagnosis and management of dementia. AAN Guideline Summary for Clinicians. Available from http://tools.aan.com/professionals/practice/pdfs/dementia_guideline.pdfGoogle Scholar
Bateman, RJ, Aisen, PS, De Strooper, B, et al. Autosomal-dominant Alzheimer's disease: a review and proposal for the prevention of Alzheimer's disease. Alzheimers Res Ther. 2011; 3.Google ScholarPubMed
Braak, H, Braak, E. Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol (Berl). 1991; 82: 239–59.Google Scholar
Beach, TG, Schneider, JA, Sue, LI, et al. Theoretical impact of florbetapir (18F) amyloid imaging on diagnosis of Alzheimer dementia and detection of preclinical cortical amyloid. J. Neuropathol Exp Neurol. 2014; 73: 948–53.Google Scholar
Zhang, S, Han, D, Tan, X, et al. Diagnostic accuracy of 18 F-FDG and 11 C-PIB-PET for prediction of short-term conversion to Alzheimer's disease in subjects with mild cognitive impairment. Int J Clin Pract. 2012; 66: 185–98.Google Scholar
Andersen, CU, Marquardsen, J, Mikkelsen, B, et al. Amaurosis fugax in a Danish community: a prospective study. Stroke. 1988; 19: 196–9.Google Scholar
Centers for Disease Control and Prevention. Primary amebic meningoencephalitis (PAM): sources of infection and risk factors. Atlanta, GA: CDC; 2013. Accessed Jan 20, 2016. Available from www.cdc.gov/parasites/naegleria/infection-sources.htmlGoogle Scholar
DynaMed Plus [Internet]. Amebic brain diseases. Ipswich, MA: EBSCO Information Services; 1995. Record No. 900886. Available from www.dynamed.com/login.aspx?direct=true&site=DynaMed&id=900886 [Registration and login required.]Google Scholar
Chow, F, Glaser, C. Emerging and reemerging neurologic infections. Neurohospitalist. 2014; 4(4): 173–84.CrossRefGoogle ScholarPubMed
Real de Asúa, D, Costa, R, Galván, JM, et al. Systemic AA amyloidosis: epidemiology, diagnosis, and management. Clin Epidemiol. 2014; 6: 369–77. DOI: 10.2147/CLEP.S39981Google Scholar
Kyle, RA, Linos, A, Beard, CM, et al. Incidence and natural history of primary systemic amyloidosis in Olmsted County, Minnesota, 1950 through 1989. Blood. 1992; 79(7): 1817–22.Google Scholar
Arvanitakis, Z, Leurgans, SE, Wang, Z, et al. Cerebral amyloid angiopathy pathology and cognitive domains in older persons. Ann Neurol. 2011; 69: 320–7.Google Scholar
Bellotti, V, Nuvolone, M, Giorgetti, S, et al. The workings of the amyloid diseases. Ann Med. 2007; 39: 200–7.Google Scholar
Greenberg, SM, Vonsattel, JP, Stakes, JW, et al. The clinical spectrum of cerebral amyloid angiopathy: presentations without lobar hemorrhage. Neurology. 1993; 43: 2073–9.CrossRefGoogle ScholarPubMed
Tsourdi, E, Därr, R, Wieczorek, K, et al. Macroglossia as the only presenting feature of amyloidosis due to MGUS. Eur J Haematol. 2014; 92: 88–9.Google Scholar
Elizan, TS, Chen, KM, Mathai, KV, Dunn, D, Kurland, LT. Amyotrophic lateral sclerosis and parkinsonism-dementia complex. A study in non-Chamorros of the Mariana and Caroline Islands. Arch Neurol. 1966; 14: 347–54.Google Scholar
Rodgers-Johnson, P, Garruto, RM, Yanagihara, R, et al. Amyotrophic lateral sclerosis and parkinsonism-dementia on Guam: a 30-year evaluation of clinical and neuropathologic trends. Neurology. 1986; 36: 7–13.Google Scholar
Plato, CC, Garruto, RM, Galasko, D, et al. Amyotrophic lateral sclerosis and parkinsonism-dementia complex of Guam: changing incidence rates during the past 60 years. Am J Epidemiol. 2003; 157(2): 149–57.Google Scholar
Hirano, A, Kurland, LT, Krooth, RS, Lessell, S. Parkinsonism-dementia complex, an endemic disease on the island of Guam. I. Clinical features. Brain. 1961; 84: 642–61.Google Scholar
Khabazian, I, Bains, JS, Williams, DE, et al. Isolation of various forms of sterol B-D-glucoside from the seed of Cycas circinalis: neurotoxicity and implications for ALS-parkinsonism dementia complex. J Neurochem. 2002; 82: 516–28.Google Scholar
Hirano, A, Kurland, LT, Krooth, RS, Lessell, S. Parkinsonism-dementia complex, an endemic disease on the island of Guam. II. Pathological features. Brain. 1961; 84: 662–70.Google Scholar
Davies, NP, Imbrici, P, Fialho, D, et al. Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation. Neurology. 2005; 65: 1083–9.Google Scholar
Yoon, G, Quitania, L, Kramer, JH, et al. Andersen-Tawil syndrome: definition of a neurocognitive phenotype. Neurology. 2006; 66: 1703–10.Google Scholar
Statland, JM, Tawil, R, Venance, SL. Andersen-Tawil syndrome. Nov 22, 2004 [Updated Sep 3, 2015]. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle, WA: University of Washington; 1993–2016. Available from www.ncbi.nlm.nih.gov/books/NBK1264/Google Scholar
Dority, JS, Oldham, JS. Subarachnoid hemorrhage: an update. Anesthesiol Clin. 2016; 34: 577–600.Google Scholar
Vlak, MH, Algra, A, Brandenburg, R, et al. Prevalence of unruptured intracranial aneurysms, with emphasis on sex, age, comorbidity, country, and time period: a systematic review and meta-analysis. Lancet Neurology. 2011; 10: 626–36.Google Scholar
Bird, LM. Angelman syndrome: review of clinical and molecular aspects. Appl Clin Genet. 2014; 7: 93–104.Google Scholar
Dagli, AI, Mueller, J, Williams, CA. Angelman syndrome. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle, WA: University of Washington; 1993–2018.Google Scholar
Williams, CA, Driscoll, DJ, Dagli, AI. Clinical and genetic aspects of Angelman syndrome. Genet Med. 2010; 12(7): 385–95.Google Scholar
Hochberg, N, Blackburn, B, Park, S, et al. Eosinophilic meningitis attributable to Angiostrongylus cantonensis infection in Hawaii: clinical characteristics and potential exposures. Am J Trop Med Hyg. 2011; 85(4): 685–90.Google Scholar
Graeff-Teixeira, C, da Silva, A, Yoshimura, K. Update on eosinophilic meningoencephalitis and its clinical relevance. Clin Microbiol Rev. 2009; 22(2): 322–48.Google Scholar
Murphy, GS, Johnson, S. Clinical aspects of eosinophilic meningitis and meningoencephalitis caused by Angiostrongylus cantonensis, the rat lungworm. Hawaii J Med Public Health. 2013; 72(6)Suppl 2: 35–40.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Mehanna, HM, Moledina, J, Travis, J. Refeeding syndrome: what it is, and how to prevent and treat it. BMJ. 2008; 336(7659): 1495–8.Google Scholar
Preti, A, Rocchi, MB, Sisti, D, et al. A comprehensive meta-analysis of the risk of suicide in eating disorders. Acta Psychiatr Scand. 2011; 124(1): 6–17.Google Scholar
Adams, RD, Victor, M, Ropper, AH, eds. The acquired metabolic disorders of the nervous system. In Principles of neurology. 6th ed. New York: McGraw-Hill; 1997, pp. 1108–37.Google Scholar
Adams, RD, Victor, M, Ropper, AH, Daroff, RB. Principles of neurology. Cogn Behav Neurol. 1997; 10(3): 220.Google Scholar
Hypothermia after Cardiac Arrest Study Group. Mild therapeutic hypothermia to improve the neurologic outcome after cardiac arrest. N Engl J Med. 2002; 346: 549–56.Google Scholar
Levy, DE, Caronna, JJ, Singer, BH, et al. Predicting outcome from hypoxic-ischemic coma. JAMA. 1985; 253(10): 1420–6.Google Scholar
Mateen, FJ, Josephs, KA, Trenerry, MR, et al. Long-term cognitive outcomes following out-of-hospital cardiac arrest: a population-based study. Neurology. 2011; 77(15): 1438–45.Google Scholar
Bogousslavsky, J, Regli, F. Anterior cerebral artery territory infarction in the Lausanne Stroke Registry. Clinical and etiologic patterns. Arch Neurol. 1990; 47(2): 144–50.Google Scholar
Gacs, G, Fox, AJ, Barnett, HJ, Vinuela, F. Occurrence and mechanisms of occlusion of the anterior cerebral artery. Stroke. 1983; 14(6): 952–9.Google Scholar
Kumral, E, Bayulkem, G, Evyapan, D, Yunten, N. Spectrum of anterior cerebral artery territory infarction: clinical and MRI findings. Eur J Neurol. 2002; 9(6): 615–24.Google Scholar
Helgason, C, Caplan, LR, Goodwin, J, Hedges, T III. Anterior choroidal artery-territory infarction: report of cases and review. Arch Neurol. 1986; 43(7): 681–6.Google Scholar
Ois, A, Cuadrado-Godia, E, Solano, A, Perich-Alsina, X, Roquer, J. Acute ischemic stroke in anterior choroidal artery territory. J Neurol Sci. 2009; 281(1–2): 80–4.Google Scholar
van Son, B, Vandevenne, J, Viaene, P. Bilateral anterior choroidal artery infarction presenting with progressive somnolence. J Stroke Cerebrovasc Dis. 2014; 23(8): e409–10.Google Scholar
de Seze, J, Stojkovid, T, Breteau, G, et al. Acute myelopathies: clinical, laboratory and outcome profiles in 79 cases. Brain. 2001; 124: 1509–21.Google Scholar
Nedeltchev, K, Loher, TJ, Stepper, F, et al. Long-term outcomes of acute spinal cord ischemia syndrome. Stroke. 2014; 35(2): 560–5.Google Scholar
Chan, TY. Herbal medicines induced anticholinergic poisoning in Hong Kong. Toxins (Basel). 2016; 8(3). PMID: 26999208Google Scholar
Ludolph, AC. Datura stramonium. In Spencer, PS, Schaumburg, HH, eds. Experimental and clinical neurotoxicology. 2nd ed. New York: Oxford University Press; 2000. pp. 466–7.Google Scholar
Hauser, A. Guillain-Barre syndrome and other immune-mediated neuropathies. In Hauser, SL, ed. Harisson's neurology in clinical medicine. 3rd ed. New York: McGraw-Hill Education/Medical; 2013.Google Scholar
Senties-Madrid, H, Vega-Boada, F. Paraneoplastic syndromes associated with Anti-Hu antibodies. IMAJ. 2001; 3: 94–103.Google Scholar
Launay, M, Delmont, E, Benaim, C, et al. Anti-MAG paraproteinemic demyelinating polyneuropathy: a clinical, biological, electrophysiological and anatomopathological descriptive study of a 13-patients’ cohort. Rev Neurol (Paris). 2009; 165(12): 1071–9.Google Scholar
Niermeijer, JM, Fischer, K, Eurelings, M, et al. Prognosis of polyneuropathy due to IgM monoclonal gammopathy: a prospective cohort study. Neurology. 2010; 74(5): 406–12.Google Scholar
Rison, RA. Paraproteinemic neuropathy: a practical review. BMC Neurology. 2016; 16: 13.Google Scholar
Martinelli, I, Passamonti, SM, Bucciarelli, P. Thrombophilic states. Handb Clin Neurol. 2014; 120: 1061–71.Google Scholar
Patnaik, MM, Moll, S. Inherited antithrombin deficiency: a review. Haemophilia. 2008; 14: 1229–39.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Kessler, RC, Ormel, J, Demler, O, Stang, PE. Comorbid mental disorders account for the role impairment of commonly occurring chronic physical disorders: results from the National Comorbidity Survey. J Occup Environ Med. 2003; 45(12): 1257–66.Google Scholar
Caselli, RJ, Hunder, GG. Neurologic aspects of giant cell (temporal) arteritis. Rheum Dis Clin North Am. 1993; 19(4): 941–53.Google Scholar
Johnson, H, Bouman, W, Pinner, G. Psychiatric aspects of temporal arteritis: a case report and review of the literature. J Geriatr Psychiatry Neurol. 1997; 10(4): 142–5.Google Scholar
Nyatsanza, F, Tipple, C. Syphilis: presentations in general medicine. Clin Med (Lond). 2016; 16(2): 184–8.Google Scholar
Hartveit, F, Lystad, H, Minken, A. The pathology of venous air embolism. Br J Exp Pathol. 1968; 49: 81–6.Google Scholar
Leblanc, FE, Charrette, EP, Dobell, AR, Branch, CL. Neurological complications of aortic coarctation. Can Med Assoc J. 1968; 99(7): 299–303.Google Scholar
Hagan, PG, Nienaber, CA, Isselbacher, EM, et al. The International Registry of Acute Aortic Dissection (IRAD): new insights into an old disease. JAMA. 2000; 283: 897–903.Google Scholar
Nallamothu, BK, Mehta, RH, Saint, S, et al. Syncope in acute aortic dissection: diagnostic, prognostic, and clinical implications. Am J Med. 2002; 113: 468–71.Google Scholar
Nienaber, CA, Fattori, R, Mehta, RH, et al. Gender-related differences in acute aortic dissection. Circulation. 2004; 109: 3014–21.Google Scholar
American Heart Association. Problem: aortic valve regurgitation. 2014. Available from www.heart.org/HEARTORG/Conditions/More/HeartValveProblemsandDisease/Problem-Aortic-Valve-Regurgitation_UCM_450611_Article.jsp. Accessed Oct 5, 2018.Google Scholar
Otto, CM, Bonow, RO. Valvular heart disease. In Mann, DL, Zipes, DP, Libby, P, Bonow, RO, Braunwald, E, eds. Braunwald's heart diseases: A textbook of cardiovascular medicine. 10th ed. Philadelphia: Elsevier/Saunders; 2015. pp. 1409–10.Google Scholar
American Heart Association. Aortic valve stenosis (AVS). 2015. Available from www.heart.org/en/health-topics/congenital-heart-defects/about-congenital-heart-defects/aortic-valve-stenosis-avs. Accessed Oct 10, 2018.Google Scholar
Eveborn, GW, Schirmer, H, Heggelund, G, et al. The evolving epidemiology of valvular aortic stenosis. The Tromsø study. Heart. 2013; 99: 396.Google Scholar
Faggiano, P, Aurigemma, GP, Rusconi, C, Gaasch, WH. Progression of valvular aortic stenosis in adults: literature review and clinical implications. Am Heart J. 1996; 132: 408.Google Scholar
Nishimura, RA, Otto, CM, Bonow, RO, et al. 2014 AHA/ACC guideline for the management of patients with valvular heart disease: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation. 2014; 129(23): 2440–92.Google Scholar
Otto, CM, Bonow, RO. Valvular heart disease. In Mann, DL, Zipes, DP, Libby, P, Bonow, RO, Braunwald, E, eds. Braunwald's heart diseases: a textbook of cardiovascular medicine. 10th ed. Philadelphia: Elsevier/Saunders; 2015. pp. 1448–58.Google Scholar
Achneck, HE, Rizzo, JA, Tranquilli, M, Elefteriades, JA. Safety of thoracic aortic surgery in the present era. Ann Thorac Surg. 2007; 84: 1180–5.Google Scholar
Dharmaraj, B, Kosai, NR, Gendeh, H, Ramzisham, AR, Das, S. A prospective cohort study on quality of life after endoscopic thoracic sympathectomy for primary hyperhidrosis. Clin Ter. 2016; 167: 67–71.Google Scholar
Messé, SR, Bavaria, JE, Mullen, , et al. Neurologic outcomes from high risk descending thoracic and thoracoabdominal aortic operations in the era of endovascular repair. Neurocrit Care. 2008; 9(3): 344–51.Google Scholar
Benjamin, ER, Tillou, A, Hiatt, JR, Cryer, HG. Blunt thoracic aortic injury. Am Surg. 2008; 74(10): 1033–7.Google Scholar
Cowley, RA, Turney, SZ, Hankins, JR, et al. Rupture of thoracic aorta caused by blunt trauma. A fifteen-year experience. J Thorac Cardiovasc Surg. 1990; 100: 652–60.Google Scholar
Fabian, TC, Richardson, JD, Croce, MA, et al. Prospective study of blunt aortic injury: multicenter trial of the American Association for the Surgery of Trauma. J Trauma. 1997; 42: 374–80.Google Scholar
Kram, HB, Appel, PL, Wohlmuth, DA, Shoemaker, WC. Diagnosis of traumatic thoracic aortic rupture: a 10-year retrospective analysis. Ann Thorac Surg. 1989; 47: 282–6.Google Scholar
CheckOrphan. Aqueductal stenosis. 2006–2018. Available from www.checkorphan.org/diseases/hydrocephalus-due-congenital-stenosis-aqueduct-sylvius. Accessed Aug 1, 2018.Google Scholar
Cinalli, G, Spennato, P, Nastro, A, et al. Hydrocephalus in aqueductal stenosis. Childs Nerv Sys. 2011; 27(10): 1621–42.Google Scholar
Millichap, JG. Temporal lobe arachnoid cyst-attention deficit disorder syndrome. Role of the electroencephalogram and diagnosis. Neurology. 1997; 48(5): 1435–9.Google Scholar
Wright, MH, Denney, LC. A comprehensive review of spinal arachnoiditis. Orthop Nurs. 2003; 22: 215–9.Google Scholar
AlShahi, R, Warlow, C. A systematic review of the frequency and prognosis of arteriovenous malformations of the brain in adults. Brain. 2001; 124: 1900–26.Google Scholar
American Society of Neuroradiology. Arteriovenous fistulae of the CNS. AJNR AM J Neuroradiol. 2001; 22: S22–5.Google Scholar
da Costa, L, Wallace, MC, Ter Brugge, KG, et al. The natural history and predictive features of hemorrhage from brain arteriovenous malformations. Stroke. 2009; 40: 100–5.Google Scholar
Gross, BA, Du, R. Natural history of cerebral arteriovenous malformations: a meta-analysis. J Neurosurg. 2013; 118: 437–43.Google Scholar
Lev, N, Maimon, S, Rappaport, ZH, Melamed, E. Spinal dural arteriovenous fistulae: a diagnostic challenge. Isr Med Assoc J. 2001; 3: 492–6.Google Scholar
Mohr, JP, KejdaScharler, J, PileSpellman, J. Diagnosis and treatment of arteriovenous malformations. Curr Neurol Neurosci Rep. 2013; 13: 324.Google Scholar
Stapf, C, Mast, H, Sciacca, RR, et al. Predictors of hemorrhage in patients with untreated brain arteriovenous malformation. Neurology. 2006; 66: 1350–5.Google Scholar
Tsai, LL. Intracranial dural arteriovenous fistulas with or without cerebral sinus thrombosis: analysis of 69 patients. J Neurol Neurosurg Psychiatry. 2004; 75: 1639–41.Google Scholar
Al-Shahi, R, Warlow, C. A systematic review of the frequency and prognosis of arteriovenous malformations of the brain in adults. Brain. 2001; 124: 1900.Google Scholar
American Heart Association. What is an arteriovenous malformation (AVM)? Reviewed Oct 23, 2012. Available from www.strokeassociation.org/STROKEORG/AboutStroke/TypesofStroke/HemorrhagicBleeds/What-Is-an-Arteriovenous-Malformation-AVM_UCM_310099_Article.jsp#.VpLPKvkrLIU. Accessed Oct 5, 2018.Google Scholar
Gross, BA, Du, R. Natural history of cerebral arteriovenous malformations: a meta-analysis. J Neurosurg. 2013; 118: 437.Google Scholar
Ross, J, Al-Shahi Salman, R. Interventions for treating brain arteriovenous malformations in adults. Cochrane Database Syst Rev. 2010; (7): CD003436.Google Scholar
Miller, NR, ed. Anterior ischemic optic neuropathy. In Walsh and Hoyt's clinical neuro-ophthalmology. 4th ed. Vol 1. Baltimore: Williams & Wilkins; 1982. pp. 212–26.Google Scholar
Russo, E, Ciriaco, M, Ventrice, P, et al. Corticosteroid-related central nervous system side effects. J Pharmacol Pharmacother. 2013; 4(Suppl 1): S94–8.Google Scholar
Kourkoumpetis, T, Desalermos, A, Muhammed, M, Mylonakis, E. Central nervous system aspergillosis. Medicine. 2012; 91(6): 328–36.Google Scholar
Shamim, M, Enam, S, Ali, R, Anwar, S. Craniocerebral aspergillosis: a review of advances in diagnosis and management. J Pak Med Assoc. 2010; 60(7): 573–9.Google Scholar
Panackal, A, Williamson, P. Fungal infections of the central nervous system. CONTINUUM (Minneap Minn). 2015; 21: 1662–78.Google Scholar
Central Brain Tumor Registry of the United States. www.CBTRUS.org. Accessed Oct 10, 2018.Google Scholar
Schwartzbaum, JA, Fisher, JL, Aldape, KD, Wrensch, M. Epidemiology and molecular pathology of glioma. Nat Clin Pract Neurol. 2006; 2: 494–503.Google Scholar
Davis, FG, Bruner, JM, Surawicz, TS. The rationale for standardized registration and reporting of brain and central nervous system tumors in population-based cancer registries. Neuroepidemiology. 1997; 16: 308–16.Google Scholar
Pan, E, Prados, MD. Glioblastoma multiforme and anaplastic astrocytoma. In Kufe, DW, Pollock, RE, Weichselbaum, RR, et al., eds. Holland-Frei cancer medicine. 6th ed. Hamilton, ON: BC Decker; 2003. Available from https://www.ncbi.nlm.nih.gov/books/NBK12526/Google Scholar
Smith, MA, Freidlin, B, Gloeckler Ries, LA, Simon, R. Trends in reported incidence of primary malignant brain tumors in children in the United States. J Natl Cancer Inst. 1998; 90: 1269–77.CrossRefGoogle ScholarPubMed
Watanabe, T, Katayama, Y, Yoshino, A, et al. Treatment of low-grade diffuse astrocytomas by surgery and human fibroblast interferon without radiation therapy. J Neurooncol. 2003; 61(2): 171–6.Google Scholar
Boden, SD, Dodge, LD, Bohlman, HH, Rechtine, GR. Rheumatoid arthritis of the cervical spine. A long-term analysis with predictors of paralysis and recovery. J Bone Joint Surg Am. 1993; 75(9): 1282–97.Google Scholar
Pueschel, SM, Scola, FH. Atlantoaxial instability in individuals with Down syndrome. Epidemiological, radiographic and clinical studies. Pediatrics. 1987; 80(4): 555–60.Google Scholar
Machado, VH, Palmini, A, Bastos, FA, Rotert, R. Long-term control of epileptic drop attacks with the combination of valproate, lamotrigine, and a benzodiazepine: a “proof of concept,” open label study. Epilepsia. 2011; 52(7): 1303–10.Google Scholar
American Heart Association. What is atrial fibrillation (AFib or AF)? 2014. Available from www.heart.org/HEARTORG/Conditions/Arrhythmia/AboutArrhythmia/What-is-Atrial-Fibrillation-AFib-or-AF_UCM_423748_Article.jsp. Accessed Oct 5, 2018.Google Scholar
Morady, F, Zipes, DP. Atrial fibrillation: clinical features, mechanisms, and management. In Mann, DL, Zipes, DP, Libby, P, Bonow, RO, Braunwald, E, eds. Braunwald's heart disease: a textbook of cardiovascular medicine. 10th ed. Philadelphia: Elsevier/Saunders; 2015. pp. 798–811.Google Scholar
Anzola, GP, Magoni, M, Guindani, M, et al. Potential source of cerebral embolism in migraine with aura: a transcranial Doppler study. Neurology. 1999; 52: 1622.Google Scholar
Del Sette, M, Angeli, S, Leandri, M, et al. Migraine with aura and right-to-left shunt on transcranial Doppler: a case-control study. Cerebrovasc Dis. 1998; 8: 327.Google Scholar
Harvey, JR, Teague, SM, Anderson, JL, et al. Clinically silent atrial septal defects with evidence for cerebral embolization. Ann Intern Med. 1986; 105: 695.Google Scholar
Kumar, V, Abbas, AK, Fausto, N, Mitchell, RN, eds. Robbins basic pathology. 8th ed. Philadelphia: Saunders/Elsevier; 2007. p. 384.Google Scholar
Lamy, C, Giannesini, C, Zuber, M, et al. Clinical and imaging findings in cryptogenic stroke patients with and without patent foramen ovale: the PFOASA Study. Atrial Septal Aneurysm. Stroke. 2002; 33: 706.Google Scholar
Meissner, I, Whisnant, JP, Khandheria, BK, et al. Prevalence of potential risk factors for stroke assessed by transesophageal echocardiography and carotid ultrasonography: the SPARC study. Stroke Prevention: Assessment of Risk in a Community. Mayo Clin Proc. 1999; 74: 862.Google Scholar
Vaughan, CJ, Basson, CT. Molecular determinants of atrial and ventricular septal defects and patent ductus arteriosus. Am J Med Genet. 2000; 97: 304.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Polanczyk, G, de Lima, MS, Horta, BL, et al. The worldwide prevalence of ADHD: a systematic review and metaregression analysis. Am J Psychiatry. 2007; 164(6): 942–48.Google Scholar
Macfarlane, TV, Blinkhorn, AS, Davies, RM, et al. Oro-facial pain in the community: prevalence and associated impact. Community Dent Oral Epidemiol. 2002; 30(1): 52–60.Google Scholar
Obermann, M, Holle, D, Katsarava, Z. Trigeminal neuralgia and persistent idiopathic facial pain. Expert Rev Neurother. 2011; 11(11): 1619–29.Google Scholar
Weiss, AL, Ehrhardt, KP, Tolba, R. Atypical facial pain: a comprehensive, evidence-based review. Curr Pain Headache Rep. 2017; 21(8): 8.CrossRefGoogle ScholarPubMed
Zakrzewska, JM. Differential diagnosis of facial pain and guidelines for management. Br J Anaesth. 2013; 111(1): 95–104.Google Scholar
Jankovic, J, Rajput, AH, McDermott, MP, Perl, DP. The evolution of diagnosis in early Parkinson disease. Parkinson Study Group. Arch Neurol. 2000; 57(3): 369–72.Google Scholar
Dąbrowska, M, Schinwelski, M, Sitek, EJ, et al. The role of neuroimaging in the diagnosis of the atypical parkinsonian syndromes in clinical practice. Neurol Neurochir Pol. 2015; 49(6): 421–31.Google Scholar
Mark, M. Lumping and splitting the Parkinson plus syndromes. Neurol Clin. 2001; 19(3): 607–27.Google Scholar
Arena, J, Weigand, SD, Whitwell, JL, et al. Progressive supranuclear palsy: progression and survival. J Neurol. 2016; 263(2): 380–9.Google Scholar
Köllensperger, M, Geser, F, Ndayisaba, JP, et al. Presentation, diagnosis, and management of multiple system atrophy in Europe: final analysis of the European multiple system atrophy registry. Mov Disord. 2010; 25(15): 2604–12.Google Scholar
McKeith, IG, Dickson, DW, Lowe, J, et al. Diagnosis and management of dementia with Lewy bodies. Third report of the DLB consortium. Neurology. 2005; 65; 1863–72.Google Scholar
Bostic, JQ, Prince, JB, Buxton, DC. Child and adolescent psychiatric disorders. In Stern, T, Fava, M, Wilens, T, Rosenbaum, J, eds. Massachusetts General Hospital comprehensive clinical psychiatry. London: Elsevier; 2015. pp. 741–45.Google Scholar
American Psychiatric Association. Autism spectrum disorder. In Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013. pp. 50–9.Google Scholar
Rutter, M. Changing concepts and findings on autism. J Autism Dev Disorder. 2013; 43: 1749–57.Google Scholar
Kasari, C. Update on behavioral interventions for autism and developmental disabilities. Curr Opin Neurol. 2015; 28: 124–9.Google Scholar
Jokiranta, E, Sourander, A, Suominen, A, et al. Epilepsy among children and adolescents with autism spectrum disorders: a population-based study. J Autism Dev Disord. 2013; 44(10): 2547–57.Google Scholar
Baribeau, DA, Anagnostou, E. An update on medication management of behavioral disorders in autism. Curr Psych Rep. 2014; 16: 437–50.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Mairs, R, Nicholls, D. Assessment and treatment of eating disorders in children and adolescents. Arch Dis Child. 2016; 101(12): 1168–75.CrossRefGoogle ScholarPubMed
Centers for Disease Control and Prevention. Babesiosis. Atlanta, GA: CDC; 2014. Available from www.cdc.gov/parasites/babesiosis/data-statistics/index.html.Google Scholar
Usmani-Brown, S, Halperin, J, Krause, P. Neurological manifestations of human babesiosis. Handb Clin Neurol. 2013; 114: 199–203.Google Scholar
Krause, P, Lepore, T, Sikand, V, et al. Atovaquone and azithromycin for the treatment of babesiosis. N Engl J Med. 2000; 343(20): 1454–58.Google Scholar
Gourmelen, J, Chastang, JF, Ozguler, A, et al. Frequency of low back pain among men and women age 30 to 64 years in France. Results of two national surveys. Med Phys. 2007; 50(8): 640–4.Google Scholar
Noonan, DJ, Garrett, WE Jr. Muscle sprain injury diagnosis and treatment. J Am Acad Orthop Surg. 1999; 7(4): 262–9.Google Scholar
Wexler, H. Bacteroides: the good, the bad, and the nitty-gritty. Clin Microbiol Rev. 2007; 20(4): 593–621.Google Scholar
Miller, N, Burton, F, Walsh, F, Hoyt, W. Walsh and Hoyt's clinical neuro-ophthalmology. Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins; 2004. p. 2714.Google Scholar
Mevorach, C, Shalev, L, Green, RJ, et al. Hierarchical processing in Balint's syndrome: a failure of flexible top-down attention. Front Hum Neurosci. 2014; 8: 113.Google Scholar
O'Reilly, RC, Munakata, Y, Frank, MJ, et al. Computational cognitive neuroscience. Wiki Book. Available from http:/ccnbook.colorado.eduGoogle Scholar
Cavina-Pratesi, C, Connolly, JD, Milner, AD. Optic ataxia as a model to investigate the role of the posterior parietal cortex in visually guided action: evidence from studies of patient M.H. Front Hum Neurosci. 2013; 7: 336.Google Scholar
Cuomo, J, Flaster, M, Biller, J. Right brain: a descriptive account of two patients’ experience with and adaptations to Balint syndrome. Neurology. 2012; 79: e95–96.Google Scholar
Becker, DA, Balcer, LJ, Galetta, SL. The neurological complications of nutritional deficiency following bariatric surgery. J Obes. 2012; 2012: 608534.Google Scholar
Juhasz-Pocsine, K, Rudnicki, SA, Archer, RL, Harik, SI. Neurologic complications of gastric bypass surgery for morbid obesity. Neurology. 2007; 68(21): 1843–50.Google Scholar
Koffman, BM, Greenfield, LJ, Ali, II, Pirzada, NA. Neurologic complications after surgery for obesity. Muscle Nerve. 2006; 33(2): 166–76.Google Scholar
Landais, A. Neurological complications of bariatric surgery. Obes Surg. 2014; 24(10): 1800–7.Google Scholar
Chaudrhry, NS, Ozpinar, A, Bi, WL, et al. Basilar invagination: case report and literature review. World Neurosurg. 2015; 83: e7–111.Google Scholar
Smith, JS, Shaffrey, CI, Abel, MF, Menezes, AH. Basilar invagination. Neurosurgery. 2010; 66: A39–A47.Google Scholar
Bushby, K. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. Lancet Neurol. 2010; 9: 77–93.Google Scholar
Hendriksen, JG, Vles, JS. Neuropsychiatric disorders in males with Duchenne muscular dystrophy: frequency rate of attention-deficit hyperactivity disorder (ADHD), autism spectrum disorder, and obsessive compulsive disorder. J Child Neurol. 2008; 23(5): 477–81.Google Scholar
Berkovic, SF. Genetics of epilepsy in clinical practice. Epilepsy Curr. 2015; 15(4): 192–6.Google Scholar
Becker, F, Schubert, J, Striano, P, et al. PRRT2-related disorders: further PKD and ICCA cases and review of the literature. J Neurol. 2013; 260(5): 1234–44.Google Scholar
Ebrahimi-Fakhari, D, Saffari, A, Westenberger, A, et al. The evolving spectrum of PRRT2-associated paroxysmal diseases. Brain. 2015; 138(Pt 12): 3476–95.Google Scholar
Nabbout, R, Dulac, O. Epileptic syndromes in infancy and childhood. Curr Opin Neurol. 2008; 21(2): 161–6.Google Scholar
Amato, AA, Russell, JA. Neuromuscular disorders. New York: McGraw-Hill; 2008. pp. 143–56.Google Scholar
Blexrud, MD, Windebank, AJ, Daube, JR. Long-term follow-up of 121 patients with benign fasciculations. Ann Neurol. 1993; 34: 622.Google Scholar
Longo, DL, Kasper, DL, Fauci, A, et al., eds. Harrison's principles of internal medicine. 17th ed. New York: McGraw-Hill; 2016. pp. 1292, 1412, 1462–1464.Google Scholar
Epley, JM. The canalith repositioning procedure: for treatment of benign paroxysmal positional vertigo. Otolaryngol Head Neck Surg. 1992; 107: 399–404.Google Scholar
Furman, JM, Cass, SP. Benign paroxysmal positional vertigo. N Engl J Med. 1999; 341(21): 1590–6.Google Scholar
Fife, TD, Iverson, DJ, Lempert, T, et al. Practice parameter: therapies for benign paroxysmal positional vertigo (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. 2008; 70(22): 2067–74.Google Scholar
Smouha, EE. Time course of recovery after Epley maneuvers for benign paroxysmal positional vertigo. Laryngoscope. 1997; 107: 187–91.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Hudson, JI, Hiripi, E, Pope, HG, et al. The prevalence and correlates of eating disorders in the National Comorbidity Survey Replication. Biol Psychiatry. 2007; 61: 348–58.Google Scholar
Hudson, JI, Lalonde, JK, Coit, CE, et al. Longitudinal study of the diagnosis of components of the metabolic syndrome in individuals with binge-eating disorder. Am J Clin Nutr. 2010; 91(6): 1568–73.Google Scholar
Olsen, C, Clasen, M. Senile dementia of the Binswanger's type. Am Fam Physician. 1998; 58(9): 2068–74.Google Scholar
Roman, GC. Senile dementia of the Binswanger type: a vascular form of dementia in the elderly. JAMA. 1987; 258: 1782–8.Google Scholar
Chedrawi, AK, Ali, A, Al Hassnan, ZN, Faiyaz-Ul-Haque, M, Wolf, B. Profound biotinidase deficiency in a child with predominantly spinal cord disease. J Child Neurol. 2008; 23(9): 1043–8. DOI: 10.1177/0883073808318062Google Scholar
Cowan, TM, Blitzer, MG, Wolf, B; Working Group of the American College of Medical Genetics Laboratory Quality Assurance Committee. Technical standards and guidelines for the diagnosis of biotinidase deficiency. Genet Med. 2010; 12(7): 464–70.Google Scholar
Grunewald, S, Champion, MP, Leonard, JV, et al. Biotinidase deficiency: a treatable leukoencephalopathy. Neuropediatrics. 2004; 35(4): 211–6.Google Scholar
Raha, S, Udani, V. Biotinidase deficiency presenting as recurrent myelopathy in a 7-year-old boy and a review of the literature. Pediatr Neurol. 2011; 45(4): 261–4. DOI: 10.1016/j.pediatrneurol.2011.06.010Google Scholar
Wolf, B. Biotinidase deficiency should be considered in individuals exhibiting myelopathy with or without and vision loss. Mol Genet Metab. 2015; 116(3): 113–8. DOI: 10.1016/j.ymgme.2015.08.012Google Scholar
Wolf, B. The neurology of biotinidase deficiency. Mol Genet Metab. 2011; 104(1–2): 27–34. DOI: 10.1016/j.ymgme.2011.06.001. Epub 2011 Jun 12.Google Scholar
Wolf, B. Biotinidase deficiency. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle, WA: University of Washington; 1993–2015.Google Scholar
Wolf, B. Biotinidase deficiency: “if you have to have an inherited metabolic disease, this is the one to have.” Genet Med. 2012; 14(6): 565–75.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Lichtenstein, P, Yip, BH, Björk, C, et al. Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study. Lancet. 2009; 373(9659): 234–9.Google Scholar
Marangell, LB, Bauer, MS, Dennehy, EB, et al. Prospective predictors of suicide and suicide attempts in 1,556 patients with bipolar disorders followed for up to 2 years. Bipolar Disord. 2006; 8(5 Pt 2): 566–75.Google Scholar
Merikangas, KR, Akiskal, HS, Angst, J, et al. Lifetime and 12-month prevalence of bipolar spectrum disorder in the National Comorbidity Survey replication. Arch Gen Psychiatry. 2007; 64(5): 543–52.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Judd, LL, Akiskal, HS, Schettler, PJ, et al. The comparative clinical phenotype and long term longitudinal episode course of bipolar I and II: a clinical spectrum or distinct disorders? J Affect Disord. 2003; 73(1–2): 19–32.Google Scholar
Merikangas, KR, Jin, R, He, JP, et al. Prevalence and correlates of bipolar spectrum disorder in the world mental health survey initiative. Arch Gen Psychiatry. 2011; 68(3): 241–51.Google Scholar
Tondo, L, Lepri, B, Baldessarini, RJ. Suicidal risks among 2826 Sardinian major affective disorder patients. Acta Psychiatr Scand. 2007; 116(6): 419–28.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Haskett, RF. Diagnostic categorization of psychiatric disturbance in Cushing's syndrome. Am J Psychiatry. 1985; 142(8): 911–6.Google Scholar
Joffe, RT, Lippert, GP, Gray, TA, et al. Mood disorder and multiple sclerosis. Arch Neurol. 1987; 44: 376–8.Google Scholar
Mustafa, B, Evrim, O, Sari, A. Secondary mania following traumatic brain injury. J Neuropsychiatry Clin Neurosci. 2005; 17(1): 122–4.Google Scholar
Robinson, RG. Neuropsychiatric consequences of stroke. Annu Rev Med. 1997; 48: 217–29.Google Scholar
Gorio, A, Di Giulio, AM. Black widow spider venom. In Spencer, PS, Schaumburg, HH, eds. Experimental and clinical neurotoxicology. 2nd ed. New York: Oxford University Press; 2000. pp. 239–43.Google Scholar
Isbister, GK, Page, CB, Buckley, NA, et al. Randomized controlled trial of intravenous antivenom versus placebo for latrodectism: the second Redback Antivenom Evaluation (RAVE-II) Study. Ann Emerg Med. 2014; 64: 620–8.Google Scholar
Monte, AA, Bucher-Bartelson, B, Heard, KJ. A US perspective of symptomatic Latrodectus spp. envenomation and treatment: a National Poison Data System review. Ann Pharmacother. 2011; 45(12): 1491–8.Google Scholar
American Cancer Society. Bladder cancer. Available from www.cancer.org/cancer/bladdercancer/#. Accessed Oct 8, 2018.Google Scholar
Mayo Clinic Staff. Bladder cancer. Dec 22, 2017. Available from www.mayoclinic.org/diseases-conditions/bladder-cancer/basics/definition/con-20027606. Accessed Oct 8, 2018.Google Scholar
Centers for Disease Control and Prevention. Blastomycosis. Atlanta, GA: CDC; 2016. Available from www.cdc.gov/fungal/diseases/blastomycosis/index.html. Accessed Oct 8, 2018.Google Scholar
Chapman, S, Dismukes, W, Proia, L, et al. Clinical practice guidelines for the management of blastomycosis: 2008 update by the Infectious Diseases Society of America. Clin Infect Dis. 2008; 46(12): 1801–12.Google Scholar
Bariola, J, Perry, P, Pappas, P, et al. Blastomycosis of the central nervous system: a multicenter review of diagnosis and treatment in the modern era. Clin Infect Dis. 2010; 50(6): 797–804.Google Scholar
Defazio, G, Hallett, M, Jinnah, HA, et al. Development and validation of a clinical scale for rating the severity of blepharospasm. Mov Disord. 2015; 30(4): 525–530.Google Scholar
Hellman, A, Torres-Russotto, D. Botulinum toxin in the management of blepharospasm: current evidence and recent developments. Ther Adv Neurol Disord. 2014; 8(2): 82–91.Google Scholar
Rana, AQ, Kabir, A, Dogu, O, Patel, A, Khondker, S. Prevalence of blepharospasm and apraxia of eyelid opening in patients with parkinsonism, cervical dystonia and essential tremor. Eur Neurol. 2012; 68(5): 318–21.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Dunai, J, Labuschagne, I, Castle, DJ, et al. Executive function in body dysmorphic disorder. Psychol Med. 2010; 40(9): 1541–8.Google Scholar
Feusner, JD, Moody, T, Hembacher, E, et al. Abnormalities of visual processing and frontostriatal systems in body dysmorphic disorder. Arch Gen Psychiatry. 2010; 67(2): 197–205.Google Scholar
Koran, LM, Abujaoude, E, Large, MD, Serpe, RT. The prevalence of body dysmorphic disorder in the United States adult population. CNS Spectr. 2008; 13(4): 316–22.Google Scholar
Phillips, KA, Wilhelm, S, Koran, LM, et al. Body dysmorphic disorder: some key issues for DSM-V. Depress Anxiety. 2010; 27(6): 573–91.Google Scholar
Hauser, S, Amato, A. Guillain-Barre syndrome and other immune-mediated neuropathies. In Hauser, SL, Josephson, SA, eds. Harrison's neurology in clinical medicine. 3rd ed. New York: McGraw-Hill Education/Medical; 2013. pp. 612–3.Google Scholar
Pegram, P, Stone, S. Botulism. In Post, TW, ed. UpToDate. Waltham, MA. Accessed Jan 21, 2016. https://www.uptodate.com/contents/botulism. Accessed Oct 12, 2018.Google Scholar
Centers for Disease Control and Prevention. Bovine spongiform encephalopathy (BSE), or mad cow disease. 2015. Available from https://www.cdc.gov/prions/bse/index.html. Accessed Oct 10, 2018.Google Scholar
Bowen, BC, Seidenwurm, DJ; for the Expert Panel on Neurologic Imaging. Plexopathy. Am J Neuroradiol. 2008; 29(2): 400–2.Google Scholar
Wittenberg, KH, Adkins, MC. MR imaging of nontraumatic brachial plexopathies: frequency and spectrum of findings. RadioGraphics. 2000; 20(4).Google Scholar
Kannan, T, Sivaram Naik, G, Sreedhar Babu, KV, Vijayalakshim Devi, B. Metastatic brachial plexopathy in breast cancer. J Clin Sci Res. 2012; 1: 196–8.Google Scholar
Bernardi, D, Tomassi, O, Stefani, M, Di Giacobbe, A. Comment on “Clinical features and course of brain metastases in colorectal cancer: an experience from a single institution.” Curr Oncol. 2013; 20(3): e278.Google Scholar
Freilich, RJ, Krol, G, Deangelis, LM. Neuroimaging and cerebrospinal fluid cytology in the diagnosis of leptomeningeal metastasis. Ann Neurol. 1995; 38(1): 51–7.Google Scholar
Fife, TD, Giza, C. Posttraumatic vertigo and dizziness. Semin Neurol. 2013; 33(3): 238–43.Google Scholar
Fitzgerald, D. Head trauma: hearing loss and dizziness. J Trauma Inj Infect Crit Care. 1996; 40(3): 488–96.Google Scholar
Katz, DI, Cohen, SI, Alexander, MP. Mild traumatic brain injury. Handb Clin Neurol. 2015; 127: 131–56.Google Scholar
Danaei, G, VanderHoorn, S, Lopez, AD, et al. Causes of cancer in the world: comparative risk assessment of nine behavioural and environmental risk factors. Lancet. 2005; 366: 1784–93.Google Scholar
World Health Organization. Breast cancer: prevention and controls. http://www.who.int/cancer/detection/breastcancer/en/. Accessed Oct 15, 2018.Google Scholar
American Cancer Society. Leading new cancer cases and deaths – 2016 estimates. Available from www.cancer.org/research/cancerfactsstatistics/cancerfactsfigures2016/index. Accessed May 4, 2016.Google Scholar
AskMayoExpert. Breast cancer. Rochester, MN: Mayo Foundation for Medical Education and Research; 2015.Google Scholar
National Cancer Institute. SEER stat fact sheet: Female breast cancer. Available from http://seer.cancer.gov/statfacts/html/breast.html. Accessed May 4, 2016.Google Scholar
National Comprehensive Cancer Network. Breast cancer. Fort Washington, PA: National Comprehensive Cancer Network. Available from www.nccn.org/professionals/physician_gls/f_guidelines.asp. Accessed Oct 10, 2018.Google Scholar
Pelosof, LC, Gerber, DE. Paraneoplastic syndromes: an approach to diagnosis and treatment. Mayo Clin Proc. 2010; 85(9), 838–54. Available from http://doi.org/10.4065/mcp.2010.0099Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Pillmann, F, Balzuweit, S, Haring, A, et al. Suicidal behavior in acute and transient psychotic disorders. Psychiatry Res. 2003; 117(3): 199–209.Google Scholar
Susser, E, Wanderling, J. Epidemiology of nonaffective acute remitting psychosis vs schizophrenia: sex and sociocultural setting. Arch Gen Psychiatry. 1994; 51(4): 294–301.Google Scholar
Abdullayev, R, Kracalik, I, Ismayilova, R, et al. Analyzing the spatial and temporal distribution of human brucellosis in Azerbaijan (1995–2009) using spatial and spatio-temporal statistics. BMC Infect Dis. 2012; 12: 185. DOI: 10.1186/1471-2334-12-185.Google Scholar
Guven, T, Ugurlu, K, Ergonul, O, et al. Neurobrucellosis: clinical and diagnostic features. Clin Infect Dis. 2013; 56(10): 1407–12.Google Scholar
Gul, H, Erdem, H, Bek, S. Overview of neurobrucellosis: a pooled analysis of 187 cases. Int J Infect Dis. 2009; 13(6): e339–43.Google Scholar
Centers for Disease Control and Prevention. Brucellosis. Updated Sep 13, 2017. Available from https://www.cdc.gov/brucellosis/index.html. Accessed Oct 16, 2018.Google Scholar
NIH. Brucellosis. Updated Dec 12, 2014. Available from https://rarediseases.info.nih.gov/diseases/5966/brucellosis. Accessed Oct 16, 2018.Google Scholar
World Health Organization. Brucellosis. Available from http://www.who.int/zoonoses/diseases/brucellosis/en/. Accessed Oct 16, 2018.Google Scholar
Calderon-Gonzalez, R, Rizzi-Hernandez, H. Buckthorn polyneuropathy N Engl J Med. 1967; 277: 69–71.Google Scholar
Weller, RO. Karwinskia humboldtiana. In Spencer, PS, Schaumburg, HH, eds. Experimental and clinical neurotoxicology. 2nd ed. New York: Oxford University Press; 2000. pp. 705–7.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Smink, FR, van Hoeken, D, Hoek, HW. Epidemiology of eating disorders: incidence, prevalence, and mortality rates. Curr Psychiatry Rep. 2012; 14(4): 406–14.Google Scholar
Steinhausen, HC, Weber, S. The outcome of bulimia nervosa: findings from one-quarter century of research. Am J Psychiatry. 2009; 166(12): 1331–41.Google Scholar
Suokas, JT, Suvisaari, JM, Gissler, M, et al. Mortality in eating disorders: a follow-up study of adult eating disorder patients treated in tertiary care, 1995–2010. Psychiatry Res. 2013; 210(3): 1101–6.Google Scholar
Blum, KA, Lozanski, G, Byrd, JC. Adult Burkitt leukemia and lymphoma. Blood. 2004; 104: 3009–20.Google Scholar
Gu, Y, Hou, Y, Zhang, X, Hu, F. Primary central nervous system Burkitt lymphoma as concomitant lesions in the third and the left ventricles: a case study and literature review. J Neurooncol. 2010; 99: 277–81.Google Scholar
Centers for Disease Control and Prevention. Campylobacter. Atlanta, GA: CDC; 2017. Available at https://www.cdc.gov/campylobacter/index.html. Accessed Oct 10, 2018.Google Scholar
Nyati, K, Nyati, R. Role of Campylobacter jejuni infection in the pathogenesis of Guillain-Barré syndrome: an update. Biomed Res Int. 2013; 2013: 1–13.Google Scholar
Pfaller, M, Diekema, D. Epidemiology of invasive candidiasis: a persistent public health problem. Clin Microbiol Rev. 2007; 20(1): 133–63.Google Scholar
Henao, N, Vagner, B. Infections of the central nervous system by candida. J Infect Dis Immun. 2011; 3(5): 79–84.Google Scholar
Coleman, JH, Tacker, HL, Evans, WE, Lemmi, H, Britton, EL. Neurological manifestations of chronic marihuana intoxication. Part I: paresis of the fourth cranial nerve. Dis Nerv Syst. 1976; 37(1): 29.Google Scholar
Macleod, J, Oakes, R, Copello, A, et al. Psychological and social sequelae of cannabis and other illicit drug use by young people: a systematic review of longitudinal, general population studies. Lancet. 2004; 363(9421): 1579–88.Google Scholar
Solowij, N, Battisti, R. The chronic effects of cannabis on memory in humans: a review. Curr Drug Abuse Rev. 2008; 1(1): 81–98.Google Scholar
Steinherz, K, Vissing, T. The medical effects of marijuana on the brain. 21st Century. 1997–1998(Winter): 59–69.Google Scholar
Herning, RI, Better, W, Cadet, JL. EEG of chronic marijuana users during abstinence: relationship to years of marijuana use, cerebral blood flow and thyroid function. Clin Neurophysiol. 2008; 119(2): 321–31. Available from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2234454/Google Scholar
Tracey, N. Marijuana withdrawal and managing marijuana withdrawal symptoms. Healthy Place. 2016. Available from www.healthyplace.com/addictions/marijuana-addiction/marijuana-withdrawal-and-managing-marijuana-withdrawal-symptoms/. Accessed Oct 10, 2018.Google Scholar
Barr, RM, Dillon, WP, Wilson, CB. Slow-flow vascular malformations of the pons: capillary telangiectasias? AJNR Am J Neuroradiol. 1996; 17(1): 71–8.Google Scholar
Lee, RR, Becher, MW, Benson, ML, Rigamonti, D. Brain capillary telangiectasia: MR imaging appearance and clinicohistopathologic findings. Radiology. 1997; 205(3): 797–805.Google Scholar
Sarwar, M, McCormick, WF. Intracerebral venous angioma. Case report and review. Arch Neurol. 1978; 35(5): 323–5.Google Scholar
Sayama, CM, Osborn, AG, Chin, SS, Couldwell, WT. Capillary telangiectasias: clinical, radiographic, and histopathological features. Clinical article. J Neurosurg. 2010; 113(4): 709–14.Google Scholar
Graham, D, Valentine, WM. Carbon disulfide. In Spencer, PS, Schaumburg, HH, eds. Experimental and clinical neurotoxicology. 2nd ed. New York: Oxford University Press; 2000. pp. 315–7.Google Scholar
Pulley, M, Berger, AR. Disorders of the peripheral nervous system (carbon disulfide). In Rosenstock, L, Cullen, MR, Brodkin, CA, Redlich, CA, eds. Textbook of clinical occupational and environmental medicine. 2nd ed. Philadelphia: Elsevier Saunders; 2005. pp. 674–5.Google Scholar
Crystal, HA, Ginsberg, MD. Carbon monoxide. In Spencer, PS, Schaumburg, HH, eds. Experimental and clinical neurotoxicology. 2nd ed. New York: Oxford University Press; 2000. pp. 318–29.Google Scholar
Kao, LW, Nañagas, KA. Carbon monoxide poisoning. Emerg Med Clin North Am. 2004; 22(4): 985–1018.Google Scholar
Buda, A, Giuliani, D, Montano, N, Perego, P, Milani, R. Primary insular carcinoid of the ovary with carcinoid heart disease: unfavourable outcome of a case. Int J Surg Case Rep. 2012; 3(2): 59–61. Available from http://doi.org/10.1016/j.ijscr.2011.10.014Google Scholar
Palaniswamy, C, Frishman, WE, Aronow, WS. Carcinoid heart disease. Cardiol Rev. 2012; 20: 1167–76. Available from https://www.ncbi.nlm.nih.gov/pubmed/22314145Google Scholar
Stewart, MJ, Willis, RA, Saram, GSW. Argentaffin carcinoma arising in ovarian teratomas – a report of two cases. J Pathol Bacteriol. 1939; 49: 207–12.Google Scholar
Telerman, A. Germ cell tumor of the ovary. In Kurman, RJ, ed. Blaunstein's pathology of the female genital tract. New York: Springer-Verlag; 2002. pp. 1006–8.Google Scholar
Chamberlain, MC. Combined-modality treatment of leptomeningeal gliomatosis. Neurosurgery. 2003; 52: 324.Google Scholar
Chamberlain, MC, Tsao-Wei, D, Groshen, S. Neoplastic meningitis-related encephalopathy: prognostic significance. Neurology. 2004; 63: 2159.Google Scholar
Lee, SH, Kong, DS, Seol, HJ, et al. Ventriculoperitoneal shunt for hydrocephalus caused by central nervous system metastasis. J Neurooncol. 2011; 104: 545.Google Scholar
Le Rhun, E, Taillibert, S, Chamberlain, MC. Carcinomatous meningitis: Leptomeningeal metastases in solid tumors. Surg Neurol Int. 2013; 4(Suppl 4): S265–88. Available from http://doi.org/10.4103/2152-7806.111304Google Scholar
Omuro, AM, Lallana, EC, Bilsky, MH, DeAngelis, LM. Ventriculoperitoneal shunt in patients with leptomeningeal metastasis. Neurology. 2005; 64: 1625.Google Scholar
Chow, GV, Marine, JE, Fleg, JL. Epidemiology of arrhythmias and conduction disorders in older adults. Clin Geriatr Med. 2012; 28(4): 539–53.Google Scholar
Morady, F. Radio-frequency ablation as treatment for cardiac arrhythmias. N Engl J Med. 1999; 340: 534.Google Scholar
Sekar, RP. Epidemiology of arrhythmias in children. Indian Pacing Electrophysiol J. 2008; 8(Suppl 1): S8–13.Google Scholar
Turner, CJ, Wren, C. The epidemiology of arrhythmia in infants: A population-based study. J Paediatr Child Health. 2013; 49: 278–81.Google Scholar
Arboix, A, Alio, J. Cardioembolic stroke: clinical features, specific cardiac disorders and prognosis. Curr Cardiol Rev. 2010; 6(3): 150–61.Google Scholar
Hornung, M, Franke, J, Gafoor, S, Sievert, H. Cardioembolic stroke and postmyocardial infarction stroke. Cardiol Clin. 2016; 34(2): 207–14.Google Scholar
Boyd, WC, Hartman, GS. Neurologic dysfunction in cardiac surgery. New Horiz. 1999; 7: 504.Google Scholar
Cheung, AT, Stecker, MM. Neurologic complications of cardiac surgery. Prog Anaesthesiol. 1998; 12: 3.Google Scholar
Gardner, TJ, Horneffer, PJ, Manolio, TA, et al. Stroke following coronary artery bypass grafting: a tenyear study. Ann Thorac Surg. 1985; 40: 574.Google Scholar
Grubb, BP. Neurocardiogenic syncope and related disorders of orthostatic intolerance. Circulation. 2005; 111(22): 2997–3006.Google Scholar
Sonobe, M, Yamazaki, T, Yonekura, M, Kikuchi, H. Small unruptured intracranial aneurysm verification study: SUAVE Study, Japan. Stroke. 2010; 41: 1969.Google Scholar
Vlak, MH, Algra, A, Brandenburg, R, Rinkel, GJ. Prevalence of unruptured intracranial aneurysms, with emphasis on sex, age, comorbidity, country, and time period: a systematic review and meta-analysis. Lancet Neurol. 2011; 10: 626.Google Scholar
Lee, VH, Brown, RD Jr, Mandrekar, JN, Mokri, B. Incidence and outcome of cervical artery dissection: a population-based study. Neurology. 2006; 67: 1809.Google Scholar
Mitsias, P, Ramadan, NM. Headache in ischemic cerebrovascular disease. Part I: Clinical features. Cephalalgia. 1992; 12: 269.Google Scholar
Müller, BT, Luther, B, Hort, W, et al. Surgical treatment of 50 carotid dissections: indications and results. J Vasc Surg. 2000; 31: 980.Google Scholar
Abou-Chebl, A, Yadav, JS, Reginelli, JP, et al. Intracranial hemorrhage and hyperperfusion syndrome following carotid artery stenting: risk factors, prevention, and treatment. J Am Coll Cardiol. 2004; 43: 1596.Google Scholar
Perkins, WJ, Lanzino, G, Brott, TG. Carotid Stenting vs Endarterectomy: New Results in Perspective. Mayo Clin Proc. 2010; 85: 1101–8.Google Scholar
Rosenfield, K, Matsumura, JS, Chaturvedi, S, et al. Randomized trial of stent versus surgery for asymptomatic carotid stenosis. N Engl J Med. 2016; 374: 10113.Google Scholar
Silver, FL, Mackey, A, Clark, WM, et al. Safety of stenting and endarterectomy by symptomatic status in the Carotid Revascularization Endarterectomy versus Stenting Trial (CREST). Stroke. 2011; 42: 6754.Google Scholar
Ellis, JA, Goldstein, H, Connolly, ES Jr., Meyers, PM. Carotid-cavernous fistulas. Neurosurg Focus. 2012; 32: E9.Google Scholar
Liang, W, Xiaofeng, Y, Weiguo, L, et al. Traumatic carotid cavernous fistula accompanying basilar skull fracture: a study on the incidence of traumatic carotid cavernous fistula in the patients with basilar skull fracture and the prognostic analysis about traumatic carotid cavernous fistula. J Trauma. 2007; 63: 1014–20Google Scholar
Meyers, PM, Halbach, VV, Dowd, CF, et al. Dural carotid cavernous fistula: definitive endovascular management and long-term follow-up. Am J Ophthalmol. 2002; 134: 85–92.Google Scholar
Connolly, SJ, Sheldon, R, Roberts, RS, Gent, M. The North American Vasovagal Pacemaker Study (VPS). A randomized trial of permanent cardiac pacing for the prevention of vasovagal syncope. J Am Coll Cardiol. 1999; 33: 16–20.Google Scholar
Sutton, R. Carotid sinus syndrome: Progress in understanding and management. Glob Cardiol Sci Pract. 2014; 2014: 1–8.Google Scholar
Kothari, M. Carpal tunnel syndrome: etiology and epidemiology. In Post, TW, ed. UpToDate. Waltham, MA. Accessed Jan 21, 2016.Google Scholar
Ropper, A, Samuels, M. Disease of the peripheral nervous system. In Adams and Victor's principles of neurology. 9th ed. New York: McGraw-Hill Education/Medical; 2009. pp. 1314–5.Google Scholar
Howlet, WP, Brubaker, GR, Mlingi, N, Rosling, H. Konzo, an epidemic upper motor neuron disease studied in Tanzania. Brain. 1990; 113: 223–35.Google Scholar
Rosling, H, Tyklesklar, T. Cassava. In Spencer, PS, Schaumburg, HH, eds. Experimental and clinical neurotoxicology. 2nd ed. New York: Oxford University Press; 2000. pp. 338–43.Google Scholar
Brian, G, Taylor, H. Cataract blindness – challenges for the 21st century. Bull World Health Org. 2001; 79(3): 249–56.Google Scholar
Frick, KD, Foster, A. The magnitude and cost of global blindness: an increasing problem that can be alleviated. Am J Ophthalmol. 2013; 135(4): 471–6.Google Scholar
Pascolini, D, Mariotti, SP. Global estimates of visual impairment: 2010. Br J Ophthalmol. 2012; 96(5): 614–8.Google Scholar
Shiels, A, Bennett, TM, Fielding Hejtmancik, J. Cat-map: putting cataract on the map. Mol Vis. 2010; 16: 2007–15.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Bush, G, Fink, M, Petrides, G, et al. Catatonia. I. Rating scale and standardized examination. Acta Psychiatr Scand. 1996; 93: 129.Google Scholar
Fink, M, Taylor, MA. Catatonia: a clinician's guide to diagnosis and treatment. Cambridge: Cambridge University Press; 2003.Google Scholar
Fink, M, Taylor, MA. The catatonia syndrome: forgotten but not gone. Arch Gen Psychiatry. 2009; 66(11): 1173.Google Scholar
Nervi, SJ. Cat scratch disease (cat scratch fever) clinical presentation. Updated Jul 24, 2017. Available from https://emedicine.medscape.com/article/214100-clinical. Accessed Oct 16, 2018.Google Scholar
Lamas, C, Curi, A, Bóia, M, Lemos, E. Human bartonellosis: seroepidemiological and clinical features with an emphasis on data from Brazil – a review. Mem Inst Oswaldo Cruz. 2008; 103(3).Google Scholar
Breitschwerdt, E, Sontakke, S, Hopkins, S. Neurological manifestations of bartonellosis in immunocompetent patients: a composite of reports from 2005–2012. J Neuroparasitol. 2012; 3: 1–15.Google Scholar
Gitelman, A, Hishme, S, Morelli, BN, et al. Cauda equina syndrome: a comprehensive review. Am J Orthop. 2008; 37(11): 556–62.Google Scholar
Al-Holou, WN, O'Lynnger, TM, Pandey, AS, et al. Natural history and imaging prevalence of cavernous malformations in children and young adults. J Neurosurg Pediatr. 2012; 9: 198–205.Google Scholar
Maraire, JN, Awad, IA. Intracranial cavernous malformations: lesion behavior and management strategies. Neurosurgery. 1995; 37: 591–605.Google Scholar
Poorthuis, MH, Klijn, CJ, Algra, A, Rinkel, GJ, Al-Shahi Salman, R. Treatment of cerebral cavernous malformations: a systematic review and meta-regression analysis. J Neurol Neurosurg Psychiatry. 2014; 85: 1319–23.Google Scholar
Agostoni, E, Aliprandi, A, Longoni, M. Review. Cerebral venous thrombosis. Expert Rev Neurother. 2009; 9: 553–64.Google Scholar
Bousser, M-G, Barnett, HJM. Cerebral venous thrombosis. In Mohr, J, Grotta, J, Wolf, P, Choi, D, Weir, B, eds. Stroke. 4th ed. Philadelphia: Churchill Livingstone; 2004. pp. 301–25.Google Scholar
Cockerham, KP. Orbital and ocular manifestations of neurological disease. In Aminoff, MJ, ed. Neurology and general medicine. 4th ed. Philadelphia: Churchill Livingstone; 2008. pp. 483–501.Google Scholar
Ebright, JR, Pace, MT, Niazi, AF. Septic thrombosis of the cavernous sinuses. Arch Intern Med. 2001; 161: 2671–6.Google Scholar
Keane, JR. Cavernous sinus syndrome. Analysis of 151 cases. Arch Neurol. 1996; 53: 967–71.Google Scholar
Kuo, JS, Chen, JC, Yu, C, et al. Gamma knife radiosurgery for benign cavernous sinus tumors: quantitative analysis of treatment outcomes. Neurosurgery. 2004; 54: 1385–93Google Scholar
Newman, S. A prospective study of cavernous sinus surgery for meningiomas and resultant common ophthalmic complications (an American Ophthalmological Society thesis). Trans Am Ophthalmol Soc. 2007; 105: 392–447.Google Scholar
Briani, C, Zara, G, Alaedini, A, et al. Neurological complications of celiac disease and autoimmune mechanisms: a prospective study. J Neuroimmunol. 2008; 195(1–2): 171–5.Google Scholar
Fasano, A, Catassi, C. Current approaches to diagnosis and treatment of celiac disease: an evolving spectrum. Gastroenterology. 2001; 120(3): 636–51.Google Scholar
Hadjivassiliou, M, Grünewald, RA, Chattopadhyay, AK, et al. Clinical, radiological, neurophysiological, and neuropathological characteristics of gluten ataxia. Lancet. 1998; 352: 1582–5.Google Scholar
Hadjivassiliou, M, Grünewald, RA, Davies-Jones, GA. Gluten sensitivity as a neurological illness. J Neurol Neurosurg Psychiatry. 2002; 72(5): 560–3.Google Scholar
Jackson, JR, Eaton, WW, Cascella, NG, Fasano, A, Kelly, DL. Neurologic and psychiatric manifestations of celiac disease and gluten sensitivity. Psychiatr Q. 2012; 83(1): 91–102.Google Scholar
Musana, A, Yale, SH. Central pontine myelinolysis: case series and review. WMJ. 2005; 104(6): 56–60.Google Scholar
Singh, TD, Fugate, JE, Rabinstein, AA. Central pontine and extrapontine myelinolysis: a systematic review. Eur J Neurol. 2014; 21: 1443–50.Google Scholar
Vermetten, E. Neuropsychiatric and neuropsychological manifestations of central pontine myelinolysis. Gen Hosp Psychiatry. 2005; 21(4): 296–302.Google Scholar
Leavitt, JA, Larson, TA, Hodge, DO, Gullerud, RE. The incidence of central retinal artery occlusion in Olmsted County, Minnesota. Am J Ophthalmol. 2011; 152: 820.Google Scholar
Rudkin, AK, Lee, AW, Aldrich, E, et al. Clinical characteristics and outcome of current standard management of central retinal artery occlusion. Clin Exp Ophthalmol. 2010; 38: 496.Google Scholar
Klein, R, Klein, BE, Moss, SE, Meuer, SM. The epidemiology of retinal vein occlusion: the Beaver Dam Eye Study. Trans Am Ophthalmol Soc. 2000; 98: 133–43.Google Scholar
The Eye Disease Case-Control Study Group. Risk factors for central retinal vein occlusion. Arch Ophthalmol. 1996; 114: 545–54.Google Scholar
Burumcek, E, Mudun, A, Karacorlu, S, Arslan, MO. Laser photocoagulation for persistent central serous retinopathy: results of long-term follow-up. Ophthalmology. 1997; 104: 616–22.Google Scholar
Kitzmann, AS, Pulido, JS, Diehl, NN, Hodge, DO, Burke, JP. The incidence of central serous chorioretinopathy in Olmsted County, Minnesota, 1980–2002. Ophthalmology. 2008; 115: 169–73.Google Scholar
Liew, G, Quin, G, Gillies, M, Fraser-Bell, S. Central serous chorioretinopathy: a review of epidemiology and pathophysiology. Clin Exp Ophthalmol. 2012; 41: 201–14.Google Scholar
Eckert, DJ, Jordan, AS, Merchia, P, et al. Central sleep apnea: pathophysiology and treatment. Chest. 2005; 131: 595–607.Google Scholar
Küpper, T, Schöffl, V, Netzer, N. Cheyne Stokes breathing at high altitude: a helpful response or a troublemaker? Sleep Breath. 2008; 12(2): 123–7.Google Scholar
Sateia, M, Berry, RB, Bornemann, MC, et al. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Tellez, HF, MacDonald-Nethercott, E, Neyte, X, et al. Sleep-related periodic breathing does not acclimatize to chronic hypobaric hypoxia: a 1-year study at high altitude in Antarctica. Am J Respir Crit Care Med. 2014; 190: 114–6.Google Scholar
Alattar, MA, Scharf, SM. Opioid-associated central sleep apnea: a case series. Sleep Breath. 2009; 13: 201–6.Google Scholar
Correa, D, Farney, RJ, Chung, F, et al. Chronic opioid use and central sleep apnea: a review of the prevalence, mechanisms, and perioperative considerations. Anesth Analg. 2015; 120: 1273–85.Google Scholar
Davis, MJ, Livingston, M, Scharf, SM. Reversal of central sleep apnea following discontinuation of opioids. J Clin Sleep Med. 2012; 8(5): 579–80.Google Scholar
Sateia, M, Berry, RB, Bornemann, MC, et al. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Walker, JM, Farney, RJ, Rhondeau, SM, et al. Chronic opioid use is a risk factor for the development of central sleep apnea and ataxic breathing. J Clin Sleep Med. 2007; 3(5): 455–61.Google Scholar
Bradley, TD, Logan, AG, Kimoff, RJ, et al. Continuous positive airway pressure for central sleep apnea and heart failure. N Engl J Med. 2005; 353: 2025–33.Google Scholar
Cowie, MR, Woehrle, H, Wegscheider, K, et al. Adaptive servo-ventilation for central sleep apnea in systolic heart failure. N Engl J Med. 2015; 373: 1095–105.Google Scholar
Dempsey, JA, Smith, CA, Przybylowski, T, et al. The ventilator responsiveness to CO2 below eupnoea as a determinant of ventilator stability in sleep. J Physiol. 2004; 560: 1–11.Google Scholar
Eckert, DJ, Jordan, AS, Merchia, P, et al. Central sleep apnea: pathophysiology and treatment. Chest. 2007; 131: 595–607.Google Scholar
Sateia, M, Berry, RB, Bornemann, MC, et al. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Fazzi, E, Signorini, SG, Bova, SM, et al. Spectrum of visual disorders in children with cerebral visual impairment. J Child Neurol. 2007; 22(3): 294–301.Google Scholar
Amato, AA, Russell, JA. Neuromuscular disorders. New York: McGraw-Hill; 2008. pp. 578, 582–3.Google Scholar
Mah, JK, Joseph, JT. An overview of congenital myopathies. Continuum (Minneap Minn). 2016; 22(6): 1932–53.Google Scholar
Izumihara, A, Ishihara, T, Iwamoto, N, Yamashita, K, Ito, H. Postoperative outcome of 37 patients with lobar intracerebral hemorrhage related to cerebral amyloid angiopathy. Stroke. 1999; 30(1): 29.Google Scholar
Maxwell, SS, Jackson, CA, Paternoster, L, et al. Genetic associations with brain microbleeds: systematic review and meta-analyses. Neurology. 2011; 77(2): 158.Google Scholar
Yamada, M. Cerebral amyloid angiopathy: emerging concepts. J Stroke. 2015; 17(1): 17–30.Google Scholar
Adib-Samii, P, Brice, G, Martin, RJ, Markus, HS. Clinical spectrum of CADASIL and the effect of cardiovascular risk factors on phenotype: study in 200 consecutively recruited individuals. Stroke. 2010; 41(4): 630–4.Google Scholar
Razvi, SS, Davidson, R, Bone, I, Muir, KW. The prevalence of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) in the west of Scotland. J Neurol Neurosurg Psychiatry. 2005; 76(5): 739–41.Google Scholar
Capute, AJ, Accardo, PJ. Developmental disabilities in infancy and childhood. Vol 2. 2nd ed. EDS. Baltimore, MD; Brooks Publishing; 2001.Google Scholar
Monster, D, Wilcox, AJ, Vollset, SE, Markestad, T, Lie, RT. Cerebral palsy long-term and post-term births. JAMA. 2010; 304(9): 976–82.Google Scholar
Shevell, MI, Bodensteiner, JB. Cerebral palsy: defining the problem. Semin Pediatric Neurol. 2004; 11(1): 2–4.Google Scholar
Volpe, JJ. Neurology of the newborn. 4th ed. Philadelphia, PA: WB Saunders; 2001. p. 41.Google Scholar
Caplan, LR, van Gijn, J, eds. Stroke syndromes. 3rd ed. Cambridge: Cambridge University Press; 2012.Google Scholar
Dunbar, K. Cerebrotendinous xanthomatosis: a treatable genetic disease not to be missed. J Clin Rheumatol. 2016; 22(2): 92–3.Google Scholar
Lorincz, MT, Rainier, S, Thomas, D, Fink, JK. Cerebrotendinous xanthomatosis: possible higher prevalence than previously recognized. Arch Neurol. 2005; 62: 1459.Google Scholar
Leffert, LR, Clancy, CR, Bateman, BT, et al. Treatment patterns and short-term outcomes in ischemic stroke in pregnancy or postpartum period. Am J Obstet Gynecol. 2016; 214(6): 723.e1–723.e11.Google Scholar
Mas, JL, Lamy, C. Stroke in pregnancy and the puerperium. Neurology. 1998; 245(6–7): 305–13.Google Scholar
Tang, SC, Jeng, JS. Management of stroke in pregnancy and the puerperium. Expert Rev Neurother. 2010; 10(2): 205–15.Google Scholar
Praemer, A, Furner, S, Rice, D. Musculoskeletal conditions in the United States. Rosemont, IL: AAOS; 1992. p 23.Google Scholar
Amato, AA, Russell, JA. Neuromuscular disorders. 2nd ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
Carette, F, Fehlings, MG. Clinical practice: Cervical radiculopathy. N Engl J Med. 2005; 353(4): 392–9.Google Scholar
Bledsoe, IO, Comella, CL. Botulinum toxin treatment of cervical dystonia. In Seminars in neurology. Stuttgart: Thieme Medical; 2016.Google Scholar
Contarino, MF, Smit, M, van den Dool, J, Volkmann, J, Tijssen, MAJ. Unmet needs in the management of cervical dystonia. Front Neurol. 2016; 7: 165.Google Scholar
Klingelhoefer, L, Martino, D, Martinez-Martin, P, et al. Nonmotor symptoms and focal cervical dystonia: observations from 102 patients. Basal Ganglia. 2014; 4: 117–20.Google Scholar
LeDoux, MS, Vemula, SR, Xiao, J, et al. Clinical and genetic features of cervical dystonia in a large multicenter cohort. Neurol Genet. 2016; 2: e69.Google Scholar
Patel, S, Martino, D. Cervical dystonia: from pathophysiology to pharmacotherapy. Behav Neurol. 2013; 26: 275–82.Google Scholar
Bovim, G, Schrader, H, Sand, T. Neck pain in the general population. Spine. 1994; 19(12): 1307–9.Google Scholar
Friedenberg, ZB, Miller, WT. Degenerative disc disease of the cervical spine. J Bone Joint Surg Am. 1963; 45: 1171–8.Google Scholar
Travell, JG, Simons, DG. Myofascial pain and dysfunction. Vol. 2. Baltimore, MD: Lippincott Williams & Wilkins; 1992.Google Scholar
Aminoff, MJ, Greenberg, DA, Simon, RP. Motor disorders. In Aminoff, MJ, Greenberg, DA, Simon, RP, eds. Clinical neurology. 9th ed. New York: McGraw-Hill; 2015.Google Scholar
Radhakrishnan, K, Litchy, WJ, O'Fallon, WM, Kurland, LT. Epidemiology of cervical radiculopathy. A population-based study from Rochester, Minnesota, 1976 through 1990. Brain. 1994; 117(Pt 2): 325.Google Scholar
McCormack, BM, Weinstein, PR. Cervical spondylosis. An update. West J Med. 1996; 165(1–2): 43–5.Google Scholar
Hu, R, Mustard, CA, Burns, C. Epidemiology of incidental CT spinal fracture in a complete population. Spine. 1996; 21: 492–9.Google Scholar
Torretti, JA, Sengupta, DK. Cervical spine trauma. Indian J Orthop. 2007; 41(4): 255–67.Google Scholar
Finsterer, J, Auer, H. Parasitoses of the human central nervous system. J Helminthol. 2013; 87(3): 257–70.Google Scholar
Salvana, EMT, Salata, RA, King, CH. Parasitic infections of the central nervous system. In Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. 5th ed. London: Academic Press; 2014: pp. 947–68.Google Scholar
World Health Organization. Chagas disease (American trypanosomiasis). www.who.int/chagas/epidemiology/en/. Accessed Oct 11, 2018.Google Scholar
Cherniack, NS, Longobardo, G, Evangelista, CJ. Causes of Cheyne-Stokes respiration. Neurocrit Care. 2005; 3(3): 271–9.Google Scholar
Giannoni, A, Emdin, M, Passino, C. Cheyne-Stokes respiration, chemoreflex, and ticagrelor-related dyspnea. N Engl J Med. 2016; 375(10): 1004–6. DOI: 10.1056/NEJMc1601662.Google Scholar
Naughton, MT. Pathophysiology and treatment of Cheyne-Stokes respiration. Thorax. 1998; 53: 514–8. DOI: 10.1136/thx.53.6.514.Google Scholar
Orr, JE, Malhotra, A, Sands, SA. Pathogenesis of central and complex sleep apnoea. Respirology. 2017; 22(1): 43–52. DOI: 10.1111/resp.12927. Epub 2016 Oct 31.Google Scholar
Wang, Y, Cao, J, Feng, J, Chen, BY. Cheyne-Stokes respiration during sleep: mechanisms and potential interventions. Br J Hosp Med (Lond). 2015; 76(7): 390–6. DOI: 10.12968/hmed.2015.76.7.390.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Ferrara, P, Guadagno, C, Sbordone, A, et al. Child abuse and neglect: A review of the literature. Curr Pediatr Rev. 2016; 12(4): 301–10.Google Scholar
National Institute for Health and Care Excellence (NICE). Clinical Guideline. Child maltreatment: when to suspect maltreatment in under 18s. July 2009. https://www.nice.org.uk/guidance/cg89. Accessed Aug 15, 2018.Google Scholar
Kronzon, I. Cholesterol embolization syndrome. Circulation. 2010; 122: 631–41. DOI: 10.1161/CIRCULATIONAHA.109.886465Google Scholar
Kranick, SM, Mowry, EM, Colcher, A, Horn, S, Golbe, L.I. Movement disorders and pregnancy: a review of the literature. Mov Disord. 2010; 25(6): 665–71.Google Scholar
Maia, DP, Fonseca, PG, Camargos, ST, et al. Pregnancy in patients with Sydenham's chorea. Parkinsonism Relat Disord. 2012; 18(5): 458–61.Google Scholar
Laughlin, RS, Dyck, PJ, Melton, LJ III, et al. Incidence and prevalence of CIDP and the association of diabetes mellitus. Neurology. 2009; 73: 39.Google Scholar
Lotan, I, Hellman, MA, Steiner, I. Diagnostic criteria of chronic inflammatory demyelinating polyneuropathy in diabetes mellitus. Acta Neurol Scand. 2015; 132: 278–83.Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. Diseases of the peripheral nerves. In Adams & Victor's principles of neurology. 10th ed. New York: McGraw-Hill; 2014.Google Scholar
Bojrab, DI, Smouha, E. Tympanic membrane perforation and tympanoplasty. In Lalwani, A, ed. Sataloff's comprehensive textbook of otolaryngology. Philadelphia, PA: JP Medical; 2015.Google Scholar
Smouha, E, Bojrab, DI. Cholesteatoma. In Lalwani, A, ed. Sataloff's comprehensive textbook of otolaryngology. Philadelphia, PA: JP Medical; 2015.Google Scholar
Butterworth, RF. Hypercapnic encephalopathy. In Siegel, GJ, Agranoff, BW, Albers, RW, et al., eds. Basic neurochemistry: molecular, cellular and medical aspects. 6th ed. Philadelphia: Lippincott-Raven; 1999. Available from: https://www.ncbi.nlm.nih.gov/books/NBK28164/Google Scholar
Incalzi, RA, Gemma, A, Marra, C, et al. Verbal memory impairment in COPD. Chest. 1997; 112(6): 1506–13. DOI: 10.1378/chest.112.6.1506Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. The acquired metabolic disorders of the nervous system. In Adams & Victor's principles of neurology, 10th ed. New York, NY: McGraw-Hill; 2014. pp. 1132–60.Google Scholar
Rycroft, CE, Heyes, A, Lanza, L, Becker, K. Epidemiology of chronic obstructive pulmonary disease: a literature review. Int J Chron Obstruct Pulmon Dis. 2012; 7: 457–94. DOI: 10.2147/COPD.S32330.Google Scholar
Scala, R. Hypercapnic encephalopathy syndrome: A new frontier for non-invasive ventilation? Respir Med. 2011; 105(8): 1109–17. DOI: 10.1016/j.rmed.2011.02.004Google Scholar
Thakur, N, Blanc, PD, Julian, LJ, et al. COPD and cognitive impairment: the role of hypoxemia and oxygen therapy. Int J Chron Obstruct Pulmon Dis. 2010; 5: 263–9.Google Scholar
Friedman, MA, Fleming, LE, Fernandez, M, et al. Ciguatera fish poisoning: treatment, prevention and management. Mar Drugs. 2008; 6(3): 456–79. PMCID: PMC2579736.Google Scholar
Kaplan, JG. Ciguatoxin. In Spencer, PS, Schaumburg, HH, eds. Experimental and clinical neurotoxicology. 2nd ed. New York: Oxford University Press; 2000. pp. 386–90.Google Scholar
Plakkal, N, Soraisham, A, Amin, H. Citrobacter freundii brain abscess in a preterm infant: a case report and literature review. Pediatr Neonatol. 2013; 54(2): 137–40.Google Scholar
Liu, H, Chang, C, Hsieh, C. Brain abscess caused by Citrobacter koseri infection in an adult. Neurosciences. 2015; 20(2): 170–2.Google Scholar
Marecos, C, Ferreira, M, Ferreira, M, Barroso, M. Sepsis, meningitis and cerebral abscesses caused by Citrobacter koseri. BMJ Case Rep. 2012; 2012.Google Scholar
Goonetilleke, A. Clostridial neurotoxins. J Neurol Neurosurg Psychiatry. 2004; 75(Suppl 3): iii35–iii39.Google Scholar
Finsterer, J, Hess, B. Neuromuscular and central nervous system manifestations of Clostridium perfringens infections. Infection. 2007; 35(6): 396–405.Google Scholar
Bahra, A, May, A, Gaodsby, PJ. Cluster headache: a prospective clinical study with diagnostic implications. Neurology. 2002; 58: 354–61.Google Scholar
Kudrow, L. Cluster headache: mechanisms and management. Oxford: Oxford University Press; 1980.Google Scholar
Manzoni, GC. Gender ratio of cluster headache over the years: a possible role of changes in lifestyle. Cephalalgia. 1998; 18: 138–42.Google Scholar
Lancé, MD. A general review of major global coagulation assays: thrombelastography, thrombin generation test and clot waveform analysis. Thomb J. 2015; 13: 1.Google Scholar
Agarwal, P. Neurologic effects of cocaine. Medscape. http://emedicine.medscape.com/article/1174408-overview#a6. Accessed Aug 15, 2018.Google Scholar
Enevoldson, TP. Recreational drugs and their neurological consequences. http://jnnp.bmj.com/content/75/suppl_3/iii9.full. Accessed Aug 15, 2018.Google Scholar
Kuriyama, H, Suyama, A. Multiple actions of cocaine on neuromuscular transmission and smooth muscle cells of the guinea-pig mesenteric artery. J Physiol. 1983; 337: 631–54. http://onlinelibrary.wiley.com/doi/10.1113/jphysiol.1983.sp014646/pdf.Google Scholar
Schwartz, BG, Rezkalla, S, Kloner, RA. Cardiovascular effects of cocaine. Circulation. 2010; 122: 2558–69.Google Scholar
Siegel, AJ, Sholar, MB, Mendelson, JH, et al. Cocaine-induced erythrocytosis and increase in von Willebrand factor: evidence for drug-related blood doping and prothrombotic effects. Arch Intern Med. 1999; 159(16): 1925–9. DOI: 10.1001/archinte.159.16.1925.Google Scholar
Venton, BJ, Seipel, AT, Phillips, PEM, et al. Cocaine increases dopamine release by mobilization of a synapsin-dependent reserve pool. J Neurosci. 2006; 26(12): 3206–9.Google Scholar
Galgiani, J, Ampel, N, Blair, J, et al. Coccidioidomycosis. Clin Infect Dis. 2005; 41(9): 1217–23.Google Scholar
DynaMed Plus [Internet]. Record No. 116164, Coccidioidomycosis. Updated Oct 26, 2015. Ipswich,MA: EBSCO InformationServices. 1995. Available from www.dynamed.com/login.aspxdirect=true&site=DynaMed&id=116164. Accessed Jan 29, 2016. Registration and login required.Google Scholar
Zunt, J, Baldwin, K. Chronic and subacute meningitis. Continuum (Minneap Minn). 2012; 18: 1290–318.Google Scholar
Bussa, M, Gutilla, D, Lucia, M, et al. Complex regional pain syndrome type 1: a comprehensive review Acta Anaesthesiol Scand. 2015; 59(6): 685–97.Google Scholar
Guthmiller, K, Dulebohn, S. Pain, complex regional pain syndrome (reflex sympathetic dystrophy, RSD, CRPS). In StatPearls [Internet]. Treasure Island, FL: StatPearls Publishing; 2017. https://www.ncbi.nlm.nih.gov/books/NBK430719/Google Scholar
Sandroni, P, Benrud-Larson, LM, McClelland, RL, Low, PA. Complex regional pain syndrome type I: incidence and prevalence in Olmsted county, a population-based study. Pain. 2003; 103(1–2): 199–207.Google Scholar
Brant, WE, Helmes Clyde, A. Benign compression fracture. Fundamentals of diagnostic radiology. 3rd ed. Philadelphia: Lippincott Williams & Wilkins; 2007. p. 302.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Mahowald, M. Non-REM arousal parasomnias. In Kryger, MH, Roth, T, Dement, WC, eds. Principles and practice of sleep medicine. 5th ed. Philadelphia: Saunders; 2010. pp. 1075–82.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Paton, JY, Swaminathan, S, Sargent, CW, Hawksworth, A, Keens, TG. Hypoxic and hypercapnic ventilatory responses in awake children with congenital central hypoventilation syndrome. Am Rev Respir Dis. 1989; 140: 368–72.Google Scholar
Cohen, TJ. Congestive heart failure. In Practical electrophysiology. Malvern, PA: HMP Communications; 2009. pp. 207–11.Google Scholar
Emory Healthcare. Heart failure statistics. 2015. Available from www.emoryhealthcare.org/heart-failure/learn-about-heart-failure/statistics.html. Accessed July 6, 2015.Google Scholar
Mayo Clinic Staff. Heart failure. 2015. Available from www.mayoclinic.org/diseases-conditions/heart-failure/basics/complications/con-20029801. Accessed July 7, 2015.Google Scholar
PubMed Health. Heart failure. June 11, 2014. Available from www.ncbi.nlm.nih.gov/pubmedhealth/PMH0063056/. Accessed July 6, 2015.Google Scholar
Kumar, N, Gross, JB Jr, Ahlskog, JE. Copper deficiency myelopathy produces a clinical picture like subacute combined degeneration. Neurology. 2004; 63: 33.Google Scholar
Naismith, RT, Shepherd, JB, Weihl, CC, et al. Acute and bilateral blindness due to optic neuropathy associated with copper deficiency. Arch Neurol. 2009; 66: 1025.Google Scholar
Gaitanis, JN, Donahue, J. Focal cortical dysplasia. Pediatr Neurol. 2013; 49(2): 79–87.Google Scholar
Lee, SK, Kim, DW. Focal cortical dysplasia and epilepsy surgery. J Epilepsy Res. 2013; 3(2): 43–7.Google Scholar
Armstrong, MJ, et al. Criteria for the diagnosis of corticobasal degeneration. Neurology. 2013; 80: 496–503.Google Scholar
McFarland, NR. Diagnostic approach to atypical parkinsonian syndromes. Continuum (Minneap Minn). 2016; 22: 1117–42.Google Scholar
Ling, H, et al. Does corticobasal degeneration exist? A clinicopathological re-evaluation. Brain. 2010; 133: 2045–57.Google Scholar
Dickson, DW, et al. Office of Rare Diseases neuropathologic criteria for corticobasal degeneration. J Neuropathol Exp Neurol. 2002; 61(11): 935–46.Google Scholar
Boeve, BF, et al. Pathologic heterogeneity in clinically diagnosed corticobasal degeneration. Neurology. 1999; 53: 795–800.Google Scholar
Alexander, SK, et al. Validation of the new consensus criteria for the diagnosis of corticobasal degeneration. J Neurol Neurosurg Psychiatry. 2014; 85(8): 925–9. DOI: 10.1136/jnnp-2013-307035.Google Scholar
DynaMed Plus [Internet]. Record No. 901254, Coxsackie virus B (CVB) infection. Ipswich, MA: EBSCO Information Services. 1995. Updated Nov 20, 2015 [about 5 screens]. Available from direct=true&site=DynaMed&id=901254. Accessed Jan 21, 2016. Registration and login required.Google Scholar
Berger, J, Chumley, W, Pittman, T, Given, C, Nuovo, G. Persistent Coxsackie B encephalitis: Report of a case and review of the literature. J Neurovirol. 2006; 12(6): 511–16.Google Scholar
Balasubramaniam, R, Ram, S. Orofacial movement disorders. Oral Maxillofac Surg Clin North Am. 2008; 20(2): 273–85.Google Scholar
Evidente, VGH, Adler, CH. Hemifacial spasm and other craniofacial movement disorders. Mayo Clin Proc. 1998; 73(1): 67–71.Google Scholar
Kraft, SP, Lang, AE. Cranial dystonia, blepharospasm and hemifacial spasm: clinical features and treatment, including the use of botulinum toxin. CMAJ. 1988; 139(9): 837–44.Google Scholar
DynaMed Plus [Internet]. Record No. 114980, Creutzfeldt-Jakob disease. Ipswich, MA: EBSCO Information Services. 1995. Updated May 01, 2015 [about 17 screens]. Available from www.dynamed.com/login.aspx?direct=true&site=DynaMed&id=114980. Accessed Jan 18, 2016. Registration and login required.Google Scholar
Rabinovici, G, Wang, P, Levin, J, et al. First symptom in sporadic Creutzfeldt-Jakob disease. Neurology. 2006; 66(2): 286–7.Google Scholar
Bolton, CF. Neuromuscular manifestations of critical illness. Muscle Nerve. 2005; 32: 140.Google Scholar
Latronico, N, Shehu, I, Seghelini, E. Neuromuscular sequelae of critical illness. Curr Opin Crit Care. 2005; 11: 381.Google Scholar
Preston, DC, Shapiro, BE. Electromyography and neuromuscular disorders: clinical-electrophysiologic correlations. 3rd ed. New York: Saunders; 2013. pp. 556–61.Google Scholar
Hermans, G, De Jonghe, B, Bruyninckx, F, Van den Berghe, G. Clinical review: Critical illness polyneuropathy and myopathy. Crit Care. 2008; 12(6): 238.Google Scholar
Zhou, C, Wu, L, Ni, F, et al. Critical illness polyneuropathy and myopathy. a systematic review. Neural Regen Res. 2014; 9: 101–10.Google Scholar
Gondim, FA, Brannagan, TH III, Sander, HW, Chin, RL, Latov, N. Peripheral neuropathy in patients with inflammatory bowel disease. Brain. 2005; 128: 867–79.Google Scholar
Gupta, G, Gelfand, JM, Lewis, JD. Increased risk for demyelinating diseases in patients with inflammatory bowel disease. Gastroenterology 2005; 129: 819–26.Google Scholar
Leibowitz, G, Eliakim, R, Amir, G, Rachmilewitz, D. Dermatomyositis associated with Crohn's disease. J Clin Gastroenterol. 1994; 18: 48–52.Google Scholar
Lossos, A, River, Y, Eliakim, A, Steiner, I. Neurologic aspects of inflammatory bowel disease. Neurology. 1995; 45: 416–21.Google Scholar
Molodecky, NA, Soon, IS, Rabi, DM, et al. Increasing incidence and prevalence of the inflammatory bowel diseases with time, based on systematic review. Gastroenterology. 2012; 142: 46–54.Google Scholar
Singh, S, Kumar, N, Loftus, EV, Kane, SV. Neurologic complications in patients with inflammatory bowel disease: increasing relevance in the era of biologics. Inflamm Bowel Dis. 2013; 19: 864–72.Google Scholar
Chang, IT, Depold Holder, A. Bilateral radial nerve compression (crutch palsy): a case report. J Neurol Neurophysiol. 2012; 3: 3.Google Scholar
Raikin, S, Froimson, MI. Bilateral brachial plexus compressive neuropathy (crutch palsy). J Orthop Trauma. 1997; 11: 136–8.Google Scholar
Ramos-Casals, M, Stone, JH, Cid, MC, Bosch, X. The cryoglobulinaemias. Lancet. 2012; 379: 348–60.Google Scholar
Tedeschi, A, Baratè, C, Minola, E, Morra, E. Cryoglobulinemia. Blood Rev 2007; 21: 183–200.Google Scholar
Zunt, J, Baldwin, K. Chronic and subacute meningitis. Continuum (Minneap Minn). 2012; 18: 1290–318.Google Scholar
Panackal, A, Williamson, P. Fungal infections of the central nervous system. Continuum (Minneap Minn). 2015; 21: 1662–78.Google Scholar
Ordúñez-García, PO, Nieto, FJ, Espinosa-Brito, AD, Caballero, B. Cuban epidemic neuropathy, 1991 to 1994: history repeats itself a century after the “amblyopia of the blockade.” Am J Public Health. 1996; 86: 738–43.Google Scholar
Haskett, R. Diagnostic categorization of psychiatric disturbance in Cushing's syndrome. Am J Psychiatry. 1985; 142(8): 911.Google Scholar
Loosen, P, Chambliss, B, DeBold, C, Shelton, R, Orth, D. Psychiatric phenomenology in Cushing's disease. Pharmacopsychiatry. 1992; 25(4): 192.Google Scholar
Newell-Price, J, Bertagna, X, Grossman, A, Nieman, L. Cushing's syndrome. Lancet. 2006; 367(9522): 1605–17.Google Scholar
Nieman, L, Biller, B, Findling, J, et al. The diagnosis of Cushing's syndrome: an Endocrine Society Clinical Practice Guidline. J Clin Endocrinol Metab. 2008; 93(5): 1526–40.Google Scholar
Abell, TL, et al. Cyclic vomiting syndrome in adults. Neurogastroenterol Motil. 2008; 20(4): 269–84.Google Scholar
Abu-Arafeh, I, Russell, G. Cyclical vomiting syndrome in children: a population-based study. J Pediatr Gastroenterol Nutr. 1995; 21(4): 454–8.Google Scholar
Li, BU, et al. North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition consensus statement on the diagnosis and management of cyclic vomiting syndrome. J Pediatr Gastroenterol Nutr. 2008; 47(3): 379–93.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Regeer, EJ, ten Have, M, Rosso, ML, et al. Prevalence of bipolar disorder in the general population: a reappraisal study of the Netherlands Mental Health Survey and Incidence Study. Acta Psychiatr Scand. 2004; 110(5): 374–82.Google Scholar
El-Beshbishi, S, Ahmed, N, Mostafa, S, El-Ganainy, G. Parasitic infections and myositis. Parasitol Res. 2011; 110(1): 1–18.Google Scholar
Garcia, H, Nash, T, Del Brutto, O. Clinical symptoms, diagnosis, and treatment of neurocysticercosis. Lancet Neurol. 2014; 13(12): 1202–15.Google Scholar
DynaMed Plus [Internet]. Record No. 906245, Cytomegalovirus (CMV) infection in immunocompetent patients. Ipswich, MA: EBSCO Information Services. 1995. Updated Mar 9, 2015 [about 9 screens]. Available from www.dynamed.com/login.aspx?direct=true&site=DynaMed&id=906245. Accessed Jan 20, 2016. Registration and login required.Google Scholar
Mamidi, A, DeSimone, J, Pomerantz, R. Central nervous system infections in individuals with HIV-1 infection. J Neurovirol. 2002; 8(3): 158–67.Google Scholar
Anders, H, Goebel, F. Neurological manifestations of cytomegalovirus infection in the acquired immunodeficiency syndrome. Int J STD AIDS. 1999; 10(3): 151–61.Google Scholar
Osenbach, RK, Menezes, AH. Diagnoses and management of the Dandy Walker Malformation: 30 years of experience. Pediatr Neurosurg. 1992; 18(4): 179–89.Google Scholar
Elliott, DH, Moon, RE. Manifestations of the decompression disorders: the physiology and medicine of diving. 4th ed. London: Saunders; 1993. p. 481.Google Scholar
Kamtchum Tatuene, J, Pignel, R, Pollak, P, et al. Neuroimaging of diving-related decompression illness: current knowledge and perspectives. AJNR Am J Neuroradiol. 2014; 35: 2039–44.Google Scholar
Kei, PL, Choong, CT, Young, T, et al. Decompression sickness: MRI of the spinal cord. J Neuroimag. 2007; 17: 378–80.Google Scholar
Newton, HB. Neurologic complications of scuba diving. Am Fam Physician. 2001; 63: 2211–8.Google Scholar
Modic, MT, Ross, JS. Lumbar degenerative disc disease. Radiology. 2007; 245(1): 43–61.Google Scholar
Bjorvatn, B, Pallesen, S. A practical approach to circadian rhythm sleep disorders. Sleep Med Rev. 2009; 13: 47–60.Google Scholar
Nesbitt, AD, Dijk, DJ. Out of synch with society: an update on delayed sleep phase disorder. Curr Opin Pulm Med. 2014; 20: 581–7.Google Scholar
Sack, RL, Auckley, D, Auger, RR, et al. Circadian rhythm sleep disorders: Part II, Advanced sleep phase disorder, delayed sleep phase disorder, free-running disorder, and irregular sleep-wake rhythm. Sleep. 2007; 30: 1484–501.Google Scholar
Sateia, M, Berry, RB, Bornemann, MC, et al. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Schrader, H, Bovim, G, Sand, T. The prevalence of delayed and advanced sleep phase disorders. J Sleep Res. 1993; 2: 51–5.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Robinson, TN, Raeburn, CD, Tran, ZV, et al. Postoperative delirium in the elderly: risk factors and outcomes. Ann Surg. 2009; 249(1): 173.Google Scholar
Witlox, J, Eurelings, LS, de Jonghe, JF, et al. Delirium in elderly patients and the risk of postdischarge mortality, institutionalization, and dementia: a meta-analysis. JAMA. 2010; 304(4): 443.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
de Portugal, E, González, N, Haro, JM, et al. A descriptive case-register study of delusional disorder. Eur Psychiatry. 2008; 23(2): 125–33.Google Scholar
Kendler, KS, McGuire, M, Gruenberg, AM, et al. The Roscommon Family Study, II: the risk of nonschizophrenic nonaffective psychoses in relatives. Arch Gen Psychiatry. 1993; 50(8): 645–52.Google Scholar
Perälä, J, Suvisaari, J, Saarni, SI, et al. Lifetime prevalence of psychotic and bipolar I disorders in a general population. Arch Gen Psychiatry. 2007; 64(1): 19–28.Google Scholar
Salvatore, P, Baldessarini, RJ, Tohen, M, et al. McLean-Harvard International First-Episode Project: two-year stability of ICD-10 diagnoses in 500 first-episode psychotic disorder patients. J Clin Psychiatry. 2011; 72(2): 183–93.Google Scholar
Jung, N, Kim, E. Cerebral phaeohyphomycosis: a rare cause of brain abscess. J Korean Neurosurg Soc. 2014; 56(5): 444.Google Scholar
Revankar, S, Sutton, D, Rinaldi, M. Primary central nervous system phaeohyphomycosis: a review of 101 cases. Clin Infect Dis. 2004; 38(2): 206–16.Google Scholar
Cox, M. Central nervous system infections due to dematiaceous fungi (cerebral phaeohyphomycosis). In Kaufman, C, ed. UpToDate. Waltham, MA. Accessed Jan 29, 2016.Google Scholar
Murray, NEA, Quam, MB, Wilder-Smith, A. Epidemiology of dengue: past, present and future prospects. Clin Epidemiol. 2013; 5: 299–309.Google Scholar
Simmons, CP, Farrar, JJ, Vinh Chau, NV, Wills, B. Dengue. New Engl J Med. 2012; 366: 1423–32.Google Scholar
Carod-Artal, FJ, Wichmann, O, Farrar, J, Gascon, J. Neurological complications of dengue virus infection. Lancet Neurol. 2013; 12: 906–19.Google Scholar
Tripathi, SM, Mishra, N. Late onset mania in dengue fever. Immunol Infect Dis. 2014; 2: 1–3.Google Scholar
Marcenes, W, Kassebaum, NJ, Bernabe, E, et al. Global burden of oral conditions in 1990–2010: a systematic analysis. J Dent Res. 2013; 92: 592–7.Google Scholar
Rugg-Gunn, A. Dental caries: strategies to control this preventable disease. Acta Med Acad. 2013; 42: 117–30. DOI: 10.5644/ama2006-124.80Google Scholar
Khan, SA, Kong, EF, Meiller, TF, Jabra-Rizk, MA. Periodontal diseases: bug induced, host promoted. PLoS Path. 2015; 11(7): e1004952. DOI: 10.1371/journal.ppat.1004952.Google Scholar
Slowik, J, Wnuk, MA, Grzech, K, et al. Periodontitis affects neurologic deficit in acute stroke. J Neurol Sci. 2010; 297: 82–4.Google Scholar
Koide, R, Ikeuchi, T, Onodera, O, et al. Unstable expansion of CAG repeat in hereditary dentarubral-pallidoluysian atrophy (DRPLA). Nat Genet. 1994; 6: 9–13.Google Scholar
Licht, DJ, Lynch, DR. Juvenile dentatorubral-pallidoluysian atrophy: new clinical features. Pediatr Neurol. 2002; 26: 51–4.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Hunter, EC, Sierra, M, David, AS. The epidemiology of depersonalisation and derealisation: a systematic review. Soc Psychiatry Psychiatr Epidemiol. 2004; 39: 9.Google Scholar
Ross, CA, Joshi, S, Currie, R. Dissociative experiences in the general population: a factor analysis. Hosp Community Psychiatry. 1991; 42: 297.Google Scholar
Spiegel, D, Loewenstein, RJ, Lewis-Fernández, R, et al. Dissociative disorders in DSM-5. Depress Anxiety. 2011; 28(9): 824–52. DOI: 10.1002/da.20874Google Scholar
Weiss, AP, Akelman, E, Tabatabai, M. Treatment of De Quervain's disease. J Hand Surg Am. 1994; 19(4): 595–8.Google Scholar
Amato, AA, Greenberg, SA. Inflammatory myopathies. Continuum (Minneap Minn). 2013; 19(6): 1615–33.Google Scholar
Low, PA, Singer, W. Management of neurogenic orthostatic hypotension: an update. Lancet Neurol. 2008; 7(5): 451–8.Google Scholar
Vinik, AI, Maser, RE, Mitchell, BD, Freeman, R. Diabetic autonomic neuropathy. Diabetes Care. 2003; 26: 1553–79.Google Scholar
Tracy, JA, Dyck, JB. The spectrum of diabetic neuropathy. Phys Med Rehabil Clin N Am. 2008; 19: 1–26.Google Scholar
Kitabchi, AE, Umpierrez, GE, Miles, JM, Fisher, JN. Hyperglycemic crises in adult patients with diabetes. Diabetes Care. 2009; 32: 1335.Google Scholar
Steenkamp, DW, Alexanian, SM, McDonnell, ME. Adult hyperglycemic crisis: a review and perspective. Curr Diab Rep. 2013; 13: 130–7.Google Scholar
Tracy, JA, Dyck, JB. The spectrum of diabetic neuropathy. Phys Med Rehabil Clin N Am. 2008; 19: 1–26.Google Scholar
Pasnoor, M, Dimachkie, MM, Barohn, RJ. Diabetic neuropathy Part 2: proximal and asymmetric phenotypes. Neurol Clin. 2013; 31(2): 447–62. DOI: 10.1016/j.ncl.2013.02.003.Google Scholar
Murray, A. Cognitive impairment in the aging dialysis and chronic kidney disease populations: an occult burden. Adv Chronic Kidney Dis. 2008; 15(2): 123–32.Google Scholar
Naganuma, T, Takemoto, Y, Shoji, T, et al. Factors associated with cerebral white matter hyperintensities in haemodialysis patients. Nephrology (Carlton). 2012; 17: 561–8.Google Scholar
Seliger, S, Gillen, D, Longstreth, W, Kestenbaum, B, Stehman-Breen, C. Elevated risk of stroke among patients with end-stage renal disease. Kidney Int. 2003; 64(2): 603.Google Scholar
Arieff, A. Dialysis disequilibrium syndrome: current concepts on pathogenesis and prevention. Kidney Int. 1994; 45(3): 629.Google Scholar
Bagshaw, SM, Peets, AD, Hameed, M, et al. Dialysis dysequilibrium syndrome: brain death and acute renal failure – A case report. BMC Nephrol. 2004; 5: 9.Google Scholar
Miyazawa, A. Ossification of the ligamentum flavum of the cervical spine. J Neurosurg Sci. 2007; 51(3): 139–44.Google Scholar
Ono, M, Russell, WJ, Kudo, S, et al. Ossification of the thoracic posterior longitudinal ligament in a fixed population. Radiological and neurosurgical manifestations. Radiology. 1982; 143(2): 469–74.Google Scholar
Center for Disease Control and Prevention: Diphtheria. Epidemiology and prevention of vaccine preventable diseases, 13th ed. Atlanta, GA: Center for Disease Control and Prevention; 2015. pp. 107–118.Google Scholar
Sanghi, V. Neurologic manifestations of diphtheria and pertussis. Handb Clin Neurol. 2014; 12: 1355–9.Google Scholar
Hadfield, TL, McEvoy, P, Polotsky, Y, Tzinserling, VA, Yakovlev, AA. The pathology of diphtheria. J Infect Dis. 2000; 181(Suppl 1): S116–20.Google Scholar
Piradov, MA, Pirogov, VN, Popova, LM, Avdunina, IA. Diphtheritic polyneuropathy. Arch Neurol. 2001; 58: 1438–42.Google Scholar
Broder, KR, Cortese, MM, Iskander, JK, et al. Preventing tetanus, diphtheria, and pertussis among adolescents: use of tetanus toxoid, reduced diphtheria toxoid and acellular pertussis vaccines: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Recomm Rep. 2006; 55(RR-3): 1–34.Google Scholar
McQuillan, GM, Kruszon-Moran, D, Deforest, A, Chu, SY, Wharton, M. Serologic immunity to diphtheria and tetanus in the United States. Ann Intern Med. 2002; 136(9): 660–6.Google Scholar
Naiditch, MJ, Bower, AG. Diphtheria: a study of 1,433 cases observed during a ten-year period at the Los Angeles County Hospital. Am J Med. 1954; 17(2): 229–45.Google Scholar
Singleton, JA, Greby, SM, Wooten, KG, Walker, FJ, Strikas, R. Influenza, pneumococcal, and tetanus toxoid vaccination of adults – United States, 1993–1997. MMWR CDC Surveill Summ. 2000; 49(9): 39–62.Google Scholar
McHenry, MC, Easley, KA, Locker, GA. Vertebral osteomyelitis: Long-term outcome for 253 patients from 7 Cleveland-Area Hospitals. Clin Infect Dis. 2002; 34: 1342–50.Google Scholar
Cebrian Parra, JL, Martinez-Aedo, ALU, Ivanez, IS, Agreda, E, Stern, LP. Management of infectious discitis. Outcome in one hundred and eight patients in a University Hospital. Int Orthop. 2012; 36: 239–44.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Lorber, MF. Psychophysiology of aggression, psychopathy, and conduct problems: a meta-analysis. Psychol Bull. 2004; 130(4): 531–52.Google Scholar
Nock, MK, Hwang, I, Sampson, NA, Kessler, RC. Mental disorders, comorbidity and suicidal behavior: results from the National Comorbidity Survey Replication. Mol Psychiatry. 2010; 15(8): 868–76.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Brotman, MA, Schmajuk, M, Rich, BA, et al. Prevalence, clinical correlates, and longitudinal course of severe mood dysregulation in children. Biol Psychiatry. 2006; 60(9): 991–7.Google Scholar
Leibenluft, E. Severe mood dysregulation, irritability, and the diagnostic boundaries of bipolar disorder in youth. Am J Psychiatry. 2011; 168(2): 129–42.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Brand, M, Eggers, C, Reinhold, N, et al. Functional brain imaging in 14 patients with dissociative amnesia reveals right inferolateral prefrontal hypometabolism. Psychiatry Res. 2009; 174(1): 32–9.Google Scholar
Cohen, NJ, Squire, LR. Preserved learning and retention of pattern-analyzing skill in amnesia: dissociation of knowing how and knowing that. Science. 1980; 210(4466): 207–10.Google Scholar
International Society for the Study of Trauma and Dissociation. Guidelines for treating dissociative identity disorder in adults, third revision. J Trauma Dissociation. 2011; 12(2): 115–87.Google Scholar
Johnson, JG, Cohen, P, Kasen, S, Brook, JS. Dissociative disorders among adults in the community, impaired functioning, and axis I and II comorbidity. J Psychiatr Res. 2006; 40(2): 131–40.Google Scholar
Kaszniak, AW, Nussbaum, PD, Berren, MR, Santiago, J. Amnesia as a consequence of male rape: a case report. J Abnorm Psychol. 1988; 97(1): 100–4.Google Scholar
Loewenstein, RJ. Psychogenic amnesia and psychogenic fugue: a comprehensive review. In Tasman, A, Goldfinger, SM, eds. The American Psychiatric Press Annual Review of Psychiatry, Vol 10. Washington, DC: American Psychiatric Press; 1991. pp. 189–222.Google Scholar
Loewenstein, RJ. Psychogenic amnesia and psychogenic fugue: a comprehensive review. In Spiegel, D, ed. Dissociative disorders: a clinical review. Baltimore, MD: The Sidran Press; 1993. pp. 45–78.Google Scholar
Witztum, E, Margalit, H, van der Hart, O. Combat-induced dissociative amnesia: review and case example of generalized dissociative amnesia. J Trauma Dissociation. 2002; 3(2): 35–55.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Ellason, JW, Ross, CA, Fuchs, DL. Lifetime Axis I and II comorbidity and childhood trauma history in dissociative identity disorder. Psychiatry. 1996; 59(3): 255–66.Google Scholar
Johnson, JG, Cohen, P, Kasen, S, Brook, JS. Dissociative disorders among adults in the community, impaired functioning, and axis I and II comorbidity. J Psychiatr Res. 2006; 40(2): 131–40.Google Scholar
Spiegel, D, Loewenstein, RJ, Lewis-Fernández, R, et al. Dissociative disorders in DSM-5. Depress Anxiety. 2011; 28(9): 824–52. DOI: 10.1002/da.20874Google Scholar
Muscular Dystrophy Association. Spinal muscular atrophy. https://www.mda.org/disease/spinal-muscular-atrophy/types. Accessed May, 2017.Google Scholar
Muthukrishnan, J, Varadarajulu, R, Mehta, SR, Singh, AP. Distal muscular atrophy: Case report. J Assoc Physicians India. 2003; 51: 113–15.Google Scholar
Kelley, SA, Kossoff, EH. Doose syndrome (myoclonic-astatic epilepsy): 40 years of progress. Dev Med Child Neurol. 2010; 52(11): 988–93.Google Scholar
Tang, S, Pal, DK. Dissecting the genetic basis of myoclonic-astatic epilepsy. Epilepsia. 2012; 53(8): 1303–13.Google Scholar
Lee, WW, Jeon, BS. Clinical spectrum of dopa-responsive dystonia and related disorders. Curr Neurol Neurosci Rep. 2014; 14(7): 1–13.Google Scholar
Wijemanne, S, Jankovic, J. Dopa-responsive dystonia: clinical and genetic heterogeneity. Nat Rev Neurol. 2015; 11(7): 414–24.Google Scholar
Centers for Disease Control and Prevention. Birth defects: data and statistics in the United States. Updated April 30, 2018. Available from www.cdc.gov/NCBDDD/birthdefects/data.html. Accessed February 26, 2014.Google Scholar
Graber, E, Chacko, E, Regelmann, MO, et al. Down syndrome and thyroid function. Endocrinol Metab Clin North Am. 2012; 41: 735–45.Google Scholar
Baumer, N, Davidson, EJ. Supporting a happy, healthy adolescence for young people with Down syndrome and other intellectual disabilities: recommendations for clinicians. Curr Opin Pediatr. 2014; 26: 428–34.Google Scholar
Yang, Q, Rasmussen, SA, Friedman, JM. Mortality associated with Down's syndrome in the USA from 1983 to 1997: a population-based study. Lancet. 2002; 359: 1019–25.Google Scholar
Davidson, MA. Primary care for children and adolescents with Down syndrome. Pediatr Clin North Am. 2008; 55: 1099–111.Google Scholar
Auvin, S, Cilio, MR, Vezzani, A. Current understanding and neurobiology of epileptic encephalopathies. Neurobiol Dis. 2016; 92(Pt A): 72–89.Google Scholar
Brigo, F, Igwe, SC. Antiepileptic drugs for the treatment of infants with severe myoclonic epilepsy. Cochrane Database Syst Rev. 2015(10): CD010483.Google Scholar
Brunklaus, A, Zuberi, SM. Dravet syndrome: from epileptic encephalopathy to channelopathy. Epilepsia. 2014; 55(7): 979–84.Google Scholar
McTague, A, Howell, KB, Cross, JH, Kurian, MA, Scheffer, IE. The genetic landscape of the epileptic encephalopathies of infancy and childhood. Lancet Neurol. 2016; 15(3): 304–16.Google Scholar
Sheldon, JH. Drop attacks in the elderly: a request for information. J Coll Gen Pract. 1962; 5(1): 107–9.Google Scholar
Stevens, DL, Matthews, WB. Cryptogenic drop attacks: an affliction of women. Br Med J. 1973; 1(5851): 439–42.Google Scholar
Goetz, CG, Dysken, MW, Klawans, HL. Assessment and treatment of drug-induced tremor. J Clin Psychiatry. 1980; 41(9): 310–5.Google Scholar
Gabellini, AS, Martinelli, P, Coccagna, G. Drug-induced tremor of the tongue. Ital J Neurol Sci. 1989; 10(1): 89–91.Google Scholar
Caroff, SN, Hurford, I, Lybrand, J, Campbell, EC. Movement disorders induced by antipsychotic drugs: implications of the CATIE schizophrenia trial. Neurol Clin. 2011; 29(1): 127–48, viii.Google Scholar
Tarsy, D, Indorf, G. Tardive tremor due to metoclopramide. Mov Disord. 2002; 17(3): 620–1.Google Scholar
Arnold, G, Trenkwalder, C, Schwarz, J, Oertel, WH. Zotepine reversibly induces akinesia and rigidity in Parkinson's disease patients with resting tremor or drug-induced psychosis. Mov Disord. 1994; 9(2): 238–40.Google Scholar
Bushby, K. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. Lancet Neurol. 2010; 9: 77–93.Google Scholar
Hendriksen, JG, Vles, JS. Neuropsychiatric disorders in males with Duchenne muscular dystrophy: frequency rate of attention-deficit hyperactivity disorder (ADHD), autism spectrum disorder, and obsessive-compulsive disorder. J Child Neurol. 2008; 23(5): 477–81.Google Scholar
Ayd, FJ Jr. A survey of drug-induced extrapyramidal reactions. JAMA. 1961; 175: 1054–60.Google Scholar
Chaudhuri, KR, Ondo, WG, Logishetty, K, Redyy, P, Sherman, R. Other movement disorders. In Chaudhuri, KR, Ondo, WG, eds. Handbook of movement disorders. London: Current Medicine Group; 2009. pp. 89–92.Google Scholar
Greene, PE. Tardive and neuroleptic-induced emergencies. In Frucht, SJ, ed. Movement disorder emergencies: diagnosis and treatment. 2nd ed. New York: Springer; 2013. pp. 141–49.Google Scholar
Horn, S. Drug induced movement disorders. Continuum (Minneap Minn). 2004; 10(3): 142–53.Google Scholar
Rosebush, PI, Mazurek, MF. Acute drug induced dystonia. In Factor, S, Lang, A, Weiner, W, eds. Drug induced movement disorders. 2nd ed. Malden, MA: Wiley-Blackwell; 2008. pp. 72–102.Google Scholar
Beal, JC, Cherian, K, Moshe, SL. Early-onset epileptic encephalopathies: Ohtahara syndrome and early myoclonic encephalopathy. Pediatr Neurol. 2012; 47(5): 317–23.Google Scholar
Khan, S, Al Baradie, R. Epileptic encephalopathies: an overview. Epilepsy Res Treat. 2012; 2012: 403592.Google Scholar
McTague, A, Howell, KB, Cross, JH, Kurian, MA, Scheffer, IE. The genetic landscape of the epileptic encephalopathies of infancy and childhood. Lancet Neurol. 2016; 15(3): 304–16.Google Scholar
Amstrong, PM, Andrealis, TG. Eastern equine encephalitis virus: old enemy, new threat. N Engl J Med. 2013; 368: 1670–3.Google Scholar
Deresiewicz, RL, Thaler, SJ, HSU, L, Zamani, AA. Clinical and neuroradiographic manifestations of Eastern equine encephalitis. N Engl J Med. 1997; 336: 1867–74.Google Scholar
Hirsh, MS, DeMara, A, Schaefer, PW, Branda, JA. Case 22–2008: a 52-year-old woman with fever and confusion. N Engl J Med. 2008; 359: 294–303.Google Scholar
McManus, DP, Gray, DJ, Zhand, W, Yang, Y. Diagnosis, treatment, and management of echinococcosis. BMJ. 2012; 344(1): 13.Google Scholar
Brunetti, E, Kern, P, Vuitton, DA. Expert consensus for the diagnosis and treatment of cystic and alveolar echinococcosis in humans. Acta Tropica. 2010; 114: 1–16.Google Scholar
Kammerer, WS. Echinococcosis affecting the central nervous system. Semin Neurol. 1993; 13(2): 144–7.Google Scholar
Neumayr, A, Tamarozzi, F, Goblirsch, S, Blum, J, Brunetti, E. Spinal cystic echinococcosis – A systematic analysis and review of the literature: Part 1. Epidemiology and Anatomy. PLoS Negl Trop Dis. 2013: 7(9): e2450. DOI: 10.1371/journal.pntd.0002450.Google Scholar
Neumayr, A, Tamarozzi, F, Goblirsch, S, Blum, J, Brunetti, E. Spinal cystic echinococcosis – A systematic analysis and review of the literature: Part 2. Treatment, follow-up and outcome. PLoS Negl Trop Dis. 2013; 7(9): e2458. DOI: 10.1371/journal.pntd.0002458.Google Scholar
Pathogen Regulation Directorate, Public Health Agency of Canada. Echovirus; 2011. https://www.canada.ca/en/public-health/services/laboratory-biosafety-biosecurity/pathogen-safety-data-sheets-risk-assessment/echovirus-pathogen-safety-data-sheet.html. Accessed Aug 15, 2018.Google Scholar
Holmes, CW, Koo, SSF, Osman, H, et al. Predominance of enterovirus B and echovirus 30 as cause of viral meningitis in a UK population. J Clin Virol. 2016; 81: 90–3.Google Scholar
Jain, S, Patel, B, Bhatt, GC. Enterovirus encephalitis in children: clinical features, pathophysiology, and treatment advances. Pathog Glob Health. 2014; 108: 216–22.Google Scholar
Dalwai, A, Ahmad, S, Al-Nakib, W. Echoviruses are a major cause of aseptic meningitis in infants and young children in Kuwait. Virol J. 2010; 7: 236–41.Google Scholar
Cipolla, MJ, Kraig, RP. Seizures in women with preeclampsia: mechanisms and management. Fetal Matern Med Rev. 2011; 22(2): 91–108.Google Scholar
Duley, L. The global impact of pre-eclampsia and eclampsia. Semin Perinatol. 2009; 33(3): 130–7.Google Scholar
Sibai, BM. Diagnosis, prevention, and management of eclampsia. Obstet Gynecol. 2005; 105(2): 402–10.Google Scholar
Hahn, I-H. MDMA toxicity. Medscape. Updated Dec 20, 2017. http://emedicine.medscape.com/article/821572-overview#a6. Accessed Aug 7, 2018.Google Scholar
Holland, J, ed. Ecstasy: The complete guide: A comprehensive look at the risks and benefits of MDMA. Rochester, VT: Inner Traditions/Bear; 2001.Google Scholar
Quednow, BB, Kühn, K-U, Hoppe, C, et al. Elevated impulsivity and impaired decision-making cognition in heavy users of MDMA (“Ecstasy”). Psychopharmacology. 2007; 189: 517. https://doi.org/10.1007/s00213-005-0256-4.Google Scholar
Wiegand, T, Thai, D, Benowitz, N. Medical consequences of the use of hallucinogens: LSD, mescaline, PCP, and MDMA (“Ecstasy”). In Brick, J, ed. Handbook of the medical consequences of alcohol and drug abuse. 2nd ed. New York: Routledge; 2008. p. 461.Google Scholar
Caplan, LR, Van Gijn, J. Clinical manifestations and diagnosis of Ehler-Danlos syndrome. UpToDate. Updated Jun 13, 2018. https://www.uptodate.com/contents/clinical-manifestations-and-diagnosis-of-ehlers-danlos-syndromes. Accessed Aug 15, 2018.Google Scholar
Ismail, N, Bloch, K, McBride, JW. Human ehrlichiosis and anaplasmosis. Clin Lab Med. 2010; 30: 261–92.Google Scholar
Ratnasamy, N, Everett, ED, Roland, WE, McDonald, G, Caldwell, C. Central nervous system manifestations of human ehrlichiosis. Clin Infect Dis. 1996; 23: 314–9.Google Scholar
Hughes, JR. A review of the relationships between Landau-Kleffner syndrome, electrical status epilepticus during sleep, and continuous spike-waves during sleep. Epilepsy Behav. 2011; 20(2): 247–53.Google Scholar
Sanchez Fernandez, I, Loddenkemper, T, Peters, JM, Kothare, SV. Electrical status epilepticus in sleep: clinical presentation and pathophysiology. Pediatr Neurol. 2012; 47(6): 390–410.Google Scholar
Hermann, RC, Dorwart, RA, Hoover, CW, Brody, J. Variation in ECT use in the United States. Am J Psychiatry. 1995; 152: 869.Google Scholar
Leiknes, KA, Jarosh-von Schweder, L, Høie, B. Contemporary use and practice of electroconvulsive therapy worldwide. Brain Behav. 2012; 2(3): 283–344. DOI: 10.1002/brb3.37.Google Scholar
Semkovska, M, McLoughlin, DM. Objective cognitive performance associated with electroconvulsive therapy for depression: a systematic review and meta-analysis. Biol Psychiatry. 2010; 68: 568.Google Scholar
National Organization for Rare Disorders. Empty sella syndrome. Available from http://rarediseases.org/rare-diseases/empty-sella-syndrome/. Accessed Dec 17, 2015.Google Scholar
Lenz, AM, Root, AW. Empty sella syndrome. Pediatr Endocrinol Rev. 2012; 9(4): 710–15. Review.Google Scholar
Granerod, J, Tam, CC, Crowcroft, NS, et al. Challenge of the unknown: a systematic review of acute encephalitis in non-outbreak situations. Neurology. 2010; 75: 924–32.Google Scholar
Armangue, T, Leypoldt, F, Dalmau, J. Auto-immune encephalitis as differential diagnosis of infectious encephalitis. Curr Opin Neurol. 2014; 27(3): 361–8.Google Scholar
Graus, F, Titulaer, MJ, Balu, R, et al. A clinical approach to diagnosis of autoimmune encephalitis. Lancet Neurol. 2016; 15(4): 391–404.Google Scholar
Solomon, T, Michael, BD, Smith, PE, et al. Management of suspected viral encephalitis in adults: Association of British Neurologists and British infection Association Guidelines. J Infect. 2012; 64(4): 347–73.Google Scholar
Thakur, KT, Motta, M, Asemota, AO, et al. Predictor of outcome in acute encephalitis. Neurology. 2013; 8(9): 793–800.Google Scholar
Dale, RC, Church, AJ, Surtees, RAH, et al. Encephalitis lethargica syndrome: 20 new cases and evidence of basal ganglia autoimmunity: Brain. 2004; 127: 21–33.Google Scholar
Cheyette, SR, Cummings, JL. Encephalitis lethargica: lessons for contemporary neuropsychiatry. J Neuropsychiatry. 1995; 7: 125–34.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Benvenga, S, Toscano, A, Rodolico, C, et al. Endocrine evaluation for muscle pain. J R Soc Med. 2001; 94(8): 405–7.Google Scholar
Rodolico, C, Toscano, A, Benvenga, S, et al. Myopathy as the persistently isolated symptomatology of primary autoimmune hypothyroidism. Thyroid. 1998; 8(11): 1033–8.Google Scholar
Ruff, RL. Endocrine myopathies. In Engel, AG, Banker, BQ, eds. Myology. New York: McGraw Hill; 1986. p. 1871.Google Scholar
Siafakas, NM, Alexopoulou, C, Bouros, D. Respiratory muscle function in endocrine diseases. Monaldi Arch Chest Dis. 1999; 54(2): 154–9.Google Scholar
Yu, J. Endocrine disorders and the neurologic manifestations. Ann Pediatr Endocrinol Metab. 2014; 19(4): 184–90.Google Scholar
Zager, J, Peeifer, S, Brown, MJ, Torosian, MH, Hackney, DB. Catamenial mononeuropathy and radiculopathy: a treatable neuropathic disorder. J Neurosurg. 1998; 88; 827–30.Google Scholar
Public Health England. Identification of Enterobacteriaceae. UK Standards forMicrobiology Investigations. ID 16, Issue 4. 2015. www.gov.uk/uk-standards-for-microbiology-investigations-smi-quality-and-consistency-in-clinical-laboratories.Google Scholar
Van Duin, D, Doi, Y. The global epidemiology of carbapenemase-producing Enterobacteriaceae. Virulence. 2017; 8(4): 460–9.Google Scholar
Vasoo, S, Barreto, JN, Tosh, PK. Emerging issues in Gram-negative bacteria resistance: an update for the practicing clinician. Mayo Clin Proc. 2015; 90: 395–403.Google Scholar
Viale, P, Giannella, M, Tedeshi, S, Lewis, R. Treatment of MDR-Gram negative infections in the 21st century: a never ending threat for clinicians. Curr Opin Pharmacol. 2015; 24: 30–7.Google Scholar
Chang, WN, Huang, CR, Lu, CH, Chien, CC. Adult Klebsiella pneumoniae meningitis in Taiwan: an overview. Acta Neurol Taiwan. 2012; 21: 87–96.Google Scholar
Huang, CC, Liu, CC, Chang, YC, et al. Neurologic complications in children with Enterovirus 71. Infection. 1999; 41(13): 936–42.Google Scholar
Jain, S, Patel, B, Bhatt, GC. Enterovirus encephalitis in children: clinical features, pathophysiology, and treatment advances. Pathog Glob Health. 2014; 108: 216–22.Google Scholar
Lugo, D, Krogstad, P. Enteroviruses in the early 21st century: new manifestations and challenges. Curr Opin Pediatr. 2016; 28: 107–13.Google Scholar
Ooi, MH, Wang, S, Lewthwaite, P, Cardosa, MJ, Solomon, T. Clinical features, diagnosis, and management of enterovirus 71. Lancet Neurol. 2010; 9: 1097–105.Google Scholar
Palacios, G, Oberste, MS. Enteroviruses as agents of emerging infectious diseases. J Neurovirol. 2005; 11: 424–33.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Robson, WL. Clinical practice. Evaluation and management of enuresis. N Engl J Med. 2009; 360(14): 1429–36.Google Scholar
Roson, WL, Leung, AK. Side effects and complications of treatment with desmopressin for enuresis. J Natl Med Assoc. 1994; 86(10): 775–7.Google Scholar
American Brain Tumor Association. Ependymoma. (n.d.). https://www.abta.org/tumor_types/ependymoma/. Accessed Oct 11, 2016.Google Scholar
CERN Foundation. Ependymoma clinical trials. (n.d.). www.cern-foundation.org/. Accessed Oct 11, 2016.Google Scholar
National Cancer Institute. Childhood ependymoma treatment. Updated July 6, 2018. Available from www.cancer.gov/types/brain/patient/child-ependymoma-treatment-pdq. Accessed Aug 3, 2018.Google Scholar
Moawad, FJ, Hartzell, JD, Biega, TJ, Lettieri, CJ. Transient blindness due to posterior reversible encephalopathy syndrome following ephedra overdose. Southern Medical Journal, May, 2006. p. 511. Academic OneFile. Available from http://go.galegroup.com/ps/anonymous?id=GALE%7CA146844361&sid=googleScholar&v=2.1&it=r&linkaccess=fulltext&issn=00384348&p=AONE&sw=w&authCount=1&isAnonymousEntry=true. Accessed Aug 3, 2018.Google Scholar
Wiegand, T, Thai, D, Benowitz, N. Medical consequences of the use of hallucinogens: LSD, mescaline, PCP, and MDMA (“Ecstasy”). In Brick, J, ed. Handbook of the medical consequences of alcohol and drug abuse. 2nd ed. New York: Routledge; 2008. p. 461.Google Scholar
Bisset, L, Beller, E, Jull, G, et al. Mobilization with movement and exercise, corticosteroid injection or wait and see for tennis elbow: randomized trial. BMJ. 2006; 333(7575): 939.Google Scholar
Chowdhury, FH, Haque, MR, Sarker, MH. Intracranial epidermoid tumor; microneurosurgical management: an experience of 23 cases. Asian J Neurosurg. 2013; 8(1): 21–8. Available from http://doi.org/10.4103/1793-5482.110276Google Scholar
Dornelles, C, da Costa, SS, Meurer, L, Schweiger, C. Some considerations about acquired adult and pediatric cholesteatomas. Braz J Otorhinolaryngol. 2005; 71(4): 536–46. DOI: 10.1590/s0034-72992005000400023.Google Scholar
Isaacson, G. Diagnosis of pediatric cholesteatoma. Pediatrics. 2007; 120(3): 603–8. DOI: 10.1542/peds.2007-0120.Google Scholar
Semaan, MT., Megerian, CA. The pathophysiology of cholesteatoma. Otolaryngol Clin North Am. 2006; 39(6): 1143–59. DOI: 10.1016/j.otc.2006.08.003.Google Scholar
Besenski, N. Traumatic injuries: imaging of head injuries. Eur Radiol. 2002; 12: 1237.Google Scholar
Bullock, MR, Chesnut, R, Ghajar, J, et al. Surgical management of acute epidural hematomas. Neurosurgery. 2006; 58: S7.Google Scholar
Matsumoto, K, Akagi, K, Abekura, M, Tasaki, O. Vertex epidural hematoma associated with traumatic arteriovenous fistula of the middle meningeal artery: a case report. Surg Neurol. 2001; 55: 302.Google Scholar
Mayer, S, Rowland, L. Head injury. In Rowland, L, ed. Merritt's neurology. Philadelphia: Lippincott Williams & Wilkins; 2000. p. 401.Google Scholar
McIver, JI, Scheithauer, BW, Rydberg, CH, Atkinson, JL. Metastatic hepatocellular carcinoma presenting as epidural hematoma: case report. Neurosurgery. 2001; 49: 447.Google Scholar
Ng, WH, Yeo, TT, Seow, WT. Non-traumatic spontaneous acute epidural haematoma – report of two cases and review of the literature. J Clin Neurosci. 2004; 11: 791.Google Scholar
Safaz, I, Alaca, R, Yasar, E, Tok, F, Yilmaz, B. Medical complications, physical function and communication skills in patients with traumatic brain injury: a single centre 5-year experience. Brain Inj. 2008; 22: 733–9.Google Scholar
Barron, KD, Hirano, A, Araki, S, Terry, RD. Experiences with metastatic neoplasms involving the spinal cord. Neurology. 1959; 9: 91–106.Google Scholar
Grant, R, Papadopoulos, SM, Sandler, HM, Greenberg, HS. Metastatic epidural spinal cord compression: current concepts and treatment. J Neurooncol. 1994; 19: 79–92.Google Scholar
Portenoy, RK, Galer, BS, Salamon, O, et al. Identification of epidural neoplasm: radiography and bone scintigraphy in the symptomatic and asymptomatic spine. Cancer. 1989; 64(11): 2207–13.Google Scholar
Schiff, D. Clinical features and diagnosis of neoplastic epidural spinal cord compression, including cauda equina syndrome. Available from www.uptodate.com/contents/clinical-features-and-diagnosis-of-neoplastic-epidural-spinal-cord-compression-including-cauda-equina-syndrome. Accessed Oct 11, 2016.Google Scholar
England, MJ, Liverman, CT, Schultz, AM, Strawbridge, LM. Epilepsy across the spectrum: promoting health and understanding. A summary of the Institute of Medicine report. Epilepsy Behav. 2012; 25(2): 266–76.Google Scholar
Fisher, RS, Acevedo, C, Arzimanoglou, A, et al. ILAE official report: a practical clinical definition of epilepsy. Epilepsia, 2014; 55(4): 475–82.Google Scholar
Jones, NC, O'Brien, TJ. Stress, epilepsy, and psychiatric comorbidity: how can animal models inform the clinic? Epilepsy Behav. 2013; 26(3): 363–9.Google Scholar
Kanner, AM. Management of psychiatric and neurological comorbidities in epilepsy. Nat Rev Neurol. 2016; 12(2): 106–16.Google Scholar
Baker, GA, Bromley, RL, Briggs, M, et al. IQ at 6 years after in utero exposure to antiepileptic drugs. Neurology. 2015; 84(4): 382–90.Google Scholar
Bangar, S, Shastri, A, El-Sayeh, H, Cavanna, AE. Women with epilepsy: clinically relevant issues. Funct Neurol. 2016; 31(3): 127–34.Google Scholar
Borgelt, LM, Hart, FM, Bainbridge, JL. Epilepsy during pregnancy: focus on management strategies. Int J Womens Health. 2016; 19(8): 505–17.Google Scholar
Kinney, MO, Craig, JJ. Pregnancy and epilepsy; meeting the challenges over the last 25 years: The rise of the pregnancy registries. Seizure. 2017; 44: 162–8.Google Scholar
Cockerell, OC, Rothwell, J, Thompson, PD, Marsden, CD, Shorvon, SD. Clinical and physiological features of epilepsia partialis continua: cases ascertained in the UK. Brain. 1996; 119(2): 393–407.Google Scholar
Eggers, C, Burghaus, L, Fink, GR, Dohmen, C. Epilepsia partialis continua responsive to intravenous levetiracetam. Seizure. 2009; 18(10): 716–8.Google Scholar
Pandian, JD, Thomas, SV, Santoshkumar, B. Epilepsia partialis continua: a clinical and electroencephalography study. Seizure. 2002; 11(7): 437–41.Google Scholar
Sinha, S, Satishchandra, P. Epilepsia partialis continua over last 14 years: experience from a tertiary care center from south India. Epilepsy Res. 2007; 74(1): 55–9.Google Scholar
Fujimoto, H, Asaoka, K, Amatzumi, T, et al. Epstein Barr virus infections of the central nervous system. Intern Med. 2003; 42: 33–40.Google Scholar
Hausler, M, Ramaekers, VT, Doenges, M, et al. Neurologic complications of acute of persistent Epstein-Barr virus infection in Paediatric patients. J Med Virol. 2002; 68: 253–63.Google Scholar
Martelius, T, Lappalainen, M, PaloMaki, M, Antilla, VJ. Clinical characterisistics of patients with Epstein Barr virus in cerebrospinal fluid. BMC Infect Dis. 2011; 11: 281.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Beutel, ME, Weidner, W, Brähler, E. Epidemiology of sexual dysfunction in the male population. Andrologia. 2006; 38(4): 115–21.Google Scholar
Prins, J, Blanker, MH, Bohnen, AM, et al. Prevalence of erectile dysfunction: a systematic review of population-based studies. Int J Impot Res. 2002; 14(6): 422–32.Google Scholar
Cardoso, F, Seppi, K, Mair, KM, Wenning, GK, Poewe, W. Seminar on choreas. Lancet Neurol. 2006; 5: 589–602.Google Scholar
Peall, KJ, Kurian, MA. Benign hereditary chorea: an update. Tremor Other Hyperkinet Mov (NY). 2015; 5: 314.Google Scholar
Harper, PS. Benign hereditary chorea: clinical and genetic aspects. Clin Genet. 1978; 13(1): 85–95.Google Scholar
Gras, D, Jonard, L, Roze, E, et al. Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene. J Neurol Neurosurg Psychiatry. 2012; 83(10): 956–62.Google Scholar
Peall, KJ, Lumsden, D, Kneen, R, et al. Benign hereditary chorea related to NKX2.1: expansion of the genotypic and phenotypic spectrum. Dev Med Child Neurol. 2014; 56(7): 642–8.Google Scholar
Inzelberg, R, Weinberger, M, Gak, E. Benign hereditary chorea: an update. Parkinsonism Relat Disord. 2011; 17(5): 301–7.Google Scholar
Caviness, JN, Brown, P. Myoclonus: current concepts and recent advances. Lancet Neurol. 2004; 3(10): 598–607.Google Scholar
Marechal, L, Raux, G, Dumanchin, C, et al. Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation. Am J Med Genet B Neuropsychiatr Genet. 2003; 119B(1): 114–7.Google Scholar
Michiels, JJ, Koudstaal, PJ, Mulder, AH, van Vliet, HH. Transient neurologic and ocular manifestations in primary thrombocythemia. Neurology. 1993; 43: 1107–10.Google Scholar
Pósfai, É, Marton, I, Szőke, A, et al. Stroke in essential thrombocythemia. J Neurol Sci. 2014; 336: 260–2.Google Scholar
Benito-León, J, Louis, ED, Mitchell, AJ, Bermejo-Pareja, F. Elderly-onset essential tremor and mild cognitive impairment: a population-based study (NEDICES). J Alzheimers Dis. 2011; 23: 727–35.Google Scholar
Bhalsing, KS, Saini, J, Pal, PK. Understanding the pathophysiology of essential tremor through advanced neuroimaging: a review. J Neurol Sci. 2013; 335(1–2): 9–13.Google Scholar
Chandran, V, Pal, PK, Reddy, JY, et al. Non-motor features in essential tremor. Acta Neurol Scand. 2012; 125(5): 332–7.Google Scholar
Deuschl, G, Raethjen, J, Hellriegel, H, Elble, R. Treatment of patients with essential tremor. Lancet Neurol. 2011; 10(2): 148–61. DOI: 10.1016/S1474-4422(10)70322-7.Google Scholar
Elble, RJ. Diagnostic criteria for essential tremor and differential diagnosis. Neurology. 2000; 54(11 Suppl 4): S2–6.Google Scholar
Fernandez, H, Machado, A, Pandya, M. Practical approach to movement disorders: diagnosis and management. 2nd ed. New York: Demos Medical; 2014.Google Scholar
Louis, ED. The primary type of tremor in essential tremor is kinetic rather than postural: cross-sectional observation of tremor phenomenology in 369 cases. Eur J Neurol. 2013; 20(4): 725–7.Google Scholar
Louis, ED. From neurons to neuron neighborhoods: the rewiring of the cerebellar cortex in essential tremor. Cerebellum. 2014; 13(4): 501–12.Google Scholar
Louis, ED, Ottman, R How many people in the USA have essential tremor? Deriving a population estimate based on epidemiological data. Tremor Other Hyperkinet Mov (N Y). 2014; 4: 259.Google Scholar
Rana, AQ, Hedera, P. Essential tremor. In Differential diagnosis of movement disorders in clinical practice. New York, NY: Springer; 2014. pp. 6–19.Google Scholar
Young, RF, Li, F, Vermeulen, S, Meier, R. Gamma knife thalamotomy for treatment of essential tremor: long-term results J Neurosurg. 2010; 112: 1311–17.Google Scholar
Brashear, A, Unverzagt, FW, Farber, MO, et al. Ethylene oxide neurotoxicity: a cluster of 12 nurses with peripheral and central nervous system toxicity. Neurology. 1996; 46(4): 992–8.Google Scholar
Bartley, GB. The differential diagnosis and classification of eyelid retraction. Ophthalmology. 1996; 103: 168–76.Google Scholar
Guimaraes, FC, Cruz, AAV. Palpebral fissure height and downgaze in patients with Graves upper eylid retraction and congenital blepharoptosis. Ophthalmology. 1995; 102: 1218–22.Google Scholar
Stout, AU, Borchert, M. Etiology of eyelid retraction in children: a retrospective study. J Pediatr Ophthalmol Strabismus. 1993; 30: 96–9.Google Scholar
Cole, AL, Lee, PJ, Hughes, DA, et al. Depression in adults with Fabry disease: a common and under-diagnosed problem. J Inherit Metab Dis. 2007; 30: 943–51.Google Scholar
Desnick, RJ, Ioannou, YA, Eng, CM. Alpha-galactosidase A deficiency: Fabry disease. In Scriver, CR, Beaudet, AL, Sly, WS, et al., eds. The metabolic and molecular bases of inherited diseases. 8th ed. New York: McGraw-Hill; 2001. pp. 3733–74.Google Scholar
Eng, CM, Fletcher, J, Wilcox, WR, et al. Fabry disease: baseline medical characteristics of a cohort of 1765 males and females in the Fabry Registry. J Inherit Metab Dis. 2007; 30: 184–92.Google Scholar
Mehta, A, Hughes, DA. Fabry disease. Aug 5, 2002 [Updated Oct 17, 2013]. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle, WA: University of Washington; 1993–2016. Available from www.ncbi.nlm.nih.gov/books/NBK1292/. Accessed Aug 6, 2018.Google Scholar
Mehta, A, Ricci, R, Widmer, U, et al. Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey. Eur J Clin Invest. 2004; 34: 236–42.Google Scholar
Sadek, J, Shellhaas, R, Camfield, CS, Camfield, PR, Burley, J. Psychiatric findings in four female carriers of Fabry disease. Psychiatr Genet. 2004; 14: 199–201.Google Scholar
Caviness, JN, Brown, P. Myoclonus: current concepts and recent advances. Lancet Neurol. 2004; 3(10): 598–607.Google Scholar
Factor, S, Lang, A, Weiner, W, eds. Drug induced movement disorders. 2nd ed. Malden, MA: Wiley-Blackwell; 2008.Google Scholar
Fahn, S, Jankovic, J. Myoclonus phenomenology, etiology, physiology, and treatment. Principles and Practice of Movement Disorders. 2nd ed. Philadelphia: Saunders; 2011. p. 447.Google Scholar
Gálvez-Jiménez, N, Tuite, P, eds. Uncommon causes of movement disorders. Cambridge, UK: Cambridge University Press; 2011.Google Scholar
Jau-Shin, L, Valls-SolÃ, J, Toro, C, Hallett, M. Facial action myoclonus in patients with olivopontocerebellar atrophy. Mov Disord. 2004; 9(2): 223–6.Google Scholar
Marcos-Salazar, S, Prim-Espada, MP, De Diego-Sastre, JI, et al. [Facial nerve tumours]. Rev Neurol. 2004; 39(12): 1120–2.Google Scholar
Shirazi, MA, Leonetti, JP, Marzo, SJ, Anderson, DE. Surgical management of facial neuromas: lessons learned. Otol Neurotol. 2007; 28(7): 958–63.Google Scholar
Szudek, J. Intratemporal tumors of the facial nerve. Updated March 11, 2016. Medscape. https://emedicine.medscape.com/article/846352-overview. Accessed Aug 15, 2016.Google Scholar
Ronthal, M. Bell's palsy: Pathogenesis, clinical features, and diagnosis in adults. UpToDate. Feb 2015. Waltham, MA. Available from www.uptodate.com/home.Google Scholar
Ronthal, M. Bell's palsy: Prognosis and treatment in adults. UpTodate. Dec 2015. Waltham, MA. Availabe from http://uptodate.com/homeGoogle Scholar
Mayersak, R. Facial trauma in adults. UpToDate. Dec 2015. Waltham, MA. Available from http://uptodate.com/homeGoogle Scholar
Fahn, S, Jankovic, J. Tics and Tourette syndrome. In Principles and practice of movement disorders. 2nd ed. Philadelphia: Saunders; 2011. pp. 350–79.Google Scholar
Martino, D, Espay, AJ, Fasano, A, Morgante, F. Tics. In Disorders of movement: a guide to diagnosis and treatment. New York: Springer; 2016. pp. 97–118.Google Scholar
Münchau, A. Tics. In Brandt, VC, ed. Neuropsychiatric symptoms of movement disorders. New York: Springer International; 2015. pp. 223–59.Google Scholar
Orrell, RW. Facioscapulohumeral dystrophy and scapuloperoneal syndromes. Handb Clin Neurol. 2011; 101: 167–80.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Reich, P, Gottfried, LA. Factitious disorders in a teaching hospital. Ann Intern Med. 1983; 99(2): 240–7.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Krahn, LE, Li, H, O'Connor, MK. Patients who strive to be ill: factitious disorder with physical symptoms. Am J Psychiatry. 2003; 160(6): 1163–8.Google Scholar
Sutherland, AJ, Rodin, GM. Factitious disorders in a general hospital setting: clinical features and a review of the literature. Psychosomatics. 1990; 31(4): 392–9.Google Scholar
Biffi, A, Greenberg, SM. Cerebral amyloid angiopathy: a systematic review. J Clin Neurol. 2011; 7(1): 1–9.Google Scholar
Caplan, LR. Factor V Leiden: clinical manifestations and diagnosis. In Bogousslavsky, K, ed. Uncommon causes of stroke. 2nd ed. Cambridge, UK: Cambridge University Press; 2008. Chapter 6.Google Scholar
Caplan, LR, ed. Uncommon causes of stroke. 2nd ed. Cambridge, UK: Cambridge University Press; 2010.Google Scholar
Black, DF. Sporadic and familial hemiplegic migraine: diagnosis and treatment. Semin Neurol. 2006; 26: 208–16.Google Scholar
Bradshaw, P, Parsons, M. Hemiplegic migraine, a clinical study. Q J Med. 1965; 34: 65–86.Google Scholar
Thomsen, LL, Eriksen, MK, Roemer, SF, et al. An epidemiological survey of hemiplegic migraine. Cephalalgia. 2002; 22: 361–75.Google Scholar
Whitty, CWM. Familial hemiplegic migraine. J Neurol Neurosurg Psychiatry. 1953; 16: 172–7.Google Scholar
Keller, A, et al. Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice. Nat Genet. 2013; 45(9): 1077–82.Google Scholar
Manyam, BV, et al. Bilateral striopallidodentate calcinosis: clinical characteristics of patients seen in a registry. Mov Disord. 2001; 16(2): 258–64.Google Scholar
Nicolas, G, et al. Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification. Neurology. 2013; 80(2): 181–7.Google Scholar
Nicolas, G, et al. Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification. Brain. 2013; 136(11): 3395–407.Google Scholar
Wang, C, Li, Y, Shi, L, et al. Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis. Nature Genet. 2012; 44(3): 254–6.Google Scholar
Harris, CM, Walker, J, Shawkat, F, Wilson, J, Russell-Eggitt, I. Eye movements in a familial vestibulocerebellar disorder. Neuropediatrics. 1993; 3: 177–22.Google Scholar
Theunissen, EJ, Huygen, PL, Verhagen, WI. Familial vestibulocerebellar dysfunction: a new syndrome? J Neurol Sci. 1989; 89: 49–155.Google Scholar
CDC. Acting fast is key with necrotizing fasciitis. June 15, 2016. https://www.cdc.gov/features/necrotizingfasciitis/index.html. Accessed Aug 15, 2019.Google Scholar
Lareau, CR, Sawyer, GA, Wang, JH, Digiovanni, CW. Plantar and medial heel pain: diagnosis and management. J Am Acad Orthoped Surg. 2014; 22(6) 372–80.Google Scholar
Ashrafi, K, Bargues, MD, O'Neill, S, Mas-Coma, S. Fascioliasis: a worldwide parasitic disease of importance in travel medicine. Travel Med Infect Dis. 2014; 12: 636–49.Google Scholar
Mas-Coma, MS, Esteban, JG, Bargues, MD. Epidemiology of human fascioliasis: a review and proposed new classification. Bull World Health Organ. 1999; 77: 340–6.Google Scholar
Saba, R, Korkmaz, M, Inan, D, et al. Human fascioliasis. Clin Microbiol Infect. 2004; 10: 385–7.Google Scholar
Arjona, R, Riancho, JA, Aguado, JM, Salesa, R, Gonzalez-Macias, J. Fascioliasis in developed countries: a review of classic aberrant forms of the disease. Medicine. 1995; 74: 13–23.Google Scholar
American Academy of Sleep Medicine. The international classification of sleep disorders. 3rd ed. Chicago, IL; American Academy of Sleep Medicine; 2014.Google Scholar
Krasnianski, A, Bartl, M, Sanchez Juan, PJ, et al. Fatal familial insomnia: Clinical features and early identification. Ann Neurol. 2008; 63(5): 658.Google Scholar
Manetto, V, Medori, R, Cortelli, P, et al. Fatal familial insomnia: clinical and pathologic study of five new cases. Neurology. 1992; 42(2): 312.Google Scholar
Mastrianni, JA, Nixon, R, Layzer, R, et al. Prion protein conformation in a patient with sporadic fatal insomnia. New Engl J Med. 1999; 340: 1630–8.Google Scholar
Peng, B, Zhang, S, Dong, H, Lu, Z. Clinical, histopathological and genetic studies in a case of fatal familial insomnia with review of the literature. Int J Clin Exp Pathol. 2015; 8: 10171–7.Google Scholar
Gupta, A, Riley, CS. Fat embolism. Contin Educ Anaesth Crit Care Pain. 2007; 7(5): 148–51. DOI: 10.1093/bjaceaccp/mkm027.Google Scholar
Baulac, S, et al. Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31. Ann Neurol. 2001; 49(6): 786–92.Google Scholar
Ashwal, S, Swaiman, KF. Swaiman's pediatric neurology. 5th ed. Edinburgh: Saunders; 2012.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Bancroft, J, Loftus, J, Long, JS. Distress about sex: a national survey of women in heterosexual relationships. Arch Sex Behav. 2003; 32(3): 193–208.Google Scholar
Woo, JS, Brotto, LA, Gorzalka, BB. The relationship between sex guilt and sexual desire in a community sample of Chinese and Euro-Canadian women. J Sex Res. 2012; 49(2–3): 290–8.Google Scholar
Rutkove, S. Overview of lower extremity peripheral nerve syndromes. Dec 2014. Uptodate. Availabe from https://www.uptodate.com/contents/overview-of-upper-extremity-peripheral-nerve-syndromes?topicRef=5278&source=see_linkGoogle Scholar
Luscher, TF, Lie, JT, Stanson, AW, et al. Arterial fibromuscular dysplasia. Mayo Clin Proc. 1987; 62(10): 931–52.Google Scholar
Gregorius, J, Sips, GJ, Wilschut, J, Smit, JM. Neuroinvasive flavivirus infections. Rev Med Virol. 2012; 22: 69–87.Google Scholar
Mackenzie, JS, Gubler, DJ, Petersen, LR. Emerging flaviviruses: the spread and resurgence of Japanese encephalitis, West Nile and dengue viruses. Nature Med. 2004; 10: S98–S109.Google Scholar
Reiman, CA, Hayes, EB, Diguiseppi, C, et al. Epidemiology of neuroinvasive arboviral disease in the United States, 1999–2007. Am J Trop Med Hyg. 2008; 79: 974–9.Google Scholar
Gallagher, RC, et al. Folinic acid-responsive seizures are identical to pyridoxine-dependent epilepsy. Ann Neurol. 2009; 65(5): 550–6.Google Scholar
Tabarki, B, Thabet, F. [Vitamin-responsive epilepsies: an update]. Arch Pediatr. 2013; 20(11): 1236–41.Google Scholar
OMIM. Fragile X mental retardation syndrome (300624). 2006. www.omim.org/entry/300624. Accessed Aug 7, 2018.Google Scholar
Saul, RA, Tarleton, JC. FMR1-related disorders. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993–2016. Available from www.ncbi.nlm.nih.gov/books/NBK1384/. Accessed Aug 7, 2018.Google Scholar
Hagerman, RJ, Hagerman, PJ. The fragile X premutation: into the phenotypic fold. Curr Opin Genet Dev. 2002; 12: 278–83.Google Scholar
Hatton, DD, Sideris, J, Skinner, M, et al. Autistic behavior in children with fragile X syndrome: prevalence, stability, and the impact of FMRP. Am J Med Genet A. 2006; 140A: 1804–13.Google Scholar
de Vries, BB, van den Ouweland, AM, Mohkamsing, S, et al. Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group. Am J Hum Genet. 1997; 61: 660–7.Google Scholar
Coffee, B, Keith, K, Albizua, I, et al. Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA. Am J Hum Genet. 2009; 85: 503–14.Google Scholar
Bear, MF, Huber, KM, Warren, ST. The mGluR theory of fragile X mental retardation. Trends Neurosci. 2004; 27: 370–7.Google Scholar
Crawford, DC, Meadows, KL, Newman, JL, et al. Prevalence of the fragile X syndrome in African-Americans. Am J Med Genet. 2002; 110: 226–33.Google Scholar
Moro, F, Pisano, T, Bernardina, BD, et al. Periventricular heterotopia in fragile X syndrome. Neurology. 2006; 67: 713–5.Google Scholar
Berry-Kravis, E, et al. Fragile X-associated tremor/ataxia syndrome: clinical features, genetics, and testing guidelines. Mov Disord. 2007; 22(14): 2018–30.Google Scholar
Hagerman, PJ, Hagerman, RJ. Fragile X-associated tremor/ataxia syndrome. Ann. NY Acad Sci. 2015; 1338: 58–70. DOI: 10.1111/nyas.12693Google Scholar
Jacquemont, S, et al. Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates. Am J Hum Genet. 2003; 72(4): 869–78.Google Scholar
Delatycki, MB, Paris, DB, Gardner, RJ, et al. Clinical and genetic study of Friedreich ataxia in an Australian population. Am J Med Genet. 1999; 87: 168–74.Google Scholar
Bidichandani, SI, Delatycki, MB. Friedreich ataxia. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993–2016. Available from www.ncbi.nlm.nih.gov/books/NBK1281/Google Scholar
Al-Mahdawi, S, Pinto, RM, Varshney, D, et al. GAA repeat expansion mutation mouse models of Friedreich ataxia exhibit oxidative stress leading to progressive neuronal and cardiac pathology. Genomics. 2006; 88(5): 580–90.Google Scholar
Delatycki, MB, Knight, M, Koenig, M, et al. G130V, a common FRDA point mutation, appears to have arisen from a common founder. Hum Genet. 1999; 105: 343–6.Google Scholar
Tsou, AY, Paulsen, EK, Lagedrost, SJ, et al. Mortality in Friedreich ataxia. J Neurol Sci. 2011; 307: 46–9.Google Scholar
Mantovan, MC, Martinuzzi, A, Squarzanti, F, et al. Exploring mental status in Friedreich's ataxia: a combined neuropsychological, behavioral and neuroimaging study. Eur J Neurol. 2006; 13: 827–35.Google Scholar
Klopper, F, Delatycki, MB, Corben, LA, et al. The test of everyday attention reveals significant sustained volitional attention and working memory deficits in Friedreich ataxia. J Int Neuropsychol Soc. 2011; 17: 196–200.Google Scholar
Lynch, DR, Farmer, JM, Tsou, AY, et al. Measuring Friedreich ataxia: complementary features of examination and performance measures. Neurology. 2006; 66: 1711–6.Google Scholar
Lynch, DR, Perlman, SL, Meier, T. A phase 3, double-blind, placebo-controlled trial of idebenone in Friedreich ataxia. Arch Neurol. 2010; 67: 941–7.Google Scholar
Lynch, DR, Regner, SR, Schadt, KA, et al. Management and therapy for cardiomyopathy in Friedreich's ataxia. Expert Rev Cardiovasc Ther. 2012; 10: 767–77.Google Scholar
Lynch, DR, Willi, SM, Wilson, RB, et al. A0001 in Friedreich ataxia: biochemical characterization and effects in a clinical trial. Mov Disord. 2012; 27: 1026–33.Google Scholar
Gold, JA, Sher, Y, Maldonado, JR. Frontal lobe epilepsy: a primer for psychiatrists and a systematic review of psychiatric manifestations. Psychosomatics. 2016; 57: 445–64.Google Scholar
Matricardi, S, Deleo, F, Ragona, F, et al. Neuropsychological profiles and outcomes in children with new onset frontal lobe epilepsy. Epilepsy Behav. 2016; 55: 79–83.Google Scholar
Knopman, DS, Roberts, RO. Estimating the number of persons with frontotemporal lobar degeneration in the US population. J Mol Neurosci. 2011: 45: 330–5.Google Scholar
Gorno-Tempini, ML, Hillis, AE, Weintraub, S, et al. Classification of primary progressive aphasia and its variants. Neurology. 2011; 76: 1006–14.Google Scholar
van Blitterswijk, M, DeJesus-Hernandez, M, Rademakers, R. How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia: can we learn from other noncoding repeat expansion disorders? Curr Opin Neurol. 2012; 25: 689–700.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
LaFrance, WC, et al. Treating nonepileptic seizures. New York: Oxford University Press; 2015.Google Scholar
Bruce, BB, Newman, NJ. Functional visual loss. Neurol Clin North Am. 2010; 28(3): 789–802.Google Scholar
Lim, SA, Siatkowski, RM, Farris, BJ. Functional visual loss in adults and children. Ophthalmology. 2005; 112: 1821–8.Google Scholar
Sharma, RR. Fungal infections of the nervous system: Current perspective and controversies in management: Int J Surg. 2010; 8: 591–601.Google Scholar
Gavito-Higuera, J, Mullins, CB, Ramos-Duran, L, et al. Fungal infections of the central nervous system: a pictorial review. J Clin Imaging Sci. 2016; 6: 24.Google Scholar
Mathur, M, Johnson, CE, Sze, G. Fungal infections of the central nervous system. Neuroimag Clin N Am. 2012; 22(4): 609–32.Google Scholar
Citron, DM. Update on the taxonomy and clinical aspects of the genus Fusobacterium. Clin Infect Dis. 2002; 35(Suppl 1): S22–7.Google Scholar
Afra, K, Laupland, K, Leal, J, Lloyd, T, Gregson, D. Incidence, risk factors, and outcomes of Fusobacterium species bacteraemia. BCM Infect Dis. 2013; 13: 264.Google Scholar
Huggan, PJ, Murdoch, DR. Fusobacterial infections: clinical spectrum and incidence of invasive disease. J Infect. 2008; 57: 283–9.Google Scholar
Nohrström, E, Mattila, T, Pettilä, V, et al. Clinical spectrum of bacteraemic Fusobacterium infections: from septic shock to nosocomial bacteraemia. Scand J Infect Dis. 2011; 43(6–7): 463–70. DOI: 10.3109/00365548.2011.565071.Google Scholar
Hsieh, MJ, Chang, WN, Lui, CC, et al. Clinical characteristics of fusobacterial brain abscess. Jpn J Infect Dis. 2007; 60: 40–4.Google Scholar
Olson, KR, Freitag, SK, Johnson, JM, Branda, JA. Case 36–2014: an 18 year-old woman with fever, pharyngitis, and double vision. N Engl J Med. 2014; 371: 2018–27. DOI: 10.1056/NEJMcpc131001.Google Scholar
Parviz, M, et al. Disorders of GABA metabolism: SSADH and GABA-transaminase deficiencies. J Pediatr Epilepsy. 2014; 3(4): 217–27.Google Scholar
Tsuji, M, et al. A new case of GABA transaminase deficiency facilitated by proton MR spectroscopy. J Inherit Metab Dis. 2010; 33(1): 85–90.Google Scholar
Katirji, B, et al. Neuromuscular disorders in clinical practice. 2nd ed. New York: Springer; 2014. DOI: 10.1007/978-1-4614-6567-6.Google Scholar
Safavi-Abbasi, S, Di Rocco, F, Chantra, K, et al. Posterior cranial fossa gangliogliomas. Skull Base. 2007; 17(4): 253–64.Google Scholar
Song, JY, Kim, JH, Cho, YH, Kim, CJ, Lee, EJ. Treatment and outcomes for gangliogliomas: a single-center review of 16 patients. Brain Tumor Res Treat. 2014; 2(2): 49–55.Google Scholar
Zentner, J, Wolf, HK, Ostertun, B, et al. Gangliogliomas: clinical, radiological, and histopathological findings in 51 patients. J Neurol Neurosurg Psychiatr. 1994; 57(12): 1497–502.Google Scholar
The American Society for Surgery of the Hand. E-Hand.com (The electronic textbook of hand surgery). The American Society for Surgery of the Hand. www.eatonhand.com/. Accessed Aug 7, 2018.Google Scholar
Lee, JL, Kang, YK, Kim, TW, et al. Leptomeningeal carcinomatosis in gastric cancer. J Neurooncol. 2004; 66(1-2): 167–74.Google Scholar
Lisenko, Y, Kumar, AJ, Yao, J, Ajani, J, Ho, L. Leptomeningeal carcinomatosis originating from gastric cancer: report of eight cases and review of the literature. Am J Clin Oncol. 2003; 26(2): 165–70.Google Scholar
Schiff, D, O'Neill, BP, Suman, VJ. Spinal epidural metastasis as the initial manifestation of malignancy: clinical features and diagnostic approach. Neurology. 1997; 49(2): 452–6.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Haas, AP, Rodgers, PL, Herman, J. Suicide attempts among transgender and gender non-conforming adults: findings of the national transgender discrimination survey. New York/Los Angeles: American Foundation for Suicide Prevention/The Williams Institute; 2014.Google Scholar
Heylens, G, De Cuypere, G, Zucker, K, et al. (2012). Gender identity disorder in twins: a review of the case report literature. J Sex Med. 2012; 8(3): 751–7.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Beesdo, K, Pine, DS, Lieb, R, Wittchen, HU. Incidence and risk patterns of anxiety and depressive disorders and categorization of generalized anxiety disorder. Arch Gen Psychiatry. 2010; 67(1): 47–57.Google Scholar
Kessler, RC, Petukhova, M, Sampson, NA, et al. Twelve-month and lifetime prevalence and lifetime morbid risk of anxiety and mood disorders in the US. Int J Methods Psychiatr Res. 2012; 21(3): 169–84.Google Scholar
Lewis-Fernández, R, Hinton, DE, Laria, AJ, et al. Culture and the anxiety disorders: recommendations for DSM-V. Depress Anxiety. 2010; 27(2): 212–29.Google Scholar
Hauser, WA, Annegers, JF, Kurland, LT. Incidence of epilepsy and unprovoked seizures in Rochester, Minnesota: 1935–1984. Epilepsia. 1993; 34(3): 453–68.Google Scholar
Ropper, A., et al. Adams and Victor's principles of neurology. 9th ed. New York: McGraw-Hill Medical; 2009.Google Scholar
Abrey, LE. Neurologic complications of female reproductive tract cancer. In Schiff, D, Kesari, S, Wen, PY, eds. Current Clinical Oncology: Cancer Neurology in Clinical Cancer. Totowa, NJ: Humana Press; 2008. pp. 449–58.Google Scholar
Packer, RJ, Cohen, BH, Coney, K. Intracranial germ cell tumors. Oncologist. 2000; 5: 312–20.Google Scholar
Rosenfeld, MR, Dalmau, J. Update on paraneoplastic neurologic disorders. Oncologist. 2010; 15: 603–17.Google Scholar
Jain, S, Sam, A, Yohannan, DI, et al. Giant cell tumor of the temporal bone: an unusual presentation. Clin Neurol Neurosurg. 2013; 115(5): 646–8.Google Scholar
Wong, RH, Thakral, B, Watkin, WG, et al. Intracranial, intra-axial metastatic giant cell tumor of bone: case report and review of literature. Clin Neurol Neurosurg. 2014; 117: 40–3.Google Scholar
Kass, MA, Heuer, DK, Higginbotham, EJ, et al. The Ocular Hypertension Treatment Study: a randomized trial determines that topical ocular hypotensive medication delays or prevents the onset of primary open-angle glaucoma. Arch Ophthalmol. 2002: 120(6): 701–13; discussion 829–30.Google Scholar
Tielsch, JM, Katz, J, Sommer, A, Quigley, HA, Javitt, JC. Hypertension, perfusion pressure, and primary open-angle glaucoma: a population-based assessment. Arch Ophthalmol. 1995: 113(2): 216–21.Google Scholar
Artigas, J, Cervos-navarro, J, Iglesias, JR, Ebhardt, G. Gliomatosis cerebri: clinical and histological findings. Clin Neuropathol. 1985; 4(4): 135–48.Google Scholar
Grisold, W, Soffietti, R, eds. Neuro-Oncology: Part I. Vol 104. 1st ed. Amsterdam: Elsevier; 2012.Google Scholar
Kim, DG, Yang, HJ, Park, IA, et al. Gliomatosis cerebri: clinical features, treatment, and prognosis. Acta Neurochir (Wien). 1998; 140(8): 755–62.Google Scholar
Kumar, K, Ahmed, R, Bajantri, B, et al. Tumors presenting as multiple cranial nerve palsies. Case Rep Neurol. 2017; 9(1): 54–61.Google Scholar
Larner, JM, Hahn, SS, Spaulding, CA, Constable, WC. Glomus jugulare tumors: long-term control by radiation therapy. Cancer. 1992; 69(7): 1813–7.Google Scholar
Blumenfeld, A, Nikolskaya, G. Glossopharyngeal neuralgia. Curr Pain Headache Rep. 2013; 17: 343.Google Scholar
Elias, J, Kuniyoshi, R, Carloni, WV, et al. Glossopharyngeal neuralgia associated with cardiac syncope. Arq Bras Cardiol. 2002; 78(5): 510–9.Google Scholar
Rey-Dios, R, Cohen-Gadol, AA. Current neurosurgical management of glossopharyngeal neuralgia and technical nuances for microvascular decompression surgery. Neurosurg Focus. 2013; 43(3): E8.Google Scholar
Singleton, AO. Glossopharyngeal neuralgia and its surgical relief. Ann Surg. 1926; 83(3): 338–44.Google Scholar
Djurendic-Brenesel, M, Stojiljkovic, G, Pilija, V. Fatal intoxication with toluene due to inhalation of glue. J Forensic Sci. 2016; 61(3): 875–8. PMID: 27122437.Google Scholar
Smith, AG, Albers, JW. n-Hexane neuropathy due to rubber cement sniffing. Muscle Nerve. 1997; 20(11): 1445–50. PMID:9342162.Google Scholar
Arino, H, et al. Paraneoplastic neurological syndromes and glutamic acid decarboxylase antibodies. JAMA Neurol. 2015; 72(8): 874–81.Google Scholar
Baizabal-Carvallo, JF, Jankovic, J. Stiff-person syndrome: insights into a complex autoimmune disorder. J Neurol Neurosurg Psychiatry. 2015; 86(8): 840–8.Google Scholar
Ryvlin, P, et al. From first unprovoked seizure to newly diagnosed epilepsy. Progress in epileptic disorders series. Montrouge: John Libbey Eurotex; 2007.Google Scholar
Gras, D, et al. GLUT1 deficiency syndrome: an update. Rev Neurol (Paris). 2014; 170(2): 91–9.Google Scholar
Heshin-Bekenstein, M, et al. Gradenigo's syndrome: Is Fusobacterium different? Two cases and review of literature. Int J Pediatr Otorhinolaryngol. 2014; 78(1): 166–9.Google Scholar
Holle, JU, Gross, WL. Neurological involvement in Wegener's granulomatosis. Curr Opin Rheumatol. 2011; 23(1): 7–11.Google Scholar
Kubaisi, B, Samra, KA, Foster, CS. Granulomatosis with polyangiitis (Wegener's disease): An updated review of ocular disease manifestations. Intractable Rare Dis Res. 2016; 5(2): 61–9.Google Scholar
Mercimek-Mahmutoglu, S, Salomons, GS. Creatine deficiency syndromes. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle, WA: University of Washington, Seattle; 1993.Google Scholar
Kouhen, F, Afif, M, El Kabous, M, et al. [Brain metastasis of endometrial cancer: report of a case and review of literature]. Pan Afr Med J. 2015; 20: 68.Google Scholar
Lesniak, MS, Olivi, A. Brain metastases from gynecologic cancers. In Intracranial metastases: current management strategies. Chichester: Wiley; 2008. pp. 331–50.Google Scholar
Ogawa, K, Yoshii, Y, Aoki, Y, et al. Treatment and prognosis of brain metastases from gynecological cancers. Neurol Med Chir (Tokyo). 2008; 48(2): 57–62.Google Scholar
Livorsi, DJ, MacNeil, JR, Cohn, AC, et al. Invasive Haemophilus influenzae in the United States, 1999–2008: epidemiology and outcomes. J Infect. 2012; 65: 496–504.Google Scholar
Centers for Disease Control and Prevention. Haemophilus influenzae type B. In Epidemiology and prevention of vaccine-preventable diseases. 13th ed. Atlanta, GA: Centers for Disease Control and Prevention; 2015. pp. 119–33.Google Scholar
Agrawal, A, Murphy, TF. Haemophilus influenzae infections in the H. influenzae type b conjugate vaccine era. J Clin Microbiol. 2011; 49: 3728–32.Google Scholar
Cugati, G, Singh, M, Pande, A, Ramamurthi, R, Vasudevan, MC. Hand Schuller Christian disease. Indian J Med Paediatr Oncol. 2011; 32(3): 183–4.Google Scholar
Jacquet, G, Plouvier, E, Billerey, C, Godard, J, Steimle, R. [Hand-Schüller-Christian disease with tumor localization in the posterior fossa]. Presse Med. 1988; 17(17): 855–7.Google Scholar
Khristov, V, Manov, A, Apostolov, P, Kolebinov, N, Nachev, S. [Long-term observation of a case of Hand-Schüller-Christian disease]. Vutr Boles. 1989; 28(5): 87–91.Google Scholar
Zaletel, K, Gaberšček, S. Hashimoto's thyroiditis: from genes to the disease. Curr Genom. 2011; 12(8): 576–88.Google Scholar
Ju, C, Zhang, L. Diplopia in a patient with Hashimoto's thyroiditis: a case report and literature review. Medicine (Baltimore). 2017; 96(26): e7330.Google Scholar
Mocellin, R, Walterfang, M, Velakoulis, D. Hashimoto's encephalopathy: epidemiology, pathogenesis and management. CNS Drugs. 2007; 21(10): 799–811.Google Scholar
Souza, PV, Bortholin, T, Pinto, WB, Santos, AJ. Progressive hearing loss and cerebellar ataxia in anti-Ma2-associated autoimmune encephalitis. Arq Neuropsiquiatr. 2017; 75(1): 74–5. https://dx.doi.org/10.1590/0004-282x20160169Google Scholar
Piantanida, E, Gallo, D, Lombardi, V, et al. Pituitary apoplexy during pregnancy: a rare, but dangerous headache. J Endocrinol Invest. 2014; 37(9): 789–97.Google Scholar
Schoen, JC, Campbell, RL, Sadosty, AT. Headache in pregnancy: an approach to emergency department evaluation and management. West J Emerg Med. 2015; 16(2): 291–301.Google Scholar
Vetvik, KG, MacGregor, EA. Sex differences in the epidemiology, clinical features, and pathophysiology of migraine. Lancet Neurol. 2017; 16(1): 76–87.Google Scholar
Von Wald, T, Walling, AD. Headache during pregnancy. Obstet & Gyn Survey. 2002; 57(3): 179–85.Google Scholar
Acikalin, MF, Oner, U, Tel, N, Paşaoğlu, O, Altinel, F. Supratentorial hemangioblastoma: a case report and review of the literature. Arch Pathol Lab Med. 2003; 127(9): e382–4.Google Scholar
Lonser, RR, Butman, JA, Huntoon, K, et al. Prospective natural history study of central nervous system hemangioblastomas in von Hippel-Lindau disease. J Neurosurg. 2014; 120(5): 1055–62.Google Scholar
Na, JH, Kim, HS, Eoh, W, et al. Spinal cord hemangioblastoma: diagnosis and clinical outcome after surgical treatment. J Korean Neurosurg Soc. 2007; 42(6): 436–40.Google Scholar
Alarcon, F, Zijlmans, JC, Duenas, G, Cevallos, N. Post-stroke movement disorders: report of 56 patients. J Neurol Neurosurg Psychiatry. 2004; 75: 1568–74.Google Scholar
Ching, LP, Chin, KP, Wah, ESA. Hyperglycemia-associated hemichorea-hemiballism: the spectrum of clinical presentation. Intern Med. 2015; 54(15): 1881–4.Google Scholar
Ghika-Schmid, F, Ghika, J, Regli, F, Bogousslavsky, J. Hyperkinetic movement disorders during and after acute stroke: the Lausanne Stroke Registry. J Neurol Sci. 1997; 146: 109–16.Google Scholar
Handley, A, Medcalf, P, Hellier, K, Dutta, D. Movement disorders after stroke. Age Ageing. 2009; 38: 260–66.Google Scholar
Kim, JS. Delayed onset mixed involuntary movements after thalamic stroke. Clinical, radiological and pathophysiological findings. Brain. 2001; 124: 299–309.Google Scholar
Bordini, C, Antonaci, F, Stovner, LJ, Schrader, H, Sjaastad, O. “Hemicrania continua”: a clinical review. Headache. 1991; 31: 20–6.Google Scholar
Cittadini, E, Goadsby, PJ. Update on hemicrania continua. Curr Pain Headache Rep. 2011; 15: 51–6.Google Scholar
Medina, JL, Diamond, S. Cluster headache variant: spectrum of a new headache syndrome. Arch Neurol. 1981; 38: 705–9.Google Scholar
Tan, NC, et al. Hemifacial spasm and involuntary facial movements. QJM. 2002; 95(8): 493–500.Google Scholar
Kim, HJ, Jeon, BS, Lee, KW. Hemimasticatory spasm associated with localized scleroderma and facial hemiatrophy. Arch Neurol. 2000; 57(4): 576–80.Google Scholar
Buchman, AS, Goetz, CG, Klawans, HL. Hemiparkinsonism with hemiatrophy. Neurology. 1988; 38: 527–30.Google Scholar
Giladi, N, Burke, RE, Kostic, V, et al. Hemiparkinsonism-hemiatrophy syndrome: clinical and neuroradiologic features. Neurology. 1990; 40(11): 1731–4.Google Scholar
Klawans, HL. Hemiparkinsonism as a late complication of hemiatrophy: a new syndrome. Neurology. 1981; 31: 625–8.Google Scholar
Wijemanne, S, Jankovic, J. Hemiparkinsonism-hemiatrophy syndrome. Neurology. 2007; 69(16): 1585–94.Google Scholar
Noris, M, Remuzzi, G. Hemolytic uremic syndrome. J Am Soc Nephrol JASN. 2005; 16: 1035–50.Google Scholar
Loirat, C, Frémeaux-Bacchi, V. Atypical hemolytic uremic syndrome. Orphanet J Rare Dis. 2011; 6: 60.Google Scholar
Inamasu, J, Nakamura, Y, Saito, R, et al. Hemorrhagic brain abscess in infective endocarditis. Emerg Radiol. 2001; 8: 308. https://doi.org/10.1007/PL00011929.Google Scholar
Thamburaj, K, Agarwal, AK, Sabat, SB, Nguyen, DT. Hemorrhage in the wall of pyogenic brain abscess on susceptibility weighted MR sequence: a report of 3 cases. Case Rep Radiol. 2014: Article ID 907584. https://doi.org/10.1155/2014/907584.Google Scholar
Berger, C, et al. Hemorrhagic transformation of ischemic brain tissue: asymptomatic or symptomatic? Stroke. 2001; 32: 1330–5.Google Scholar
Zhang, J, et al. Hemorrhagic transformation after cerebral infarction: current concepts and challenges. Ann Transl Med. 2014; 2(8): 81.Google Scholar
Kondziolka, D, Bernstein, M, Resch, L, et al. Significance of hemorrhage into brain tumors: clinicopathological study. J Neurosurg. 1987; 67(6): 852–7.Google Scholar
Lieu, AS, Hwang, SL, Howng, SL, Chai, CY. Brain tumors with hemorrhage. J Formos Med Assoc. 1999; 98(5): 365–7.Google Scholar
Wakai, S, Yamakawa, K, Manaka, S, Takakura, K. Spontaneous intracranial hemorrhage caused by brain tumor: its incidence and clinical significance. Neurosurgery. 1982; 10(4): 437–44.Google Scholar
Bérubé, MD, Blais, N, Lanthier, S. Neurological manifestations of Henoch-Schonlein purpura. Handb Clin Neurol. 2014; 120: 1101–11. DOI: 10.1016/B978-0-7020-4087-0.00074-7.Google Scholar
Caplan, LR, ed. Uncommon causes of stroke. 2nd ed. Cambridge, UK: Cambridge University Press; 2010.Google Scholar
Garzoni, L, et al. Nervous system dysfunction in Henoch-Schonlein syndrome: systematic review of the literature. Rheum (Oxford). 2009; 48(12): 1524–9.Google Scholar
Alving, BM. How I treat heparin-induced thrombocytopenia and thrombosis. Blood. 2003; 101: 31–7.Google Scholar
Datar, S, Wijdicks, EF. Neurologic manifestations of acute liver failure. Handb Clin Neurol. 2014; 120: 645–59.Google Scholar
Fridman, V, Galetta, SL, Pruitt, AA, Levine, JM. MRI findings associated with acute liver failure. Neurology. 2009; 72(24): 2130–1.Google Scholar
White, H. Neurologic manifestations of acute and chronic liver disease. Continuum (Minneap Minn). 2014; 20(3 Neurology of Systemic Disease): 670–80.Google Scholar
Wijdicks, EF, Hocker, SE. Neurologic complications of liver transplantation. Handb Clin Neurol. 2014; 121: 1257–66.Google Scholar
Wijdicks, EF, Plevak, DJ, Wiesner, RH, Steers, JL. Causes and outcome of seizures in liver transplant recipients. Neurology. 1996; 47(6): 1523–30.Google Scholar
Cocito, D, Maule, S, Paolasso, I, et al. High prevalence of neuropathies in patients with end-stage liver disease. Acta Neurol Scand. 2010; 122(1): 36–40.Google Scholar
Ferro, JM, Oliveira, S. Neurologic manifestations of gastrointestinal and liver diseases. Curr Neurol Neurosci Rep. 2014; 14(10): 487.Google Scholar
Sureka, B, Bansal, K, Patidar, Y, et al. Neurologic manifestations of chronic liver disease and liver cirrhosis. Curr Probl Diagn Radiol. 2015; 44(5): 449–61.Google Scholar
Utku, U, Asil, T, Balci, K, et al. Hepatic myelopathy with spastic paraparesis. Clin Neurol Neurosurg. 2005; 107(6): 514–16.Google Scholar
White, H. Neurologic manifestations of acute and chronic liver disease. Continuum (Minneap Minn). 2014; 20(3 Neurology of Systemic Disease): 670–80.Google Scholar
Wijdicks, EF, Hocker, SE. Neurologic complications of liver transplantation. Handb Clin Neurol. 2014; 121: 1257–66.Google Scholar
Sellner, J, Steiner, I. Neurologic complications of hepatic viruses. Handb Clin Neurol. 2014; 123: 647–61.Google Scholar
Acharya, JN, Pacheco, VH. Neurologic complications of hepatitis C. Neurologist. 2008; 14(3): 151–6.Google Scholar
Sellner, J, Steiner, I. Neurologic complications of hepatic viruses. Handb Clin Neurol. 2014; 123: 647–61.Google Scholar
Thames, AD, Castellon, SA, Singer, EJ, et al. Neuroimaging abnormalities, neurocognitive function, and fatigue in patients with hepatitis C. Neurol Neuroimmunol Neuroinflamm. 2015; 2(1): e59.Google Scholar
Yong, HT, Son, R. Hepatitis A virus: a general overview. Int Food Res J. 2009; 16: 455–67.Google Scholar
Lee, JJ, Kang, K, Park, JM, Kwon, O, Kim, BK. Encephalitis associated with acute hepatitis A. J Epilepsy Res. 2011; 1: 27–8.Google Scholar
Bromberg, K, NewHall, DN, Peter, G. Hepatitis A and meningoencephalitis. JAMA. 1982; 247: 815.Google Scholar
Mathew, T, Aroor, S, Nadig, R, Sarma, G. Focal meningoencephalitis of hepatitis A: a clinico-radiologic picture. Pediatr Neurol. 2012; 47: 222–3.Google Scholar
Chonmaitree, P, Methawasin, K. Transverse myelitis in acute hepatitis A infection: the rare co-occurrence of hepatology and neurology. Case Rep Gastroenterol. 2016; 10: 44–9.Google Scholar
Stubgen, JP. Neuromuscular complications of hepatitis A virus infection and vaccines. J Neurol. Sci. 2011; 300: 2–8.Google Scholar
Guillevin, L, Lhote, F, Cohen, P, et al. Polyarteritis nodosa related to hepatitis B virus. A prospective study of long term observation of 41 patients. Medicine. 1995; 74: 238–53.Google Scholar
Guillevin, L, Mahr, A, Callard, P, et al. Hepatitis B virus-associated polyarteritis nodosa: clinical characteristics, outcome and impact of treatment in 115 patients. Medicine. 2005; 84: 313–22.Google Scholar
Wada, Y, Yanagihara, C, Nishimura, Y, Oka, N. Hepatitis B virus-related vasculitis manifesting as severe neuropathy following influenza vaccination. Clin Neurol Neurosurg. 2008; 110: 750–2.Google Scholar
Verma, R, Lalla, R, Babu, S. Mononeuritis multiplex and painful ulcers as the initial manifestation of hepatitis B infection. BMJ Case Rep. 2013: 1–4. DOI: 10.1136/bcr-2013- 009666Google Scholar
Fleischer, RD, Lok, ASF. Myopathy and neuropathy with nucleo(t)ide analog therapy for hepatitis B. J Hepatol. 2009; 51: 787–91.Google Scholar
Stubgen, JP. Neuromuscular disorders associated with hepatitis B virus infection. J Clin Neuromusc Dis. 2011; 13: 26–34.Google Scholar
Baig, S, Alamgir, M. The extrahepatic manifestation of hepatitis B virus. J Coll Physicians Surg Pak. 2008; 18: 451–7.Google Scholar
Mathew, S, Faheem, M, Ibrahim, SM, et al. Hepatitis C virus and neurological damage. World J Hepatol. 2016; 8: 545–56.Google Scholar
Adinolfi, LE, Nevola, R, Lus, G, et al. Chronic hepatitis C virus infection and neurological and psychiatric disorders: An overview. World J Gastroenterol. 2015; 21: 2269–80.Google Scholar
Monaco, S, Ferrari, S, Gajofatto, A, Zanusso, G, Mariotto, S. HCV-related nervous system disorders. Clin Developmental Immunol. 2012; 2012: 236148. DOI: 10.1155/236148.Google Scholar
Hehir, MK 2nd, Logigian, EL. Infectious neuropathies. Continuum (Minneap Minn). 2014; 20(5 Peripheral Nervous System Disorders): 1274–92.Google Scholar
Stubgen, JP. Neuromuscular disorders associated with hepatitis B virus infection. J Clin Neuromuscul Dis. 2011; 13(1): 26–37.Google Scholar
Stubgen, JP. Neuromuscular diseases associated with chronic hepatitis C virus infection. J Clin Neuromuscul Dis. 2011; 13(1): 14–25.Google Scholar
Katirji, B, Kaminski, HJ, Ruff, RL. Neuromuscular disorders in clinical practice. 2nd ed. New York: Springer-Verlag New York; 2014.Google Scholar
Mathis, S, Goizet, C, Tazir, M, et al. Charcot-Marie-Tooth diseases: an update and some new proposals for the classification. J Med Genet. 2015; 52(10): 681–90.Google Scholar
Miller, LJ, Saporta, AS, Sottile, SL, et al. Strategy for genetic testing in Charcot-Marie-disease. Acta Myol. 2011; 30(2): 109–16.Google Scholar
Plante-Bordeneuve, V, Said, G. Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy. Muscle Nerve. 2002; 26(5): 608–21.Google Scholar
US Department of Health and Human Services. Genetics Home Reference. Refsum disease. 2016. Available from https://ghr.nlm.nih.gov/condition/refsum-disease. Accessed Aug 24, 2018.Google Scholar
Fink, JK. Hereditary spastic paraplegia: clinical principles and genetic advances. Semin Neurol. 2014; 34(3): 293–305.Google Scholar
Katirji, B, Kaminski, HJ, Ruff, RL. Neuromuscular disorders in clinical practice. 2nd ed. New York: Springer-Verlag New York; 2014.Google Scholar
Salinas, S, Provkakis, C, Crosby, A, Warner, TT. Hereditary spastic paraplegia: Clinical features and pathogenetic mechanisms. Lancet Neurol. 2008; 7(12): 1127–38.Google Scholar
Windsor, RE. Frequency of asymptomatic cervical disc protrusion. Cervical disc injuries. eMedicine; 2006. https://emedicine.medscape.com/article/93635-overview. Accessed Aug 14, 2018.Google Scholar
Sahrakar, K. Lumbar disc disease. Medscape. Updated Dec 12, 2017. https://emedicine.medscape.com/article/249113-overview. Accessed Aug 24, 2018.Google Scholar
Enevoldson, T. Recreational drugs and their neurological consequences. J Neurol Neurosurg Psychiatry. 2004; 75: iii9–iii15. DOI: 10.1136/jnnp.2004.045732.Google Scholar
Habal, R. Heroin toxicity. Medscape. Updated Dec 26, 2017. http://emedicine.medscape.com/article/166464-overview#a6. Accessed Aug 14, 2018.Google Scholar
Neuromuscular Disease Center. Myotoxic myopathy. http://neuromuscular.wustl.edu/mother/myotox.htm. Accessed Aug 14, 2018.Google Scholar
Pascual Calvet, J, Pou, A, Pedro-Botet, J, Gutiérrez Cebollada, J. [Non-infective neurologic complications associated to heroin use.] Arch Neurobiol (Madr). 1989; 52(Suppl 1): 155–61.Google Scholar
The Discovery House. The truth about marijuana abuse vs. heroin addiction. April 20, 2015. https://www.linkedin.com/pulse/truth-marijuana-abuse-vs-heroin-addiction-the-discovery-house. Accessed Aug 14, 2018.Google Scholar
American Addiction Centers. Heroin withdrawal timeline, symptoms and treatment.http://americanaddictioncenters.org/withdrawal-timelines-treatments/heroin/. Accessed Aug 8, 2018.Google Scholar
Options Behavioral Health System. Heroin abuse & addiction treatment. 2018. www.optionsbehavioralhealthsystem.com/addiction/heroin. Accessed Aug 24, 2018.Google Scholar
Bradley, H, Markowitz, LE, Gibson, T, McGuillan, GM. Seroprevalence of herpes virus type 1 and 2 – United States, 1999–2010. J Infect Dis. 2014; 209(3): 325–33.Google Scholar
Bradshaw, MJ, Venkatesan, A. Herpes simplex virus-1 encephalitis in adults: pathophysiology, diagnosis, and management. Neurotherapeutics. 2016; 13(3): 493–508.Google Scholar
Singh, TD, Fugate, JE, Rabinstein, AA. The spectrum of acute encephalitis: causes, management, and predictors of outcome. Neurology. 2015; 84: 359–66.Google Scholar
Bradley, H, Markowitz, LE, Gibson, T, McGuillan, GM. Seroprevalence of herpes virus type 1 and 2 – United States, 1999–2010. J Infect Dis. 2014; 209(3): 325–33.Google Scholar
Berger, RJ, Houff, S. Neurologic complications of herpes simplex virus type 2 infection. Arch Neurol. 2008; 65: 596–600.Google Scholar
Zis, P, Stritsou, P, Angelidakis, P, Tavernarakis, A. Herpes simplex virus type 2 encephalitis as a cause of ischemic stroke: case report and systematic review of the literature. J Stroke Cerebrovasc Dis. 2016; 25(2): 335–9.Google Scholar
Gilden, D, Nagel, M, Cohrs, R, Mahalingam, R, Baird, N. Varicella zoster virus in the nervous system. F1000Res 2015a; 4. PMID 26918131Google Scholar
Whitley, RJ. Varicella-zoster virus. In Mandell, GL, Bennett, JE, Dolin, R, eds. Principles and practice of infectious diseases. 4th ed. New York: Churchill-Livingstone; 1995. pp. 1345–51.Google Scholar
Agency for Toxic Substances and Disease Registry. Public Health Statement for n-Hexane. Jan 21, 2015. Available from: https://www.atsdr.cdc.gov/phs/phs.asp?id=391&tid=68. Accessed Aug 30, 2018.Google Scholar
Committee on Acute Exposure Guideline Levels; Committee on Toxicology; Board on Environmental Studies and Toxicology; Division on Earth and Life Studies; National Research Council. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Hexane: acute exposure guideline levels. Vol 14. Washington, DC: National Academies Press (US); Apr 26, 2013. Available from: https://www.ncbi.nlm.nih.gov/books/NBK201488/. Accessed Aug 30, 2018.Google Scholar
Brown, GD, Swanson, EA, Nercessian, OA. Neurologic injuries after total hip arthroplasty. Am J Orthop (Belle Mead NJ). 2008; 37(4): 191–7.Google Scholar
Schmalzried, TP, Noordin, S, Amstutz, HC. Update on nerve palsy associated with total hip replacement. Clin Orthop Relat Res. 1997; 344: 188–206.Google Scholar
Hariri, OR, Minasian, T, Quadri, SA, et al. Histoplasmosis with deep CNS involvement: case presentation with discussion and literature review. J Neurol Surg Rep. 2015; 76(1): e167–72. DOI: 10.1055/s-0035-1554932.Google Scholar
Harris, EA, Roos, KL. Medlink Neurology. Histoplasmosis of the nervous system. Originally released Aug 11, 2005; last updated Jan 4, 2016. www.medlink.com/article/histoplasmosis_of_the_nervous_system. Accessed Aug 30, 2018.Google Scholar
Benjamin, LA. HIV infection and stroke: current perspectives and future directions. Lancet Neurol. 2012; 11(10): 878–90.Google Scholar
Maartens, G, et al. HIV infection: epidemiology, pathogenesis, treatment, and prevention. Lancet. 2014; 384(9939): 258–71.Google Scholar
NIH. Guidelines for the use of antiretroviral agents in adults and adolescents living with HIV. Updated Oct 17, 2017. https://aidsinfo.nih.gov/guidelines/html/1/adult-and-adolescent-arv-guidelines/31/adverse-effects-of-arv. Accessed Aug 16, 2018.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Grisham, JR, Frost, RO, Steketee, G, et al. Age of onset of compulsive hoarding. J Anxiety Disord. 2006; 20(5): 675–86.Google Scholar
Landau, D, Iervolino, AC, Pertusa, A, et al. Stressful life events and material deprivation in hoarding disorder. J Anxiety Disord. 2011; 25(2): 192–202.Google Scholar
Nordsletten, AE, Reichenberg, A, Hatch, SL, et al. Epidemiology of hoarding disorder. Br J Psychiatry. 2013; 203: 445.Google Scholar
Pertusa, A, Frost, RO, Fullana, MA, et al. Refining the diagnostic boundaries of compulsive hoarding: a critical review. Clin Psychol Rev. 2010; 30(4): 371–86.Google Scholar
Samuels, J, Bienvenu, OJ 3rd, Pinto, A, et al. Hoarding in obsessive-compulsive disorder: results from the OCD Collaborative Genetics Study. Behav Res Ther. 2007; 45(4): 673–86.Google Scholar
Bahatia, P, Singh, N. Homocysteine excess: delineating the possible mechanism of neurotoxicity and depression. Fundam Clin Pharmacol. 2015; 29(6): 522–8.Google Scholar
Kang, SS, Wong, PW, Susmano, A, et al. Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease. Am J Hum Genet. 1991; 48(3): 536–45.Google Scholar
Yoo, JH, Chung, CS, Kang, SS. Relation of plasma homocysteine to cerebral infarction and cerebral atherosclerosis. Stroke. 1998; 29(12): 2478–83.Google Scholar
Bahatia, P, Singh, N. Homocysteine excess: delineating the possible mechanism of neurotoxicity and depression. Fundam Clin Pharmacol. 2015; 29(6): 522–8.Google Scholar
Walter, J, Jahnke, N. Newborn screen for homocystinuria. Cochrane Database System Rev. Oct 2015. DOI: 10.1002/14651858.CD008840.pub4.Google Scholar
Yoo, JH, Chung, CS, Kang, SS. Relation of plasma homocysteine to cerebral infarction and cerebral atherosclerosis. Stroke. 1998; 29(12): 2478–83.Google Scholar
Liedholm, LJ, Eeg-Olofsson, O, Ekenberg, BE, Nicolaysen, RB, Torbergsen, T. Acute postasthmatic amyotrophy (Hopkins' syndrome). Muscle Nerve. 1994; 17(7): 769–72.Google Scholar
Matsuzaki, T, Nakagawa, M, Nagai, M, et al. HTLV-I-associated myelopathy (HAM)/tropical spastic paraparesis (TSP) with amyotrophic lateral sclerosis-like manifestations. J Neurovirol. 2000; 6(6): 544–8.Google Scholar
Oger, J, Reder, AT. HTLV-1 associated myelopathy. Medlink Neurology. Originally released April 3, 2001; last updated June 9, 2016. www.medlink.com/article/htlv-1_associated_myelopathy. Accessed Aug 16, 2018.Google Scholar
Olindo, S, Cabre, P, Lezin, A, et al. Natural history of human T-lymphotropic virus 1-associated myelopathy: a 14-year follow-up study. Arch Neurol. 2006; 63(11): 1560–6. PMID 17101824.Google Scholar
Agut, H. Deciphering the clinical impact of acute human herpesvirus 6 (HHV-6) infections. J Clin Virol. 2011; 52(3): 164–71.Google Scholar
Pellett, PE, Ablashi, DV, Ambros, PF, et al. Chromosomally integrated human herpesvirus 6: questions and answers. Rev Med Virol. 2012; 22(3): 144–55.Google Scholar
Wheeless, CR. Wheeless' textbook of orthopaedics. [Internet] Duke University Medical Center's Division of Orthopedic Surgery and Data Trace Internet Publishing, LLC; 2015. Available from www.wheelessonline.com/. Accessed Aug 30, 2018.Google Scholar
Hout, P, Levesque, M, Parent, A. The fate of striatal dopaminergic neurons in Parkinson's disease and Huntington's chorea. Brain. 2007; 130(1): 222–32.Google Scholar
Nopoulos, PC, Aylward, EH, Ross, CA, et al. Cerebral cortex structure in prodromal Huntington disease. 2010; 40(3): 544–54.Google Scholar
Pringsheim, T, Wiltshire, K, Day, L, et al. The incidence and prevalence of Huntington's disease: a systematic review and meta-analysis. Mov Disord. 2012; 27(9): 1083–91.Google Scholar
Salpietro, V, Polizzi, A, Di Rosa, G, et al. Adrenal disorders and the paediatric brain: pathophysiological considerations and clinical implications. Int J Endocrinol. 2014; 2014: 282489.Google Scholar
Sharma, V, Borah, P, Basumatary, LJ, et al. Myopathies of endocrine disorders: a prospective clinical and biochemical study. Ann Indian Acad Neurol. 2014; 17: 298–302.Google Scholar
Sweeney, AT, Griffing, GT. Pheochromocytoma. eMedicine. August 2, 2011. Available from https://emedicine.medscape.com/article/124059-overview. Accessed Aug 30, 2018.Google Scholar
DeWolfe, JL, Knowlton, RC, Beasley, MT, et al. Hyperammonemia following intravenous valproate loading. Epilepsy Res. 2009; 85(1): 65–71.Google Scholar
Haeberle, J, Boddaert, N, Burlina, A, et al. Suggested guidelines for the diagnosis and management of urea cycle disorders. Orphanet J Rare Dis. 2012; 7(1): 32.Google Scholar
Lichter-Konecki, U, Mangin, JM, Gordish-Dressman, H, Hoffman, EP, Gallo, V. Gene expression profiling of astrocytes from hyperammonemic mice reveals altered pathways for water and potassium homeostasis in vivo. Glia. 2008; 56(4): 365–77.Google Scholar
Durrington, HJ, Flubacher, M. Initial oxygen management in patients with an exacerbation of chronic obstructive pulmonary disease. QJM. 2005; 98(7): 499–504.Google Scholar
Pal, P, Chen, R. Breathing and the nervous system. In Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. London, UK: Elsevier; 2014. pp. 3–23.Google Scholar
Roufosse, FE, Goldman, M, Cogan, E. Hypereosinophilic syndromes. Orphanet J Rare Dis. 2007; 2: 37.Google Scholar
Lee, D, Ahn, T-B. Central nervous system involvement of hypereosinophilic syndrome: a report of 10 cases and a literature review. J Neurol Sci. 2014; 347: 281–7.Google Scholar
Ducat, L, Philipson, LH, Anderson, BJ. The mental health comorbidities of diabetes. JAMA. 2014; 312(7): 691–2.Google Scholar
Dyck, PJ, Kratz, KM, Karnes, JL, et al. The prevalence by staged severity of various types of diabetic neuropathy, retinopathy, and nephropathy in a population-based cohort: The Rochester Diabetic Neuropathy Study. Neurology. 1993; 43: 817.Google Scholar
Edwards, JL, Vincent, AM, Cheng, HT, Feldman, EL. Diabetic neuropathy: mechanisms to management. Pharmacol Ther. 2008; 120(1): 1.Google Scholar
Ewing, DJ. Recent advances in the non-invasive investigation of diabetic autonomic neuropathy. In Bannister, R, ed. Autonomic failure. Oxford: Oxford University Press; 1988. p. 667.Google Scholar
Wilbourn, AJ. Diabetic entrapment and compression neuropathies. In Dyck, PJ, Thomas, PK, eds. Diabetic neuropathy, 2nd ed. Toronto: WB Saunders; 1999. p. 481.Google Scholar
World Health Organization. Global status report on noncommunicable diseases 2014. Geneva: World Health Organization; 2014.Google Scholar
Lonn, E, Yusuf, S, Arnold, MJ, et al. Homocysteine lowering with folic acid and B vitamins in vascular disease. N Engl J Med. 2006; 354: 1567–77.Google Scholar
Wierzbicki, AS. Homocysteine and cardiovascular disease: a review of the evidence. Diab Vasc Dis Res. 2007; 4: 143–50.Google Scholar
Goldman, L, Schafer, A. Muscle diseases. In Goldman's Cecil medicine. 24th ed. Philadelphia, PA: Saunders; 2011. Chapter 429.Google Scholar
Kerchner, G, Ptacek, L. Channelopathies: episodic and electrical disorders of the nervous system. In Daroff, RB, et al., eds. Bradley's Neurology in Clinical Practice. 6th ed. Philadelphia, PA: Saunders; 2012. Chapter 64.Google Scholar
Moxley, R, Heatwole, C. Channelopathies. In Swaiman, KF, ed. Swaiman's pediatric neurology: principles and practice. Philadelphia, PA: Saunders; 2012. pp. 1667–89.Google Scholar
Riggs, J. Neurologic complications of electrolytes disturbances. In Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. 5th ed. London, UK: Elsevier; 2014. pp. 317–26.Google Scholar
Hay, O, Dar, G, Abbas, J, et al. The lumbar lordosis in males and females, revisited. Plos One. Aug 24, 2015. https://doi.org/10.1371/journal.pone.0133685.Google Scholar
Riggs, J. Neurologic manifestations of electrolyte disturbances. Neurol Clin. 2002; 20: 227–39.Google Scholar
Riggs, J. Neurologic complications of electrolyte disturbances. In Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. London, UK: Elsevier; 2014. pp. 317–26.Google Scholar
Riggs, J. Neurologic manifestations of electrolyte disturbances. Neurol Clin. 2002; 20: 227–39.Google Scholar
Riggs, J. Neurologic complications of electrolyte disturbances. In Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. London, UK: Elsevier; 2014. pp. 317–26.Google Scholar
Brown, R, Fischman, A, Showalter, C. Primary hyperparathyroidism, hypercalcemia, paranoid deluisons, homicide and attempted murder. J Foren Sci. 1987; 32(4): 1460–3.Google Scholar
Fuleihan, G, Silverberg, S. Primary hyperparathyroidism: Clinical manifestations. UpToDate. 2015. Available from www.uptodate.com/contents/primary-hyperparathyroidism-clinical-manifestations. Accessed Aug 16, 2018.Google Scholar
Lockwood, A. Toxic and metabolic encephalopathies. In Daroff, RB, et al., eds. Bradley's neurology in clinical practice. 6th ed. Philadelphia, PA: Saunders; 2012. Chapter 56.Google Scholar
Schipper, H, Jay, C, Abrams, G. Sex hormone, pituitary, parathyroid, and adrenal disorders and the nervous system. In Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. 5th ed. London, UK: Elsevier; 2014. pp. 369–397.Google Scholar
Wysolmerski, J, Insogna, K. The parathyroid glands, hypercalcemia, and hypocalcemia. In Goldman's Cecil medicine. 24th ed. Philadelphia, PA: Saunders; 2011. Chapter 253.Google Scholar
Catli, G, Abaci, A, Altincik, A. Hyperprolactinemia in children: clinical features and long-term results. J Pediatr Endocrinol Metab. 2012; 25(11–12): 1123–8. DOI: 10.1515/jpem-2012-0130.Google Scholar
Ou, H-Y, Hsiao, S-H, Yu, EH, Wu, T-J. Etiologies and clinical manifestations of hyperprolactinemia in a medical center in Southern Taiwan. Department of Internal Medicine, Department of Pharmacy National Cheng Kung University Hospital, Tainan, Taiwan.Google Scholar
Wong, A, Eloy, JA, Couldwell, WT, Liu, JK. Update on prolactinomas. Part 1: Clinical manifestations and diagnostic challenges. J Clin Neurosci. 2015; 22(10): 1562–7. DOI: 10.1016/j.jocn.2015.03.058.Google Scholar
Zahajszky, J, Quinn, DK, Smith, FA, et al. Cognitive and perceptual disturbances in a young man. Prim Care Companion J Clin Psychiatry. 2007; 9: 59–63. [PMC free article][PubMed].Google Scholar
Biller, J. The interface of neurology and internal medicine. Philadephia, PA: Wolters Kluwer. 2007.Google Scholar
Biller, J. The interface of neurology and internal medicine. Philadephia, PA: Wolters Kluwer. 2007.Google Scholar
Hollowell, JG, Staehling, NW, Flanders, WD, et al. Serum TSH, T(4), and thyroid antibodies in the United States population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III). J Clin Endocrinol Metab. 2002; 87(2): 489–99.Google Scholar
Asvold, BO, Bjøro, T, Nilsen, TI, Vatten, LJ. Tobacco smoking and thyroid function: a population-based study. Arch Intern Med. 2007; 167(13): 1428–32. DOI: 10.1001/archinte.167.13.1428.Google Scholar
Aiello, DP, DuPlessis, AJ, Pattishall, EG 3rd, Kulin, HE. Thyroid storm. Presenting with coma and seizures in a 3-year-old girl. Clin Pediatr (Phila). 1989; 28: 571–4.Google Scholar
Awad, AG. The thyroid and the mind and emotions/thyroid dysfunction and mental disorders. Thyroid Foundation of Canada. 2000. Available from https://thyroid.ca/resource-material/articles/e-10-f/. Accessed Aug 16, 2018.Google Scholar
Martin, FI, Deam, DR. Hyperthyroidism in elderly hospitalised patients. Clinical features and treatment outcomes. Med J Aust. 1996; 164: 200.Google Scholar
Seeherunvong, T, Diamantopoulos, S, Berkovitz, GD. A nine year old girl with thyrotoxicosis, ataxia, and chorea. Brain Dev. 2007; 29: 660–1.Google Scholar
Cleveland Clinic. Septal myectomy. June, 2009. Available from http://my.clevelandclinic.org/services/heart/disorders/septal_myectomy Accessed June 22, 2015.Google Scholar
Maron, BJ, Olivotto, I. Hypertrophic cardiomyopathy. In Mann, DL, Zipes, D, Libby, P, Bonow, RO, Braunwald, E, eds. Braunwald's heart disease: A textbook of cardiovascular medicine. 10th ed. Philadelphia, PA: Elsevier/Saunders; 2015. pp. 1574–86.Google Scholar
Mayo Clinic Staff. Hypertrophic cardiomyopathy. Feb 18, 2015. Available from www.mayoclinic.org/diseases-conditions/hypertrophic-cardiomyopathy/home/ovc-20122102. Accessed June 22, 2015.Google Scholar
Cowley, DS, Roy-Byrne, PP. Hyperventilation and panic disorder. Am J Med. 1987; 83: 929.Google Scholar
Lewis, RA, Howell, JB. Definition of the hyperventilation syndrome. Bull Eur Physiopathol Respir. 1986; 22: 201.Google Scholar
Pfortmueller, CA, Pauchard-Neuwerth, SE, Leichtle, AB, et al. Primary hyperventilation in the emergency department: a first overview. PLoS One. 2015; 10: e0129562.Google Scholar
Saisch, SG, Wessely, S, Gardner, WN. Patients with acute hyperventilation presenting to an inner-city emergency department. Chest. 1996; 110: 952.Google Scholar
Lewis, MA, Hendrickson, AW, Moynihan, TJ. Oncologic emergencies: Pathophysiology, presentation, diagnosis, and treatment. CA Cancer J Clin. 2011; 61: 287–314.Google Scholar
Stone, MJ, Bogen, SA. Evidence-based focused review of management of hyperviscosity syndrome. Blood. 2012; 119: 2205–8.Google Scholar
Fong, J, Khan, A. Hypocalcemia: updates in diagnosis and management for primary care. Canad Fam Physician. 2012; 58(2): 158–62.Google Scholar
Lockwood, A. Toxic and metabolic encephalopathies. In Daroff, RB, et al., eds. Bradley's neurology in clinical practice. 6th ed. Philadelphia, PA: Saunders; 2012. Chapter 56.Google Scholar
Riggs, J. Neurologic complications of electrolyte disturbances. In Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. London, UK: Elsevier; 2014. pp. 317–26.Google Scholar
Wysolmerski, J, Insogna, K. The parathyroid glands, hypercalcemia, and hypocalcemia. In Goldman's Cecil medicine. 24th ed. Philadelphia, PA: Saunders; 2011. Chapter 253.Google Scholar
Lin, HC, Barkhaus, PE. Cranial nerve XII: the hypoglossal nerve. Semin Neurol. 2009; 29(1): 45–52.Google Scholar
Goldman, L, Schafer, A. Hypoglycemia. In Goldman's Cecil medicine. 24th ed. Philadelphia, PA: Saunders; 2011. pp. 237–8.Google Scholar
Lockwood, A. Toxic and metabolic encephalopathies. In Daroff, RB, et al., eds. Bradley's neurology in clinical practice. 6th ed. Philadelphia, PA: Saunders; 2012. Chapter 56.Google Scholar
Sircar, M, Bhatia, A, Munshi, M. Review of hypoglycemia in the older adult: clinical implications and management. Can J Diabetes. 2016; 40(1): 66–72. DOI: 10.1016/j.jcjd.2015.10.004. Epub Dec 29, 2015.Google Scholar
Zochodne, D, Toth, C. Diabetes and the nervous system. In Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. London, UK: Elsevier; 2014. pp. 351–68.Google Scholar
Goldman, L, Schafer, A. Muscle diseases. In Goldman's Cecil medicine. 24th ed. Philadelphia, PA: Saunders; 2011. Chapter 429.Google Scholar
Kerchner, G, Ptacek, L. Channelopathies: episodic and electrical disorders of the nervous system. In Daroff, RB, et al., eds. Bradley's neurology in clinical practice. 6th ed. Philadelphia, PA: Saunders; 2012. Chapter 64.Google Scholar
Moxley, R, Heatwole, C. Channelopathies. In Swaiman, KF, ed. Swaiman's pediatric neurology: principles and practice. Philadelphia, PA: Saunders; 2012. pp. 1667–89.Google Scholar
Riggs, J. Neurologic complications of electrolytes disturbances. In Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. London, UK: Elsevier; 2014. pp. 317–26.Google Scholar
Riggs, J. Neurologic complications of electrolytes disturbances. In Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. London, UK: Elsevier; 2014. pp. 317–26.Google Scholar
Decaux, G, Soupart, A. Treatment of symptomatic hyponatremia. Am J Med Sci. 2003; 326(1): 25–30.Google Scholar
Spasovaski, G, Vanholder, R, Allolio, B, et al. Clinical practice guideline on diagnosis and treatment of hyponatremia. Nephrol Dial Transplant. 2014; 170(3): G1–47.Google Scholar
Sterns, RH, Riggs, JE, Schochet, SS. Osmotic demyelination syndrome following correction of hyponatremia. N Engl J Med. 1986; 314: 1535.Google Scholar
Al-Azem, H, Khan, AA; Hypoparathyroidism. Best Pract Res Clin Endocrinol Metab. 2012; 26(4): 517–22. DOI: 10.1016/j.beem.2012.01.004.Google Scholar
Bhadada, SK, Bhansali, A, Upreti, V, Subbiah, S, Khandelwal, N. Spectrum of neurological manifestations of idiopathic hypoparathyroidism and pseudohypoparathyroidism. Neurol India. 2011; 59: 586–9.Google Scholar
Clarke, BL, Brown, EM, Collins, MT, et al. Epidemiology and diagnosis of hypoparathyroidism. J Clin Endocrinol Metab. 2016; 101(6): 2284–99. DOI: 10.1210/jc.2015-3908.Google Scholar
Fonseca, OA, Calverley, JR. Neurological manifestations of hypoparathyroidism. Arch Intern Med. 1967; 120(2): 202–6. DOI: 10.1001/archinte.1967.00300020074009.Google Scholar
Felsenfeld, A, Levine, B. Approach to treatment of hypophosphatemia. Am J Kidney Dis. 2012; 60(4): 655–61.Google Scholar
Subramanian, R, Khardori, R. Severe hypophosphatemia: pathophysiologic implications, clinical presentations, and treatment. Medicine. 2009; 79(1): 1–8.Google Scholar
Alchanatis, M, Zias, N, Deligiorgis, N, et al. Sleep apnea-related cognitive deficits and intelligence: an implication of cognitive reserve theory. J Sleep Res. 2005; 14, 69–75.Google Scholar
Bruce, AS, Aloia, MS, Ancoli-Israel, S. Neuropsychological assessment of neuropsychiatric and neuromedical disorders. Oxford: Oxford University Press; 2009.Google Scholar
Kozora, E, Filley, C, Julian, L, Cullum, C. Cognitive functioning in patients with chronic obstructive pulmonary disease and mild hypoxemia compared with patients with mild Alzheimer disease and controls. J Neuropsychiatry Neuropsychol Behav Neurol. 1999; 12: 178–83.Google Scholar
Martin, DS, Grocott, M. Oxygen therapy in critical illness. Crit Care Med. 2013; 41(2): 423–32.Google Scholar
Rothenhausler, HB, Ehrentraut, S, Stoll, C, Schelling, G, Kapfammer, HP. The relationship between cognitive performance and employment and health status in long-term survivors of the acute respiratory distress syndrome: Results of an exploratory study. Gen Hosp Psychiatry. 2001; 23(2): 90–6.Google Scholar
Fuh, JL, Kuo, KH, Wang, SJ. Primary stabbing headache in a headache clinic. Cephalalgia. 2007; 27(9): 1005–9.Google Scholar
Mathew, NT. Indomethacin responsive headache syndromes. Headache. 1981; 21(4): 147–50.Google Scholar
Ali, M, Auger, RR, Slocumb, NL, Morganthaler, TI. Idiopathic hypersomnia: clinical features and response to treatment. J Clin Sleep Med. 2009; 5: 562–8.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Anderson, KN, Pilsworth, S, Sharples, RD, Smith, IE, Shneerson, JM. Idiopathic hypersomnia: a study of 77 cases. Sleep. 2007; 30: 1274–81.Google Scholar
Mayer, G, Benes, H, Young, P, Bitterlich, M, Rodenbeck, A. Modafinil in the treatment of idiopathic hypersomnia without long sleep time: a randomized, double-blind, placebo-controlled study. J Sleep Res. 2015; 24: 74–81.Google Scholar
Rye, DB, Bliwise, DL, Parker, K, et al. Modulation of vigilance in the primary hypersomnias by endogenous enhancement of GABAA receptors. Sci Trans Med. 2012; 21: 161.Google Scholar
Friedman, DI. Papilledema and idiopathic intracranial hypertension. Continuum (Minneap Minn). 2014; 20(4): 857–76.Google Scholar
Markey, K, Mollan, S, Jensen, R, Sinclair, A. Understanding idiopathic intracranial hypertension: mechanisms, management and future directions. Lancet Neurol. 2016; 15(1): 78–91.Google Scholar
Pérez, MA, Bialer, OY, Bruce, BB, Newman, NJ, Biousse, V. Primary spontaneous cerebrospinal fluid leaks and idiopathic intracranial hypertension. J Neuroophthalmol. 2013; 33(4): 330–7.Google Scholar
Wall, M, Kupersmith, MJ, Kieburtz, KD, et al. The idiopathic intracranial hypertension treatment trial: clinical profile at baseline. JAMA Neurol. 2014; 71(6): 693–701.Google Scholar
Fogarty, PF, Segal, JB. The epidemiology of immune thrombocytopenic purpura. Curr Opin Hematol. 2007; 14(5): 515–9.Google Scholar
Marie, I, Maurey, G, Hervé, F, Hellot, MF, Levesque, H. Intravenous immunoglobulin-associated arterial and venous thrombosis: report of a series and review of the literature. Br J Dermatol. 2006; 155(4): 714–21.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Noyes, R Jr, Stuart, S, Langbehn, DR, et al. Childhood antecedents of hypochondriasis. Psychosomatics. 2002; 43(4): 282–9.Google Scholar
Noyes, R Jr, Carney, CP, Hillis, SL, et al. Prevalence and correlates of illness worry in the general population. Psychosomatics. 2005; 46(6): 529–39.Google Scholar
Go, CY, et al. Evidence-based guideline update: medical treatment of infantile spasms. Report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology. 2012; 78(24): 1974–80.Google Scholar
Taghdiri, MM, Nemati, H. Infantile spasm: a review article. Iran J Child Neurol. 2014; 8(3): 1–5.Google Scholar
Werz, MA, Pita-Garcia, IL. Epilepsy syndromes. Philadelphia, PA: Saunders/Elsevier; 2010.Google Scholar
Baddour, LM, Freeman, WK, Suri, RM, Wilson, WR. Cardiovascular infections. In Mann, DL, Zipes, D, Libby, P, Bonow, RO, Braunwald, E, eds. Braunwald's heart disease: A textbook of cardiovascular medicine. 10th ed. Philadelphia, PA: Elsevier/Saunders; 2015. pp. 1524–43.Google Scholar
Mayo Clinic Staff. Endocarditis. June 14, 2014. Available from www.mayoclinic.org/diseases-conditions/endocarditis/basics/definition/con-20022403. Accessed June 21, 2015.Google Scholar
Ekstrand, JJ. Neurologic complications of influenza. Semin Pediatr Neurol. 2012; 19(3): 96–100.Google Scholar
Mizuguchi, M. Influenza encephalopathy and related neuropsychiatric syndromes. Influenza Other Respir Viruses. 2013; 7(Suppl. 3): 67–71.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders, 3rd ed. Darien, IL: American Academy of Sleep Medicine, 2014.Google Scholar
Bonnet, MH, Arand, DL, Javaheri, S. Cardiovascular implications of poor sleep. Sleep Med Clin. 2007; 2: 529.Google Scholar
Buscemi, N, Vendermeer, B, Friesen, C, et al. The efficacy and safety of drug treatments for chronic insomnia in adults: a meta-analysis of RCTs. J Gen Intern Med. 2007; 22: 1335.Google Scholar
Kripke, DF, Langer, RD, Kline, LE. Hypnotics' association with mortality or cancer: a matched cohort study. BMJ Open. 2012; 2: e000850.Google Scholar
LeBlanc, M, Merette, C, Savard, J, et al. Incidence and risk factors of insomnia in a population-base sample. Sleep. 2009; 32: 1027.Google Scholar
Vgontzas, AN, Liao, D, Bixler, EO, Chrousos, GP, Vela-Bueno, A. Insomnia with objective short sleep duration is associated with a high risk for hypertension. Sleep. 2009; 32: 491.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Ellis, JG, Gehrman, P, Espie, CA, et al. Acute insomnia: Current conceptualizations and future directions. Sleep Med Rev. 2012; 16: 5–14.Google Scholar
Nofzinger, EA, Nissen, C, Germain, A, et al. Regional cerebral metabolic correlates of WASO during sleep in insomnia. J Clin Sleep Med. 2006; 2: 316–22.Google Scholar
American Academy of Sleep Medicine. The international classification of sleep disorders. 3rd ed. Chicago, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Knutson, KL. Sleep duration and cardiometabolic risk: a review of the epidemiologic evidence. Best Pract Res Clin Endocrinol Metab. 2010; 24: 731–43.Google Scholar
Tucker, AM, Whitney, P, Belenky, G, Hinson, JM, Van Dongen, HPA. Effects of sleep deprivation on dissociated components of executive functioning. Sleep. 2010; 33: 45–57.Google Scholar
Al-Aama, T, Brymer, C, Gutmanis, I, et al. Melatonin decreases delirium in elderly patients: A randomized, placebo-controlled trial. Int J Geriatr Psychiatry. 2011; 26(7): 687–94.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Cavallazzi, R, Saad, M, Marik, PE. Delirium in the ICU: an overview. Ann Intens Care. 2012; 2(1): 1.Google Scholar
Ely, E, Gautam, S, Margolin, R, et al. The impact of delirium in the intensive care unit on hospital length of stay. Intensive Care Med. 2001; 27(12): 1892–1900.Google Scholar
Ely, EW, Shintani, A, Truman, B, et al. Delirium as a predictor of mortality in mechanically ventilated patients in the intensive care unit. JAMA. 2004; 291(14): 1753–62.Google Scholar
Girard, TD, Pandharipande, PP, Ely, EW. Delirium in the intensive care unit. Crit Care. 2008; 12(Suppl 3): S3.Google Scholar
Inouye, SK, Bogardus, ST Jr, Charpentier, PA, et al. A multicomponent intervention to prevent delirium in hospitalized older patients. New Engl J Med. 1999; 340(9): 669–76.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Best, M, Williams, JM, Coccaro, EF. Evidence for a dysfunctional prefrontal circuit in patients with an impulsive aggressive disorder. Proc Nat Acad Sci. 2002; 99(12): 8448–53.Google Scholar
Coccaro, EF, Lee, EF, Kavoussi, RJ. A double-blind, randomized, placebo-controlled trial of fluoxetine in patients with intermittent explosive disorder. J Clin Psychiatry. 2009; 70(5): 653–62.Google Scholar
Davanzo, P, Yue, K, Thomas, MA, et al. Proton magnetic resonance spectroscopy of bipolar disorder versus intermittent explosive disorder in children and adolescents. Am J Psychiatry. 2003; 160(8): 1442–52.Google Scholar
Jones, RM, Arlidge, J, Gillham, R, et al. Efficacy of mood stabilisers in the treatment of impulsive or repetitive aggression: systematic review and meta-analysis. Br J Psychiatry. 2011; 198(2): 93–8.Google Scholar
Kant, R, Chalansani, R, Chengappa, KR, Dieringer, MF. The off-label use of clozapine in adolescents with bipolar disorder, intermittent explosive disorder, or posttraumatic stress disorder. J Child Adolesc Psychopharmacol. 2004; 14(1): 57–63.Google Scholar
McCloskey, MS, Noblett, KL, Deffenbacher, JL, Gollan, JK, Coccaro, EF. Cognitive-behavioral therapy for intermittent explosive disorder: a pilot randomized clinical trial. J Consult Clin Psychol. 2008; 76(5): 876.Google Scholar
Murray-Close, D, Ostrov, JM, Nelson, DA, Crick, NR, Coccaro, EF. Proactive, reactive, and romantic relational aggression in adulthood: Measurement, predictive validity, gender differences, and association with Intermittent Explosive Disorder. J Psychiatr Res. 2010; 44(6): 393–404.Google Scholar
Mahé, G, Kaladji, A, Le Faucheur, A, Jaquinandi, V. Internal iliac artery stenosis: diagnosis and how to manage it in 2015. Front Cardiovasc Med. 2015; 2: 33. DOI: 10.3389/fcvm.2015.00033.Google Scholar
Shin, RK, Stecker, MM, Imbesi, SG. Peripheral nerve ischaemia after internal iliac artery ligation. J Neurol Neurosurg Psychiatry 2001; 70: 411–12. DOI: 10.1136/jnnp.70.3.411.Google Scholar
Sen, S, et al. Complications after unintentional intra-arterial injection of drugs: risks, outcomes, and management strategies. Mayo Clin Proc. 2005; 80(6): 783–95.Google Scholar
Jeng, J-S, et al. Epidemiology, diagnosis and management of intracranial atherosclerotic disease. Expert Rev Cardiovasc Ther. 2010; 8(10): 1423–32.Google Scholar
Arenillas, JF. Intracranial atherosclerosis: current concepts. Stroke. 2011; 42: S20–3.Google Scholar
Beristain, X, Azzarelli, B. The neurological masquerade of intravascular lymphomatosis. Arch Neurol. 2002; 59(3): 439–43.Google Scholar
Fonkem, E, Dayawansa, S, Stroberg, E, et al. Neurological presentations of intravascular lymphoma (IVL): meta-analysis of 654 patients. BMC Neurol. 2016; 16: 9.Google Scholar
Mihaljevic, B, Sternic, N, Skender Gazibara, M, et al. Intravascular large B-cell lymphoma of central nervous system: a report of two cases and literature review. Clin Neuropathol. 2010; 29(4): 233–8.Google Scholar
Hanley, DF. Intraventricular hemorrhage: severity factor and treatment target in spontaneous intracerebral hemorrhage. Stroke. 2009; 40: 1533–8.Google Scholar
Abbott, SM, Zee, PC. Irregular sleep-wake rhythm disorder. Sleep Med Clin. 2015; 10: 517–22.Google Scholar
Ancoli-Israel, S, Gehrman, P, Martin, JL, et al. Increased light exposure consolidates sleep and strengthens circadian rhythms in severe Alzheimer's disease patients. Behav Sleep Med. 2003; 1: 22–36.Google Scholar
Auger, RR, Burgess, HJ, Emens, JS, et al. Clinical practice guideline for the treatment of intrinsic circadian rhythm sleep-wake disorders: Advanced sleep-wake phase disorder (ASWPD), delayed sleep-wake phase disorder (DSWPD), non-24-hour sleep-wake rhythm disorder (N24SWD), and irregular sleep-wake rhythm disorder (ISWRD). An update for 2015: An American Academy of Sleep Medicine Clinical Practice Guideline. J Clin Sleep Med. 2015; 11: 1199–236.Google Scholar
Bjorvatn, B, Pallesen, S. A practical approach to circadian rhythm sleep disorders. Sleep Med Rev. 2009; 13: 47–60.Google Scholar
Sack, RL, Auckley, D, Auger, RR, et al. Circadian rhythm sleep disorders: Part II, Advanced sleep phase disorder, delayed sleep phase disorder, free-running disorder, and irregular sleep-wake rhythm. Sleep. 2007; 30: 1484–501.Google Scholar
Sateia, M, Berry, RB, Bornemann, MC, et al. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Greenberg, SM, Vonsattel, JP. Diagnosis of cerebral amyloid angiopathy. Sensitivity and specificity of cortical biopsy. Stroke. 1997; 28: 1418.Google Scholar
Hébert, R, Brayne, C. Epidemiology of vascular dementia. Neuroepidemiology. 1995; 14: 240.Google Scholar
Lipton, RB, Bigal, ME, Diamond, M, et al. Migraine prevalence, disease burden, and the need for preventive therapy. Neurology. 2007; 68: 343.Google Scholar
Rodriguez, V, Shah, D, Gover, V, et al. Ischemic monomelic neuropathy: a disguised diabetic neuropathy. Pract Neurol. March/April 2013. http://practicalneurology.com/2013/04/ischemic-monomelic-neuropathy-a-disguised-diabetic-neuropathy/. Accessed Aug 30, 2018.Google Scholar
Sheetal, S, Byju, P, Manoj, P. Ischemic monomelic neuropathy. J Postgrad Med. 2017; 63(1): 42–3. DOI: 10.4103/0022-3859.194221.Google Scholar
Ullery, BW, Cheung, AT, Fairman, RM, et al. Risk factors, outcomes, and clinical manifestations of spinal cord ischemia following thoracic endovascular aortic repair. J Vasc Surg. 2011; 54(3): 677–84.Google Scholar
Garg, RK, Greenlee, JE. Japanese encephalitis. Medlink Neurology. Originally released August 17, 2000; last updated July 21, 2017. Available from www.medlink.com/article/japanese_encephalitis. Accessed Aug 20, 2018.Google Scholar
Solomon, T. Current concepts: Flavivirus encephalitis. New Engl J Med. 2004; 351: 370–8. PMID 15269317.Google Scholar
Solomon, T, Cardosa, MJ. Emerging arboviral encephalitis. BMJ. 2000; 321: 1484–5. PMID 11118162.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders, 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Burgess, HJ, Crowley, SJ, Gazda, CJ, et al. Preflight adjustment to eastward travel: 3 days of advancing sleep with and without morning bright light. J Biol Rhythms. 2003; 18: 318.Google Scholar
Herxheimer, A, Petrie, KJ. Melatonin for the prevention and treatment of jet lag. Cochrane Database Syst Rev. 2002; 2: CD001520.Google Scholar
Jamieson, AO, Zammit, GK, Rosenberg, RS, et al. Zolpidem reduces the sleep disturbance of jet lag. Sleep Med. 2001; 2: 423.Google Scholar
Morris, HH 3rd, Estes, ML. Traveler's amnesia. Transient global amnesia secondary to triazolam. JAMA. 1987; 258: 945.Google Scholar
Rosenberg, RP, Bogan, RK, Tiller, JM, et al. A phase 3, double-blind, randomized, placebo-controlled study of armodafinil for excessive sleepiness associated with jet lag disorder. Mayo Clin Proc. 2010; 85: 630.Google Scholar
Sack, RL, Auckley, D, Auger, RR, et al. Circadian rhythm sleep disorders: Part I, basic principles, shift work and jet lag disorders. Sleep. 2007; 30: 1460–83.Google Scholar
Asadi-Pooya, AA, Farazdaghi, M. Seizure outcome in patients with juvenile absence epilepsy. Neurol Sci. 2016; 37(2): 289–92.Google Scholar
Trinka, E, et al. Long-term prognosis for childhood and juvenile absence epilepsy. J Neurol. 2004; 251(10): 1235–41.Google Scholar
Werz, MA, Pita-Garcia, IL. Epilepsy syndromes. Philadelphia, PA: Saunders/Elsevier; 2010. p. ix, 216.Google Scholar
de Araujo Filho, GM, Yacubian, EM. Juvenile myoclonic epilepsy: psychiatric comorbidity and impact on outcome. Epilepsy Behav. 2013; 28(Suppl 1): S74–80.Google Scholar
Swaiman, KF. Pediatric neurology: principles and practice. 5th ed. Edinburgh: Elsevier Saunders; 2012.Google Scholar
Wolf, P, et al. Juvenile myoclonic epilepsy: A system disorder of the brain. Epilepsy Res. 2015; 114: 2–12.Google Scholar
Shaheen, B, Bakir, M, Jain, S. Corneal nerves in health and disease. Surv Ophthalmol. 2014; 59(3): 263–85.Google Scholar
American Academy of Pediatrics Clinical Practice Guideline Subcommittee on Hyperbilirubinemia. Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation. Pediatrics. 2004; 114: 297–316.Google Scholar
Bhutani, VK, Johnson, L. Review: kernicterus in the 21st century: frequently asked questions. J Perinatol. 2009; 29: S20–4.Google Scholar
Shapiro, SM. Definition of the clinical spectrum of kernicterus and bilirubin-induced neurologic dysfunction (BIND). J Perinatol. 2005; 25: 54–9.Google Scholar
Hoffman, RJ. Ketamine poisoning. UpToDate. Updated Aug 15, 2017. https://www.uptodate.com/contents/ketamine poisoning?source=search_result&search=Ketamine%20abuse&selectedTitle=1∼150. Accessed Aug 20, 2018.Google Scholar
Wang, C, Zheng, D, Xu, J, Lam, W, Yew, DT. Brain damages in ketamine addicts as revealed by magnetic resonance imaging. Front Neuroanat. July 17, 2013. http://journal.frontiersin.org/article/10.3389/fnana.2013.00023/fullGoogle Scholar
Zhou, Z-S, Zhao, ZQ. Ketamine blockage of both tetrodotoxin (TTX)-sensitive and TTX-resistant sodium channels of rat dorsal root ganglion neurons. Brain Res Bull. 2000; 52(5): 427–33.Google Scholar
American Academy of Sleep Medicine. The international classification of sleep disorders. 3rd ed. Chicago, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Arnulf, I, Lin, I, Gadoth, N, et al. Kleine-Levin syndrome: a systematic study of 108 patients. Ann Neurol. 2008; 63: 482–93.Google Scholar
Billiard, M, Jaussent, I, Dauvilliers, Y, Besset, A. Recurrent hypersomnia: a review of 339 cases. Sleep Med Rev. 2011; 15: 247–57.Google Scholar
Dauvilliers, Y, Mayer, G, Lecendreux, M, et al. Kleine-Levin syndrome. An autoimmune hypothesis based on clinical and genetic analyses. Neurology. 2002; 59: 1739–45.Google Scholar
Bonomi, M, Rochira, V, Pasquali, D, et al.; ItaliaN Group (KING). Klinefelter syndrome (KS): genetics, clinical phenotype and hypogonadism. J Endocrinol Invest. 2017; 40(2): 123–34.Google Scholar
Freund, G. Chronic central nervous system toxicity of alcohol. Annu Rev Pharmacol. 1973; 13: 217.Google Scholar
Gregory, MC, Hammond, ME, Brewer, ED. Renal deposition of cytomegalovirus antigen in immunoglobulin-A nephropathy. Lancet. 1988; 1: 11.Google Scholar
Parkin, AJ, Blunden, J, Rees, JE, Hunkin, NM. Wernicke-Korsakoff syndrome of nonalcoholic origin. Brain Cogn. 1991; 15: 69.Google Scholar
Pittella, JE, de Castro, LP. Wernicke's encephalopathy manifested as Korsakoff's syndrome in a patient with promyelocytic leukemia. South Med J. 1990; 83: 570.Google Scholar
Engel, PA, Grunnet, M, Jacobs, B. Wernicke-Korsakoff syndrome complicating T-cell lymphoma: unusual or unrecognized? South Med J. 1991; 84: 253.Google Scholar
Becker, JT, Furman, JM, Panisset, M, Smith, C. Characteristics of the memory loss of a patient with Wernicke-Korsakoff's syndrome without alcoholism. Neuropsychologia. 1990; 28: 171.Google Scholar
Beatty, WW, Bailly, RC, Fisher, L. Korsakoff-like amnesic syndrome in a patient with anorexia and vomiting. Int J Clin Neuropsychol. 1988; 11: 55.Google Scholar
Victor, M, Adams, RA, Collins, GH. The Wernicke-Korsakoff syndrome and related disorders due to alcoholism and malnutrition. Philadelphia: F. A. Davis; 1989.Google Scholar
Harper, C. The incidence of Wernicke's encephalopathy in Australia: a neuropathological study of 131 cases. J Neurol Neurosurg Psychiatry. 1983; 46: 593.Google Scholar
Blansjaar, BA, Van Dijk, JG. Korsakoff minus Wernicke syndrome. Alcohol Alcohol. 1992; 27: 435.Google Scholar
Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
Eckardt, MJ, Martin, PR. Clinical assessment of cognition in alcoholism. Alcohol Clin Exp Res. 1986; 10: 123.Google Scholar
Harding, A, Halliday, G, Caine, D, Kril, J. Degeneration of anterior thalamic nuclei differentiates alcoholics with amnesia. Brain. 2000; 123(Pt 1): 141.Google Scholar
Phillips, BK, Ingram, MV, Grammer, GG. Wernicke-Korsakoff syndrome and galantamine. Psychosomatics. 2004; 45: 366.Google Scholar
Cochrane, M, Cochrane, A, Jauhar, P, Ashton, E. Acetylcholinesterase inhibitors for the treatment of Wernicke-Korsakoff syndrome: three further cases show response to donepezil. Alcohol Alcohol. 2005; 40: 151.Google Scholar
Rustembegović, A, Kundurović, Z, Sapcanin, A, Sofic, E. A placebo-controlled study of memantine (Ebixa) in dementia of Wernicke-Korsakoff syndrome. Med Arh. 2003; 57: 149.Google Scholar
Gaillard, F, Weerakkody, Y. Krabbe disease. Radiopaedia.org. Available from http://radiopaedia.org/articles/krabbe-disease. Accessed Mar 30, 2016.Google Scholar
Tappino, B, Biancheri, R, Mort, M, et al. Identification and characterization of 15 novel GALC gene mutations causing Krabbe disease. Hum Mutat. 2010; 31: E1894–914.Google Scholar
Wenger, DA. Krabbe disease. In: Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 2000 [Updated Mar 31, 2011]. pp. 1993–2016.Google Scholar
Nitzschke, E, Hildenbrand, M. [Epidemiology of kyphosis in school children.] Z Orthop Ihre Grenzgeb. 1990; 128(52): 477–81.Google Scholar
Song, KS, Chang, BS, Yeom, JS, et al. Surgical treatment of severe angular kyphosis with myelopathy, anterior and posterior approach with pedicle screw instrumentation. Spine. 2008; 33(11): 1229–35. DOI: 10.1097/BRS.0b013e31817152b3.Google Scholar
Centers for Disease Control and Prevention. La Crosse encephalitis. Apr 13, 2016. https://www.cdc.gov/lac/tech/symptoms.html. Accessed Aug 21, 2018.Google Scholar
McJunkin, JE, et al. La Crosse encephalitis in children. N Engl J Med. 2001; 344: 801–7. DOI: 10.1056/NEJM200103153441103.Google Scholar
Agranoff, AB. Lacunar stroke. Medscape. Updated May 23, 2017. https://emedicine.medscape.com/article/322992-overview. Accessed Aug 30, 2018.Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. Adams and Victor's principles of neurology. 10th ed. New York: McGraw-Hill Education/Medical; 2014. Chapter 34.Google Scholar
Bataller, L, Dalmau, J. Paraneoplastic disorders of the nervous system. Continuum (Minneap Minn). 2005; 11(5, Neuro-Oncology): 69–92. DOI: 10.1212/01.con.0000293680.24426.ae.Google Scholar
Katirji, B, Kaminski, HJ, Ruff, RL. Neuromuscular disorders in clinical practice. 2nd ed. New York: Springer-Verlag; 2014.Google Scholar
Lancaster, E. Paraneoplastic disorders. Continuum (Minneap Minn). 2015; 21(2, Neuro-Oncology): 452–75. DOI: 10.1212/01.CON.0000464180.89580.88.Google Scholar
Nicolle, MW. Myasthenia gravis and Lambert-Eaton myasthenic syndrome. Continuum (Minneap Minn). 2016; 22(6, Muscle and Neuromuscular Junction Disorders): 1978–2005. DOI: 10.1212/CON.0000000000000415.Google Scholar
Vernino, S. Paraneoplastic disorders affecting the neuromuscular junction or anterior horn cell. Continuum (Minneap Minn). 2009; 15(1, Myasthenic Disorders and ALS): 132–46. DOI: 10.1212/01.CON.0000300011.79845.eb.Google Scholar
Hughes, JR. A review of the relationships between Landau–Kleffner syndrome, electrical status epilepticus during sleep, and continuous spike-waves during sleep. Epilepsy Behav. 2011; 20(2): 247–53.Google Scholar
Sanchez Fernandez, I, et al. Electrical status epilepticus in sleep: clinical presentation and pathophysiology. Pediatr Neurol. 2012; 47(6): 390–410.Google Scholar
Tuft, M, et al. Landau–Kleffner syndrome. Tidsskr Nor Laegeforen. 2015; 135(22): 2061–4.Google Scholar
Rubens, O, Logina, I, Kravale, I, Eglite, M, Donaghy, M. Peripheral neuropathy in chronic occupational inorganic lead exposure: a clinical and electrophysiologic study. J Neurol Neurosurg Psychiatry. 2001; 71: 200–4. PMID 11459892.Google Scholar
Spencer, PS, Schaumburg, HH. Experimental and clinical neurotoxicology. 2nd ed. Oxford, UK: Oxford University Press; 2000. pp. 315–17.Google Scholar
Brown, MD, Sun, F, Wallace, DC. Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage. Am J Hum Genet. 1997; 60: 381.Google Scholar
Newman, NJ, Lott, MT, Wallace, DC. The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation. Am J Ophthalmol. 1991; 111: 750.Google Scholar
Uemura, A, Osame, M, Nakagawa, M, et al. Leber's hereditary optic neuropathy: mitochondrial and biochemical studies on muscle biopsies. Br J Ophthalmol. 1987; 71: 531.Google Scholar
Wallace, DC, Singh, G, Lott, MT, et al. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science. 1988; 242: 1427.Google Scholar
Bogousslavsky, J, Regli, F. Anterior cerebral artery territory infarction in the Lausanne Stroke Registry: clinical and etiologic patterns. Arch Neurol. 1990; 47(2): 144–50.Google Scholar
Gacs, G, Fox, AJ, Barnett, HJ, Vinuela, F. Occurrence and mechanisms of occlusion of the anterior cerebral artery. Stroke. 1983; 14(6): 952–9.Google Scholar
Kumral, E, Bayulkem, G, Evyapan, D, Yunten, N. Spectrum of anterior cerebral artery territory infarction: clinical and MRI findings. Eur J Neurol. 2002; 9(6): 615–24.Google Scholar
Finsterer, J. Leigh and Leigh-like syndrome in children and adults. Pediatr Neurol. 2008; 39(4): 223–35. DOI: 10.1016/j.pediatrneurol.2008.07.013.Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. Inherited metabolic diseases of the nervous system. In Adams & Victor's principles of neurology, 10th ed. New York, NY: McGraw-Hill; 2014. Chapter 37.Google Scholar
Arzimanoglou, A., et al. Lennox–Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology. Lancet Neurol. 2009; 8(1): 82–93.Google Scholar
Kerr, M, Kluger, G, Philip, S. Evolution and management of Lennox–Gastaut syndrome through adolescence and into adulthood: are seizures always the primary issue? Epileptic Disord. 2011; 13(Suppl 1): S15–26.Google Scholar
Montouris, GD, Wheless, JW, Glauser, TA. The efficacy and tolerability of pharmacologic treatment options for Lennox–Gastaut syndrome. Epilepsia. 2014; 55(Suppl 4): 10–20.Google Scholar
Werz, MA, Pita-Garcia, IL. Epilepsy syndromes. Philadelphia, PA: Saunders/Elsevier; 2010. pp. ix, 216 p.Google Scholar
Chandra, A, Charteris, D. Molecular pathogenesis and management strategies of ectopia lentis. Eye. 2014; 28(2): 162–8.Google Scholar
Lastória, JC, de Abreu, MAMM. Leprosy: review of the epidemiological, clinical, and etiopathogenic aspects – Part 1. An Bras Dermatol. 2014; 89(2): 205–18. http://doi.org/10.1590/abd1806–4841.20142450.Google Scholar
Su, TW, Wu, LL, Lin, CP. The prevalence of dementia and depression in Taiwanese institutionalized leprosy patients, and the effectiveness evaluation of reminiscence therapy: a longitudinal, single-blind, randomized control study. Int J Geriatr Psychiatry. 2012; 27(2): 187–96.Google Scholar
Day, N. Epidemiology, microbiology, clinical manifestations, and diagnosis of leptospirosis. In Post, TW, ed. UpToDate. Waltham, MA. https://www.uptodate.com/contents/leptospirosis-epidemiology-microbiology-clinical-manifestations-and-diagnosis?search=Epidemiology,%20microbiology,%20clinical%20manifestations,%20and%20diagnosis%20of%20leptospirosis&source=search_result&selectedTitle=1∼77&usage_type=default&display_rank=1. Accessed Aug 30, 2018.Google Scholar
Day, N. Leptospirosis: treatment and prevention. In Post, TW, ed. UpToDate. Waltham, MA. https://www.uptodate.com/contents/leptospirosis-treatment-and-prevention?topicRef=5527&source=see_link. Accessed Aug 30, 2018.Google Scholar
Singh, R, et al. Cerebellar ataxia due to leptospirosis: a case report. BMC Infect Dis. 2016; 16: 748.Google Scholar
Vale, TC, et al. Weil syndrome: a rare cause of cerebral venous thrombosis. JAMA Neurol. 2014; 71(2): 238–9.Google Scholar
European Medicines Agency. Public summary of opinion on orphan designation. Ecopipam for the treatment of Lesch–Nyhan disease. Mar 2, 2010. www.ema.europa.eu/docs/en_GB/document_library/Orphan_designation/2010/03/WC500075166.pdf. Accessed Aug 21, 2018.Google Scholar
Jinnah, HA. Lesch–Nyhan disease: from mechanism to model and back again. Dis Model Mech. 2009; 2: 116–21; DOI: 10.1242/dmm.002543.Google Scholar
Nyhan, WL, O'Neill, JP, Jinnah, HA, Harris, JC. Lesch–Nyhan syndrome. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. Updated May 15, 2014. Gene Reviews®. Seattle (WA): University of Washington, Seattle; 1993–2016. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1149/. Accessed Aug 21, 2018.Google Scholar
Armentrout, SA, Ulrich, RF. Neurological manifestations of acute granulocytic leukemia. West J Med. 1974; 121(1): 1–5.Google Scholar
Narayanaswamy, AS, Prakash, MP, Kakkar, R. Neurological manifestations of leukemia: clinical and pathological findings. J Assoc Physicians India. 1992; 40(11): 740–2.Google Scholar
National Cancer Institute. Cancer stat facts: leukemia. https://seer.cancer.gov/statfacts/html/leuks.html. Accessed Aug 30, 2018.Google Scholar
Gomperts, SN. Lewy body dementias: dementia with Lewy bodies and Parkinson disease dementia. Continuum (Minneap Minn). 2016; 22: 435–63.Google Scholar
Tsuboi, Y, Dickson, DW. Dementia with Lewy bodies and Parkinson's disease with dementia: are they different? Parkinsonism Relat Disord. 2005; 11; S47–51.Google Scholar
Braak, H, Del Tredici, K, Rüb, U, et al. Staging of brain pathology related to sporadic Parkinson's disease. Neurobiol Aging. 2003; 24: 197–211.Google Scholar
Aarsland, D, Andersen, K, Larsen, JP, Lolk, A, Kragh-Sørensen, P. Prevalence and characteristics of dementia in Parkinson disease: an 8-year prospective study. Arch Neurol. 2003; 60: 387–92.Google Scholar
Govindan, A, Premkumar, S, Alapatt, JP. Lhermitte–Duclos disease (dysplastic gangliocytoma of the cerebellum) as a component of Cowden syndrome. Indian J Pathol Microbiol. 2012; 55(1): 107–8.Google Scholar
Nayil, K, Wani, M, Ramzan, A, et al. Lhermitte–Duclos disease with syrinx: case report and literature review. Turk Neurosurg. 2011; 21(4): 651–4.Google Scholar
Rivera, M, Lara-Del Rio, JA, Di Pasquale-Guadalupe, L, Zequeira, J. Silent presentation of a solid pseudopapillary neoplasm of the pancreas. Am J Case Rep. 2017; 18: 656–9.Google Scholar
Andrews, CJ, Cooper, MA, Darveniza, M. Lightening injuries: Electrical, medical, and legal aspects. Boca Raton, FL: CRC Press; 1992.Google Scholar
Center for Disease Control and Prevention. Lightening associated deaths – United States, 1980–1995. MMWR Morb Mortal Wkly Rep. 1998; 47(19): 391–4.Google Scholar
Charlier, C, et al. Clinical features and prognostic factors of listeriosis: the MONALISA national prospective cohort study. Lancet Infect Dis. 2017; 17(5): 510–19.Google Scholar
de Noordhout, CM, et al. The global burden of listeriosis: a systematic review and meta-analysis. Lancet Infect Dis. 14(11): 1073–82.Google Scholar
Aguilar, MI, Freeman, WD. Spontaneous intracerebral hemorrhage. Semin Neurol. 2010; 30(5): 555–64. DOI: 10.1055/s–0030–1268865. Epub 2011 Jan 4.Google Scholar
Patterson, JR, Grabois, M. Locked-in syndrome: a review of 139 cases. Stroke. 1986; 17: 758–64.Google Scholar
Roussea, M-C, et al. Quality of life in patients with locked-in syndrome: Evolution over a 6-year period. Orphanet J Rare Dis. 2015; 10: 88.Google Scholar
Klion, AD. Loiasis (Loa loa infection). In Post, TW, ed. UpToDate. Waltham, MA. Updated May 4, 2017.Google Scholar
Padgett, JJ, Jacobsen, KH. Loiasis: African eye worm. Trans R Soc Trop Med Hyg. 2008; 102(10): 983–9. DOI: 10.1016/j.trstmh.2008.03.022.Google Scholar
Kirkaldy-Willis, WH, ed. The pathology and pathogenesis of low back pain. In Managing low back pain. New York, NY: Churchill Livingstone; 1988. p. 49.Google Scholar
Newman, PH. Spondylolisthesis, its cause and effect. Ann R Coll Surg Engl. 1955; 16(5): 305–23. PMC 2377893.Google Scholar
O'Neill, TW, McCloskey, VE, Kanis, JA, et al. The distribution determinants and clinical correlates of vertebral osteophytosis: a population based survey. J Rheumatol. 1999; 26(4): A42–8.Google Scholar
O'Neill, TW, McCloskey, VE, Kanis, JA, et al. The distribution determinants and clinical correlates of vertebral osteophytosis: a population based survey. J Rheumatol. 1999; 26(4): A42–8.Google Scholar
Keene, JS, Albert, MS, Springer, SL, Drummond, DS, Clancy, WG Jr. Back injuries in college athletes. J Spinal Disord. 1989; 2(3): 190–5.Google Scholar
Lee, SY, Kim, T-H, Oh, JK, Lee, SJ, Park, MS. Lumbar stenosis: a recent update by review of literature. Asian Spine J. 2015; 9(5): 818–28. DOI: 10.4184/asj.2015.9.5.818.Google Scholar
Dyck, PJ, Norell, JE, Dyck, PJ. Non-diabetic lumbosacral radiculoplexus neuropathy: natural history, outcome and comparison with the diabetic variety. Brain. 2001; 124(6): 1197–207.Google Scholar
Katirji, B, Kaminski, HJ, Ruff, RL. Neuromuscular disorders in clinical practice. 2nd ed. New York: Springer-Verlag; 2014.Google Scholar
Castellanos, AM, Glass, JP, Yung, WK. Regional nerve injury after intra-arterial chemotherapy. Neurology. 1987; 37(5): 834–7.Google Scholar
Stohr, M, Dichgans, J, Dorstelmann, D. Ischaemic neuropathy of the lumbosacral plexus following intragluteal injection. J Neurol Neurosurg Psychiatry. 1980; 43(6): 489–94.Google Scholar
Wilbourn, AJ, Furlan, AJ, Hulley, W, Ruschhaupt, W. Ischemic monomelic neuropathy. Neurology. 1983; 33(4): 447–51.Google Scholar
Wohlgemuth, WA, Rottach, KG, Stoehr, M. Intermittent claudication due to ischaemia of the lumbosacral plexus. J Neurol Neurosurg Psychiatry. 1999; 67(6): 793–5.Google Scholar
Katirji, B, Kaminski, HJ, Ruff, RL. Neuromuscular disorders in clinical practice. 2nd ed. New York: Springer-Verlag; 2014.Google Scholar
Katirji, B, Kaminski, HJ, Ruff, RL. Neuromuscular disorders in clinical practice. 2nd ed. New York: Springer-Verlag; 2014.Google Scholar
Giglio, P, Gilbert, MR. Neurologic complications of cancer and its treatment. Curr Oncol Rep. 2010; 12(1): 50–9.Google Scholar
Höftberger, R, Rosenfeld, MR, Dalmau, J. Update on neurological paraneoplastic syndromes. Curr Opin Oncol. 2015; 27(6): 489–95.Google Scholar
Halperin, JJ. Nervous system Lyme disease. In Post, TW, ed. UpToDate. Waltham, MA. www.uptodate.com/contents/nervous-system-lyme-disease. Accessed May 18, 2017.Google Scholar
Koedel, U, et al. Lyme neuroborreliosis: epidemiology, diagnosis and management. Nat Rev Neurol. 2015; 11(8): 446–56.Google Scholar
Schwenkenbecher, P, Pul, R, Wurster, U, et al. Common and uncommon neurological manifestations of neuroborreliosis leading to hospitalization. BMC Infect Dis. 2017; 17(1): 90.Google Scholar
Steere, AC. Lyme borreliosis. In Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015. p. 1401.Google Scholar
Bonthius, DJ. Lymphocytic choriomeningitis virus: an underrecognized cause of neurologic disease in the fetus, child, and adult. Semin Pediatr Neurol. 2012; 19(3): 89–95.Google Scholar
Kunz, S, Rojek, JM, Roberts, AJ, et al. Altered central nervous system gene expression caused by congenitally acquired persistent infection with lymphocytic choriomeningitis virus. J Virol. 2006; 80: 9082–92.Google Scholar
Cetin, B, Benekli, M, Akyurek, N, et al. Isolated primary lymphomatoid granulomatosis of central nervous system. Indian J Hematol Blood Transfus. 2013; 29(1): 39–42.Google Scholar
Kermode, AG, Robbins, PD, Carroll, WM. Cerebral lymphomatoid granulomatosis. J Clin Neurosci. 1996; 3(4): 346–53.Google Scholar
Olmes, DG, Agaimy, A, Kloska, S, Linker, RA. Fatal lymphomatoid granulomatosis with primary CNS involvement in an immunocompetent 80-year-old woman. BMJ Case Rep. 2014; DOI: 10.1136/bcr-2014-206825.Google Scholar
Wiegand, T, Thai, D, Benowitz, N. Medical consequences of the use of hallucinogens: LSD, mescaline, PCP, and MDMA (“Ecstasy”). In Brick, J, ed. Handbook of the medical consequences of alcohol and drug abuse. 2nd ed. New York: Routledge; 2008. p. 461.Google Scholar
Giugliani, RV, Villareal, MLS, Valdez, C, et al. Guidelines for diagnosis and treatment of Hunter Syndrome for clinicians in Latin America. Genet Mol Biol. 2014; 37(2): 315–29. https://dx.doi.org/10.1590/S1415-47572014000300003.Google Scholar
Raluy-Callado, M, Chen, WH, Whiteman, DA, Fang, J, Wiklund, I. The impact of Hunter syndrome (mucopolysaccharidosis type II) on health-related quality of life. Orphanet J Rare Dis. 2013; 8: 101. DOI: 10.1186/1750-1172-8-101.Google Scholar
Scarpa, M, Almassy, Z, Beck, M, et al. Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease. Orphanet J Rare Dis. 2011; 6: 72. DOI: 10.1186/1750-1172-6-72.Google Scholar
Age-Related Eye Disease Study Research Group. A randomized, placebo-controlled, clinical trial of high-dose supplementation with vitamins C and E, beta carotene, and zinc for age-related macular degeneration and vision loss. Arch Ophthalmol. 2001; 119(10): 1417–36.Google Scholar
Schadlu, AP, Schadlu, R, Shepherd, JB. Charles Bonnet syndrome: a review. Curr Opin Ophthalmol. 2009: 20(3): 219–22.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Beauregard, M, Paquette, V, Levesque, J. Dysfunction in the neural circuitry of emotional self-regulation in major depressive disorder. Neuroreport. 2006; 17(8): 843–6.Google Scholar
Belmaker, RH, Agam, G. Major depressive disorder. New Engl J Med. 2008; 358(1): 55–68.Google Scholar
Cotter, D, Mackay, D, Landau, S, Kerwin, R, Everall, I. Reduced glial cell density and neuronal size in the anterior cingulate cortex in major depressive disorder. Arch Gen Psychiatry. 2001; 58(6): 545–53.Google Scholar
Holmes, AJ, Pizzagalli, DA. Spatiotemporal dynamics of error processing dysfunctions in major depressive disorder. Arch Gen Psychiatry. 2008; 65(2): 179–88.Google Scholar
Lee, H, Halverson, S, Ezinwa, N. Mosquito-borne diseases. Prim Care. 2018; 45(3): 393–407.Google Scholar
Salvana, EMT, Salata, RA, King, CH. Parasitic infections of the central nervous system. In Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. 5th ed. London: Academic Press; 2014. pp. 947–51.Google Scholar
World Health Organization. World malaria report 2017. Geneva (Switzerland): World Health Organization; 2017.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Meuleman, EJ, Van Lankveld, JJ. Hypoactive sexual desire disorder: An underestimated condition in men. BJU Int. 2005; 95(3): 291–6.Google Scholar
Segraves, KB, Segraves, RT. Hypoactive sexual desire disorder: Prevalence and comorbidity in 906 subjects. J Sex Marital Ther. 1991; 17(1): 55–8.Google Scholar
Stoléru, S, Redouté, J, Costes, N, et al. Brain processing of visual sexual stimuli in men with hypoactive sexual desire disorder. Psychiatry Res. 2003; 124(2): 67–86.Google Scholar
Rosenbaum, HK. Malignant hyperthermia. MedLink Neurology. Updated Jun 8, 2015. San Diego: MedLink Corporation. Available from www.medlink.com/article/malignant_hyperthermia. Accessed Aug 24, 2018.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Mittenberg, W, Patton, C, Canyock, EM, Condit, DC. Base rates of malingering and symptom exaggeration. J Clin Exp Neuropsychol. 2002; 24(8): 1094–102.Google Scholar
Pankratz, L, Erickson, RC. Two views of malingering. Clin Neuropsychol. 1990; 4(4): 379–89.Google Scholar
Rogers, R, ed. Clinical assessment of malingering and deception. New York: Guilford Press; 2008.Google Scholar
Stern, T, et al. Massachusetts General Hospital handbook of general hospital psychiatry. Philadephia, PA: Saunders; 2010.Google Scholar
Cersosimo, MG, Koller, WC. The diagnosis of manganese-induced parkinsonism. Neurotoxicology. 2006; 27(3): 340–6. PMID:16325915.Google Scholar
Chu, N-S, Huang, C-C, Calne, DB. Manganese. In Spencer, PS, Schaumburg, HH, eds. Experimental and clinical neurotoxicology. 2nd edition. Oxford, UK: Oxford University Press; 2000. pp. 752–5.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
McDonald, WM, Krishnan, KR, Doraiswamy, PM, et al. Occurrence of subcortical hyperintensities in elderly subjects with mania. Psychiatry Res. 1991; 40(4): 211–20.Google Scholar
Pares, P. Mania following deep brain stimulation for Parkinson's disease. Neurology. 2002; 59(9): 1421–4.Google Scholar
Peet, M. Induction of mania with selective serotonin re-uptake inhibitors and tricyclic antidepressants. Br J Psychiatry. 1994; 164(4): 549–50.Google Scholar
Starkstein, SE, Mayberg, HS, Berthier, ML, et al. Mania after brain injury: neuroradiological and metabolic findings. Ann Neurol. 1990; 27(6): 652–9.Google Scholar
Young, RC, Biggs, JT, Ziegler, VE, Meyer, DA. A rating scale for mania: reliability, validity and sensitivity. Br J Psychiatry. 1978; 133(5): 429–35.Google Scholar
Frazier, DM, et al. Nutrition management guideline for maple syrup urine disease: An evidence- and consensus-based approach. Mol Genet Metab. 2014; 112(3): 210–17.Google Scholar
NORD. Maple syprup urine disease. http://rarediseases.org/rare-diseases/maple-syrup-urine-disease/. Accessed Jun 20, 2016.Google Scholar
Strauss, KA, Puffenberger, EG, Morton, DH. Maple syrup urine disease. Jan 30, 2006. Updated May 9, 2013. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. Gene Reviews®. Seattle (WA): University of Washington, Seattle; 1993–2016. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1319/. Accessed Aug 25, 2018.Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. Diseases of the nervous system caused by nutritional deficiency. In Adams & Victor's principles of neurology, 10th ed. New York, NY: McGraw-Hill; 2014. Chapter 41.Google Scholar
Rosa, A, Demiati, M, Cartz, L, Mizon, JP. Marchiafava-Bignami disease, syndrome of interhemispheric disconnection, and right-handed agraphia in a left-hander. Arch Neurol. 1991; 48: 986.Google Scholar
Marom, T, et al. Trends in otitis media-related health care utilization in the United States, 2001–2011. JAMA Pediatr. 2014; 168(1): 68–75.Google Scholar
Wald, ER. Acute mastoiditis in children: Clinical features and diagnosis. In Post, TW, ed. UpToDate. Waltham, MA. Last updated Jan 3, 2017. https://www.uptodate.com/contents/acute-mastoiditis-in-children-clinical-features-and-diagnosis. Accessed Aug 25, 2018.Google Scholar
Centers for Disease Control and Prevention. Measles. In Hamborsky, J, et al., eds. Epidemiology and prevention of vaccine-preventable diseases (The Pink Book). 13th ed. Washington DC: Public Health Foundation; 2015. Chapter 13.Google Scholar
Gans, H, Maldonado, YA. Measles: Epidemiology and transmission. Last updated May 25, 2017. In Post, TW, ed. UpToDate. Waltham, MA. https://www.uptodate.com/contents/measles-epidemiology-and-transmission. Accessed Aug 25, 2018.Google Scholar
Demicheli, V, Rivetti, A, Debalini, MG, Di Pietrantonj, C. Vaccines for measles, mumps and rubella in children. Cochrane Database Syst Rev. 2012: CD004407.Google Scholar
Elliman, D, Sengupta, N, El Bashir, H, Bedford, H. Measles, mumps, and rubella: prevention. BMJ Clin Evid. 2007; 2007: pii: 0316.Google Scholar
Hendriksz, T, Malouf, P, Foy, JE. Advisory Committee on Immunization Practices (ACIP) of the Centers for Disease Control and PreventionVaccines for measles, mumps, rubella, varicella, and herpes zoster: immunization guidelines for adults. J Am Osteopath Assoc. 2011; 111(10 Suppl 6): S10–2.Google Scholar
McLean, HQ, Fiebelkorn, AP, Temte, JL, et al. Prevention of measles, rubella, congenital rubella syndrome, and mumps, 2013: summary recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Recomm Rep. 2013; 62: 1.Google Scholar
White, SJ, Boldt, KL, Holditch, SJ, Poland, GA, Jacobson, RM. Measles, mumps, and rubella. Clin Obstet Gynecol. 2012; 55(2): 550–9. DOI: 10.1097/GRF.0b013e31824df256.Google Scholar
Kristoffersen, ES, Lundqvist, C. Medication-overuse headache: a review. J Pain Res. 2014; 7: 367–78. DOI: 10.2147/JPR.S46071.Google Scholar
Kudrow, L. Paradoxical effects of frequent analgesic use. Adv Neurol. 1982; 33: 335–41.Google Scholar
Mathew, NT, Kurman, R, Perez, F. Drug induced refractory headache: clinical features and management. Headache. 1990; 30(10): 634–8.Google Scholar
Mehuys, E, Paemeleire, K, Van Hees, T, et al. Self-medication of regular headache: a community pharmacy-based survey. Eur J Neurol. 2012; 19(8): 1093–9.Google Scholar
De Bont, JM, Packer, RJ, Michiels, EM, Den Boer, ML, Pieters, R. Biological background of pediatric medulloblastoma and ependymoma: a review from a translational research perspective. Neuro-oncology. 2008; 10(6): 1040–60.Google Scholar
Kieffer-Renaux, V, Bulteau, C, Grill, J, et al. Patterns of neuropsychological deficits in children with medulloblastoma according to craniospatial irradiation doses. Dev Med Child Neurol. 2000; 42(11): 741–5.Google Scholar
Taran, SJ, Taran, R, Malipatil, N, Haridas, K. Paediatric medulloblastoma: an updated review. West Indian Med J. 2016; 65(2): 363–8.Google Scholar
Balasubramaniam, R, Ram, S. Orofacial movement disorders. Oral Maxillofac Surg Clin North Am. 2008: 20(2): 273–85.Google Scholar
Colosimo, C, Suppa, A, Fabbrini, G, Bologna, M, Berardelli, A. Craniocervical dystonia: clinical and pathophysiological features. Eur J Neurol. 2010; 17(s1): 15–21.Google Scholar
Kraft, SP, Lang, AE. Cranial dystonia, blepharospasm and hemifacial spasm: clinical features and treatment, including the use of botulinum toxin. CMAJ: Can Med Assoc J. 1988; 139(9): 837.Google Scholar
Choi, KN, Withers, HR, Rotman, M. Intracranial metastases from melanoma. Clinical features and treatment by accelerated fractionation. Cancer. 1985; 56(1): 1–9.Google Scholar
Hayward, RD. Malignant melanoma and the central nervous system. A guide for classification based on the clinical findings. J Neurol Neurosurg Psychiatr. 1976; 39(6): 526–30.Google Scholar
Raizer, JJ, Hwu, WJ, Panageas, KS, et al. Brain and leptomeningeal metastases from cutaneous melanoma: survival outcomes based on clinical features. Neuro-oncology. 2008; 10(2): 199–207.Google Scholar
Harcourt, J, Barraclough, K, Bronstein, AM. Meniere's disease. BMJ. 2014; 349. PMID: 25391837.Google Scholar
Silverstein, H, Smouha, E, Jones, R. Natural history vs. surgery for Meniere's disease. Otolaryngol Head Neck Surg. 1989; 100: 6–16.Google Scholar
Gerganov, V, Bussarsky, V, Romansky, K, et al. Cerebellopontine angle meningiomas. Clinical features and surgical treatment. J Neurosurg Sci. 2003; 47(3): 129–35.Google Scholar
Jiang, XB, Ke, C, Han, ZA, et al. Intraparenchymal papillary meningioma of brainstem: case report and literature review. World J Surg Oncol. 2012; 10: 10.Google Scholar
Wofford, JL, Moran, WP, Wilson, TA, Velez, R. Clinical presentation of meningioma in the elderly. J Am Geriatr Soc. 1993; 41(2): 122–6.Google Scholar
Kaler, SG. ATP7A-related copper transport disorders. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. Gene Reviews®. Updated Aug 18, 2016. Seattle, WA: University of Washington, Seattle; 1993–2017. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1413/.Google Scholar
Delgado, J. Intoxication from LSD and other common hallucinogens. UpToDate. Updated Sep 20, 2017. https://www.uptodate.com/contents/intoxication-from-lsd-and-other-common-hallucinogens?source=machineLearning&search=mescaline&selectedTitle=1∼4§ionRank=1&anchor=H15#H15. Accessed Aug 28, 2018.Google Scholar
Cendes, F. Febrile seizures and mesial temporal sclerosis. Curr Opin Neurol. 2004; 17(2): 161–4.Google Scholar
Garcia, CS. Depression in temporal lobe epilepsy: a review of prevalence, clinical features, and management considerations. Epilepsy Res Treat. 2012; 2012: 809843.Google Scholar
Lewis, DV. Losing neurons: selective vulnerability and mesial temporal sclerosis. Epilepsia. 2005; 46(Suppl 7): 39–44.Google Scholar
Spano, VR, Mikulis, DJ. Mesial temporal sclerosis in epilepsy. CMAJ. 2011; 183(15): E1151.Google Scholar
Gustavson, KH, Hagberg, B. The incidence and genetics of metachromatic leucodystrophy in northern Sweden. Acta Paediatr Scand. 1971; 60: 585.Google Scholar
Heinisch, U, Zlotogora, J, Kafert, S, Gieselmann, V. Multiple mutations are responsible for the high frequency of metachromatic leukodystrophy in a small geographic area. Am J Hum Genet. 1995; 56: 51.Google Scholar
Holve, S, Hu, D, McCandless, SE. Metachromatic leukodystrophy in the Navajo: fallout of the American-Indian wars of the nineteenth century. Am J Med Genet. 2001; 101: 203.Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. Inherited metabolic diseases of the nervous system. In Adams & Victor's principles of neurology, 10th ed. New York, NY: McGraw-Hill; 2014. Chapter 37.Google Scholar
Von Figura, K, Gieselmann, V, Jacken, J. Metachromatic leukodystrophy. In Scriver, CR, Beaudet, AL, Sly, WS, et al., eds. The metabolic and molecular bases of inherited diseases. 8th ed. New York: McGraw-Hill; 2001. p. 3695.Google Scholar
Zlotogora, J, Bach, G, Barak, Y, Elian, E. Metachromatic leukodystrophy in the habbanite Jews: high frequency in a genetic isolate and screening for heterozygotes. Am J Hum Genet. 1980 32: 663.Google Scholar
Ardakani, RK, Nahangi, H, Yadegari, M, Hosseini-Sharifabad, M. The effects of long-term administration of methamphetamine on the cerebellum of the male mice: a stereological study. The Neuroscience Journal of Shefaye Khatam. www.shefayekhatam.ir/browse.php?a_id=453&sid=1&slc_lang=en. Accessed Aug 28, 2018.Google Scholar
Foroughipour, M, Farzadfard, M, Aghaee, M, Ghabeli-Juibary, A, Rezaietalab, F. Methamphetamine related radiculopathy: case series and review of literature. Asia Pacific J Med Toxicol. 2013; 2(2): 71–5. DOI: 10.22038/apjmt.2013.894.Google Scholar
Gonzalez-Usigli, HA. Chorea, athetosis, and hemiballismus. MSD Manuals. Revised Feb 2017. Available from https://www.merckmanuals.com/professional/neurologic-disorders/movement-and-cerebellar-disorders/chorea,-athetosis,-and-hemiballismus. Accessed Aug 28, 2018.Google Scholar
NIDA. Methamphetamine. National Institute on Drug Abuse website. https://www.drugabuse.gov/publications/research-reports/methamphetamine. September 19, 2013. Accessed August 28, 2018.Google Scholar
Won, S, Hong, RA, Shohet, RV, Seto, TB, Parikh, NI. Methamphetamine-associated cardiomyopathy. Clin Cardiol. 2013; 36(12): 737–42. DOI: 10.1002/clc.22195.Google Scholar
Aminoff, MJ, Josephson, SA. Aminoff's neurology and general medicine. London, UK: Academic Press; 2014.Google Scholar
Jahnke, K, Korfel, A, Martus, P, et al. High-dose methotrexate toxicity in elderly patients with primary central nervous system lymphoma. Ann Oncol. 2005; 16(3): 445–9.Google Scholar
Wernick, R, Smith, DL. Central nervous system toxicity associated with weekly low-dose methotrexate treatment. Arthritis Rheum. 1989; 32(6): 770–5.Google Scholar
Warburg, M. Classification of microphthalmos and coloboma. J Med Genet. 1993; 30: 664–9.Google Scholar
Charles, A, Hansen, JM. Migraine aura: new ideas about cause, classification and clinical significance. Curr Opin Neurol. 2015; 28: 255–60.Google Scholar
Petrusic, I, Zidverc-Trajkovic, J. Cortical spreading depression; origins and paths as inferred from the sequence of events during migraine aura. Funct Neurol. 2014; 29: 207–12.Google Scholar
Reede, DL, Garcon, E, Smoker, WR, Kardon, R. Horner's syndrome: clinical and radiographic evaluation. Neuroimaging Clin N Am. 2008; 18(2): 369–85.Google Scholar
American Heart Association. Problem: mitral valve regurgitation. Feb 18, 2013. Available from www.heart.org/HEARTORG/Conditions/More/HeartValveProblemsandDisease/Problem-Mitral-Valve-Regurgitation_UCM_450612_Article.jsp. Accessed Jun 23, 2015.Google Scholar
Mayo Clinic Staff. Mitral valve regurgitation. Feb 18, 2015. Available from www.mayoclinic.org/diseases-conditions/mitral-valve-regurgitation/home/ovc-20121849. Accessed Jun 23, 2015.Google Scholar
Otto, CM, Bonow, RO. Valvular heart disease. In Mann, DL, Zipes, DP, Libby, P, Bonow, RO, Braunwald, E, eds. Braunwald's heart diseases: a textbook of cardiovascular medicine. 10th ed. Philadelphia: Elsevier/Saunders; 2015. pp. 1479–94.Google Scholar
American Heart Association. Problem: mitral valve stenosis. Aug 4, 2014. Available from www.heart.org/HEARTORG/Conditions/More/HeartValveProblemsandDisease/Problem-Mitral-Valve-Stenosis_UCM_450370_Article.jsp. Accessed Jun 23, 2015.Google Scholar
Mayo Clinic Staff. Mitral valve stenosis. Aug 22, 2014. Available from www.mayoclinic.org/diseases-conditions/mitral-valve-stenosis/basics/definition/con-20022582. Accessed Jun 23, 2015.Google Scholar
Otto, CM, Bonow, RO. Valvular heart disease. In Mann, DL, Zipes, DP, Libby, P, Bonow, RO, Braunwald, E, eds. Braunwald's heart diseases: a textbook of cardiovascular medicine. 10th ed. Philadelphia: Elsevier/Saunders; 2015. pp. 1469–79.Google Scholar
American Heart Association. Problem: mitral valve prolapse. Apr 24, 2015. Available from www.heart.org/HEARTORG/Conditions/More/HeartValveProblemsandDisease/Problem-Mitral-Valve-Prolapse_UCM_450441_Article.jsp. Accessed Jun 23, 2015.Google Scholar
Mayo Clinic Staff. Mitral valve prolapse. Apr 5, 2014. Available from www.mayoclinic.org/diseases-conditions/mitral-valve-prolapse/basics/definition/con-20024748. Accessed Jun 23, 2015.Google Scholar
Otto, CM, Bonow, RO. Valvular heart disease. In Mann, DL, Zipes, DP, Libby, P, Bonow, RO, Braunwald, E, eds. Braunwald's heart diseases: a textbook of cardiovascular medicine. 10th ed. Philadelphia: Elsevier/Saunders; 2015; pp. 1494–1497.Google Scholar
Farazmand, P, Woolley, PD, Kinghorn, GR. Mollaret's meningitis and HSV2 infections. Int J STD AIDS. 2011; 22(6): 306–7. DOI: 10.1258/ijsa.2010.010405.Google Scholar
Poulikakos, PJ, Sergi, EE, Margaritas, AS, et al. A case of recurrent benign lymphocytic (Mollaret's) meningitis and review of the literature. J Infect Public Health. 2010; 3(4): 192–5. Copyright © 2010 King Saud Bin Abdulaziz University for Health Sciences.Google Scholar
Steel, JG, Dix, RD, Baringer, JR. Isolation of herpes simplex type 1 in recurrent (Mollarets) meningitis. Trans Am Neurol Assoc. 1981; 106: 37–42.Google Scholar
Bindu, PS. Encephalopathy due to sulfite oxidase deficiency. Orphanet rare diseases portal. Updated Jan 2012. Available from www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=833. Accessed Aug 28, 2018.Google Scholar
Veldman, A, Santamaria-Araujo, JA, Sollazzo, S, et al. Successful treatment of molybdenum cofactor deficiency type A with cPMP. Pediatrics. 2010; 125(5): e1249–54. DOI: 10.1542/peds.2009–2192. Epub Apr 12, 2010.Google Scholar
Di Troia, A, Carpo, M, Meucci, N, et al. Clinical features and anti-neural reactivity in neuropathy associated with IgG monoclonal gammopathy of undetermined significance. J Neurol Sci. 1999; 164: 64–71.Google Scholar
Nobile-Orazio, E, Manfredini, E, Carpo, M, et al. Frequency and clinical correlates of anti-neural IgM antibodies in neuropathy associated with IgM monoclonal gammopathy. Ann Neurol. 1994; 36: 416–24.Google Scholar
Grover, A, Clark-Bilodeau, C, D'Ambrosio, CM. Restless leg syndrome in pregnancy. Obstet Med. 2015; 8(3): 121–5.Google Scholar
Kranick, SM, Mowry, EM, Colcher, A, Horn, S, Golbe, LI. Movement disorders and pregnancy: a review of the literature. Mov Disord. 2010; 25(6): 665–71.Google Scholar
Manconi, M, Govoni, V, De Vito, A, et al. Pregnancy as a risk factor for restless legs syndrome. Sleep Med. 2004; 5(3): 305–8.Google Scholar
Pathania, M, Upadhayaya, S, Lali, BS, Sharma, A. Chorea gravidarum: a rarity in West still haunts pregnant women in the East. BMJ Case Rep. 2013; pii: bcr2012008096. DOI: 10.1136/bcr-2012-008096.Google Scholar
Robottom, BJ, Reich, SG. Exposure to high dosage trihexyphenidyl during pregnancy for treatment of generalized dystonia: case report and literature review. Neurologist. 2011; 17(6): 340–1.Google Scholar
Singhal, AB. Moyamoya disease. Medlink Neurology. Updated Dec 1, 2015. San Diego: MedLink Corporation. Available from www.medlink.com.Google Scholar
Centers for Disease Control and Prevention. Mucormycosis. Available from www.cdc.gov/fungal/diseases/mucormycosis/index.html. Accessed Aug 28, 2018.Google Scholar
Gonzalez, CE, Rinaldi, MG, Sugar, AM. Mucormycosis. Infect Dis Clin North Am. 2002; 16: 895–914.Google Scholar
Petrikkos, G, Skiadda, A, Lortholary, O, et al. Epidemiology and clinical manifestations of mucormycosis. Clin Infect Dis. 2012; 4(suppl_1): S23–S34.Google Scholar
Spellberg, B, Edwards, J Jr, Ibrahim, A. Novel perspectives on mucormycosis: pathophysiology, presentation, and management. Clin Microbiol Rev. 2005; 18(3): 556–69.Google Scholar
Katirji, B, Kaminski, HJ, Ruff, RL. Neuromuscular disorders in clinical practice. 2nd ed. New York: Springer-Verlag New York; 2014.Google Scholar
Katirji, B, Kaminski, HJ, Ruff, RL. Neuromuscular disorders in clinical practice. 2nd ed. New York: Springer-Verlag New York; 2014.Google Scholar
Denier, C, Lozeron, P, Adams, D, et al. Multifocal neuropathy due to plasma cell infiltration of peripheral nerves in multiple myeloma. Neurology. 2006; 66(6): 917–8.Google Scholar
Dispenzieri, A, Kyle, RA. Neurological aspects of multiple myeloma and related disorders. Best Pract Res Clin Haematol. 2005; 18(4): 673–88.Google Scholar
Schluterman, KO, Fassas, AB, Van Hemert, RL, Harik, SI. Multiple myeloma invasion of the central nervous system. Arch Neurol. 2004; 61(9): 1423–9.Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. Multiple sclerosis and other inflammatory demyelinating diseases. In Adams & Victor's principles of neurology, 10th ed. New York, NY: McGraw-Hill; 2014. Chapter 36.Google Scholar
Alonso, A, Hernán, MA. Temporal trends in the incidence of multiple sclerosis: A systematic review. Neurology. 2008; 71(2): 129–35.Google Scholar
Alroughani, A, Altintas, A, Jumah, MA, et al. Pregnancy and the use of disease-modifying therapies in patients with multiple sclerosis: benefits versus risks. Mult Scler Int. 2016; 2016: 1034912.Google Scholar
Coyle, PK. Management of women with multiple sclerosis through pregnancy and after childbirth. Ther Adv Neurol Disord. 2016(3): 198–210.Google Scholar
Jankovic, J, Rajput, AH, McDermott, MP, Perl, DP. The evolution of diagnosis in early Parkinson disease. Parkinson Study Group. Arch Neurol. 2000; 57(3): 369–72.Google Scholar
Dąbrowska, M, Schinwelski, M, Sitek, EJ, et al. The role of neuroimaging in the diagnosis of the atypical parkinsonian syndromes in clinical practice. Neurol Neurochir Pol. 2015; 49(6): 421–31.Google Scholar
Iodice, V, Lipp, A, Ahlskog, JE, et al. Autopsy confirmed multiple system atrophy cases: Mayo experience and role of autonomic function tests. J Neurol Neurosurg Psychiatry. 2012; 83: 453–9.Google Scholar
Köllensperger, M, Geser, F, Ndayisaba, JP, et al. Presentation, diagnosis, and management of multiple system atrophy in Europe: final analysis of the European multiple system atrophy registry. Mov Disord. 2010; 25(15): 2604–12.Google Scholar
Tada, M, Onodera, O, Tada, M, et al. Early development of autonomic dysfunction may predict poor prognosis in patients with multiple system atrophy. Arch Neurol. 2007; 64(2): 256–60.Google Scholar
Wenning, GK, Stefanova, N. Recent developments in multiple system atrophy. J Neurol. 2009; 256: 1791–808.Google Scholar
Fanciulli, A, Wenning, GK. Multiple-system atrophy. New Engl J Med. 2015; 372: 249–63.Google Scholar
Lin, DJ, Hermann, KL, Schmahmann, JD. Multiple system atrophy of the cerebellar type: Clinical state of the art. Mov Disord. 2014; 29(4): 294–304.Google Scholar
Lin, IS, Wu, RM, Lee-Chen, GJ, Shan, DE, Gwinn-Hardy, K. The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairment. Parkinsonism Relat Disord. 2007; 13(4): 246–9.Google Scholar
Wenning, GK, Stefanova, N. Recent developments in multiple system atrophy. J Neurol. 2009; 256: 1791–808.Google Scholar
Anderson, LJ, Seward, JF. Mumps epidemiology and immunity: the anatomy of a modern epidemic. Pediatr Infect Dis J. 2008; 27: S75.Google Scholar
Bruyn, HB, Sexton, HM, Brainerd, HD. Mumps meningoencephalitis: a clinical review of 119 cases with one death. Calif Med. 1957; 86(3): 153–60.Google Scholar
Centers for Disease Control and Prevention. Mumps cases and outbreaks. Updated June 27, 2018. https://www.cdc.gov/mumps/outbreaks.html. Accessed Apr 6, 2017.Google Scholar
Dourado, I, Cunha, S, Teixeira, MG et al. Outbreak of aseptic meningitis associated with mass vaccination with a urabe-containing measles-mumps-rubella vaccine: implications for immunization programs. Am J Epidemiol. 2000; 151(5): 524–30.Google Scholar
Johnstone, JA, Ross, CAC, Dunn, M. Meningitis and encephalitis associated with mumps infection: a 10-year survey. Arch Dis Child. 1972; 47(254): 647–51.Google Scholar
Mclean, DM, Bach, RD, Larke, RP, McNaughton, GA. Mumps meningoencephalitis, Toronto, 1963. Can Med Assoc J. 1964; 90: 458.Google Scholar
World Health Organization. Mumps reported cases. Jul 15, 2018. http://apps.who.int/immunization_monitoring/globalsummary/timeseries/tsincidencemumps.html. Accessed Sep 6, 2018.Google Scholar
Amato, AA, Russell, JA. Neuromuscular disorders. New York: McGraw-Hill; 2008. pp. 143–56Google Scholar
Longo, DL, Kasper, DL, Fauci, A, et al., eds. Harrison's principles of internal medicine. 17th ed. New York: McGraw-Hill Education/Medical; 2016. pp. 1292, 1412, 1462–4.Google Scholar
Amato, AA, Russell, JA. Neuromuscular disorders. 2nd ed. New York: McGraw-Hill Medical; 2016.Google Scholar
Katirji, B, Kaminski, HJ, Ruff, RL. Neuromuscular disorders in clinical practice. 2nd ed. New York: Springer-Verlag New York; 2014.Google Scholar
Chaudhry, SA, Vignarajah, B, Koren, G. Myasthenia gravis during pregnancy. Can Fam Physician. 2012; 58(12): 1346–9.Google Scholar
Sanders, DB, Wolfe, GI, Benatar, M, et al. International consensus guidance for management of myasthenia gravis: Executive summary. Neurology. 2016; 87(4): 419–25.Google Scholar
Wolfe, GI, Kaminski, HJ, Aban, IB, et al.; MGTX Study Group. Randomized trial of thymectomy in myasthenia gravis. N Engl J Med. 2016; 375(6): 511–22.Google Scholar
Bitnun, A, Ford-Jones, E, Blaser, S, Richardson, S. Mycoplasma pneumoniae encephalitis. Semin Pediatr Infect Dis. 2003; 14: 96.Google Scholar
Daxboeck, F. Mycoplasma pneumoniae central nervous system infections. Curr Opin Neurol. 2006; 19: 374.Google Scholar
Foy, HM, Kenny, GE, Cooney, MK, Allan, ID. Long-term epidemiology of infections with Mycoplasma pneumoniae. J Infect Dis. 1979; 139: 681.Google Scholar
Gücüyener, K, Simşek, F, Yilmaz, O, et al. Methyl-prednisolone in neurologic complications of Mycoplasma pneumonia. Indian J Pediatr. 2000; 67(6): 467–9.Google Scholar
Tsiodras, S, Kelesidis, T, Kelesidis, I, et al. Mycoplasma pneumoniae-associated myelitis: a comprehensive review. Eur J Neurol. 2006; 13: 112.Google Scholar
Chun, JY, Smith, W, Halbach, VV, et al. Current multimodality management of infectious intracranial aneurysms. Neurosurgery. 2001; 48(6): 1203–13; discussion 1213–4.Google Scholar
Mandell, G. Infective endarteritis and mycotic aneurysms. In Mandell, G, Bennett, J, Dolin, R, eds. Principles and practice of infectious disease. Philadelphia: Churchill Livingstone; 2000. pp. 888–92.Google Scholar
American Heart Association. About heart attacks. May 15, 2015. Available from www.heart.org/HEARTORG/Conditions/HeartAttack/AboutHeartAttacks/About-Heart-Attacks_UCM_002038_Article.jsp. Accessed Jun 23, 2015.Google Scholar
Mayo Clinic Staff. Heart attack. Nov 15, 2014. Available from www.mayoclinic.org/diseases-conditions/heart-attack/basics/definition/con-20019520. Accessed Jun 23, 2015.Google Scholar
Scirica, BM, Morrow, DA. ST-elevation myocardial infarction: pathology, pathophysiology, and clinical features. In Mann, DL, Zipes, D, Libby, P, Bonow, RO, Braunwald, E, eds. Braunwald's heart disease: A textbook of cardiovascular medicine. 10th ed. Philadelphia, PA: Elsevier/Saunders; 2015; pp. 1071–85.Google Scholar
Amato, AA, Russell, JA. Neuromuscular disorders. New York: McGraw-Hill; 2008. pp. 143–56.Google Scholar
DiMauro, S, Hirano, M. MERRF. GeneReviews®. Jun 3, 2003. Updated Jan 29, 2015. Seattle (WA): University of Washington, Seattle; 1993–2017.Google Scholar
Tobon, A. Metabolic myopathies. Continuum (Minneap Minn). 2013; 19(6 Muscle Disease): 1571–97.Google Scholar
Hess, CW, Raymond, D, Aguiar Pde, C, Frucht, S, et al. Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers. Neurology. 2007; 68: 522–4.Google Scholar
Kinugawa, K, Vidailhet, M, Clot, F, et al. Myoclonus-dystonia: An update. Mov Disord. 2009; 24: 479–89.Google Scholar
Raymond, D, Ozelius, L. Myoclonus-dystonia. May 21, 2003. Updated Jan 26, 2012. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2016.Google Scholar
Zimprich, A, Grabowski, M, Asmus, F, et al. Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome. Nat Genet. 2001; 29: 66–9.Google Scholar
Goldstein, J, Austin, S, Kishnani, P, et al. Phosphorylase kinase deficiency. May 31, 2011. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2016.Google Scholar
Luica, A, Nogales-Gadea, G, Pérez, M, et al. McArdle disease – what do neurologists need to know? Nat Clin Pract Neurol. 2008; 4(10): 568–77. DOI: 10.1038/ncpneuro0913Google Scholar
Martín, MA, Lucía, A, Arenas, J, et al. Glycogen storage disease type V. Apr 19, 2006. Updated Jun 26, 2014. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2016.Google Scholar
Udd, B. The myotonic dystrophies: molecular, clinical, and therapeutic challenges. Lancet Neurol. 2012; 11(10): 891–905.Google Scholar
Wicklund, MP. The muscular dystrophies. Continuum (Minneap Minn). 2013; 19(6): 1535–70.Google Scholar
Udd, B. The myotonic dystrophies: molecular, clinical, and therapeutic challenges. Lancet Neurol. 2012; 11(10): 891–905.Google Scholar
Wicklund, MP. The muscular dystrophies. Continuum (Minneap Minn). 2013; 19(6): 1535–70.Google Scholar
Fassone, E, Shamima, R. REVIEW Complex I deficiency: clinical features, biochemistry and molecular genetics. J Med Genet. 2012; 49: 578–90.Google Scholar
Gorman, GS, Schaefer, AM, Ng, Y, et al. Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease. Ann Neurol. 2015; 77(5): 753–9. DOI: 10.1002/ana.24362.Google Scholar
Lightowlers, RN, Taylor, RW, Turnbull, DM. Mutations causing mitochondrial disease: What is new and what challenges remain? Science. 2015; 349(6255): 1494–9. DOI: 10.1126/science.aac7516.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Andlauer, O, Moore, IVH, Hong, SC, et al. Predictors of hypocretin (orexin) deficiency in narcolepsy without cataplexy. Sleep. 2012; 35: 1247–55.Google Scholar
Dauvilliers, Y, Arnulf, I, Mignot, E. Narcolepsy with cataplexy. Lancet. 2007; 369: 499–511.Google Scholar
Wang, J, Greenberg, H. Status cataplecticus precipitated by abrupt withdrawal of venlafaxine. J Clin Sleep Med. 2013; 9(7): 715–6.Google Scholar
Zeman, A, Britton, T, Douglas, N, et al. Narcolepsy and excessive daytime sleepiness. BMJ. 2004; 329: 724.Google Scholar
American Cancer Society. What are the key statistics about nasopharyngeal cancer? Updated Aug 8, 2016. Available from https://www.cancer.org/cancer/nasopharyngeal-cancer/about/key-statistics.html. Accessed Sep 9, 2018.Google Scholar
Rosenbaum, HE, Seaman, WB. Neurologic manifestations of nasopharyngeal tumors. Neurology. 1955; 5(12): 868–74.Google Scholar
Turgman, J, Braham, J, Modan, B, Goldhammer, Y. Neurological complications in patients with malignant tumors of the nasopharynx. Eur Neurol. 1978; 17(3): 149–54.Google Scholar
Clouston, PD, Sharpe, DM, Corbett, AJ, Kos, S, Kennedy, PJ. Perineural spread of cutaneous head and neck cancer. Its orbital and central neurologic complications. Arch Neurol. 1990; 47(1): 73–7.Google Scholar
Heroiu Cataloiu, AD, Danciu, CE, Popescu, CR. Multiple cancers of the head and neck. Maedica (Buchar). 2013; 8(1): 80–5.Google Scholar
Ruzevick, J, Olivi, A, Westra, WH. Metastatic squamous cell carcinoma to the brain: an unrecognized pattern of distant spread in patients with HPV-related head and neck cancer. J Neurooncol. 2013; 112(3): 449–54.Google Scholar
Brandtzaeg, P, Ovstebøo, R, Kierulf, P. Compartmentalization of lipopolysaccharide production correlates with clinical presentation in meningococcal disease. J Infect Dis. 1992; 166: 650.Google Scholar
Centers for Disease Control and Prevention. Meningococcal disease. Updated Apr 9, 2018. https://www.cdc.gov/meningococcal/index.html. Accessed Sep 9, 2018.Google Scholar
Heckenberg, SG, de Gans, J, Brouwer, MC, et al. Clinical features, outcome, and meningococcal genotype in 258 adults with meningococcal meningitis: a prospective cohort study. Medicine (Baltimore). 2008; 87: 185.Google Scholar
Julayanont, P, Ruthirago, D, DeToledo, JC. Bacterial meningitis and neurological complications in adults. SWRCCC. 2016; 4(14): 5–16.Google Scholar
Ropper, A, Samuels, M. Disease of the peripheral nervous system. In Adams and Victor's principles of neurology. 9th ed. New York: McGraw-Hill Education/Medical; 2009.Google Scholar
Amato, AA, Russell, JA. Neuromuscular disorders. New York: McGraw-Hill; 2008. pp. 578, 582–583.Google Scholar
Mah, JK, Joseph, JT. An overview of congenital myopathies. Continuum (Minneap Minn). 2016; 22(6): 1932–53.Google Scholar
Jung, HH, Danek, A, Walker, RH. Neuroacanthocytosis syndromes. Orphanet J Rare Dis. 2011; 6: 68.Google Scholar
Walker, RH. Untangling the thorns: advances in the neuroacanthocytosis syndromes. J Mov Disord. 2015; 8: 41–54.Google Scholar
Walker, RH, Jung, HH, Danek, A. Neuroacanthocytosis. Handb Clin Neurol. 2011; 100: 141–51.Google Scholar
Lee, J, Hegele, RA. Abetalipoproteinemia and homozygous hypobetalipoproteinemia: a framework for diagnosis and management. J Inherit Metab Dis. 2014; 37: 333–9.Google Scholar
Chinnery, PF. Neuroferritinopathy. Apr 25, 2005. Updated Dec 23, 2010. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2016. Available from: www.ncbi.nlm.nih.gov/books/NBK1141/. Accessed Aug 30, 2018.Google Scholar
Crompton, DE, Chinnery, PF, Bates, D, et al. Spectrum of movement disorders in neuroferritinopathy. Mov Disord. 2005; 20: 95–9.Google Scholar
McNeill, A, Birchall, D, Hayflick, SJ, et al. T2 and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulation. Neurology. 2008; 70: 1614–9.Google Scholar
OMIM. Neurodegeneration with brain iron accumulation 3; NBIA3 (606159). https://www.omim.org/entry/606159. Accessed Sep 9, 2018.Google Scholar
Wills, AJ, Sawle, GV, Guilbert, PR, Curtis, AR. Palatal tremor and cognitive decline in neuroferritinopathy. J Neurol Neurosurg Psychiatry. 2002; 73: 91–2.Google Scholar
Batista, PB, Bertollo, EM, de Souza, Costa D, et al. Neurofibromatosis: part 2 – clinical management. Arq Neuropsiquiatr. 2015; 73(6): 531–43.Google Scholar
Fox, CJ, Tomajian, S, Kaye, AJ, et al. Perioperative management of neurofibromatosis type 1. Ochsner J. 2012; 12(2): 111–21.Google Scholar
Pastar, Z, Lipozencić, J, Budimcić, D, Tomljanović-veselski, M. Neurofibromatosis: review of the literature and case report. Acta Dermatovenerol Croat. 2006; 14(3): 167–71.Google Scholar
Asthagiri, AR, Parry, DM, Butman, JA, et al. Neurofibromatosis type 2. Lancet. 2009; 373(9679): 1974–86.Google Scholar
Mathieu, D, Kondziolka, D, Flickinger, JC, et al. Stereotactic radiosurgery for vestibular schwannomas in patients with neurofibromatosis type 2: an analysis of tumor control, complications, and hearing preservation rates. Neurosurgery. 2007; 60(3): 460–8.Google Scholar
Pastar, Z, Lipozencić, J, Budimcić, D, Tomljanović-Veselski, M. Neurofibromatosis: review of the literature and case report. Acta Dermatovenerol Croat. 2006; 14(3): 167–71.Google Scholar
Bick, A, Meiner, Z, Gotkine, M, Levin, N. Using advanced methods to study neurolathyrism. IMAJ. 2016; 18: 341–5.Google Scholar
Ngudi, D. Research on motor neuron diseases konzo and neurolathyrism: trends from 1990 to 2010. PloS Negl Trop Dis. 2012; 6(7): 11759.Google Scholar
Tan, RY, Xing, G-Y, Zhou, G-M, et al. Toxin β-ODAP activates integrin β1 and focal adhesion: A critical pathway to cause neurolathyrism. Sci Rep. 2017; 7: 40677.Google Scholar
Asgari, N, Lillevang, ST, Skejoe, HP, et al. A population-based study of neuromyelitis optica in Caucasians. Neurology. 2011; 76: 1589.Google Scholar
Cabrera-Gómez, JA, Kurtzke, JF, González-Quevedo, A, Lara-Rodríguez, R. An epidemiological study of neuromyelitis optica in Cuba. J Neurol. 2009; 256: 35.Google Scholar
Crout, T, Parks, LP, Majithia, V. Neuromyelitis optica (Devic's syndrome): an appraisal. Curr Rheumatol Rep. 1999; 18(8): 54.Google Scholar
Flanagan, EP, Cabre, P, Weinshenker, BG, et al. Epidemiology of aquaporin-4 autoimmunity and neuromyelitis optica spectrum. Ann Neurol. 2016; Feb 17. DOI: 10.1002/ana.24617. [Epub ahead of print]Google Scholar
Jung, JS, Bhat, RV, Preston, GM, et al. Molecular characterization of an aquaporin cDNA from brain: candidate osmoreceptor and regulator of water balance. Proc Natl Acad Sci USA. 1994; 91: 13052.Google Scholar
Mealy, MA, Wingerchuk, DM, Greenberg, BM, Levy, M. Epidemiology of neuromyelitis optica in the United States: a multicenter analysis. Arch Neurol. 2012; 69: 1176.Google Scholar
Papais-Alvarenga, RM, Carellos, SC, Alvarenga, MP, et al. Clinical course of optic neuritis in patients with relapsing neuromyelitis optica. Arch Ophthalmol. 2008; 126: 12.Google Scholar
Sellner, J, Boggild, M, Clanet, M, et al. EFNS guidelines on diagnosis and management of neuromyelitis optica. Eur J Neurol. 2010; 17: 1019.Google Scholar
Uzawa, A, Mori, M, Kuwabara, S. Neuromyelitis optica: concept, immunology and treatment. J Clin Neurosci. 2014; 21: 12.Google Scholar
Amato, AA, Russell, JA. Neuromuscular disorders. New York: McGraw-Hill; 2008. pp. 144–56.Google Scholar
Cugati, S, Varma, DD, Chen, CS, Lee, AW. Treatment options for central retinal artery occlusion. Curr Treat Options Neurol. 2013; 15(1): 63–77.Google Scholar
Digre, KB. Neuro-ophthalmology and pregnancy: what does a neuro-ophthalmologist need to know? J Neuroophthalmol. 2011; 31(4): 381–7.Google Scholar
Errera, M, Kohly, RP, da Cruz, L. Pregnancy-associated retinal diseases and their management. Surv Ophthalmol. 2013; 58(2): 127–42.Google Scholar
Grant, AD, Chung, SM. The eye in pregnancy: ophthalmologic and neuro-ophthalmologic changes. Clin Obstet Gynecol. 2013; 56(2): 397–412.Google Scholar
Bradshaw, AD, Advincula, AP. Postoperative neuropathy in gynecologic surgery. Obstet Gynecol Clin North Am. 2010; 37(3): 451–9.Google Scholar
Padua, L, Aprile, I, Caliandro, P, et al.; Italian CTS Study Group. Carpal tunnel syndrome in pregnancy. Neurology. 2002; 59(10): 1643–6.Google Scholar
Sax, TW, Rosenbaum, RB. Neuromuscular disorders in pregnancy. Muscle Nerve. 2006; 34: 559–71.Google Scholar
Yoram, C, Lavie, O, Granovsky-Grisaru, S, Aboulafia, Y, Diamant, YZ. Bell palsy complicating pregnancy. Obs Gyn Survey. 2000; 55(3): 184–8.Google Scholar
Katirji, B, Kaminski, HJ, Ruff, RL. Neuromuscular disorders in clinical practice. 2nd ed. New York: Springer-Verlag New York; 2014.Google Scholar
Campagnolo, M, et al. Polyneuropathy with anti-sulfatide and anti-MAG antibodies: Clinical, neurophysiological, pathologic features and response to treatment. J Neuroimmunol. 2015; 281: 1–4.Google Scholar
Neuromuscular Disease Center. Anti-sulfatide antibodies in sensory-motor neuropathies. http://neuromuscular.wustl.edu/antibody/sulfatide.html. Accessed Aug 31, 2018.Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. Adams and Victor's principles of neurology. 10th ed. New York: McGraw-Hill Education/Medical; 2014.Google Scholar
Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
Wan, P, Moat, S, Anstey, A. Pellagra: a review with emphasis on photosensitivity. Br J Dermatol. 2011; 164: 1188.Google Scholar
Bomb, BS, Bedi, HK, Bhatnagar, LK. Post-ischaemic paresthesiae in pellagrins. J Neurol Neurosurg Psychiatry. 1977; 40: 265.Google Scholar
Ishii, N, Nishihara, Y. Pellagra among chronic alcoholics: Clinical and pathological study of 20 necropsy cases. J Neurol Neurosurg Psychiatry. 1981; 44: 209.Google Scholar
Jolliffe, N, Bowman, KM, Rosenblum, LA, Fein, HD. Nicotinic acid deficiency encephalopathy. JAMA. 1940; 114: 307.Google Scholar
Altschul, R, Hoffer, A, Stephen, JD. Influence of nicotinic acid on serum cholesterol in man. Arch Biochem Biophys. 1955; 54: 558.Google Scholar
Gharavi, AG, Diamond, JA, Smith, DA, Phillips, RA. Niacin-induced myopathy. Am J Cardiol. 1994; 74: 841.Google Scholar
Vilter, RW, Mueller, JF, Bean, WB. The therapeutic effect of tryptophane in human pellagra. J Lab Clin Med. 1949; 34: 409.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Hobson, JA, McCarley, RW. The brain as a dream state generator: an activation-synthesis hypothesis of the dream process. Am J Psychiatry. 1977; 134: 1335–48.Google Scholar
Krakow, B, Hollifield, M, Johnston, L, et al. Imagery rehearsal therapy for chronic nightmares in sexual assault survivors with posttraumatic stress disorder: a randomized controlled trial. JAMA. 2001; 286: 537–45.Google Scholar
Nadorff, MR, Lambdin, KK, Germain, A. Pharmacological and non-pharmacological treatments for nightmare disorder. Int Rev Psychiatry. 2014; 26: 225–36.Google Scholar
Nielsen, T, Zadra, A. Idiopathic nightmares and dream disturbances associated with sleep-wake transitions. In Kryger, MH, Roth, T, Dement, WC, eds. Principles and practice of sleep medicine. 5th ed. Philadelphia: Saunders; 2010. pp. 1106–15.Google Scholar
Becker, DE, Rosenberg, M. Nitrous oxide and the inhalation anesthetics. Anesth Progr. 2008; 55(4): 124–31. DOI: 10.2344/0003-3006-55.4.124.Google Scholar
Drug Addiction Treatment. Health effects of nitric oxide abuse. www.drugaddictiontreatment.com/types-of-addiction/club-drugs/health-effects-of-nitrous-oxide-abuse/. Accessed Aug 31, 2018.Google Scholar
McCann, SM, Kimura, M, Karanth, S, Yu, WH, Rettori, V. Nitric oxide controls the hypothalamic-pituitary response to cytokines. Neuroimmunomodulation. 1997; 4: 98–106. DOI: 10.1159/000097327.Google Scholar
Shoults, K. Case report: Neurologic complications of nitrous oxide abuse. BCMJ. 2016; 58(4): 192–4.Google Scholar
Anagnostou, T, Arvanitis, M, Kourkoumpetis, TK, et al. Nocardiosis of the central nervous system: experience from a general hospital and review of 84 cases from the literature. Medicine (Baltimore). 2014; 93(1): 19–32.Google Scholar
Brown-Elliott, BA, Brown, JM, Conville, PS, Wallace, RJ Jr. Clinical and laboratory features of the Nocardia spp. based on current molecular taxonomy. Clin Microbiol Rev. 2006; 19: 259.Google Scholar
Centers of Disease Control and Prevention. Nocardiosis. Updated Feb 24, 2017. https://www.cdc.gov/nocardiosis/. Accessed Aug 31, 2018.Google Scholar
Mamelak, AN, Obana, WG, Flaherty, JF, Rosenblum, ML. Nocardial brain abscess: treatment strategies and factors influencing outcome. Neurosurgery. 1994; 35: 622.Google Scholar
Johnson, LN, Guy, ME, Krohel, GB, Madsen, RW. Levodopa may improve vision loss in recent-onset, nonarteritic anterior ischemic optic neuropathy. Ophthalmology. 2000; 107: 521–6.Google Scholar
Levin, LA, Danesh-Meyer, HV. Hypothesis: a venous etiology for nonarteritic anterior ischemic optic neuropathy. Arch Ophthalmol. 2008; 126: 1582–5.Google Scholar
Miller, NR, ed. Anterior ischemic optic neuropathy. In Walsh and Hoyt's clinical neuro-ophthalmology. Vol 1. Baltimore: Williams & Wilkins; 1982. pp. 212–26.Google Scholar
Fernandez-Torre, JL, Kaplan, PW, Hernandez-Hernandez, MA. New understanding of nonconvulsive status epilepticus in adults: treatments and challenges. Expert Rev Neurother. 2015; 15(12): 1455–73.Google Scholar
Meierkord, H, Holtkamp, M. Non-convulsive status epilepticus in adults: clinical forms and treatment. Lancet Neurol. 2007; 6(4): 329–39.Google Scholar
Trinka, E, Cock, H, Hesdorffer, D, et al. A definition and classification of status epilepticus: Report of the ILAE Task Force on Classification of Status Epilepticus. Epilepsia. 2015; 56(10): 1515–23.Google Scholar
Alchanatis, M, Zias, N, Deligiorgis, N, et al. Sleep apnea-related cognitive deficits and intelligence: an implication of cognitive reserve theory. J Sleep Res. 2005; 14: 69–75.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Engleman, HM, Douglas, NJ. Sleepiness, cognitive function, and quality of life in obstructive sleep apnoea/hypopnoea syndrome. Thorax. 2004; 59: 618–22.Google Scholar
Engleman, HM, Ringshott, RN, Martin, SE, Douglas, NJ. Cognitive function in the sleep apnea/hypopnea syndrome (SAHS). [Abstract]. Sleep. 2000; 15(23): 102–8.Google Scholar
Littleton, SW, Mokhlesi, B. The Pickwickian syndrome – obesity hypoventilation syndrome. Clin Chest Med. 2009; 30(3): 467–78. DOI: 10.1016/j.ccm.2009.05.004Google Scholar
Mokhlesi, B. Obesity hypoventilation syndrome: a state-of-the-art review. Respir Care. 2010; 55(10): 1347–62.Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. The acquired metabolic disorders of the nervous system. In Adams and Victor's principles of neurology. 10th ed. New York: McGraw-Hill; 2014. p. 1132.Google Scholar
Abramowitz, JS, Taylor, S, McKay, D. Obsessive-compulsive disorder. Lancet. 2009; 374(9688): 491–9.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Baxter, LR, Phelps, ME, Mazziotta, JC, et al. Local cerebral glucose metabolic rates in obsessive-compulsive disorder: a comparison with rates in unipolar depression and in normal controls. Arch Gen Psychiatry. 1987; 44(3): 211–18.Google Scholar
Baxter, LR, Schwartz, JM, Bergman, KS, et al. Caudate glucose metabolic rate changes with both drug and behavior therapy for obsessive-compulsive disorder. Arch Gen Psychiatry. 1992; 49(9): 681–9.Google Scholar
Hirschtritt, ME, Lee, PC, Pauls, DL, et al.; Tourette Syndrome Association International Consortium for Genetics. Lifetime prevalence, age of risk, and genetic relationships of comorbid psychiatric disorders in Tourette syndrome. JAMA Psychiatry. 2015; 72(4): 325–33.Google Scholar
Spinello, C, Laviola, G, Macrì, S. Pediatric autoimmune disorders associated with streptococcal infections and Tourette's syndrome in preclinical studies. Front Neurosci. 2016; 10: 310.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Peppard, PE, Young, T, Barnet, JH, et al. Increased prevalence of sleep-disordered breathing in adults. Am J Epidemiol. 2013; 177: 1006–14.Google Scholar
Piazzini, A, et al. Visuoperceptive impairment in adult patients with occipital lobe epilepsies. Epilepsy Behav. 2009; 15(2): 256–9.Google Scholar
Polat, M, et al. Neurocognitive evaluation in children with occipital lobe epilepsy. Seizure. 2012; 21(4): 241–4.Google Scholar
Yang, PF, et al. Intractable occipital lobe epilepsy: clinical characteristics, surgical treatment, and a systematic review of the literature. Acta Neurochir (Wien). 2015; 157(1): 63–75.Google Scholar
Afridi, SK, Shields, KG, Bhola, R, Goadsby, PJ. Greater occipital nerve injection in primary headache syndromes: prolonged effects from a single injection. Pain. 2006; 122: 126–9.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
FitzGerald, PM, Jankovic, J. Tardive oculogyric crises. Neurology, 1989; 39(11): 1434.Google Scholar
Lee, MS, Kim, YD, Lyoo, CH. Oculogyric crisis as an initial manifestation of Wilson's disease. Neurology. 1999; 52(8): 1714–5.Google Scholar
Leigh, RJ, Foley, JM, Remler, BF, Civil, RH. Oculogyric crisis: a syndrome of thought disorder and ocular deviation. Ann Neurol. 1987; 22(1): 13–17.Google Scholar
Beal, JC, Cherian, K, Moshe, SL. Early-onset epileptic encephalopathies: Ohtahara syndrome and early myoclonic encephalopathy. Pediatr Neurol. 2012; 47(5): 317–23.Google Scholar
Alvarez, JA, Cohen, ML, Hlavin, ML. Primary intrinsic brainstem oligodendroglioma in an adult. J Neurosurg. 1996; 85(6): 1165–9. DOI: 10.3171/jns.1996.85.6.1165.Google Scholar
Bunevicius, A, Deltuva, VP, Deltuviene, D, Tamasauskas, A, Bunevicius, R. Brain lesions manifesting as psychiatric disorders: eight cases. CNS Spectr. 2008; 13(11): 950–8.Google Scholar
Hodges, SD, Malafronte, P, Gilhooly, J, et al. Rare brainstem oligodendroglioma in an adult patient: Presentation, molecular characteristics and treatment response. J Neurol Sci. 2015; 355(1-2): 209–10. DOI: 10.1016/j.jns.2015.05.019.Google Scholar
Lachi, PK, Irrakula, M, Ahmed, SF, et al. Clinical profile and outcomes in brainstem glioma: An institutional experience. Asian J Neurosurg. 2015; 10(4): 298–302. DOI: 10.4103/1793-5482.162709.Google Scholar
Mohindra, S, Savardekar, A, Bal, A. Pediatric brainstem oligodendroglioma. J Neurosci Rural Pract. 2012; 3(1): 52–4. DOI: 10.4103/0976-3147.91940.Google Scholar
Centers for Disease Control and Prevention. Parasites – Onchocerciasis (also known as river blindness). Aug 10, 2015. https://www.cdc.gov/parasites/onchocerciasis/index.html. Accessed Sep 2, 2018.Google Scholar
Johnson, T, Tyagi, R, Lee, P, et al. Nodding syndrome may be an autoimmune reaction to the parasitic worm Onchocerca volvulus. Sci Transl Med. 2017; 9(377): eaaf6953.Google Scholar
Njamnshi, A, Bisseck, AZ, Etya'ale, D. Onchocerciasis: neurological involvement. In Bentivoglio, M, Cavalheiro, E, Kristensson, K, Patel, N, eds. Neglected tropical diseases and conditions of the nervous system. New York, NY: Springer; 2014. pp. 147–64.Google Scholar
Twum-Danso, NA, Meredith, S. Variation in incidence of serious adverse events after onchocerciasis treatment with ivermectin in areas of Cameroon co-endemic for loiasis. Trop Med Int Health. 2003; 8(9): 820–31.Google Scholar
WHO. Signs, symptoms and treatment of onchocerciasis. www.who.int/onchocerciasis/symptoms/en/. Accessed Sep 2, 2018.Google Scholar
Ambrosetto, P, Nicolini, F, Zoli, M, et al. Ophthalmoplegic migraine: from questions to answers. Cephalalgia. 2014; 34(11): 914–19.Google Scholar
Friedman, A, Harter, D, Merritt, H. Ophthalmoplegic migraine. Arch Neurol. 1962; 7: 320–7.Google Scholar
Lal, V. Ophthalmoplegic migraine: Past, present and future. Neurol India. 2010; 58: 15–19.Google Scholar
Delta Medical Center. Opioid abuse signs, symptoms and effects. www.deltamedcenter.com/addiction/opiates/effects-symptoms-signs. Accessed Sept 2, 2018.Google Scholar
Hazelden Betty Ford Foundation. Signs of addiction. www.hazeldenbettyford.org/articles/addictive-substances-effects-and-withdrawal-symptoms. Accessed Sept 2, 2018.Google Scholar
Narconon. What parts of the body may be severely damaged by painkiller abuse? www.narconon.org/drug-abuse/prescription/painkillers/body-damage.html. Accessed Sept 2, 2018.Google Scholar
Symptoma. Opioid withdrawal. https://www.symptoma.com/en/info/opioid-withdrawal. Accessed Sept 2, 2018.Google Scholar
American Addiction Centers. Opioid withdrawal timelines. http://americanaddictioncenters.org/withdrawal-timelines-treatments/opiate/. Accessed Sep 9, 2018.Google Scholar
Compton, WM, Yolkow, ND. Abuse of prescription drugs and the risk of addiction. Drug Alcohol Depend. 2006; 83(Suppl 1): S4–S7.Google Scholar
NIH. Opiate and opioid withdrawal. Update Aug 14, 2018. https://medlineplus.gov/ency/article/000949.htm. Accessed Sep 9, 2018.Google Scholar
Lee, AG, Chau, FY, Golnik, KC, Kardon, RH, Wall, M. The diagnostic yield of the evaluation for isolated unexplained optic atrophy. Ophthalmology. 2005; 112(5): 757–9.Google Scholar
Van Stavern, GP, Newman, NJ. Optic neuropathies. An overview. Ophthalmol Clin North Am. 2001; 14(1): 61–71.Google Scholar
Parsa, CF, Hoyt, CS, Lesser, RL, et al. Spontaneous regression of optic gliomas: thirteen cases documented by serial neuroimaging. Arch Ophthalmol. 2001; 119(4): 516–29.Google Scholar
Eggenberger, ER. Inflammatory optic neuropathies. Ophthalmol Clin North Am. 2001; 14(1): 73–82.Google Scholar
Optic Neuritis Study Group. The clinical profile of optic neuritis. Experience of the Optic Neuritis Treatment Trial. Arch Ophthalmol. 1991; 109(12): 1673–8.Google Scholar
Percy, AK, Nobrega, FT, Kurland, LT. Optic neuritis and multiple sclerosis. An epidemiologic study. Arch Ophthalmol. 1972; 87: 135.Google Scholar
Rodriguez, M, Siva, A, Cross, SA, et al. Optic neuritis: a population-based study in Olmsted County, Minnesota. Neurology. 1995; 45: 244.Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. Disturbances of vision. In Adams & Victor's principles of neurology. 10th ed. New York, NY: McGraw-Hill; 2014. Chapter 13.Google Scholar
Van Stavern, GP, Newman, NJ. Optic neuropathies. An overview. Ophthalmol Clin North Am. 2001; 14(1): 61–71.Google Scholar
Frankefort, N, Salu, P, Van Tussenbfoek, F. Orbital arteriovenous fistula with symptoms contralateral to the arterial supply. A case report. Bull Soc Belge Ophthalmol. 2005; 296: 63–7.Google Scholar
Ohtsuka, K, Hashimoto, M. Clinical findings in a patient with spontaneous arteriovenous fistulas of the orbit. Am J Ophthalmol. 1999; 127(6): 736–7.Google Scholar
Lima, V, Burt, B, Leibovitch, I, et al. Orbital compartment syndrome: the ophthalmic surgical emergency. Surv Ophthalmol. 2009; 54(4): 441–9.Google Scholar
Moin, M, Kersten, RC, Bernardini, F, et al. Spontaneous hemorrhage in an intraorbital arteriovenous malformation. Ophthalmology. 2000; 107(12): 2215–9.Google Scholar
Popat, H, Doyle, PT, Davies, SJ. Blindness following retrobulbar haemorrhage: it can be prevented. Br J Oral Maxillofac Surg. 2007; 45(2): 163–4.Google Scholar
Demirci, H, Shields, CL, Shields, JA, et al. Orbital tumors in the older adult population. Ophthalmology. 2002; 109(2): 243–8.Google Scholar
Rootman, J, Robertson, W, Lapointe, JS. Inflammatory diseases. In Rootman, J, ed. Diseases of the orbit: a multidisciplinary approach. Philadelphia: J.B. Lippincott; 1988. pp. 143–204.Google Scholar
Hatef, E, Roberts, D, McLaughlin, P, Pro, B, Esmaeli, B. Prevalence and nature of systemic involvement and stage at initial examination in patients with orbital and ocular adnexal lymphoma. Arch Ophthalmol. 2007; 125(12): 1663–7.Google Scholar
Shields, JA, Shields, CL, Scartozzi, R. Survey of 1264 patients with orbital tumors and simulating lesions. The 2002 Montgomery Lecture, Part 1. Ophthalmology. 2004; 111: 997–1008.Google Scholar
Balasubramaniam, R, Ram, S. Orofacial movement disorders. Oral Maxillofac Surg Clin North Am. 2008; 20(2): 273–85.Google Scholar
Evidente, VGH, Adler, CH. Hemifacial spasm and other craniofacial movement disorders. Mayo Clin Proc. 1998; 73(1): 67–71.Google Scholar
Kraft, SP, Lang, AE. Cranial dystonia, blepharospasm and hemifacial spasm: clinical features and treatment, including the use of botulinum toxin. CMAJ. 1988; 139(9): 837–44.Google Scholar
Gerschlager, W, Brown, P. Orthostatic tremor – a review. Handb Clin Neurol. 2011; 100: 457–62.Google Scholar
McDonald, J, Bayrak-Toydemir, P, Pyeritz, RE. Hereditary hemorrhagic telangiectasia: An overview of diagnosis, management, and pathogenesis. Genet Med. 2011; 13: 607–16. DOI: 10.1097/GIM.0b013e3182136d32.Google Scholar
Arden, N, Blanco, F, Cooper, C, et al. Atlas of osteoarthritis. New York: Springer Healthcare Communications. 2015; p. 21.Google Scholar
Mayo Clinic. Swollen knee. https://www.mayoclinic.org/diseases-conditions/swollen-knee/symptoms-causes/syc-20378129. Accessed Sep 3, 2018.Google Scholar
Stavridis, SI, Pingel, A, Schnake, KJ, Kandziora, F. Diagnosis and treatment of a C2-osteoblastoma encompassing the vertebral artery. Eur Spine J. 2013; 22(11): 2504–12. DOI: 10.1007/s00586-013-2875-5.Google Scholar
Kandziora, F, Pingel, A. Posterior-anterior resection of a cervical spine osteoblastoma. Eur Spine J. 2010; 19(6): 1041–3. DOI: 10.1007/s00586-010-1461-3.Google Scholar
Gutteck, N, Mendel, T, Held, A, Wohlrab, D. Cervical spine osteoblastoma in children: selective diagnostics as the basis for effective surgical management. Orthopade. 2010; 39(1): 92–6. DOI: 10.1007/s00132-009-1530-7.Google Scholar
Samdani, A, Torre-Healy, A, Chou, D, Cahill, AM, Storm, PB. Treatment of osteoblastoma at C7: a multidisciplinary approach. A case report and review of the literature. Eur Spine J. 2009; 18(Suppl 2): 196–200. DOI: 10.1007/s00586-008-0806-7.Google Scholar
Miller, C, Khan, R, Lemole, GM Jr, Jacob, A. Osteoblastoma of the lateral skull base: work-up, surgical management, and a review of the literature. J Neurol Surg Rep. 2013; 74(1): 37–42. Epub 2013 Jun 13. DOI: 10.1055/s-0033-1346978.Google Scholar
Han, X, Dong, Y, Sun, K, Lu, Y. A huge occipital osteoblastoma accompanied with aneurysmal bone cyst in the posterior cranial fossa. Clin Neurol Neurosurg. 2008; 110(3): 282–5. Epub 2007 Dec 4.Google Scholar
Boaro, A, Marton, E, Mazzucco, GM, Longatti, P. Osteoblastoma mimicking an idiopathic intracranial hypertension syndrome. J Pediatr Neurosci. 2017; 12(1): 87–90. DOI: 10.4103/jpn.JPN_167_16.Google Scholar
Miller, C, Khan, R, Lemole, GM Jr, Jacob, A. Osteoblastoma of the lateral skull base: Work-up, surgical management, and a review of the literature. J Neurol Surg Rep. 2013; 74: 37–42.Google Scholar
Castro-Castro, J, Rodiño-Padín, J, Touceda-Bravo, A, Castro-Bouzas, D, Pinzón-Millán, A. Cervical spine osteochondroma presenting with torticollis and hemiparesis. Neurocirugia (Astur). 2014; 25(2): 94–7. Epub 2013 Oct 16.Google Scholar
Certo, F, Sciacca, G, Caltabiano, R, et al. Anterior, extracanalar, cervical spine osteochondroma associated with DISH: description of a very rare tumor causing bilateral vocal cord paralysis, laryngeal compression and dysphagia. Case report and review of the literature. Eur Rev Med Pharmacol Sci. 2014; 18(1 Suppl): 34–40.Google Scholar
Herget, GW, Kontny, U, Saueressig, U, et al. Osteochondroma and multiple osteochondromas: recommendations on the diagnostics and follow-up with special consideration to the occurrence of secondary chondrosarcoma. Radiologe. 2013; 53(12): 1125–36.Google Scholar
Huegel, J, Sgariglia, F, Enomoto-Iwamoto, M, et al. Heparan sulfate in skeletal development, growth, and pathology: the case of hereditary multiple exostoses. Dev Dyn. 2013; 242(9): 1021–32. Epub 2013 Jul 29.Google Scholar
Mnif, H, Koubaa, M, Zrig, M, Zammel, N, Abid, A. Peroneal nerve palsy resulting from fibular head osteochondroma. Orthopedics. 2009; 32(7): 528.Google Scholar
Sciubba, DM, Macki, M, Bydon, M, et al. Long-term outcomes in primary spinal osteochondroma: a multicenter study of 27 patients. J Neurosurg Spine. 2015; 22(6): 582–8. DOI: 10.3171/2014.10.SPINE14501.Google Scholar
Tian, Y, Yuan, W, Chen, H, Shen, X. Spinal cord compression secondary to a thoracic vertebral osteochondroma. J Neurosurg Spine. 2011; 15(3): 252–7. Epub 2011 May 20.Google Scholar
Mankin, HJ. Rickets, osteomalacia and renal osteodystrophy. An update. Orthop Clin North Am. 1990; 21(1): 81–96.Google Scholar
Kaplan, SL. Osteomyelitis in children. Infect Dis Clin North Am. 2005; 19(4): 787–97, vii.Google Scholar
Zimmerli, W. Clinical practice. Vertebral osteomyelitis. N Engl J Med. 2010; 362(11): 1022–9.Google Scholar
Lynn, SG, Sinaki, M, Westerlind, KC. Balance characteristics of persons with osteoporosis. Arch Phys Med Rehabil. 1997; 78(3): 273–7.Google Scholar
Fischgrund, JS, ed. Orthopaedic knowledge update 9. Rosemont, IL: American Academy of Orthopaedic Surgeons; 2008.Google Scholar
Huvos, AG. Bone tumors: diagnosis treatment and prognosis. Vol 2. Philadelphia: W.B. Saunders. Co; 1991.Google Scholar
Katonis, P, et al. Spinal osteosarcoma. Clin Med Insights Oncol. 2013; 7: 199–208. PMC. Web. Jun 5, 2017.Google Scholar
McIntyre, JF, Smith-Sorensen, B, Friend, SH, et al. Germline mutations of the p53 tumor suppressor gene in children with osteosarcoma. J Clin Oncol. 1994; 12: 925–30.Google Scholar
Mirabello, L, Troisi, RJ, Savage, SA. Osteosarcoma incidence and survival rates from 1973 to 2004: data from the Surveillance, Epidemiology, and End Results Program. Cancer. 2009; 115(7): 1531–43.Google Scholar
Ozaki, T, Flege, S, Liljenqvist, U, et al. Osteosarcoma of the spine: experience of the Cooperative Osteosarcoma Study Group. Cancer. 2002; 94(4): 1069–77.Google Scholar
Causse, JB, Causse, JR, Cezard, R, et al. Vertigo in postoperative follow-up of otosclerosis. Am J Otol. 1988; 9: 246–55.Google Scholar
Grayeli, AB, Sterkers, O, Toupet, M. Audiovestibular function in patients with otosclerosis and balance disorders. Otol Neurotol. 2009; 30: 1085–91.Google Scholar
Hlzll, Ö, Kaya, S, Schachern, PA, et al. Quantitative assessment of vestibular otopathology in otosclerosis: A temporal bone study. Laryngoscope. 2016; 126: E118–22.Google Scholar
Lin, KY, Young, YH. Role of ocular VEMP test in assessing the occurrence of vertigo in otosclerosis patients. Clin Neurophysiol. 2015; 126: 187–93.Google Scholar
Breast Cancer Linkage Consortium. Cancer risks in BRCA2 mutation carriers. J Natl Cancer Inst. 1999; 91(15): 1310–6.Google Scholar
Newton, HB, Malkin, MG. Neurological complications of systemic cancer and antineoplastic therapy. (Neurological Disease and Therapy series: Vol 96). Boca Raton, FL: CRC Press; 2016. p. 307.Google Scholar
Reid, BM, Permuth, JB, Sellers, TA. Epidemiology of ovarian cancer: a review. Cancer Biol Med. 2017; 14(1): 9–32.Google Scholar
Wentzensen, N, Poole, EM, Trabert, B, et al. Ovarian cancer risk factors by histologic subtype: an analysis from the Ovarian Cancer Cohort Consortium. J Clin Oncol. 2016; 34(24): 2888–98. Epub 2016 Jun 20.Google Scholar
Dove, J. Complete fracture of the femur in Paget's disease of the bone. J Bone Joint Surg Br. 1980; 62–B(1): 12–7.Google Scholar
Lyles, KW, Siris, ES, Singer, FR, Meunier, PJ. A clinical approach to diagnosis and management of Paget's disease of bone. J. Bone Miner Res. 2001; 16(8): 1379–87.Google Scholar
Deuschl, G, Mischke, G, Schenck, E, Schulte-Monting, J, Lucking, CH. Symptomatic and essential rhythmic palatal myoclonus. Brain. 1990; 113: 1645–72.Google Scholar
Zadikoff, C, Lang, AE, Klein, C. The ‘essentials’ of essential palatal tremor: a reappraisal of the nosology. Brain. 2006; 129: 832–40.Google Scholar
Vieregge, P, Klein, C, Gehrking, E, Kurtke, D. The diagnosis of ‘essential’ palatal tremor. Neurology. 1997; 49: 248–9Google Scholar
Deuschl, G, Toro, C, Hallett, M. Symptomatic and essential palatal tremor. 2. Differences of palatal movements. Mov Disord. 1994; 9(6): 676–8.Google Scholar
Kadakia, S, McAbee, G. Volitional control of palatal myoclonus. Mov Disord. 1990; 5: 182–3.Google Scholar
Lemke, J, Scheele, J, Kapapa, T, et al. Brain metastasis in pancreatic cancer. Int J Mol Sci. 2013; 14(2): 4163–73. DOI: 10.3390/ijms14024163.Google Scholar
Makarova-Rusher, OV, Ulahannan, S, Greten, TF, Duffy, A. Pancreatic squamous cell carcinoma: a population-based study of epidemiology, clinicopathologic characteristics and outcomes. Pancreas. 2016; 45(10): 1432–7.Google Scholar
Newton, HB, Malkin, MG. Neurological complications of systemic cancer and antineoplastic therapy. (Neurological Disease and Therapy series: Vol 96). Boca Raton, FL: CRC Press; 2016. p. 330.Google Scholar
Patchell, RA, Tibbs, PA, Walsh, JW, et al. A randomized trial of surgery in the treatment of single metastases to the brain. N Engl J Med. 1990; 322: 494–500.Google Scholar
Rana-Guajardo, AC, Cámara-Lemarroy, CR, Rendón-Ramírez, EJ, et al. Wernicke encephalopathy presenting in a patient with severe acute pancreatitis. JOP. 2012; 13: 104.Google Scholar
Ruggieri, RM, Lupo, I, Piccoli, F. Pancreatic encephalopathy: a 7-year follow-up case report and review of the literature. Neurol Sci. 2002; 23: 203–5.Google Scholar
Tsai, HH, Hsieh, CH, Liou, CW, et al. Encephalopathy and acute axonal sensorimotor polyneuropathy following acute pancreatitis: a case report and review of the literature. Pancreas. 2005; 30(3): 285–7.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Breslau, N, Schultz, LR, Stewart, WF, Lipton, R, Welch, KMA. Headache types and panic disorder: Directionality and specificity. Neurology. 2001; 56(3): 350–4.Google Scholar
Cox, BJ, Swinson, RP, Endler, NS, Norton, GR. The symptom structure of panic attacks. Compr Psychiatry. 1994; 35(5): 349–53.Google Scholar
Ley, R. Agoraphobia, the panic attack and the hyperventilation syndrome. Behav Res Ther. 1985; 23(1): 79–81.Google Scholar
Reiman, EM, Raichle, ME, Butler, FK, Herscovitch, P, Robins, E. A focal brain abnormality in panic disorder, a severe form of anxiety. Nature. 1984; 310(5979): 683–5.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Beletsky, V, Mirsattari, SM. Epilepsy, Mental health disorders, or both? Epilepsy Res Treat. 2012; Article ID 163731. http://dx.doi.org/10.1155/2012/163731.Google Scholar
Cassem, NH, Stern, TA, Rosenbaum, JF, Jellinek, MS, Fricchione, GL. Massachusetts General Hospital handbook of general hospital psychiatry. 6th ed. St. Louis, MO: Mosby; 2004.Google Scholar
Kessler, RC, Chiu, WT, Jin, R, et al. The epidemiology of panic attacks, panic disorder, and agoraphobia in the National Comorbidity Survery Replication. Arch Gen Psychiatry. 2006; 63(4): 415–24.Google Scholar
Lyketsos, CG, Kozauer, N, Rabins, PV. Psychiatric manifestations of neurologic disease: Where are we headed? Dialog Clin Neurosci. 2007; 9(2): 111–24.Google Scholar
Nadarajan, V, Perry, RJ, Johnson, J, Werring, DJ. Transient ischemic attack: mimics and chameleons. Pract Neurol. 2013; 14: 23–31.Google Scholar
Rizzo, M, Eslinger, PJ. Principles and practice of behavioral neurology and neuropsychology. Philadelphia, PA: W.B. Saunders; 2004.Google Scholar
Gordon, N. Pantothenate kinase-associated neurodegeneration (Hallevorden-Spatz syndrome). Eur Paediatr Neurol Soc. 2002; (6): 243–7.Google Scholar
Gregory, A, Hayflick, SJ. Neurodegeneration with brain iron accumulation. Folia Neuropathol. 2005; 43(4): 286–96.Google Scholar
Mikati, MA, Yehya, A, Darwish, H, Karam, P, Comair, Y. Deep brain stimulation as a mode of treatment of early onset pantothenate kinase-associated neurodegeneration. Eur J Pediatr Neurol. 2008; 13(1): 61–4.Google Scholar
Shields, DC, Sharma, N, Gale, JT, Eskandar, EN. Pallidal stimulation for dystonia in pantothenate kinase-associated neurodegeneration. Pediatr Neurol. 2007; 37(6): 442–5.Google Scholar
de Almeida, SM. Central nervous system paracoccidioidomycosis: an overview. Braz J Infect Dis. 2005; 9(2): 126–33.Google Scholar
Martinez, R. Epidemiology of paracoccidioidomycosis. Rev Inst Med Trop Sao Paulo. 2015: 57(Suppl 19): 11–20.Google Scholar
Abermil, N, Guillaud-Bataille, M, Burnichon, N, et al. TMEM127 screening in a large cohort of patients with pheochromocytoma and/or paraganglioma. J Clin Endocrinol Metab. 2012; 97: E805–9.Google Scholar
Anderson, J, Gulant, RW. Paraganglioma of the cauda equina: a case report. J Neurol Neurosurg Psychiatry. 1987; 50: 100–3.Google Scholar
Bayley, JP, Kunst, HP, Cascon, A, et al. SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma. Lancet Oncol. 2010; 11: 366–72.Google Scholar
Kirmani, S, Young, WF. Hereditary paraganglioma-pheochromocytoma syndromes. May 21, 2008. Updated Nov 6, 2014. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2017.Google Scholar
Papathomas, TG, de Krijger, RR, Tischler, AS. Paragangliomas: update on differential diagnostic considerations, composite tumors, and recent genetic developments. Semin Diagn Pathol. 2013; 30(3): 207–23. DOI: 10.1053/j.semdp.2013.06.006.Google Scholar
Centers for Disease Control and Prevention. Paragonimiasis. www.cdc.gov. Accessed Sep 4, 2018.Google Scholar
Johnson, RJ, Jong, EC, Dunning, SB, et al. Paragonimiasis: diagnosis and the use of praziquantel in treatment. Rev Infect Dis 1985; 7: 200.Google Scholar
Kim, MK, Cho, BM, Yoon, DY. Imaging features of intradural spinal paragonimiasis: A case report Br J Radiol. 2011 Apr; 84(1000): e72–e74.Google Scholar
Xia, Y, Ju, Y, Chen, J, You, C. Cerebral paragonimiasis: a retrospective analysis of 27 cases. J Neurosurg Pediatr 2015; 15: 101.Google Scholar
Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. 5th ed. London, UK: Elsevier; 2014.Google Scholar
Ka, A, Britton, P, Troedson, C, et al. Mild encephalopathy with reversible splenial lesion: An important differential of encephalitis. Eur J Paediatr Neurol. 2015; 19(3): 377–82.Google Scholar
Fry, AM, Curns, AT, Harbour, K, et al. Seasonal trends of human parainfluenza viral infections: United States, 1990–2004. Clin Infect Dis. 2006; 43(8): 1016–22. Epub 2006 Sep 13.Google Scholar
Bataller, L, Dalmau, J. Paraneoplastic disorders of the nervous system. Continuum (Minneap Minn). 2005; 11(5, Neuro-Oncology): 69–92. DOI: 10.1212/01.con.0000293680.24426.ae.Google Scholar
Honnorat, J, Antoine, J-C. Paraneoplastic neurological syndromes. Orphanet J Rare Dis. 2007; 2: 22. DOI: 10.1186/1750-1172-2-22.Google Scholar
Lancaster, E. Paraneoplastic disorders. Continuum (Minneap Minn). 2015; 21(2, Neuro-Oncology): 452–75. DOI: 10.1212/01.CON.0000464180.89580.88.Google Scholar
Muppidi, S, Vernino, S. Paraneoplastic neuropathies. Continuum (Minneap Minn). 2014; 20(5, Peripheral Nervous System Disorders): 1359–72. DOI: 10.1212/01.CON.0000455876.53309.ec.Google Scholar
Bataller, L, Dalmau, J. Paraneoplastic disorders of the nervous system. Continuum (Minneap Minn). 2005; 11(5, Neuro-Oncology): 69–92. DOI: 10.1212/01.con.0000293680.24426.ae.Google Scholar
Honnorat, J, Antoine, J-C. Paraneoplastic neurological syndromes. Orphanet J Rare Dis. 2007; 2: 22. DOI: 10.1186/1750-1172-2-22.Google Scholar
Lancaster, E. Paraneoplastic disorders. Continuum (Minneap Minn). 2015; 21(2, Neuro-Oncology): 452–75. DOI: 10.1212/01.CON.0000464180.89580.88.Google Scholar
Muppidi, S, Vernino, S. Paraneoplastic neuropathies. Continuum (Minneap Minn). 2014; 20(5, Peripheral Nervous System Disorders): 1359–72. DOI: 10.1212/01.CON.0000455876.53309.ec.Google Scholar
Bataller, L, Dalmau, J. Paraneoplastic disorders of the nervous system. Continuum (Minneap Minn). 2005; 11(5, Neuro-Oncology): 69–92. DOI: 10.1212/01.con.0000293680.24426.ae.Google Scholar
Honnorat, J, Antoine, J-C. Paraneoplastic neurological syndromes. Orphanet J Rare Dis. 2007; 2: 22. DOI: 10.1186/1750-1172-2-22.Google Scholar
Lancaster, E. Paraneoplastic disorders. Continuum (Minneap Minn). 2015; 21(2, Neuro-Oncology): 452–75. DOI: 10.1212/01.CON.0000464180.89580.88.Google Scholar
Muppidi, S, Vernino, S. Paraneoplastic neuropathies. Continuum (Minneap Minn). 2014; 20(5, Peripheral Nervous System Disorders): 1359–72. DOI: 10.1212/01.CON.0000455876.53309.ec.Google Scholar
Rosenfeld, MR, Dalmau, JO. Paraneoplastic disorders of the CNS and autoimmune synaptic encephalitis. Continuum (Minneap Minn). 2012; 18(2, Neuro-Oncology): 366–83. DOI: 10.1212/01.CON.0000413664.42798.aa.Google Scholar
Turk, HM, et al. Paraneoplastic motor neuron disease resembling amyotrophic lateral sclerosis in a patient with renal cell carcinoma. Med Princ Pract. 2009; 18(1): 73–5.Google Scholar
Arroyo, HA, Tringler, N. Opsoclonus-myoclonus syndrome. Medicina (B Aires). 2009; 69(1 Pt 1): 64–70.Google Scholar
Bataller, L, Dalmau, J. Paraneoplastic disorders of the nervous system. Continuum (Minneap Minn). 2005; 11(5, Neuro-Oncology): 69–92. DOI: 10.1212/01.con.0000293680.24426.ae.Google Scholar
Blumkin, L, Lerman-Sagie, T. Opsoclonus myoclonus ataxia syndrome in Israel. Harefuah. 2010; 149(1): 24–8, 63.Google Scholar
Catsman-Berrevoets, CE, Aarsen, FK, van Hemsbergen, ML, et al. Improvement of neurological status and quality of life in children with opsoclonus myoclonus syndrome at long-term follow-up. Pediatr Blood Cancer. 2009; 53(6): 1048–53.Google Scholar
Honnorat, J, Antoine, J-C. Paraneoplastic neurological syndromes. Orphanet J Rare Dis. 2007; 2: 22. DOI: 10.1186/1750-1172-2-22.Google Scholar
Matsumoto, H, Ugawa, Y. Paraneoplastic opsoclonus-myoclonus syndrome: a review. Brain Nerve. 2010; 62(4): 365–9.Google Scholar
Bataller, L, Dalmau, J. Paraneoplastic disorders of the nervous system. Continuum (Minneap Minn). 2005; 11(5, Neuro-Oncology): 69–92. DOI: 10.1212/01.con.0000293680.24426.ae.Google Scholar
Honnorat, J, Antoine, J-C. Paraneoplastic neurological syndromes. Orphanet J Rare Dis. 2007; 2: 22. DOI: 10.1186/1750-1172-2-22.Google Scholar
Lancaster, E. Paraneoplastic disorders. Continuum (Minneap Minn). 2015; 21(2, Neuro-oncology): 452–75. DOI: 10.1212/01.CON.0000464180.89580.88.Google Scholar
Nicolle, MW. Myasthenia gravis and Lambert-Eaton myasthenic syndrome. Continuum (Minneap Minn). 2016; 22(6, Muscle and Neuromuscular Junction Disorders): 1978–2005. DOI: 10.1212/CON.0000000000000415.Google Scholar
Bataller, L, Dalmau, J. Paraneoplastic disorders of the nervous system. Continuum (Minneap Minn). 2005; 11(5, Neuro-Oncology): 69–92. DOI: 10.1212/01.con.0000293680.24426.ae.Google Scholar
Honnorat, J, Antoine, J-C. Paraneoplastic neurological syndromes. Orphanet J Rare Dis. 2007; 2: 22. DOI: 10.1186/1750-1172-2-22.Google Scholar
Lancaster, E. Paraneoplastic disorders. Continuum (Minneap Minn). 2015; 21(2, Neuro-oncology): 452–75. DOI: 10.1212/01.CON.0000464180.89580.88.Google Scholar
Muppidi, S, Vernino, S. Paraneoplastic neuropathies. Continuum (Minneap Minn). 2014; 20(5, Peripheral Nervous System Disorders): 1359–72. DOI: 10.1212/01.CON.0000455876.53309.ec.Google Scholar
Nicolle, MW. Myasthenia gravis and Lambert-Eaton myasthenic syndrome. Continuum (Minneap Minn). 2016; 22(6, Muscle and Neuromuscular Junction Disorders): 1978–2005. DOI: 10.1212/CON.0000000000000415.Google Scholar
Vernino, S. Paraneoplastic disorders affecting the neuromuscular junction or anterior horn cell. Continuum (Minneap Minn). 2009; 15(1, Myasthenic Disorders and ALS): 132–46. DOI: 10.1212/01.CON.0000300011.79845.eb.Google Scholar
Kim, DW, et al. Parietal lobe epilepsy: the semiology, yield of diagnostic workup, and surgical outcome. Epilepsia. 2004; 45(6): 641–9.Google Scholar
Baloh, RW, Furman, JM, Yee, RD. Dorsal midbrain syndrome: Clinical and oculographic findings. Neurology. 1985; 35: 54.Google Scholar
Lee, AG, Brazis, PW. Clinical pathways in neuro-ophthalmology: an evidence-based approach. New York: Thieme; 1998.Google Scholar
Pringsheim, T, Jette, N, Frolkis, A, Steeves, TD. The prevalence of Parkinson's disease: a systematic review and meta-analysis. Mov Disord. 2014; 29: 1583.Google Scholar
de Lau, LM, Breteler, MM. Epidemiology of Parkinson's disease. Lancet Neurol. 2006; 5: 525.Google Scholar
Braak, H, Del Tredici, K, Rub, U, de Vos, RAI et al. Staging of brain pathology related to sporadic Parkinson's disease. Neurobiol. Aging. 2003; 24: 197–211.Google Scholar
Gelb, DJ, Oliver, E, Gilman, S. Diagnostic criteria for Parkinson disease. Arch Neurol. 1999; 56: 33.Google Scholar
Gardner, RC, Burke, JF, Nettiksimmons, J, et al. Traumatic brain injury in later life increases risk for Parkinson disease. Ann Neurol. 2015; 77(6): 987–95.Google Scholar
Klein, C, Schneider, SA, Lang, AE. Hereditary parkinsonism: Parkinson disease look-alikes – an algorithm for clinicians to “PARK” genes and beyond. Mov Disord. 2009; 24: 2042.Google Scholar
Gaeta, M, Frosina, P, Loria, G, Di Pietro, A, De Renzis, C. A case of perineural metastatic diffusion along the facial nerve: its computed tomographic demonstration and the radiotherapy considerations. Radiol Med. 1994; 87(6): 870–2.Google Scholar
Kumar, PP, Patil, AA, Ogren, FP, Johansson, SL, Reeves, MA. Intracranial skip metastasis from parotid and facial skin tumors: mechanism, diagnosis, and treatment. J Nat Med Assoc. 1993; 85(5) 369–74.Google Scholar
Newton, HB, Malkin, MG. Neurological complications of systemic cancer and antineoplastic therapy. (Neurological Disease and Therapy series: Vol 96). Boca Raton, FL: CRC Press; 2016. p. 80.Google Scholar
Renehan, AG, Gleave, EN, Slevin, NJ, McGurk, M. Clinico-pathological and treatment-related factors influencing survival in parotid cancer. Br J Cancer. 1999; 80(8): 1296–300.Google Scholar
Tullio, A, Marchetti, C, Sesenna, E, et al. Treatment of carcinoma of the parotid gland: The results of a multicenter study. J Oral Maxillofac Surg. 2001; 59(3): 263–70.Google Scholar
Antonaci, F, Sjaastad, O. Chronic paroxysmal hemicrania (CPH): a review of the clinical manifestations. Headache. 1989; 29: 648–56.Google Scholar
Boes, CJ, Matharu, MS, Goadsby, PJ. The paroxysmal hemicraniatic syndrome. Cephalalgia. 2003; 23: 24–8.Google Scholar
Cittadini, E, Matharu, MS, Goadsby, PJ. Paroxysmal hemicrania: a prospective clinical study of 31cases. Brain. 2008; 131(Pt4): 1142–55.Google Scholar
Prakash, S, Patell, R. Paroxysmal hemicrania: an update. Curr Pain Headache Rep. 2014; 18: 407.Google Scholar
Bruno, MK, Hallett, M, Gwinn-Hardy, K, et al. Critical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria. Neurology. 2004; 63(12): 2280–7.Google Scholar
Bhatia, KP. Familial (idiopathic) paroxysmal dyskinesias: an update. Semin Neurol. 2001; 21(1): 69–74.Google Scholar
Van Rootselaar, AF, van Westrum, SS, Velis, DN, Tijssen, MA. The paroxysmal dyskinesias. Pract Neurol. 2009; 9(2): 102–9.Google Scholar
Gardiner, AR, Jaffer, F, Dale, RC, et al. The clinical and genetic heterogeneity of paroxysmal dyskinesias. Brain. 2015; 138(12): 3567–80.Google Scholar
Wang, JL, Cao, L, Li, XH, et al. Identification of Prrt2 as the causative gene of paroxysmal kinesigenic dyskinesias. Brain. 2011; 134(12): 3493–501.Google Scholar
Hur, YJ, Hwang, T. Secondary paroxysmal dyskinesia associated with 2009 H1N1 infection. Korean J Pediatr. 2013; 56(1): 42–4.Google Scholar
Meppiel, E, Crassard, I, Peffault de Latour, R, et al. Cerebral venous thrombosis in paroxysmal nocturnal hemoglobinuria: a series of 15 cases and review of the literature. Medicine (Baltimore). 2015; 94: e362.Google Scholar
Schrezenmeier, H, Muus, P, Socié, G, et al. Baseline characteristics and disease burden in patients in the International Paroxysmal Nocturnal Hemoglobinuria Registry. Haematologica. 2014; 99: 922–9.Google Scholar
Mayo Clinic Staff. Patent ductus arteriosus (PDA). Dec 16, 2014. Available from www.mayoclinic.org/diseases-conditions/patent-ductus-arteriosus/basics/complications/con-20028530 Accessed Jul 6, 2015.Google Scholar
Webb, GD, Smallhorn, J, Therrien, J, Redington, AN. Congenital heart disease. In Mann, DL, Zipes, DP, Libby, P, Bonow, RO, Braunwald, E, eds. Braunwald's heart disease: A textbook of cardiovascular medicine. 10th ed. Philadelphia, PA: Elsevier/Saunders; 2015. pp. 1413–14.Google Scholar
Mayo Clinic Staff. Patent foramen ovale. Jul 16, 2015. Available from www.mayoclinic.org/diseases-conditions/patent-foramen-ovale/basics/causes/con-20028729. Accessed Jul 19, 2015.Google Scholar
Webb, GD, Smallhorn, J, Therrien, J, Redington, AN. Congenital heart disease. In Mann, DL, Zipes, DP, Libby, P, Bonow, RO, Braunwald, E, eds. Braunwald's heart disease: A textbook of cardiovascular medicine. 10th ed. Philadelphia, PA: Elsevier/Saunders; 2015. pp. 1409–10.Google Scholar
Benke, T. Peduncular hallucinosis: A syndrome of impaired reality monitoring. J Neurol. 2006; 253: 1561–71.Google Scholar
Penney, L, Galameau, D. Peduncular hallucinosis: A case report. Oschner J. 2014(Fall); 14(3): 456–8.Google Scholar
Friedland, DR, Wackym, PA. Clinical forum: a critical appraisal of spontaneous perilymphatic fistulas of the inner ear. Am J Otol. 1999; 20: 261–76.Google Scholar
Minor, LB. Labyrinthine fistulae: pathobiology and management. Curr Opin Otolaryngol Head Neck Surg. 2003; 11: 340–6.Google Scholar
Smouha, EE, Bojrab, DI. Lateral semicircular canal fistula. In Cholesteatoma. New York, NY: Thieme; 2011. p. 88.Google Scholar
Sorenson, EJ, Sima, AA, Blaivas, M, Sawchuk, K, Wald, JJ. Clinical features of perineuritis. Muscle Nerve. 1997; 20(9): 1153–7.Google Scholar
Gaultney, JF. The prevalence of sleep disorders in college students: impact on academic performance. J Am Coll Health. 2010; 59(2): 91–7.CrossRefGoogle ScholarPubMed
Petrov, ME, Lichstein, KL, Baldwin, CM. Prevalence of sleep disorders by sex and ethnicity among older adolescents and emerging adults: Relations to daytime functioning, working memory and mental health. J Adolesc. 37; 2014: 587–97.Google Scholar
Moore, H, Winkelmann, J, Lin, L, et al. Periodic leg movements during sleep are associated with polymorphisms in BTBD9, TOX3/BC034767, MEIS1, MAP2K5/SKOR1, and PTPRD. Sleep. 2014; 37(9): 1535–42.Google Scholar
Aurora, RN, Kristo, DA, Bista, SR, et al. The treatment of restless legs syndrome and periodic limb movement disorder in adults – an update for 2012: practice parameters with an evidence-based systematic review and meta-analyses. Sleep. 2012; 35(8): 1039–62.Google Scholar
Merikangas, KR, Zhang, J, Emsellem, H, et al. The structured Diagnostic Interview for Sleep Patterns and Disorders: rationale and initial evaluation. Sleep Med. 2014; 15: 530–5.Google Scholar
Ke, Q, Luo, B, Qi, M, et al. Gender differences in penetrance and phenotype in hypokalemic periodic paralysis. Muscle Nerve. 2013; 47: 41.Google Scholar
Miller, TM, Dias da Silva, MR, Miller, HA, et al. Correlating phenotype and genotype in the periodic paralyses. Neurology. 2004; 63: 1647.CrossRefGoogle ScholarPubMed
Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
Ober, KP. Thyrotoxic periodic paralysis in the United States. Report of 7 cases and review of the literature. Medicine (Baltimore). 1992; 71: 109.Google Scholar
Links, TP, Zwarts, MJ, Wilmink, JT, et al. Permanent muscle weakness in familial hypokalaemic periodic paralysis: Clinical, radiological and pathological aspects. Brain. 1990; 113(6): 1873.Google Scholar
Venance, SL, Cannon, SC, Fialho, D, et al. The primary periodic paralyses: diagnosis, pathogenesis and treatment. Brain. 2006; 129: 8.Google Scholar
Chen, YC, Fang, JT, Chang, CT, Chou, HH. Thyrotoxic periodic paralysis in a patient abusing thyroxine for weight reduction. Ren Fail. 2001; 23: 139.Google Scholar
Pompeo, A, Nepa, A, Maddestra, M, et al. Thyrotoxic hypokalemic periodic paralysis: An overlooked pathology in western countries. Eur J Intern Med. 2007; 18: 380.Google Scholar
Hannon, MJ, Behan, LA, Agha, A. Thyrotoxic periodic paralysis due to excessive L-thyroxine replacement in a Caucasian man. Ann Clin Biochem. 2009; 46: 423.Google Scholar
Chou, HK, Tsao, YT, Lin, SH. An unusual cause of thyrotoxic periodic paralysis: triiodothyronine-containing weight reducing agents. Am J Med Sci. 2009; 337: 71.Google Scholar
Manoukian, MA, Foote, JA, Crapo, LM. Clinical and metabolic features of thyrotoxic periodic paralysis in 24 episodes. Arch Intern Med. 1999; 159: 601.Google Scholar
Pothiwala, P, Levine, SN. Analytic review: thyrotoxic periodic paralysis: a review. J Intens Care Med. 2010; 25: 71.Google Scholar
Hsieh, MJ, Lyu, RK, Chang, WN, et al. Hypokalemic thyrotoxic periodic paralysis: clinical characteristics and predictors of recurrent paralytic attacks. Eur J Neurol. 2008; 15: 559.Google Scholar
Shiang, JC, Cheng, CJ, Tsai, MK, et al. Therapeutic analysis in Chinese patients with thyrotoxic periodic paralysis over 6 years. Eur J Endocrinol. 2009; 161: 911.Google Scholar
Griggs, RC, Bender, AN, Tawil, R. A puzzling case of periodic paralysis. Muscle Nerve. 1996; 19: 362.Google Scholar
Lu, KC, Hsu, YJ, Chiu, JS, et al. Effects of potassium supplementation on the recovery of thyrotoxic periodic paralysis. Am J Emerg Med. 2004; 22: 544.Google Scholar
Birkhahn, RH, Gaeta, TJ, Melniker, L. Thyrotoxic periodic paralysis and intravenous propranolol in the emergency setting. J Emerg Med. 2000; 18: 199.Google Scholar
Conway, MJ, Seibel, JA, Eaton, P. Thyrotoxicosis and periodic paralysis: improvement with beta blockade. Ann Intern Med. 1974; 81: 332.Google Scholar
Jurkat-Rott, K, Lehmann-Horn, F. Genotype-phenotype correlation and therapeutic rationale in hyperkalemic periodic paralysis. Neurotherapeutics. 2007; 4: 216.Google Scholar
Venance, SL, Cannon, SC, Fialho, D, et al. The primary periodic paralyses: diagnosis, pathogenesis and treatment. Brain. 2006; 129: 8.Google Scholar
Gould, RJ, Steeg, CN, Eastwood, AB, et al. Potentially fatal cardiac dysrhythmia and hyperkalemic periodic paralysis. Neurology. 1985; 35: 1208.Google Scholar
Bradley, WG, Taylor, R, Rice, DR, et al. Progressive myopathy in hyperkalemic periodic paralysis. Arch Neurol. 1990; 47: 1013.Google Scholar
McManis, PG, Lambert, EH, Daube, JR. The exercise test in periodic paralysis. Muscle Nerve. 1986; 9: 704.Google Scholar
Kuntzer, T, Flocard, F, Vial, C, et al. Exercise test in muscle channelopathies and other muscle disorders. Muscle Nerve. 2000; 23: 1089.3.0.CO;2-Q>CrossRefGoogle ScholarPubMed
Hanna, MG, Stewart, J, Schapira, AH, et al. Salbutamol treatment in a patient with hyperkalaemic periodic paralysis due to a mutation in the skeletal muscle sodium channel gene (SCN4A). J Neurol Neurosurg Psychiatry. 1998; 65: 248.Google Scholar
Bendheim, PE, Reale, EO, Berg, BO. beta-Adrenergic treatment of hyperkalemic periodic paralysis. Neurology. 1985; 35: 746.Google Scholar
Riggs, JE, Griggs, RC, Moxley, RT 3rd, Lewis, ED. Acute effects of acetazolamide in hyperkalemic periodic paralysis. Neurology. 1981; 31: 725.Google Scholar
Cannon, SC, George, AL. Pathophysiology of myotonia and periodic paralysis. In Asbury, AK, McKhann, GM, McDonald, WI, et al., eds. Diseases of the nervous system. 3rd ed. Cambridge, UK: Cambridge University Press; 2002. p. 1183.Google Scholar
Klingler, W, Lehmann-Horn, F, Jurkat-Rott, K. Complications of anaesthesia in neuromuscular disorders. Neuromuscul Disord. 2005; 15: 195.Google Scholar
Brazis, PW, et al., eds. Peripheral nerves. In Localization in clinical neurology. 6th ed. Philadelphia, PA: Lippincott Williams and Wilkins; 2011. Chapter 2.Google Scholar
Stewart, JD. Foot drop: where, why and what to do? Pract Neurol. 2008; 8(3): 158–69. DOI: 10.1136/jnnp.2008.149393.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Thase, ME, Fava, M, Halbreich, U, et al. A placebo-controlled, randomized clinical trial comparing sertraline and imipramine for the treatment of dysthymia. Arch Gen Psychiatry. 1996; 53(9): 777–84.Google Scholar
van Elst, LT, Woermann, FG, Lemieux, L, Trimble, MR. Amygdala enlargement in dysthymia – a volumetric study of patients with temporal lobe epilepsy. Biol Psychiatry. 1999; 46(12): 1614–23.Google Scholar
Weissman, MM, Leaf, PJ, Bruce, ML, Florio, L. The epidemiology of dysthymia in five communities: rates, risks, comorbidity, and treatment. Am J Psychiatry. 1988; 145(7): 815–19.Google Scholar
Williams, JW Jr, Barrett, J, Oxman, T, et al. Treatment of dysthymia and minor depression in primary care: a randomized controlled trial in older adults. JAMA. 2000; 284(12): 1519–26.Google Scholar
Multi-Society Task Force on PVS. Medical aspects of the persistent vegetative state. N Engl J Med. 1994; 330: 1499–579.Google Scholar
Kinney, HC, Korein, J, Panigrahy, A, Dikkes, P, Goode, R. Neuropathological findings in the brain of Karen Ann Quinlan: the role of the thalamus in the persistent vegetative state. N Engl J Med. 1994; 330: 1469–75.Google Scholar
Posner, JB, Saper, CB. Plum and Posner's diagnosis of stupor and coma. 4th ed. Oxford: Oxford University Press; 2007.Google Scholar
Quality Standards Subcommittee of the American Academy of Neurology. Practice parameters: Assessment and management of patients in the persistent vegetative state (Summary statement). Neurology. 1995; 45: 1015–18.Google Scholar
No authors listed. Position of the American Academy of Neurology on certain aspects of the care and management of the persistent vegetative state patient. Neurology. 1989; 39: 125–6Google Scholar
Larriviere, D, Bonnie, RJ. Terminating artificial nutrition and hydration in persistent vegetative state patients: Current and proposed state laws. Neurology. 2006; 66: 1624–8.Google Scholar
Giacino, JT, et al. The minimally conscious state: definition and diagnostic criteria. Neurology. 2002; 58(3): 349–53.Google Scholar
Cherry, JD, Heininger, U. Pertussis and other Bordetella infections. In Feigin, RD, Cherry, JD, Demmler-Harrison, GJ, et al., eds. Textbook of pediatric infectious diseases. Vol. 1. Philadelphia, PA: Saunders/Elsevier; 2009. pp. 1683–706.Google Scholar
Sanghi, V. Neurologic manifestations of diphtheria and pertussis. In Biller, J, Ferro, JM, eds. Neurologic aspects of systemic disease Part III. Handbook of Clinical Neurology. Vol 121. 3rd Series. Philadelphia, PA: Elsevier; 2014.Google Scholar
Brenner, S. PCP toxicity. Updated Feb 1, 2018. https://emedicine.medscape.com/article/1010821-overview. Accessed Sep 17, 2018.Google Scholar
Hallucinogens.com. PCP effects on the brain. http://hallucinogens.com/pcp/pcp-effects-on-the-brain/. Accessed Sep 6, 2018.Google Scholar
National Institute of Drug Abuse. What are the effects of common dissociative drugs on the brain and body? Feb 2015. https://www.drugabuse.gov/publications/research-reports/hallucinogens-dissociative-drugs/what-are-effects-common-dissociative-drugs-brain-body. Accessed Sep 6, 2018.Google Scholar
Leuzzi, V, et al. Biochemical, clinical and neuroradiological (MRI) correlations in late-detected PKU patients. J Inherit Metab Dis. 1995; 18(5): 624–34.Google Scholar
Leuzzi, V, et al. The pathogenesis of the white matter abnormalities in phenylketonuria. A multimodal 3.0 Tesla MRI and magnetic resonance spectroscopy (1H MRS) study. J Inherit Metab Dis. 2007; 30(2): 209–16.Google Scholar
Rahja, R, et al. Mental health and social functioning in early treated phenylketonuria: the PKU-COBESO study. Mol Genet Metab. (2013); 110(Suppl): S57–S61.Google Scholar
Smith, I, Knowles, J. Behavior in early treated PKU: a systematic review. Eur J Pediatr. 2000; 159(2): S89–93.Google Scholar
Abermil, N, Guillaud-Bataille, M, Burnichon, N, et al. TMEM127 screening in a large cohort of patients with pheochromocytoma and/or paraganglioma. J Clin Endocrinol Metab. 2012; 97: E805–9.Google Scholar
Anderson, J, Gulant, RW. Paraganglioma of the cauda equina: a case report. J Neurol Neurosurg Psychiatry. 1987; 50: 100–3.Google Scholar
Bayley, JP, Kunst, HP, Cascon, A, et al. SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma. Lancet Oncol. 2010; 11: 366–72.Google Scholar
Fishbein, L. Pheochromocytoma and paraganglioma: genetics, diagnosis, and treatment. Hematol Oncol Clin North Am. 2016; 30(1): 135–50. DOI: 10.1016/j.hoc.2015.09.006. Epub 2015 Oct 23.Google Scholar
Hrabovsky, EE, McLellan, D, Horton, JA, Klingberg, WG. Catheter embolization: preparation of patient with pheochromocytoma. J Pediatr Surg. 1982; 17(6): 849–50.Google Scholar
Kirmani, S, Young, WF. Hereditary paraganglioma-pheochromocytoma syndromes. May 21, 2008. Updated Nov 6, 2014. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2017.Google Scholar
Naguib, M, Caceres, M, Thomas, CR Jr, Herman, TS, Eng, TY. Radiation treatment of recurrent pheochromocytoma of the bladder: case report and review of literature. Am J Clin Oncol. 2002; 25(1): 42–4.Google Scholar
Papathomas, TG, de Krijger, RR, Tischler, AS. Paragangliomas: update on differential diagnostic considerations, composite tumors, and recent genetic developments. Semin Diagn Pathol. 2013; 30(3): 207–23. DOI: 10.1053/j.semdp.2013.06.006.Google Scholar
You, D, Ren, R, Chen, E, et al. Radiotherapy for urinary bladder pheochromocytoma with invasion of the prostate: A case report and literature review. Mol Clin Oncol. 2016; 4(6): 1060–2. Epub 2016 Mar 17.Google Scholar
Beck, G, Shinzawa, K, Hayakawa, H, et al. Deficiency of calcium-independent phospholipase A2 beta induces brain iron accumulation through upregulation of divalent metal transporter 1. PLoS One. 2015; 10(10): e0141629. DOI: 10.1371/journal.pone.0141629.Google Scholar
Bernardi, B. MRI findings in patients with clinical onset consistent with infantile neuroaxonal dystrophy (INAD), literature review, clinical and MRI follow-up. Neuroradiol J. 2011; 24(2): 202–14. Epub 2011 May 11.Google Scholar
Illingworth, MA, Meyer, E, Chong, WK, et al. PLA2G6-associated neurodegeneration (PLAN): Further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease. Mol Genet Metab. 2014; 112(2): 183–9. DOI: 10.1016/j.ymgme.2014.03.008.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Bhatia, MS, Gupta, R. Pica responding to SSRI: An OCD spectrum disorder? World J Biol Psychiatry. 2009; 10(4–3): 936–8.Google Scholar
Ruddock, JC. Lead poisoning in children: with special reference to pica. J Am Med Assoc. 1924; 82(21): 1682–4.Google Scholar
Singhi, S, Singhi, P, Adwani, GB. Role of psychosocial stress in the cause of pica. Clin Pediatr. 1981; 20(12): 783–5.Google Scholar
Amato-Watkins, AC, Lammie, A, Hayhurst, C, Leach, P. Pineal parenchymal tumours of intermediate differentiation: An evidence-based review of a new pathological entity. Br J Neurosurg. 2016; 30(1): 11–5. DOI: 10.3109/02688697.2015.1096912.Google Scholar
Ito, T, Kanno, H, Sato, K, et al. Clinicopathologic study of pineal parenchymal tumors of intermediate differentiation. World Neurosurg. 2014; 81(5–6): 783–9. DOI: 10.1016/j.wneu.2013.02.007.Google Scholar
Kwak, J, Shim, JK, Kim, DS, et al. Isolation and characterization of tumorspheres from a recurrent pineoblastoma patient: Feasibility of a patient-derived xenograft. Int J Oncol. 2016; 49(2): 569–78. DOI: 10.3892/ijo.2016.3554.Google Scholar
Raleigh, DR, Solomon, DA, Lloyd, SA, et al. Histopathologic review of pineal parenchymal tumors identifies novel morphologic subtypes and prognostic factors for outcome. Neuro Oncol. 2017; 19(1): 78–88. DOI: 10.1093/neuonc/now105.Google Scholar
Schild, SE, Scheithauer, BW, Schomberg, PJ, et al. Pineal parenchymal tumors. Clinical, pathologic, and therapeutic aspects. Cancer. 1993; 72(3): 870–80.Google Scholar
Al-Hussaini, M, Sultan, I, Gajjar, AJ, Abuirmileh, N, Qaddoumi, I. Pineal gland tumors: experience from the Seer database. J Neurooncol. 2009; 94(3): 351–8. DOI: 10.1007/s11060-009-9881-9.Google Scholar
Ito, T, Kanno, H, Sato, K, et al. Clinicopathologic study of pineal parenchymal tumors of intermediate differentiation. World Neurosurg. 2014; 81(5–6): 783–9. DOI: 10.1016/j.wneu.2013.02.007.Google Scholar
Kwak, J, Shim, JK, Kim, DS, et al. Isolation and characterization of tumorspheres from a recurrent pineoblastoma patient: Feasibility of a patient-derived xenograft. Int J Oncol. 2016; 49(2): 569–78. DOI: 10.3892/ijo.2016.3554.Google Scholar
Mottolese, C, Szathmari, A, Beuriat, PA. Incidence of pineal tumours. A review of the literature. Neurochirurgie. 2015; 61(2–3): 65–9. DOI: 10.1016/j.neuchi.2014.01.005.Google Scholar
Raleigh, DR, Solomon, DA, Lloyd, SA, et al. Histopathologic review of pineal parenchymal tumors identifies novel morphologic subtypes and prognostic factors for outcome. Neuro Oncol. 2017; 19(1): 78–88. DOI: 10.1093/neuonc/now105.Google Scholar
Schild, SE, Scheithauer, BW, Schomberg, PJ, et al. Pineal parenchymal tumors. Clinical, pathologic, and therapeutic aspects. Cancer. 1993; 72(3): 870–80.3.0.CO;2-X>CrossRefGoogle ScholarPubMed
Cass, S. Piriformis syndrome: a cause of nondiscogenic sciatica. Curr Sports Med Rep. 2015; 14(1): 41–4. DOI: 10.1249/JSR.0000000000000110. Review.Google Scholar
Smoll, NR. Variations of the piriformis and sciatic nerve with clinical consequence: a review. Clin Anat. 2010; 23(1): 8–17.Google Scholar
Nawar, RN, AbdelMannan, D, Selman, WR, Arafah, BM. Pituitary tumor apoplexy: a review. J Intens Care Med. 2008; 23(2): 75–90.Google Scholar
Vaphiades, MS. Pituitary apoplexy. Medscape. Updated Sep 20, 2017. Available from https://emedicine.medscape.com/article/1198279-overview. Available from https://emedicine.medscape.com/article/1198279-overview. Accessed Sep 25, 2018.Google Scholar
Arafah, BM, Nasrallah, MP. Pituitary tumors: pathophysiology, clinical manifestations and management. Endocr Relat Cancer. 2001; 8(4): 287–305.CrossRefGoogle ScholarPubMed
Chaudhary, V, Bano, S. Imaging of the pituitary: Recent advances. Ind J Endocrinol Metab. 2011; 15(Suppl 3): S216–23. DOI: 10.4103/2230-8210.84871.Google ScholarPubMed
Ironside, JW. Best practice No 172: Pituitary gland pathology. J Clin Pathol. 2003; 56: 561–8.Google Scholar
Huguet, I, Clayton, R. Pituitary-hypothalamic tumor syndromes: Adults. Endotext [Internet]. South Dartmouth, MA: MDText.com, Inc.; 2000. Available from https://www.ncbi.nlm.nih.gov/books/NBK278946/. Accessed Jul 3, 2015.Google Scholar
Robertson, GL. Diabetes insipidus: differential diagnosis and management. Best Pract Res Clin Endocrinol Metab. 2016; 30(2): 205–18.Google Scholar
Utz, AL, Klibanski, A. Pituitary disorders. Continuum (Minneap Minn). 2009; 15(2, Neurology): 17–36.Google Scholar
Malkani, RG, Tallman, M, Gottardi-Littell, N, et al. Bing-Neel syndrome: an illustrative case and a comprehensive review of the published literature. J Neurooncol. 2010; 96: 301–12.Google Scholar
Sobol, U, Stiff, P. Neurologic aspects of plasma cell disorders. Handb Clin Neurol. 2014; 120: 1083–99.Google Scholar
Nobile-Orazio, E. Neuropathy and monoclonal gammopathy. Handb Clin Neurol. 2013; 115: 443–59.Google Scholar
Dispenzieri, A, Kyle, RA, Lacy, MQ, et al. POEMS syndrome: definitions and long-term outcome. Blood. 2003; 101: 2496.Google Scholar
Dupont, SA, Dispenzieri, A, Mauermann, ML, et al. Cerebral infarction in POEMS syndrome: incidence, risk factors, and imaging characteristics. Neurology. 2009; 73: 1308.Google Scholar
Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. 5th ed. London, UK: Elsevier; 2014.Google Scholar
Aylward, RB, Linkins, J. Polio eradication: mobilizing and managing the human resources. Bull World Health Org. 2005; 83(4): 268–73.Google ScholarPubMed
Grist, NR, Bell, EJ. Paralytic poliomyelitis and nonpolio enteroviruses: studies in Scotland. Rev Infect Dis. 1984; 6(Suppl 2): S385–6.Google Scholar
Robbins, FC, Nightingale, EO. Selective primary health care: Strategies for control of disease in the developing world. IX. Poliomyelitis. Rev Infect Dis. 1983; 5(5): 957–68.Google Scholar
Ramachandran, TS, Roos, RP. Periarteritis nodosa. Medlink Neurology. Updated Nov 14, 2017. San Diego: Medlink Corporation. Available from https://emedicine.medscape.com/article/330717-overview. Accessed Nov 25, 2018.Google Scholar
Cao, M, Olsen, RJ, Zu, Y. Polycythemia vera: new clinicopathologic perspectives. Arch Pathol Lab Med. 2006; 130: 1126–32.Google Scholar
Buttgereit, F, Dejaco, C, Matteson, EL, Dasgupta, B. Polymyalgia rheumatica and giant cell arteritis: a systematic review. JAMA. 2016; 315(22): 2442–58.Google Scholar
Caylor, TL, Perkins, A. Recognition and management of polymyalgia rheumatica and giant cell arteritis. Am Fam Physician. 2013; 88(10): 676–84.Google Scholar
Amato, AA, Greenberg, SA. Inflammatory myopathies. Continuum (Minneap Minn). 2013; 19(6): 1615–33.Google Scholar
Brazis, PW, et al., eds. Peripheral nerves. In Localization in clinical neurology. 6th ed. Philadelphia, PA: Lippincott Williams and Wilkins; 2011. Chapter 2.Google Scholar
Hanewinckel, R, van Oijen, M, Ikram, MA, van Doorn, PA. The epidemiology and risk factors of chronic polyneuropathy. Eur J Epidemiol. 2016; 31: 5–20. DOI: 10.1007/s10654-015-0094-6.Google Scholar
Visser, N. Chronic idiopathic axonal polyneuropathy is associated with the metabolic syndrome. Diabetes Care. 2013; 36(4): 817–22.Google Scholar
Arboix, A, Arbe, C, Garcia-Eroles, L, et al. Infarctions in the vascular territory of the posterior cerebral artery: clinical features in 232 patients. BMC Res Notes. 2011; 4: 329–35.Google Scholar
Cereda, C, Carrera, E. Posterior cerebral artery territory infarctions. Front Neurol Neurosci. 2012; 30: 128–31.Google Scholar
Arboix, A, Arbe, C, Garcia-Eroles, L, et al. Infarctions in the vascular territory of the posterior cerebral artery: clinical features in 232 patients. BMC Res Notes. 2011; 4: 329–35.Google Scholar
Cereda, C, Carrera, E. Posterior cerebral artery territory infarctions. Front Neurol Neurosci. 2012; 30: 128–31.Google Scholar
Rodriguez Frontal, M, Kerrison, JB, Garcia, R, Oria, V. Ischemic optic neuropathy. Semin Neurol. 2007; 27(3): 221–32Google Scholar
Fischer, M, Schmutzhard, E. Posterior reversible encephalopathy syndrome. J Neurol. 2017; 264(8): 1608–16.Google Scholar
Hinchey, J, Chaves, C, Appignani, B, et al. A reversible posterior leukoencephalopathy syndrome. N Engl J Med. 1996; 334: 494.Google Scholar
Christo, PJ, et al. Post-herpetic neuralgia in older adults: evidence-based approaches to clinical management. Drugs Aging. 2007; 24(1): 1–19.Google Scholar
Denny-Brown, D, et al. Pathologic features of herpes zoster: A note on ‘geniculate herpes’. Arch Neurol Psychiatr. 1944; 51: 216.Google Scholar
Johnson, R. Herpes zoster and postherpetic neuralgia. Expert Rev Vaccines. 2010; 9(Suppl 3): 21–6.Google Scholar
Alper, G. Acute disseminated encephalomyelitis. J Child Neurol. 2012; 27(11): 1408–25.CrossRefGoogle ScholarPubMed
Huynh, W, Cordato, DJ, Kehdi, E, Masters, LT, Dedousis, C. Post-vaccination encephalomyelitis: literature review and illustrative case. J Clin Neurosci. 2008; 15(12): 1315–22.Google Scholar
Alper, G. Acute disseminated encephalomyelitis. J Child Neurol. 2012; 27(11): 1408–25.Google Scholar
Wingerchuk, DM. Postinfectious encephalomyelitis. Curr Neurol Neurosci Rep. 2003; 3(3): 256–64.Google Scholar
Ahmed, SV, Jayawarna, C, Jude, E. Post lumbar puncture headache: diagnosis and management. Postgrad Med J. 2006; 82: 713–16Google Scholar
Kuntz, KM, Kokmen, E, Stevens, JC, et al. Post-lumbar puncture headaches: experience in 501 consecutive procedures. Neurology. 1992; 42: 1884–7.Google Scholar
Niall, CT, Globerson, JA, de Rosayro, MA. Epidural blood patch for postdural puncture headache: it's never too late. Anesth Anal. 1986; 65: 895–6.Google Scholar
Olsen, J, Bousser, M-G, Diener, H-C, et al. The international classification of headache disorders: 2nd edition. Cephalalgia. 2004; 24: 9–160.Google Scholar
Thomas, S-R, Jamieson, D-R, Muir, K-W. Randomised controlled trial of atraumatic versus standard needles for diagnostic lumbar puncture. BMJ (Clin Res Ed). 2000; 3210: 986–90.Google Scholar
Turnbull, DK, Shepherd, DB. Post-dural puncture headache: pathogenesis, prevention and treatment. Br J Anaesth. 2003; 91: 718–29.CrossRefGoogle ScholarPubMed
Padovan, CS, Sostak, P, Straube, A. [Neurological complications after organ transplantation]. Der Nervenarzt. 2000; 71(4): 249–58.Google Scholar
Živković, SA. Neurologic complications after liver transplantation. World J Hepatol. 2013; 5(8): 409–16. DOI: 10.4254/wjh.v5.i8.409.Google Scholar
Bashir, . Neurologic complications of organ transplantation. Curr Treat Options Neurol. 2001; 3(6): 543–54.Google Scholar
Mathew, RM, Rosenfeld, MR. Neurologic complications of bone marrow and stem-cell transplantation in patients with cancer. Curr Treat Options Neurol. 2007; 9(4): 308–31.Google Scholar
Patchell, RA. Neurological complications of organ transplantation and immunosuppressive agents. In Aminoff, M, ed. Neurology and general medicine. 4th ed. London: Churchill Livingstone; 2007. pp. 873–85.Google Scholar
Pruitt, AA, Grus, F, Rosenfeld, MR. Neurological complications of solid organ transplantation. The Neurohospitalist. 2012; 3(3): 152–66.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Rauch, SL, van der Kolk, BA, Fisler, RE, et al. A symptom provocation study of posttraumatic stress disorder using positron emission tomography and script-driven imagery. Arch Gen Psychiatry. 1996; 53(5): 380–7.Google Scholar
Shin, LM, Wright, CI, Cannistraro, PA, et al. A functional magnetic resonance imaging study of amygdala and medial prefrontal cortex responses to overtly presented fearful faces in posttraumatic stress disorder. Arch Gen Psychiatry. 2005; 62(3): 273–81.Google Scholar
Taylor, HR. Prazosin for treatment of nightmares related to post traumatic stress disorder. Am J Health Syst Pharm. 2008; 65(8): 716–22.Google Scholar
Yule, W. Posttraumatic stress disorder. In Ollendick, , King, NJ, Yule, W, eds. International handbook of phobic and anxiety disorders in children and adolescents. New York: Springer US; 1994. pp. 223–40.Google Scholar
Zarei, MR, Shabani, M, Chamani, G, et al. Migraine patients have higher prevalence of PTSD symptoms in comparison to chronic tension type headache and healthy subjects: a case control study. Acta Odontol Scand. 2016; 74(8): 633–5.Google Scholar
Jacob, G, Costa, F, Shannon, JR, et al. The neuropathic postural tachycardia syndrome. N Engl J Med. 2000; 343: 1008–14.Google Scholar
Raj, SR. Postural orthostatic tachycardia syndrome (POTS). Circulation. 2013; 127(23): 2336–42.Google Scholar
Thieben, MJ, Sandroni, P, Sletten, DM, et al. Postural orthostatic tachycardia syndrome: the Mayo Clinic experience. Mayo Clin Proc. 2007; 82: 308–13.Google Scholar
Tena Rosser, AP. Pediatric neurology: a case based review. Lippincott Williams & Wilkins; 2007.Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. The myotonias, periodic paralyses, cramps, spasms, and states of persistent muscle fiber activity. In Adams & Victor's principles of neurology. 10th ed. New York, NY: McGraw-Hill; 2014. Chapter 50.Google Scholar
Patcek, LJ, Tawil, R, Griggs, RC, Storvick, D, Leppert, M. Linkage of atypical myotonia congenita to a sodium channel locus. Neurology. 1992; 42(2): 431.Google Scholar
Science Direct. Potassium-aggravated myotonia. Available from https://www.sciencedirect.com/topics/neuroscience/potassium-aggravated-myotonia. Accessed Sep 25, 2018.Google Scholar
Trudell, RG, Kaiser, KK, Griggs, R. Actetazolamide-responsive myotonia congenita. Neurology. 1987; 37(3): 488.Google Scholar
Driscoll, DJ, Miller, JL, Schwartz, S, et al. Prader–Willi syndrome. Oct 6, 1998. Updated Feb 4, 2016. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2016. Available from: www.ncbi.nlm.nih.gov/books/NBK1330/. Accessed Sep 11, 2018.Google Scholar
Miller, J, Kranzler, J, Liu, Y, et al. Neurocognitive findings in Prader-Willi syndrome and early-onset morbid obesity. J Pediatr. 2006; 149: 192–8.Google Scholar
Descheemaeker, MJ, Govers, V, Vermeulen, P, Fryns, JP. Pervasive developmental disorders in Prader-Willi syndrome: the Leuven experience in 59 subjects and controls. Am J Med Genet A. 2006; 140: 1136–42.Google Scholar
Wigren, M, Hansen, S. ADHD symptoms and insistence on sameness in Prader-Willi syndrome. J Intellect Disabil Res. 2005; 49: 449–56.Google Scholar
Iughetti, L, Bosio, L, Corrias, A, et al. Pituitary height and neuroradiological alterations in patients with Prader-Labhart-Willi syndrome. Eur J Pediatr. 2008; 167: 701–2.Google Scholar
Bartsch, E, Medcalf, KE, Park, AL, Ray, JG. High Risk of Pre-eclampsia Identification Group. Clinical risk factors for pre-eclampsia determined in early pregnancy: systematic review and meta-analysis of large cohort studies. BMJ. 2016; 353: i1753. DOI: 10.1136/bmj.i1753.Google Scholar
Duhig, KE, Shennan, AH. Recent advances in the diagnosis and management of pre-eclampsia. F1000Prime Rep. 2015; 7: 24. DOI: 10.12703/P7-24.Google Scholar
Powe, CE, Levine, RJ, Karumanchi, SA. Preeclampsia, a disease of the maternal endothelium: the role of antiangiogenic factors and implications for later cardiovascular disease. Circulation. 2011; 123(24): 2856–69. DOI: 10.1161/CIRCULATIONAHA.109.853127.Google Scholar
WHO. Recommendations for prevention and treatment of pre-eclampsia and eclampsia. Geneva: World Health Organization; 2011.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Hatzimouratidis, K, Amar, E, Eardley, I, et al. Guidelines on male sexual dysfunction: erectile dysfunction and premature ejaculation. Eur Urol. 2010; 57(5): 804–14.Google Scholar
Waldinger, MD. The neurobiological approach to premature ejaculation. J Urol. 2002; 168(6): 2359–67.Google Scholar
Waldinger, MD, Hengeveld, MW, Zwinderman, AH. Paroxetine treatment of premature ejaculation: a double-blind, randomized, placebo-controlled study. Am J Psychiatry. 1994; 151(9): 1377–9.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Epperson, CN, Haga, K, Mason, GF, et al. Cortical γ-aminobutyric acid levels across the menstrual cycle in healthy women and those with premenstrual dysphoric disorder: A proton magnetic resonance spectroscopy study. Arch Gen Psychiatry. 2002; 59(9): 851–8.Google Scholar
Grady-Weliky, T. Premenstrual dysphoric disorder. New Engl J Med. 2003; 348(5): 433–8.Google Scholar
Yonkers, KA, Halbreich, U, Freeman, E, et al. Symptomatic improvement of premenstrual dysphoric disorder with sertraline treatment: a randomized controlled trial. JAMA. 1997; 278(12): 983–8.Google Scholar
Yonkers, KA, Brown, C, Pearlstein, TB, et al. Efficacy of a new low-dose oral contraceptive with drospirenone in premenstrual dysphoric disorder. Obstet Gynecol. 2005; 106(3): 492–501.Google Scholar
El-Hattab, AW. Systemic primary carnitine deficiency. Mar 15, 2012. Updated Jun 26, 2014. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2015. Available from: www.ncbi.nlm.nih.gov/books/NBK84551/. Accessed Sep 12, 2018.Google Scholar
Magoulas, PL, El-Hattab, AW. Systemic primary carnitine deficiency: an overview of clinical manifestations, diagnosis, and management. Orphanet J Rare Dis. 2012; 7: 68. DOI: 10.1186/1750-1172-7-68.Google Scholar
Online Mendelian Inheritance in Man (OMIM). Carnitine deficiency, systemic primary; CDSP. McKusick, VA, ed. Johns Hopkins University. Updated Jul 7, 2014. Entry Number 212140. Available at http://omim.org/entry/212140. Accessed Sep 12, 2018.Google Scholar
Dempsey, JA, Smith, CA, Przybylowski, T, et al. The ventilator responsiveness to CO2 below eupnoea as a determinant of ventilator stability in sleep. J Physiol. 2004; 560: 1–11.Google Scholar
Eckert, DJ, Jordan, AS, Merchia, P, et al. Central sleep apnea: Pathophysiology and treatment. Chest. 2007; 131: 595–607.Google Scholar
Sateia, M, Berry, RB, Bornemann, MC, et al. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Quinzii, CM, Dimauro, S, Hirano, M. Human coenzyme Q10 deficiency. Neurochem Res. 2007; 32: 723–7.Google Scholar
Rodriguez-Pla, A, Monoch, DA. Primary angiitis of the central nervous system in adults and children. Rheum Dis Clin North Am. 2015; 41(1): 47–62.Google Scholar
Al Bahrani, B, Henderson, C, Delaney, G. Primary central nervous system lymphoma and subcutaneous metastases. J Neurooncol. 2000; 47(2): 141–4.Google Scholar
Carnevale, J, Rubenstein, JL. The challenge of primary central nervous system lymphoma. Hematol Oncol Clin North Am. 2016; 30(6): 1293–316.Google Scholar
Fitzsimmons, A, Upchurch, K, Batchelor, T. Clinical features and diagnosis of primary central nervous system lymphoma. Hematol Oncol Clin North Am. 2005; 19(4): 689–703, vii.Google Scholar
Herrlinger, U, Schabet, M, Bitzer, M, Petersen, D, Krauseneck, P. Primary central nervous system lymphoma: from clinical presentation to diagnosis. J Neurooncol. 1999; 43(3): 219–26.Google Scholar
Ko, JH, Lu, PH, Tang, TC, Hsu, YH. Metastasis of primary CNS lymphoma along a ventriculoperitoneal shunt. J Clin Oncol. 2011; 29(34): e823–4Google Scholar
Korfel, A, Schlegel, U. Diagnosis and treatment of primary CNS lymphoma. Nat Rev Neurol. 2013; 9(6): 317–27.Google Scholar
Masroujeh, R, Otrock, ZK, Yamout, B, Jabbour, MN, Bazarbachi, A. Myasthenia gravis developing in a patient with CNS lymphoma. Int J Hematol. 2010; 91(3): 522–4Google Scholar
Matsuyama, J, Ichikawa, M, Oikawa, T, et al. Primary CNS lymphoma arising in the region of the optic nerve presenting as loss of vision: 2 case reports, including a patient with a massive intracerebral hemorrhage. Brain Tumor Pathol. 2014; 31(3): 222–8Google Scholar
Nayak, L, Pentsova, E, Batchelor, TT. Primary CNS lymphoma and neurologic complications of hematologic malignancies. Continuum (Minneap Minn). 2015; 21(2): 355–72.Google Scholar
Rees, J, Wen, P, eds. Blue books of neurology: Neuro-oncology. Vol 36. Elsevier Inc. 2010; pp. 201–17.Google Scholar
Cutrer, FM, Boes, CJ. Cough, exertional, and sex headaches. Neurol Clin North Am. 2004; 22: 133–49.Google Scholar
Headache Classification Subcommittee of the International Headache Society. The international classification of headache disorders. 2nd ed. Cephalalgia. 2004; 24(Suppl 1): 1–160.Google Scholar
Cutrer, FM, Boes, CJ. Cough, exertional, and sex headaches. Neurol Clin North Am. 2004; 22: 133–49.Google Scholar
Grace, A, Horgan, J, Breathnach, K, et al. Anginal headache and its basis. Cephalalgia. 1997; 17: 195–6.Google Scholar
Rasmussen, BK, Olesen, J. Symptomatic and nonsymptomatic headaches in a general population. Neurology. 1992; 42: 1225–31.Google Scholar
Lance, JW. Headaches related to sexual activity. J Neurol Neurosurg Psychiatry. 1976; 39: 1226.Google Scholar
Gomez-Tortosa, E, et al. Familial primary lateral sclerosis or dementia associated with ARG573Gly TBK1 mutation. J Neurol Neurosurg Psychiatry. 2017; 88(11): 996–7. Post Script letter.Google Scholar
Wais, V, et al. The concept and diagnostic criteria of primary lateral sclerosis. Acta Neurol Scand. 2017; 136(3): 204–11.Google Scholar
Albanese, A, Bhatia, K, Bressman, S, et al. Phenomenology and classification of dystonia: a consensus update. Mov Disord. 2013; 28: 863–73.Google Scholar
Bressman, SB. Dystonia genotypes, phenotypes, and classification. Adv Neurol. 2004; 94: 101–7.Google Scholar
Fernandez, H, Machado, A, Pandya, M. Practical approach to movement disorders: diagnosis and management. 2nd ed. New York, US: Demos Medical; 2014.Google Scholar
Fuchs, T, Gavarini, S, Saunders-Pullman, R, et al. Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia. Nat Genet. 2009; 41(3): 286–8.Google Scholar
Phibbs, FT, Hedera, P. Update on the genetics of movement disorders. Continuum (Minneap Minn). 2010; 16(1, Neurology): 77–95.Google Scholar
Saunders-Pullman, R. Genetics of dystonia. Continuum (Minneap Minn). 2008; 14(2, Neurology): 65–89.Google Scholar
Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. 5th ed. London, UK: Elsevier; 2014.Google Scholar
Bauer, J, Gold, R, Adams, O, Lassmann, H. Progressive multifocal leukoencephalopathy and immune reconstitution inflammatory syndrome (IRIS). Acta Neuropathologica [Online]. 2015; 130(6): 751–64.Google Scholar
Malek, N, Stewart, W, Greene, J. The progressive myoclonic epilepsies. Pract Neurol. 2015; 15(3): 164–71.Google Scholar
McFarland, NR. Diagnostic approach to atypical parkinsonian syndromes. Continuum (Minneap Minn). 2016; 22: 1117–42.Google Scholar
Kobylecki, C, et al. Cognitive-behavioural features of progressive supranuclear palsy syndrome overlap with frontotemporal dementia. J Neurol. 2015; 262: 916–22.Google Scholar
Josephs, KA, et al. Atypical progressive supranuclear palsy underlying progressive apraxia of speech and nonfluent aphasia. Neurocase. 2005; 11: 283–96.Google Scholar
Averbuch-Heller, L, Steiner, I, Abramsky, O. Neurologic manifestations of progressive systemic sclerosis. Arch Neurol. 1992; 49: 1292.Google Scholar
Denton, CP, Khanna, D. Systemic sclerosis. Lancet. 2017; 390(10103): 1685–99. DOI: 10.1016/S0140-6736(17)30933-9.Google Scholar
Hietaharju, A, Jääskeläinen, S, Kalimo, H, Hietarinta, M. Peripheral neuromuscular manifestations in systemic sclerosis (scleroderma). Muscle Nerve. 1993; 16: 1204.Google Scholar
Longo, DL, Kasper, DL, Fauci, A, et al., eds. Harrison's principles of internal medicine. 17th ed. New York: McGraw-Hill; 2016. pp. 2906–106.Google Scholar
Ciccarelli, A, Daly, AF, Beckers, A. The epidemiology of prolactinomas. Pituitary. 2005; 8(1): 3–6.Google Scholar
Wong, A, Eloy, JA, Couldwell, WT, Liu, JK. Update on prolactinomas. Part 1: clinical manifestations and diagnostic challenges. J Clin Neurosci. 2015; 22: 1562–67.Google Scholar
Wong, A, Eloy, JA, Couldwell, WT, Liu, JK. Update on prolactinomas. Part 2: treatment and management strategies. J Clin Neurosci. 2015; 22: 1568–74.Google Scholar
Vincent, GM. The long QT syndrome. Indian Pacing Electrophysiol J. 2002; 2(4): 127–42.Google Scholar
Brazis, PW, et al., eds. Peripheral nerves. In Localization in clinical neurology. 6th ed. Philadelphia, PA: Lippincott Williams and Wilkins; 2011. Chapter 2.Google Scholar
Rodner, CM, Tinsley, BA, O'Malley, MP. Pronator syndrome and anterior interosseous nerve syndrome. J Am Acad Orthop Surg. 2013; 21(5): 268–75.Google Scholar
Roze, E, Bounolleau, P, Ducreux, D, et al. Propriospinal myoclonus revisited: Clinical, neurophysiologic, and neuroradiologic findings. Neurology. 2009; 72(15): 1301–9.Google Scholar
Brown, P. Propriospinal myoclonus: where do we go from here? Mov Disord. 2014; 29(9): 1092–3.Google Scholar
Brown, P, Rothwell, JC, Thompson, PD, Marsden, CD. Propriospinal myoclonus: evidence for spinal “pattern” generators in humans. Mov Disord. 1994; 9(5): 571–6.Google Scholar
Chokroverty, S, Walters, A, Zimmerman, T, Picone, M. Propriospinal myoclonus: a neurophysiologic analysis. Neurology. 1992; 42(8): 1591–5.Google Scholar
Antelmi, E, Provini, F. Propriospinal myoclonus: The spectrum of clinical and neurophysiological phenotypes. Sleep Med Rev. 2015; 22: 54–63.Google Scholar
Attard, G, Parker, C, Eeles, RA, et al. Prostate cancer. Lancet. 2016; 387(10013): 70–82.Google Scholar
Benjamin, R. Neurologic complications of prostate cancer. Am Fam Physician. 2002; 65(9): 1834–40. Review.Google Scholar
Cuzick, J, Thorat, MA, Andriole, G, et al. Prevention and early detection of prostate cancer. Lancet Oncol. 2014; 15(11): e484–92.Google Scholar
Hong, MK, Kong, J, Namdarian, B, et al. Paraneoplastic syndromes in prostate cancer. Nat Rev Urol. 2010; 7(12): 681–92.Google Scholar
Karden, EM. Prosthetic heart valves. Feb 18, 2015. Available from http://emedicine.medscape.com/article/780702-overview#a4. Retrieved Jul 27, 2017.Google Scholar
Otto, CM, Bonow, RO. Valvular heart disease. In Mann, DL, Zipes, DP, Libby, P, Bonow, RO, Braunwald, E, eds. Braunwald's heart diseases: a textbook of cardiovascular medicine. 10th ed. Philadelphia: Elsevier/Saunders; 2015; p. 1505.Google Scholar
Papadakis, MA, McPhee, SJ. Current medical diagnosis and treatment. 58th ed. New York: McGraw-Hill Education; in press.Google Scholar
Ropper, AH, Samuels, MA, Klein, JP. Adams & Victor's principles of neurology. 10th ed. New York, NY: McGraw-Hill; 2014.Google Scholar
Goldenberg, NA, Manco-Johnson, MJ. Protein C deficiency. Haemoph Off J World Fed Hemoph. 2008; 14: 1214–21.Google Scholar
D'Angelo, A, Viganò D'Angelo, S. Protein S deficiency. Haematologica. 2008; 93: 498–501.Google Scholar
Kershaw, P, Freeman, R, Templeton, D, et al. Pseudallescheria boydii infection of the central nervous system. Arch Neurol. 1990; 47(4): 468–72.Google Scholar
Long, S, Pickering, LK, Prober, CG, eds. Principles and practice of pediatric infectious disease. 4th ed. Edinburgh: Elsevier/Saunders; 2012.Google Scholar
Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. 5th ed. London, UK: Elsevier; 2014.Google Scholar
Roberts, J, Larson-Williams, L, Ibrahim, F, Hassoun, A. Malignant otitis externa (MOE) causing cerebral abscess and facial nerve palsy. J Hosp Med. 2010; 5(7): E6–8.Google Scholar
Longo, LP, Johnson, B. Addiction: Part I. Benzodiazepines – side effects, abuse risk and alternatives. Am Fam Physician. 2000; 61(7): 2121–8.Google Scholar
Wiegand, TJ, Burns, MM, Wiley, JF. Clinical manifestations and evaluation of mushroom poisoning. Updated Dec 9, 2016. UpToDate. Waltham, MA. https://www.uptodate.com/contents/clinical-manifestations-and-evaluation-of-mushroom-poisoning?source=search_result&search=psilocybin&selectedTitle=2∼8. Accessed Aug 8, 2018.Google Scholar
Mallick, IH, Thoufeeq, MH, Rajendran, TP. Iliopsoas abscesses. Postgrad Med J. 2004; 80(946): 459.Google Scholar
Mückley, T, Schütz, T, Kirschner, M, et al. Psoas abscess: the spine as a primary source of infection. Spine (Phila Pa 1976). 2003; 28(6): E106.Google Scholar
Lefevre, N, Bohu, Y, Klouche, S, Chewla, N, Herman, S. Complete paralysis of the quadriceps secondary to post-traumatic iliopsoas hematoma: A systematic review. Eur J Orthopaed Surg Traumatol. 2015; 25(1): 39–43.Google Scholar
Parner, SS, Carpenter, JP, Fairman, RM, Velazquez, OC, Mitchell, ME. Femoral neuropathy following retroperitoneal hemorrhage: case series and review of the literature. Ann Vasc Surg. 2006; 20(4): 536–40.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Barofsky, I, Buchholz, D, Edwin, D, Jones, B, Ravich, W. Characteristics of patients who have difficulties initiating swallowing. Annual Meeting of the Dysphagia Research Society, Lake Geneva, WI, September, 1993.Google Scholar
Leopold, NA. Dysphagia in drug-induced parkinsonism: a case report. Dysphagia. 1996; 11(2): 151–3.Google Scholar
Ravich, WJ, Wilson, RS, Jones, B, Donner, MW. Psychogenic dysphagia and globus: reevaluation of 23 patients. Dysphagia. 1989; 4(1): 35–8.Google Scholar
Tanidir, C, Hergüner, S. Mirtazapine for choking phobia: report of a pediatric case. J Child Adolesc Psychopharmacol. 2015; 25(8): 659–60.Google Scholar
Benbadis, SR, Agrawal, V, Tatum, WO. How many patients with psychogenic nonepileptic seizures also have epilepsy? Neurology. 2001; 57(5): 915–17.Google Scholar
Benbadis, SR, Hauser, WA. An estimate of the prevalence of psychogenic non-epileptic seizures. Seizure. 2000; 9(4): 280–1.Google Scholar
Diprose, W, Sundram, F, Menkes, DB. Psychiatric comorbidity in psychogenic nonepileptic seizures compared with epilepsy. Epilepsy Behav. 2016; 56: 123–30.Google Scholar
Ettinger, AB, Devinsky, O, Weisbrot, DM, et al. Headaches and other pain symptoms among patients with psychogenic non-epileptic seizures. Seizure. 1999; 8: 424.Google Scholar
Ettinger, AB, Devinsky, O, Weisbrot, DM, Ramakrishna, RK, Goyal, A. A comprehensive profile of clinical, psychiatric, and psychosocial characteristics of patients with psychogenic nonepileptic seizures. Epilepsia. 1999; 40(9): 1292–8.Google Scholar
Ettinger, AB, Dhoon, A, Weisbrot, DM, Devinsky, O. Predictive factors for outcome of nonepileptic seizures after diagnosis. J Neuropsychiatry Clin Neurosci. 1999; 11: 458.Google Scholar
Meierkord, H, Shorvon, S. The clinical features and prognosis of pseudoseizures diagnosed using video-EEG telemetry. Neurology. 1991; 41(10): 1643–3.Google Scholar
American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders (DSM-5). 5th ed. American Psychiatric Pub; 2013.Google Scholar
Engel, GL. “Psychogenic” pain and the pain-prone patient. Am J Med. 1959; 26(6): 899–918.Google Scholar
Ilgen, MA, Kleinberg, F, Ignacio, RV, et al. Noncancer pain conditions and risk of suicide. JAMA Psychiatry. 2013; 70(7): 692–7.Google Scholar
Merskey, HE. Classification of chronic pain: Descriptions of chronic pain syndromes and definitions of pain terms. Pain. 1986; Suppl 3: 226.Google Scholar
Sriram, T.G, Chaturvedi, SK, Gopinath, PS, Shanmugam, V. Controlled study of alexithymic characteristics in patients with psychogenic pain disorder. Psychother Psychosomat. 1987; 47(1): 11–17.Google Scholar
Siegel, AJ. Hyponatremia in psychiatric patients: update on evaluation and management. Harv Rev Psychiatry. 2008; 16(1): 13–24. DOI: 10.1080/10673220801924308.Google Scholar
Bremner, AJ, Regan, A. Intoxicated by water. Polydipsia and water intoxication in a mental handicap hospital. Br J Psychiatry. 1991; 158: 244–50.Google Scholar
Whitchurch, FT, Alexander, J. Psychogenic polydipsia: Hidden or underdiagnosed? Aust N Z J Psychiatry. 2011; 45(9): 789–90. DOI: 10.3109/00048674.2011.585457.Google Scholar
Dundas, B, Harris, M, Narasimhan, M. Psychogenic polydipsia review: Etiology, differential, and treatment. Curr Psychiatry Rep. 2007; 9(3): 236–41. DOI: 10.1007/s11920-007-0025-7.Google Scholar
Hawken, ER, Crookall, JM, Reddick, D, et al. Mortality over a 20-year period in patients with primary polydipsia associated with schizophrenia: A retrospective study. Schizophr Res. 2009; 107(2–3): 128–33. DOI: 10.1016/j.schres.2008.09.029.Google Scholar
Stuart, CA, Neelon, FA, Lebovitz, HE. Disordered control of thirst in hypothalamic-pituitary sarcoidosis. N Engl J Med. 1980; 303(19): 1078.Google Scholar
Ödman, M, Maire, R. Chronic subjective dizziness. Acta Oto-laryngologica. 2008; 128(10): 1085–8.Google Scholar
Staab, JP. Chronic dizziness: the interface between psychiatry and neuro-otology. Curr Opin Neurol. 2006; 19(1): 41–8.Google Scholar
Strupp, M, Brandt, T. Diagnosis and treatment of vertigo and dizziness. Dtsch Arztebl Int. 2008; 105(10): 173–80. http://doi.org/10.3238/arztebl.2008.0173.Google Scholar
Fernandez, HH, Friedman, JH, Jacques, C, Rosenfeld, M. Quetiapine for the treatment of drug-induced psychosis in Parkinson's disease. Mov Disord. 1999; 14: 484.Google Scholar
Popeo, D, Kellner, CH. ECT for Parkinson's disease. Med Hypotheses. 2009; 73(4): 468–9. DOI: 10.1016/j.mehy.2009.06.053. PubMed PMID: 19660875.Google Scholar
Rabey, JM, Treves, TA, Neufeld, MY, et al. Low-dose clozapine in the treatment of levodopa-induced mental disturbances in Parkinson's disease. Neurology. 1995; 45: 432.Google Scholar
Ravina, B, Marder, K, Fernandez, HH, et al. Diagnostic criteria for psychosis in Parkinson's disease: report of an NINDS, NIMH work group. Mov Disord. 2007; 22(8): 1061–8.Google Scholar
Williams-Gray, CH, Foltynie, T, Lewis, SJG, Barker, RA. Cognitive deficits and psychosis in Parkinson's disease: a review of pathophysiology and therapeutic options. CNS Drugs. 2006; 20(6): 477–505. DOI: 10.2165/00023210-200620060-00004.Google Scholar
Wolters, E. Intrinsic and extrinsic psychosis in Parkinson's disease. J Neurol. 2001; 248(Suppl 3): 22–8.Google Scholar
Zahodne, LB, Fernandez, HH. Pathophysiology and treatment of psychosis in Parkinson's disease: a review. Drugs Aging. 2008; 25(8): 665–82. DOI: 10.2165/00002512-200825080-00004.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Greene, KA, Dickman, CA, Smith, KA, Kinder, EJ, Zabramski, JM. Self-inflicted orbital and intracranial injury with a retained foreign body, associated with psychotic depression: case report and review. Surg Neurol. 1993; 40(6): 499–503.Google Scholar
Johnson, J, Horwath, E, Weissman, MM. The validity of major depression with psychotic features based on a community study. Arch Gen Psychiatry. 1991; 48: 1075.Google Scholar
Ohayon, MM, Schatzberg, AF. Prevalence of depressive episodes with psychotic features in the general population. Am J Psychiatry. 2002; 159: 1855.Google Scholar
Shagass, C, Naiman, J, Mihalik, J. An objective test which differentiates between neurotic and psychotic depression. AMA Archiv Neurol Psychiatry. 1993; 75(5): 461–71.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Cummings, J. Organic psychoses. Delusion disorders and secondary mania. Psychiatr Clin North Am. 1996; 9(2): 293–311.Google Scholar
Keshavan, MS, Kaneko, Y. Secondary psychoses: An update. World Psychiatry. 2013; 12(1): 4–15. DOI: 10.1002/wps.20001.Google Scholar
Stern, TA, Fricchione, GL, Cassem, NH, Jellinek, M, Rosenbaum, JF. Massachusetts General Hospital handbook of general hospital psychiatry. Philadephia, PA: Saunders; 2010.Google Scholar
Weisholtz, DS, Dworetzky, BA. Epilepsy and psychosis. J Neurol Disord Stroke. 2014; 2(3): 1069.Google Scholar
Bever, C, Aquino, AV, Penn, AS, et al. Prognosis of ocular myasthenia gravis. Ann Neurol. 1998; 14: 516–9.Google Scholar
Defazio, G, Livrea, P, Lamberi, P, et al. Isolated so-called paraxis of eyelid opening: Report of 10 cases and a review of the literature. Eur Neurol. 1998; 39(4): 204–10.Google Scholar
Ferguson-Myrthil, N. Droxidopa for symptomatic neurogenic hypotension. Cardiol Rev. 2017; 25(5): 241–6. DOI: 10.1097/CRD.0000000000000151.Google Scholar
Idiaquez, J. Pure autonomic failure. Bradbury Eggleston syndrome: Case report. Rev Med Chil. 2005; 133(2): 215–8. Epub Apr 7, 2005.Google Scholar
Kuritzky, L, Espay, AJ, Gelblum, J, Payne, R, Dietrich, E. Diagnosing and treating neurogenic orthostatic hypotension in primary care. Postgrad Med. 2015; 127(7): 702–15, DOI: 10.1080/00325481.2015.1050340.Google Scholar
Feve, AP, Fenelon, G, Wallays, C, Remy, P, Guillard, A. Axial motor disturbances after hypoxic lesions of the globus pallidus. Mov Disord. 1993; 8(3): 321–6.Google Scholar
Galati, S, Stadler, C. Schizophrenia symptoms relieved by CO-induced pallidal lesion: a case report. J Neuropsychiatry Clin Neurosci. 2013; 25(2): E52–3.Google Scholar
Alquist, CR, McGoey, R, Bastian, F, Newman, W, 3rd. Bilateral globus pallidus lesions. J La State Med Soc. 2012; 164(3): 145–6.Google Scholar
Bucher, SF, Seelos, KC, Dodel, RC, et al. Pallidal lesions: structural and functional magnetic resonance imaging. Arch Neurol. 1996; 53: 682–6.Google Scholar
Aizawa, H, Kwak, S, Shimizu, T, et al. A case of adult onset pure pallidal degeneration. I. Clinical manifestations and neuropathological observations. J Neurol Sci. 1991; 102(1): 76–82.Google Scholar
Aizawa, H, Kwak, S, Shimizu, T, Mannen, T, Shibasaki, H. A case of adult onset pure pallidal degeneration. II. Analysis of neurotransmitter markers, with special reference to the termination of pallidothalamic tract in human brain. J Neurol Sci. 1991; 102(1): 83–91.Google Scholar
Bickels, J, Ben-Sira, L, Kessler, A, Wientroub, S. Primary pyomyositis. J Bone Joint Surg Am. 2002; 84–A: 2277.Google Scholar
Combs, GF. The vitamins: fundamental aspects in nutrition and health. San Diego: Elsevier; 2008. pp. 313–29.Google Scholar
Basura, GJ, et al. Clinical features and the management of pyridoxine-dependent and pyridoxine-responsive seizures: review of 63 North American cases submitted to a patient registry. Eur J Pediatr. 2009; 168(6): 697–704.Google Scholar
Bok, LA, et al. Long-term outcome in pyridoxine-dependent epilepsy. Dev Med Child Neurol. 2012; 54(9): 849–54.Google Scholar
van Karnebeek, CD, Jaggumantri, S. Current treatment and management of pyridoxine-dependent epilepsy. Curr Treat Options Neurol. 2015; 17(2): 335.Google Scholar
Combs, GF. The vitamins: fundamental aspects in nutrition and health. San Diego: Elsevier; 2008. pp. 313–29.Google Scholar
Perry, TA, Weerasuriya, A, Mouton, PR, Holloway, HW, Greig, NH. Pyridoxine-induced toxicity in rats: a stereological quantification of the sensory neuropathy. Exp Neurol. 2004; 190(1): 133–44.Google Scholar
Schwartz, M, Hocherman, S. Antipsychotic-induced rabbit syndrome: epidemiology, management and pathophysiology. CNS Drugs. 2004; 18(4): 213–20.Google Scholar
Fornazzari, L, Ichise, M, Remington, G, Smith, I. Rabbit syndrome, antidepressant use, and cerebral perfusion SPECT scan findings. J Psychiatry Neurosci. 1991; 16(4): 227–9.Google Scholar
Wada, Y, Yamaguchi, N. The rabbit syndrome and antiparkinsonian medication in schizophrenic patients. Neuropsychobiology. 1992; 25(3): 149–52.Google Scholar
Catena Dell'osso, M, Fagiolini, A, Ducci, F, et al. Newer antipsychotics and the rabbit syndrome. Clin Pract Epidemiol Ment Health. 2007; 3: 6.Google Scholar
Deshmukh, DK, Joshi, VS, Agarwal, MR. Rabbit syndrome: a rare complication of long-term neuroleptic medication. Br J Psychiatry. 1990; 157: 293.Google Scholar
Villeneuve, A. The rabbit syndrome. A peculiar extrapyramidal reaction. Can Psychiatr Assoc J. 1972; 17(2, Suppl 2):SS69.Google Scholar
Hankins, DG, Rosekrans, JA. Overview, prevention, and treatment of rabies. Mayo Clin Proc. 2004; 79(5): 671–6.Google Scholar
World Health Organization. WHO expert consultation on rabies. WHO Tech Rep Ser 2005;Abstract 931: 88.Google Scholar
Brazis, PW, et al., eds. Peripheral nerves. In Localization in clinical neurology. 6th ed. Philadelphia, PA: Lippincott Williams and Wilkins; 2011. Chapter 2.Google Scholar
Gouse, M. Incidence and predictors of radial nerve palsy with the anterolateral brachialis splitting approach to the humeral shaft. Chin J Traumatol. 2016; 19(4): 217–20.Google Scholar
Posner, JB. Side effects of radiation therapy. In DeAngelis, LM, Posner, JB, eds. Neurologic complications of cancer. Philadelphia, PA: FA Davis; 1995. pp. 311–37.Google Scholar
Posner, JB. Side effects of radiation therapy. In Neurologic complications of cancer. Philadelphia, PA: FA Davis; 1995. pp. 311–37.Google Scholar
Alexander, C. Lumbosacral radiculopathy. StatPearls. Treasure Island, FL: StatPearls Publishing; Jun 29, 2017.Google Scholar
Brazis, PW, et al., eds. Peripheral nerves. In Localization in clinical neurology. 6th ed. Philadelphia, PA: Lippincott Williams and Wilkins; 2011. Chapter 2.Google Scholar
Warren, M. Cervical radiculopathy. StatPearls. Treasure Island, FL: StatPearls Publishing; Jun 25, 2017.Google Scholar
Goadsby, PJ. Raeder's syndrome: paratrigeminal paralysis of the oculopupillary sympathetic system. J Neurol Neurosurg Psychiatry. 2002; 72(3): 297.Google Scholar
Mokri, B. Raeder's paratrigeminal syndrome. Original concept and subsequent deviations. Arch Neurol. 1982; 39(7): 395.Google Scholar
Tatsui, C. Raeder's syndrome after embolization of a giant intracavernous carotid artery aneurysm: pathophysiological considerations. Arq Neuropsiquiatr. 2005; 63(3A): 676–80.Google Scholar
Dobyns, WB, Ozelius, LJ, Kramer, PL, et al. Rapid-onset dystonia-Parkinsonism. Neurology. 1993; 43: 2596–602.Google Scholar
Pittock, SJ, Joyce, C, O'Keane, V, et al. Rapid-onset dystonia parkinsonism: a clinical and genetic analysis of a new kindred. Neurology. 2000; 55: 991–5.Google Scholar
Charlesworth, G, Bhatia, KP, Wood, NW. The genetics of dystonia: New twists in an old tale. Brain. 2013; 136(7): 2017–37.Google Scholar
Sweney, MT, Newcomb, TM, Swoboda, KJ. The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, alternating hemiplegia of childhood, rapid onset dystonia parkinsonism, CAPOS and beyond. Pediatr Neurol. 2015; 52(1): 56–64.Google Scholar
de Carvalho Aguiar, P, Sweadner, KJ, Penniston, J, et al. Mutations in the Na+/K+-ATPase α3 gene ATP1A3 are associated with rapid onset dystonia parkinsonism. Neuron. 2004; 43: 169–75.Google Scholar
Brashear, A, Dobyns, WB, de Carvalho Aguiar, P, et al. The phenotypic spectrum of rapid onset dystonia-parkinsonism (RDP) and mutations in the ATPIA3 gene. Brain. 2007; 130(3): 828–35.Google Scholar
Daroff, RB, Bradley, WG, eds. Bradley's neurology in clinical practice. 6th ed. Philadelphia, PA: Saunders; 2012.Google Scholar
Varadkar, S, et al. Rasmussen's encephalitis: clinical features, pathobiology, and treatment advances. Lancet Neurol. 2014; 13(2): 195–205.Google Scholar
Carter, JD, Hudson, AP. Reactive arthritis: clinical aspects and medical management. Rheum Dis Clin North Am. 2009; 35(1): 21–44.Google Scholar
Kaarela, K, Jäntti, JK, Kotaniemi, KM. Similarity between chronic reactive arthritis and ankylosing spondylitis. A 32–35-year follow-up study. Clin Exp Rheumatol. 2009; 27(2): 325–8.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders. 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Schenck, C, Mahowald, M. REM sleep parasomnias in adults. In Barkoukis, TJ, et al., eds. Therapy in sleep medicine. Philadelphia, PA: Elsevier; 2012. pp. 540–58.Google Scholar
Sharpless, BA, Barber, JP. Lifetime prevalence rates of sleep paralysis: a systematic review. Sleep Med Rev. 2011; 15: 311–5.Google Scholar
Brockington, IF. Menstrual psychosis: a bipolar disorder with a link to the hypothalamus. Curr Psychiatry Rep. 2011; 13(3): 193.Google Scholar
Dennerstein, L, Judd, F, Davies, B. Psychosis and the menstrual cycle. Med J Aust. 1983; 1(11): 524–6.Google Scholar
Felthous, AR, Robinson, DB, Conroy, RW. Prevention of recurrent menstrual psychosis by an oral contraceptive. Am J Psychiatry. 1980; 137(2): 245–6.Google Scholar
Kramer, MS. Menstrual epileptoid psychosis in an adolescent girl. Am J Dis Child. 1977; 131(3): 316–17.Google Scholar
Chopra, R, Chaudhary, N, Kay, J. Relapsing polychondritis. Rheum Dis Clin N Am. 2013; 39(2): 263–76.Google Scholar
Langford, CA. Relapsing polychondritis. In Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015. p. 389.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders, 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Boeve, BF, Silber, MH, Ferman, TJ, et al. Clinicopathologic correlations in 172 cases of rapid eye movement sleep behavior disorder with or without a coexisting neurologic disorder. Sleep Med. 2013; 14: 754–62.Google Scholar
Devnani, P, Fernandes, R. Management of REM sleep behavior disorder: An evidence based review. Ann Indian Acad Neurol. 2015; 18: 1–5.Google Scholar
Holtbernd, F, Gagnon, JF, Postuma, RB, et al. Abnormal metabolic network activity in REM sleep behavior disorder. Neurology. 2014; 82: 620–7.Google Scholar
Giglio, P, Gilbert, MR. Neurologic complications of cancer and its treatment. Curr Oncol Rep. 2010; 12(1): 50–9.Google Scholar
Palapattu, GS, Kristo, B, Rajfer, J. Paraneoplastic syndromes in urologic malignancy: the many faces of renal cell carcinoma. Rev Urol. 2002; 4(4): 163–70.Google Scholar
Traul, DE, Schiff, D. Neurologic complications of genitourinary cancer. Current Clinical Oncology: Cancer Neurology in Clinical Cancer. Totowa, NJ: Humana Press; 2008.Google Scholar
Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
Brouns, R, De Deyn, PP. Neurological complications in renal failure: a review. Clin Neurol Neurosurg. 2004; 107: 1–16.Google Scholar
Burn, DJ, Bates, B. Neurology and the kidney. J Neurol Neurosurg Psychiatry. 1998; 65: 810–21.Google Scholar
Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
Lacerda, G, Krummel, T, Hirsch, E. Neurologic presentations of renal diseases. Neurol Clin. 2010; 28: 45–59.Google Scholar
Byl, N. Treatment effectiveness for patients with a history of repetitive hand use and focal hand dystonia: a planned, prospective follow-up study. J Hand Ther. 2000; 13(4): 289–301.Google Scholar
Ioannou, C. Objective evaluation of performance stress in musicians with focal hand dystonia: a case series. J Mot Behav. 2016; 48(6): 562–72.Google Scholar
Edwards, AO. Clinical features of congenital vitreoretinopathies. Eye. 2008; 22: 1233–42.Google Scholar
Corbett, JJ. Neuro-ophthalmic complications of migraine and cluster headaches. Neurol Clin. 1983; 1: 973–95.Google Scholar
Grosbert, BM, Solomon, S, Lipton, RB. Retinal migraine. Curr Pain and Headache Rep. 2005; 9: 268–71.Google Scholar
Rothrock, J, Walicke, P, Swenson, MR, et al. Migrainous stroke. Arch Neurol. 1988; 45: 63–7.Google Scholar
Massof, RW, Fishman, GA. How strong is the evidence that nutritional supplements slow the progression of retinitis pigmentosa? Arch Ophthalmol. 2010; 128(4): 493–95. DOI: 10.1001/archophthalmol.2010.46.Google Scholar
Pruett, RC. Retinitis pigmentosa: clinical observations and correlations. Trans Am Ophthalmol Soc. 1983; 81: 693–735.Google Scholar
Laurvick, CL, de Klerk, N, Bower, C, et al. Rett syndrome in Australia: a review of the epidemiology. J Pediatr. 2006; 148: 347–52.Google Scholar
Christodoulou, J, Ho, G. MECP2-related disorders. Oct 3, 2001. Updated Jun 28, 2012. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2018. Available from www.ncbi.nlm.nih.gov/books/NBK1497/. Accessed Sep 15, 2018.Google Scholar
Calabrese, LH, Dodick, DW, Schwedt, TJ, Singhal, AB. Narrative review: reversible cerebral vasoconstriction syndromes. Ann Intern Med. 2007; 146(1): 34–44.Google Scholar
Chen, SP, Fuh, JL, Chang, FC, et al. Transcranial color Doppler study for reversible cerebral vasoconstriction syndromes. Ann Neurol. 2008; 63(6): 751–7.Google Scholar
Ducros, A. [Reversible cerebral vasoconstriction syndrome]. Presse Med. 2010; 39(3): 312–22.Google Scholar
Ducros, A. Reversible cerebral vasoconstriction syndrome. Lancet Neurol. 2012; 10: 906–17.Google Scholar
Ducros, A, Boukobza, M, Porcher, R, et al. The clinical and radiological spectrum of reversible cerebral vasoconstriction syndrome. A prospective series of 67 patients. Brain. 2007; 130(Pt 12): 3091–101.Google Scholar
Fugate, JE, Rabinstein, AA. Posterior reversible encephalopathy syndrome: clinical and radiological manifestations, pathophysiology, and outstanding questions. Lancet Neurol. 2015; 14(9): 914–25.Google Scholar
Larry, C, Oppenheim, C, Mas, JL. Posterior reversible encephalopathy syndrome. Handb Clin Neurol. 2014; 121: 1687–701.Google Scholar
Rykken, B, McKinney, AM. Posterior reversible encephalopathy syndrome. Semin Ultrasound CT MR. 2014; 35(2): 118–35.Google Scholar
Huerta-Alardín, AL, Varon, J, Marik, PE. Bench-to-bedside review: Rhabdomyolysis – an overview for clinicians. Crit Care. 2005; 9: 158.Google Scholar
Vanholder, R, Sever, MS, Erek, E, Lameire, N. Rhabdomyolysis. J Am Soc Nephrol. 2000; 11(8): 1553–61.Google Scholar
Warren, JD, Blumbergs, PC, Thompson, PD. Rhabdomyolysis: a review. Muscle Nerve. 2002; 25: 332.Google Scholar
Bland, EF, Duckett Jones, T. Rheumatic fever and rheumatic heart disease; a twenty year report on 1000 patients followed since childhood. Circulation. 1951; 4(6): 836.Google Scholar
GBD 2013 Mortality and Causes of Death Collaborators. Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990–2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet. 2015; 385(9963): 117.Google Scholar
Meira, ZM, Goulart, EM, Colosimo, EA, Mota, CC. Long term follow up of rheumatic fever and predictors of severe rheumatic valvar disease in Brazilian children and adolescents. Heart. 2005; 91(8): 1019.Google Scholar
Tibazarwa, KB, Volmink, JA, Mayosi, BM. Incidence of acute rheumatic fever in the world: a systematic review of population-based studies. Heart. 2008; 94(12): 1534.Google Scholar
Majithia, V, Geraci, SA. Rheumatoid arthritis: diagnosis and management. Am J Med. 2007; 120(11): 936–9.Google Scholar
Scott, DL, Wolfe, F, Huizinga, TW. Rheumatoid arthritis. Lancet. 2010; 376(9746): 1094–108.Google Scholar
Turesson, C. Extra-articular rheumatoid arthritis. Curr Opin Rheumatol. 2013; 25(3): 360–6.Google Scholar
Turesson, C, O'Fallon, WM, Crowson, CS, Gabriel, SE, Matteson, EL. Extra-articular disease manifestations in rheumatoid arthritis: incidence trends and risk factors over 46 years. Ann Rheum Dis. 2003; 62(8): 722–7.Google Scholar
Biller, J, Ferro, JM, ed. Neurologic aspects of systemic disease, Part III. Handbook of Clinical Neurology, Vol 121 (3rd Series). San Diego: Elsevier; 2014.Google Scholar
Centers for Disease Control and Prevention. Rocky mountain spotted fever. Updated Aug 6, 2018. https://www.cdc.gov/rmsf/index.html. Accessed Sep 15, 2018.Google Scholar
Atkins, L, Miller, WL, Salam, M. A ring-20 chromosome. J Med Genet. 1972; 9(3): 377–80.Google Scholar
Inoue, Y, et al. Ring chromosome 20 and nonconvulsive status epilepticus. A new epileptic syndrome. Brain. 1997; 120(Pt 6): 939–53.Google Scholar
Nishiwaki, T, et al. Mosaicism and phenotype in ring chromosome 20 syndrome. Acta Neurol Scand. 2005; 111(3): 205–8.Google Scholar
Ferrante, M. Brachial plexopathies: classification, causes and consequences. Muscle Nerve. 2004; 30(5): 547–68.Google Scholar
Zhong, L. Microanatomy of the brachial plexus roots and its clinical significance Surg Radiol Anat. 2017; 39(6): 601–10.Google Scholar
Adeleye, AO, Amir, G, Fraifeld, S, et al. Diagnosis and management of Rosai-Dorfman disease involving the central nervous system. Neurol Res. 2010; 32(6): 572–8.Google Scholar
Dalia, S, Sagatys, E, Sokol, L, Kubal, T. Rosai-Dorfman disease: tumor biology, clinical features, pathology, and treatment. Cancer Control. 2014; 21(4): 322–7.Google Scholar
Kroft, S. Rosai-Dorfman disease: Familiar yet enigmatic. Semin Diagn Pathol. 2016; 33(5): 244–53.Google Scholar
Sandoval-Sus, JD, Sandoval-Leon, AC, Chapron, JR, et al. Rosai-Dorfman disease of the central nervous system: report of six cases and review of the literature. Medicine (Baltimore). 2014; 93(3): 165–75.Google Scholar
Tian, Y, Wang, J, Ge, Jz, Ma, Z, Ge, M. Intracranial Rosai-Dorfman disease mimicking multiple meningiomas in a child: a case report and review of the literature. Childs Nerv Syst. 2015; 31(2): 317–23.Google Scholar
Jauch, EC, Saver, JL, Adams, HP Jr, et al. American Heart Association Stroke Council; Council on Cardiovascular Nursing; Council on Peripheral Vascular Disease; Council on Clinical Cardiology. Guidelines for the early management of patients with acute ischemic stroke: a guideline for healthcare professionals from the American Heart Association/American Stroke Association. Stroke. 2013; 44: 870–947.Google Scholar
Biller, J, Ferro, JM, ed. Neurologic aspects of systemic disease, Part III. Handbook of Clinical Neurology, Vol 121 (3rd Series). San Diego: Elsevier; 2014.Google Scholar
Pan American Health Organization. Americas region is declared the world's first to eliminate rubella. April 29, 2015. www.paho.org.ezproxy.med.nyu.edu/hq/index.php?option=com_content&view=article&id=10798%3Aamericas-free-of-rubella&catid=740%3Anews-press-releases&Itemid=1926&lang=en. Accessed Feb 1, 2017.Google Scholar
Spena, S, Gervasini, C, Milani, D. Ultra-rare syndromes: the example of Rubinstein–Taybi syndrome. J Pediatr Genet. 2015; 4(3): 177–86.Google Scholar
Stevens, CA. Rubinstein-Taybi syndrome. Aug 30, 2002. Updated Aug 7, 2014. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2018. https://www.ncbi.nlm.nih.gov/books/NBK1526/. Accessed Sep 17, 2018.Google Scholar
Fedele, AO. Sanfilippo syndrome: causes, consequences, and treatments. Appl Clin Genet. 2015; 8: 269–81. DOI: 10.2147/TACG.S57672.Google Scholar
Chatham, W. Rheumatic manifestations of systemic disease: sarcoidosis. Curr Opin Rheumatol. 2010; 22: 85–90.Google Scholar
Fayad, F, Lioté, F, Berenbaum, F, Orcel, P, Bardin, T. Muscle involvement in sarcoidosis: a retrospective and follow-up studies. J Rheumatol. 2006; 33: 98–103.Google Scholar
Le Roux, K, Streichenberger, N, Vial, C, et al. Granulomatous myositis: a clinical study of thirteen cases. Muscle Nerve. 2007; 35: 171–77.Google Scholar
Nemoto, I, Shimizu, T, Fujita, Y, et al. Tumour-like muscular sarcoidosis. Clin Exp Dermatol. 2007; 32: 298–300.Google Scholar
Balcer, LJ, Galetta, SL, Cornblath, WT, Liu, GT. Neuro-ophthalmologic manifestations of Maffucci's syndrome and Ollier's disease. J Neuroophthalmol. 1999; 19(1): 62–6.Google Scholar
Bloch, OG, Jian, BJ, Yang, I, et al. A systematic review of intracranial chondrosarcoma and survival. J Clin Neurosci. 2009; 16(12): 1547–51.Google Scholar
Galy-Bernadoy, C, Garrel, R. Head and neck soft-tissue sarcoma in adults. Eur Ann Otorhinolaryngol Head Neck Dis. 2016; 133(1): 37–42.Google Scholar
Gliem, M, Panayotopoulos, D, Feindt, P, et al. Cerebellar degeneration as presenting symptom of recurrent endometrial stromal sarcoma with sex-cord elements. Case Rep Neurol. 2011; 3(1): 54–61.Google Scholar
Hui, JY. Epidemiology and etiology of sarcomas. Surg Clin North Am. 2016; 96(5): 901–14.Google Scholar
Joseph, JR, Wilkinson, DA, Bailey, NG, et al. Aggressive myeloid sarcoma causing recurrent spinal cord compression. World Neurosurg. 2015; 84(3): 866. e7–10.Google Scholar
Kramer, ED, Lewis, D, Raney, B, Womer, R, Packer, RJ. Neurologic complications in children with soft tissue and osseous sarcoma. Cancer. 1989; 64(12): 2600–3.Google Scholar
Thomas, DM, Ballinger, ML. Etiologic, environmental and inherited risk factors in sarcomas. J Surg Oncol. 2015; 111(5): 490–5.Google Scholar
Wang, L, Deng, H, Mao, M. Paraneoplastic pemphigus and myasthenia gravis, associated with inflammatory pseudotumor-like follicular dendritic cell sarcoma: response to rituximab. Clin Case Rep. 2016; 4(8): 797–9.Google Scholar
Yamashiro, K, Funabe, S, Tanaka, R, et al. Primary aortic sarcoma: A rare but critical cause of stroke. Neurology. 2015; 84; 755–6.Google Scholar
Fayer, R, Esposito, DH, Dubey, JP. Human infections with Sarcocystis species. Clin Microbiol Rev. 2015; 28(2): 295–311.Google Scholar
Brazis, PW, et al., eds. Peripheral nerves. In Localization in clinical neurology. 6th ed. Philadelphia, PA: Lippincott Williams and Wilkins; 2011. Chapter 2.Google Scholar
Han, BR, et al. Clinical features of wrist drop caused by compressive radial neuropathy and its anatomical considerations. J Korean Neurosurg Soc. 2014; 55(3): 148–51. DOI: 10.3340/jkns.2014.55.3.148.Google Scholar
Kimbrough, D, et al. Case of the season: saturday night palsy. Semin Roentgenol. 2013; 48(2): 108–10.Google Scholar
Nascimento-Carvalho, CM, Moreno-Carvalho, OA. Neuroschistosomiasis due to Schistosoma mansoni: a review of pathogenesis, clinical syndromes and diagnostic approaches. Rev Inst Med Trop Sao Paulo. 2005; 47(4): 179.Google Scholar
Silva, LC, Maciel, PE, Ribas, JG, et al. Treatment of schistosomal myeloradiculopathy with praziquantel and corticosteroids and evaluation by magnetic resonance imaging: a longitudinal study. Clin Infect Dis. 2004; 39(11): 1618–24. Epub Nov 8, 2004.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Beatty, WW, Jocic, Z, Monson, N, Staton, RD. Memory and frontal lobe dysfunction in schizophrenia and schizoaffective disorder. J Nerv Ment Dis. 1993; 181(7): 448–53.Google Scholar
Bilder, RM, Goldman, RS, Volavka, J, et al. Neurocognitive effects of clozapine, olanzapine, risperidone, and haloperidol in patients with chronic schizophrenia or schizoaffective disorder. Am J Psychiatry. 2002; 159(6): 1018–28.Google Scholar
Kane, JM, Carson, WH, Saha, AR, et al. Efficacy and safety of aripiprazole and haloperidol versus placebo in patients with schizophrenia and schizoaffective disorder. J Clin Psychiatry. 2002; 63(9): 763–71.Google Scholar
Stoll, AL, Banov, M, Kolbrener, M, et al. Neurologic factors predict a favorable valproate response in bipolar and schizoaffective disorders. J Clin Psychopharmacol. 1994; 14(5): 311–13.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Crow, TJ, Ball, J, Bloom, SR, et al. Schizophrenia as an anomaly of development of cerebral asymmetry: a postmortem study and a proposal concerning the genetic basis of the disease. Arch Gen Psychiatry. 1989; 46(12): 1145–50.Google Scholar
Endicott, J, Spitzer, RL. A diagnostic interview: the schedule for affective disorders and schizophrenia. Arch Gen Psychiatry. 1978; 35(7): 837–44.Google Scholar
Friston, KJ, Liddle, PF, Frith, CD, Hirsch, SR, Frackowiak, RSJ. The left medial temporal region and schizophrenia: a PET study. Brain. 1992; 115(2): 367–82.Google Scholar
Kapur, S, Zipursky, R, Jones, C, Remington, G, Houle, S. Relationship between dopamine D2 occupancy, clinical response, and side effects: a double-blind PET study of first-episode schizophrenia. Am J Psychiatry. 2000; 157(4): 514–20.Google Scholar
Kay, SR, Flszbein, A, Opfer, LA. The positive and negative syndrome scale (PANSS) for schizophrenia. Schizophr Bull. 1987; 13(2): 261.Google Scholar
Maurer, K, Maurer, K, Löffler, W, Riecher-Rössler, A. The influence of age and sex on the onset and early course of schizophrenia. Br J Psychiatry. 1993; 162(1): 80–6.Google Scholar
Weinberger, DR, Berman, KF, Zec, RF. Physiologic dysfunction of dorsolateral prefrontal cortex in schizophrenia: I. Regional cerebral blood flow evidence. Arch Gen Psychiatry. 1986; 43(2): 114–24.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Dazzan, P, Murray, RM. Neurological soft signs in first-episode psychosis: a systematic review. Br J Psychiatry. 2002; 181(43): s50–s57.Google Scholar
Rubin, P, Holm, S, Friberg, L, et al. Altered modulation of prefrontal and subcortical brain activity in newly diagnosed schizophrenia and schizophreniform disorder: A regional cerebral blood flow study. Arch Gen Psychiatry. 1991; 48(11): 987–95.Google Scholar
Weinberger, DR, DeLisi, LE, Perman, GP, Targum, S, Wyatt, RJ. Computed tomography in schizophreniform disorder and other acute psychiatric disorders. Arch Gen Psychiatry. 1982; 39(7): 778–83.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Chemerinski, E, Triebwasser, J, Roussos, P, Siever, LJ. Schizotypal personality disorder. J Pers Disord. 2013; 27(5): 652.Google Scholar
Ettinger, U, Williams, SC, Meisenzahl, EM, et al. Association between brain structure and psychometric schizotypy in healthy individuals. World J Biol Psychiatry. 2012; 13(7): 544–9.Google Scholar
Goldberg, SC, Schulz, SC, Schulz, PM, et al. Borderline and schizotypal personality disorders treated with low-dose thiothixene vs placebo. Arch Gen Psychiatry. 1986; 43(7): 680–6.Google Scholar
Gruzelier, JH. Syndromes of schizophrenia and schizotypy, hemispheric imbalance and sex differences: implications for developmental psychopathology. Int J Psychophysiol. 1994; 18(3): 167–78.Google Scholar
Herpertz, SC, Zanarini, M, Schulz, CS, et al.; WFSBP Task Force on Personality Disorders. World Federation of Societies of Biological Psychiatry (WFSBP) guidelines for biological treatment of personality disorders. World J Biol Psychiatry. 2007: 8(4): 212–44.Google Scholar
Koenigsberg, HW, Reynolds, D, Goodman, M, et al. Risperidone in the treatment of schizotypal personality disorder. J Clin Psychiatry. 2003; 64(6): 628–34.Google Scholar
Larrison, AL, Ferrante, CF, Briand, KA, Sereno, AB. Schizotypal traits, attention and eye movements. Progr Neuropsychopharmacol Biol Psychiatry. 2000; 24(3): 357–72.Google Scholar
Raine, A, Benishay, D. The SPQ-B: A brief screening instrument for schizotypal personality disorder. J Pers Disord. 1995; 9(4): 346–55.Google Scholar
Lloyd, SKW, King, AT, Rutherford, SA, et al. Hearing optimisation in neurofibromatosis type 2: A systematic review. Clin Otolaryngol. 2017; 42(6): 1329–37.Google Scholar
Park, JK, Vernick, DM, Ramakrishna, N. Vestibular schwannoma. UpToDate. Available at https://www.uptodate.com/contents/vestibular-schwannoma-acoustic-neuroma. Accessed Sep 18, 2018.Google Scholar
de Fidelix, TS, Vieira, LA, de Freitas, D, Trevisani, VF. Biologic therapy for refractory scleritis: a new treatment perspective. Int Ophthalmol. 2015; 35(6): 903–12.Google Scholar
Sims, J. Scleritis: presentations, disease associations and management. Postgrad Med J. 2012; 88(1046): 713–8.Google Scholar
Averbuch-Heller, L, Steiner, I, Abramsky, O. Neurologic manifestations of progressive systemic sclerosis. Arch Neurol. 1992; 49: 1292.Google Scholar
Amaral, TN, Peres, FA, Lapa, AT, Marques-Neto, JF, Appenzeller, S. Neurologic involvement in scleroderma: a systematic review. Semin Arthritis Rheum. 2013; 43(3): 335–47.Google Scholar
Weinstein, SL. Zavala, DC, Ponseti, IV. Idiopathic scoliosis: long-term follow-up and prognosis in untreated patients. J Bone Joint Surg Am. 1981; 63(5): 702–12.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Bergman, RL, Piacentini, J, McCracken, JT. Prevalence and description of selective mutism in a school-based sample. J Am Acad Child Adolesc Psychiatry. 2002; 41(8): 938–46.Google Scholar
Dummit, ES, Klein, RG, Asche, B, Martin, J, Tancer, NK. Fluoxetine treatment of children with selective mutism: an open trial. J Am Acad Child Adolesc Psychiatry. 1996; 35(5): 615–21.Google Scholar
Gray, RM, Jordan, CM, Ziegler, RS, Livingston, RB. Two sets of twins with selective mutism: neuropsychological findings. Child Neuropsychol. 2002; 8(1): 41–51.Google Scholar
Kristensen, H. Non-specific markers of neurodevelopmental disorder/delay in selective mutism. Eur Child Adolesc Psychiatry. 2002; 11(2): 71–8.Google Scholar
Finley, JW, Penland, JG. Adequacy or deprivation of dietary selenium in healthy men: Clinical and psychological findings. J Trace Elem Exp Med. 1998; 11: 11.Google Scholar
Hawkes, WC, Hornbostel, L. Effects of dietary selenium on mood in healthy men living in a metabolic research unit. Biol Psychiatry. 1996; 39: 121.Google Scholar
Ishida, T, Himeno, K, Torigoe, Y, et al. Selenium deficiency in a patient with Crohn's disease receiving long-term total parenteral nutrition. Intern Med. 2003; 42: 154.Google Scholar
Kasper, DL, Fauci, AS, Hauser, SL, et al. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
Mazokopakis, EE, Papadakis, JA, Papadomanolaki, MG, et al. Effects of 12 months treatment with L-selenomethionine on serum anti-TPO levels in patients with Hashimoto's thyroiditis. Thyroid. 2007; 17: 609.Google Scholar
No authors listed. Observations on effect of sodium selenite in prevention of Keshan disease. Chin Med J (Engl). 1979; 92: 471.Google Scholar
Spallholz, JE, Boylan, LM, Larsen, HS. Advances in understanding selenium's role in the immune system. Ann N Y Acad Sci. 1990; 587: 123.Google Scholar
Taylor, EW, Nadimpalli, RG, Ramanathan, CS. Genomic structures of viral agents in relation to the biosynthesis of selenoproteins. Biol Trace Elem Res. 1997; 56: 63.Google Scholar
van Rij, AM, Thomson, CD, McKenzie, JM, Robinson, MF. Selenium deficiency in total parenteral nutrition. Am J Clin Nutr. 1979; 32: 2076.Google Scholar
Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. 5th ed. London, UK: Elsevier; 2014.Google Scholar
Bolton, CF, Young, GB, Zochodne, DW. The neurological complications of sepsis. Ann Neurol. 1993; 33(1): 94.Google Scholar
Eidelman, LA, Putterman, D, Putterman, C, Sprung, CL. The spectrum of septic encephalopathy. Definitions, etiologies, and mortalities. JAMA. 1996; 275(6): 470.Google Scholar
Grabowski, M, Hryniewiecki, T, Janas, J, Stępińska, J. Clinically overt and silent cerebral embolism in the course of infective endocarditis. J Neurol. 2011; 258: 1133.Google Scholar
Molavi, A. Endocarditis: recognition, management, and prophylaxis. Cardiovasc Clin. 1993; 23: 139.Google Scholar
Iqbal, MM, Basil, MJ, Kaplan, J, Iqbal, T. Overview of serotonin syndrome. Ann Clin Psychiatry. 2012; 24(4): 310–18.Google Scholar
Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
American Academy of Sleep Medicine International classification of sleep disorders, 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Boggild, H, Knutsson, A. Shift work, risk factors and cardiovascular disease. Scand J Work Environ Health. 1999; 25: 85–99.Google Scholar
Morgenthaler, TI, Lee-Chiong, T, Alessi, C, et al. Practice parameters for the clinical evaluation and treatment of circadian rhythm sleep disorders. An American Academy of Sleep Medicine report. Sleep. 2007; 30: 1445.Google Scholar
Sack, RL, Auckley, D, Auger, RR, et al. Circadian rhythm sleep disorders: Part I, basic principles, shift work and jet lag disorders. Sleep. 2007; 30: 1460–83.Google Scholar
Vyas, MV, Garg, AX, Iansavichus, AV, et al. Shift work and vascular events: systematic review and meta-analysis. BMJ. 2012; 345: e4800.Google Scholar
d'Azzo, A, Machado, E, Annunziata, I. Pathogenesis, emerging therapeutic targets and treatment in sialidosis. Expert Opin Orphan Drugs. 2015; 3(5): 491–504.Google Scholar
Lu, CS, Ng, SH, Lai, SC, et al. Cortical damage in the posterior visual pathway in patients with sialidosis type 1. Brain Imaging Behav. 2016; 11(1): 214–23.Google Scholar
Berkowitz, AL, Samuels, MA. The neurology of Sjogren's syndrome and the rheumatology of peripheral neuropathy and myelitis. Pract Neurol. 2014; 14(1): 14–22.Google Scholar
Chai, J, Logigian, EL. Neurological manifestations of primary Sjogren's syndrome. Curr Opin Neurol. 2010; 23(5): 509–13.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders, 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Chiaro, G, Caletti, MT, Provini, F. Treatment of sleep-related eating disorder. Curr Treat Options Neurol. 2015; 17: 361.Google Scholar
Rand, CS, Macgregor, AM, Stunkard, AJ. The night eating syndrome in the general population and among postoperative obesity surgery patients. Int J Eat Disord. 1997; 22: 65–9.Google Scholar
Winkelman, JW, Herzog, DB, Fava, M. The prevalence of sleep-related eating disorder in psychiatric and non-psychiatric populations. Psychol Med. 1999; 29: 1461–6.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders, 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Fois, C, Wright, MA, Sechi, G, Walker, MC, Eriksson, SH. The utility of polysomnography for the diagnosis of NREM parasomnias: an observational study over 4 years of clinical practice. J Neurol. 2015; 262: 385–93.Google Scholar
American Academy of Sleep Medicine. International classification of sleep disorders, 3rd ed. Darien, IL: American Academy of Sleep Medicine; 2014.Google Scholar
Attarian, H, Zhu, L. Treatment options for disorders of arousal: a case series. Int J Neurosci. 2013; 123: 623–5.Google Scholar
Mahowald, M, Cramer Bornemann, MA. Non-REM arousal parasomnias. In Kryger, M, Roth, T, Dement, W, eds. Principles and Practice of Sleep Medicine. 5th ed. St. Louis: Elsevier Saunders; 2011. pp. 1075–82.Google Scholar
Popat, S, William, W. While you were sleepwalking: science and neurobiology of sleep disorders & the enigma of legal responsibilty of violence during parasomnia. Neuroethics. 2015; 8(2): 203–14.Google Scholar
Breman, JG, Henderson, DA. Diagnosis and management of smallpox. N Engl J Med. 2002; 346: 1300.Google Scholar
Casey, CG, Iskander, JK, Roper, MH, et al. Adverse events associated with smallpox vaccination in the United States, January-October 2003. JAMA. 2005; 294: 2734.Google Scholar
Centers for Disease Control and Prevention (CDC). Update: adverse events following civilian smallpox vaccination – United States, 2003. MMWR Morb Mortal Wkly Rep. 2004; 53: 106.Google Scholar
Centers for Disease Control and Prevention (CDC). Supplemental recommendations on adverse events following smallpox vaccine in the pre-event vaccination program: recommendations of the Advisory Committee on Immunization Practices. MMWR Morb Mortal Wkly Rep. 2003; 52: 282.Google Scholar
Miller, ER, Moro, PL, Cano, M, Shimabukuro, TT. Deaths following vaccination: What does the evidence show? Vaccine. 2015; 33(29): 3288–92. DOI: 10.1016/j.vaccine.2015.05.023. Epub May 23, 2015.Google Scholar
WHO. The global eradication of smallpox: Final report of the global commission for the certification of smallpox eradication. History of International Public Health, No. 4. Geneva: World Health Organization; 1980.Google Scholar
Wu, S, Yu, Z, Liang, H. Sneddon's syndrome: a comprehensive review of the literature. Orphanet J Rare Dis. 2014; 9: 215.Google Scholar
Chen, HF, Chen, SW, Chen, P, et al. Chronic glue sniffing with transient central hypothyroidism and hypergonadotropism. J Chin Med Assoc. 2003; 66(12): 747–51.Google Scholar
Hormes, JT, Filley, CM, Rosenberg, NL. Neurologic sequelae of chronic solvent vapor abuse. Neurology. 1986; 36(5): 698–702.Google Scholar
Perry, H. Inhalant abuse in children and adolescents. Updated May 9, 2018. Available from https://www.uptodate.com/contents/inhalant-abuse-in-children-and-adolescents?source=search_result&search=aerosol%20inhalation%20abuse&selectedTitle=2∼133.Accessed Sep 18, 2018.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Creed, F, Barsky, A. A systematic review of the epidemiology of somatisation disorder and hypochondriasis. J Psychosom Res. 2004; 56(4): 391–408.Google Scholar
Fink, P, Ewald, H, Jensen, J, et al. Screening for somatization and hypochondriasis in primary care and neurological in-patients: a seven-item scale for hypochondriasis and somatization. J Psychosom Res. 1999; 46(3): 261–73.Google Scholar
Lipowski, ZJ. Somatization: the concept and its clinical application. Am J Psychiatry. 1988; 145(11): 1358–68.Google Scholar
Stern, T, et al. Massachusetts General Hospital handbook of general hospital psychiatry. Philadephia, PA: Saunders; 2010.Google Scholar
Van der Kolk, BA, Pelcovitz, D, Roth, S, Mandel, FS. Dissociation, somatization, and affect dysregulation. Am J Psychiatry. 1996; 153(7): 83.Google Scholar
NIH. NIDCD Fact Sheet: Spasmodic Dysphonia. NIH Publication No. 10-4214. Updated Oct 2010.Google Scholar
Schweinfurth, JM, Billante, M, Courey, MS. Risk factors and demographics in patients with spasmodic dysphonia. Laryngoscope. 2002; 112(2): 220–3.Google Scholar
Jinnah, HA, Berardelli, A, Comella, C, et al. The focal dystonias: current views and challenges for future research. Mov Disord. 2013; 28(7): 926–43.Google Scholar
Stamelou, M, Charlesworth, G, Cordivari, C, et al. The phenotypic spectrum of DYT24 due to ANO3 mutations. Mov Disord. 2014; 29(7): 928–34.Google Scholar
Lapsiwala, SB, Iskandar, BJ. The tethered cord syndrome in adults with spina bifida occulta. Neurol Res. 2004; 26(7): 235–40.Google Scholar
Finsterer, J, Soraru, G. Onset manifestations of spinal and bulbar muscular atrophy (Kennedy's disease). J Mol Neurosci. 2016; 58: 321–9.Google Scholar
Cheshire, WP, Santos, CC, Massey, EW, Howard, JF Jr. Spinal cord infarction: etiology and outcome. Neurology. 1996; 47(2): 321–30.Google Scholar
Rigney, L, Cappelen-Smith, C, Sebire, D, Beran, RG, Cordato, D. Nontraumatic spinal cord ischaemic syndrome. J Clin Neurosci. 2015; 22(10): 1544–9.Google Scholar
Sendi, P, Bregenzer, T, Zimmerli, W. Spinal epidural abscess and clinical practice. QJM. 2008; 101(1): 1–12.Google Scholar
Hussenbocus, SM, Wilby, MJ, Cain, C, Hali, D. Spontaneous spinal epidural hematoma: a case report and literature review. J Emerg Med. 2012; 42(2): 31–4.Google Scholar
Moftakhar, P, Hefts, SW, Ko, NU. Vascular myelopathies. Semin Neurol. 2012; 32(2): 146–53.Google Scholar
Rajput, D, Srivastava, AK, Kumar, R. Spinal epidural lipomatosis: An unusual cause of relapsing and remitting paraparesis. J Pediatr Neurosci. 2010; 5(2): 150–2.Google Scholar
Rustom, D, Gupta, D, Chakrabortty, S. Epidural lipomatosis: A dilemma in interventional pain management for the use of epidural steroid. J Anaesthesiol Clin Pharmacol. 2013; 29(3): 410–41. DOI: 10.4103/0970-9185.117070.Google Scholar
Conway, JE, Chou, D, Clatterbuck, RE, et al. Hemangioblastomas of the central nervous system in von Hippel-Lindau syndrome and sporadic disease. Neurosurgery. 2001; 48(1): 55–63.Google Scholar
Gläsker, S, Van Velthoven, V. Risk of hemorrhage in hemangioblastomas of the central nervous system. Neurosurgery. 2005; 57(1): 71–6.Google Scholar
Lonser, RR, Oldfield, EH. Spinal cord hemangioblastomas. Neurosurg Clin North Am. 2006; 17(1): 37–44.Google Scholar
Lonser, RR, Weil, RJ, Wanebo, JE, Devroom, HL, Oldfield, EH. Surgical management of spinal cord hemangioblastomas in patients with von Hippel-Lindau disease. J Neurosurg. 2003; 98(1): 106–16.Google Scholar
Markowitz, JA, Singh, P, Darra, BT. Spinal muscular atrophy: a clinical and research update. Pediatr Neurol. 2012; 46(1): 1–12.Google Scholar
Prior, TW, Finanger, E. Spinal muscular atrophy. Feb 24, 2000. Updated Dec 22, 2016. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2018. Available from https://www.ncbi.nlm.nih.gov/books/NBK1352/. Accessed 5/2017.Google Scholar
Hayat, MA. Tumors of the central nervous system: Volume 6, Spinal tumors, Part 1. Dordrecht: Springer; 2012.Google Scholar
Krings, T, Geibprasert, S. Spinal dural arteriovenous fistulas. Am J Neuroradiol. 2009; 30(4): 639–48.Google Scholar
Moftakhar, P, Hefts, SW, Ko, NU. Vascular myelopathies. Semin Neurol. 2012; 32(2): 146–53.Google Scholar
Domenicucci, M, Eramieri, A, Paolini, S, et al. Spinal subarachnoid hemorrhage: our experience and literature review. Acta Neurochir (Wein). 2005; 147(7): 741–50.Google Scholar
Kim, JS, Lee, SH. Spontaneous spinal subarachnoid hemorrhage with spontaneous resolution. J Korean Neurosurg Soc. 2009; 45(4): 253–5.Google Scholar
Madhugiri, VS, Ambekar, S, Roopesh Kumar, VR, Sasidharan, GM, Nanda, A. Spinal aneurysms: clinicoradiological features and management paradigms. J Neurosurg Spine. 2013; 19(1): 34–48.Google Scholar
Khan, MA. Ankylosing spondylitis and related spondyloarthropathies: the dramatic advances in the past decade. Rheumatology. 2011; 50(4): 637–9. https://doi.org/10.1093/rheumatology/keq433.Google Scholar
Wright, KA, Crowson, CS, Michet, CJ, Matteson, EL. Time trends in incidence, clinical features and cardiovascular disease in ankylosing spondylitis over 3 decades: a population based study. Arthritis Care Res. 2015; 67(6): 836–41. DOI: 10.1002/acr.22512.Google Scholar
Freitas, DF, de Siqueira Hoagland, B, do Valle, AC, et al. Sporotrichosis in HIV-infected patients: report of 21 cases of endemic sporotrichosis in Rio de Janeiro, Brazil. Med Mycol. 2012; 50(2): 170–8. Epub Aug 23, 2011.Google Scholar
Hessler, C, Kauffman, CA, Chow, FC. The upside of bias: a case of chronic meningitis due to Sporothrix schenckii in an immunocompetent host. Neurohospitalist. 2017; 7(1): 30–34.Google Scholar
Aguilar, J, Urday-Cornejo, V, Donabedian, S, et al. Staphylococcus aureus meningitis: case series and literature review. Medicine (Baltimore). 2010; 89(2): 117.Google Scholar
Biller, J, Ferro, JM, ed. Neurologic aspects of systemic disease, Part III. Handbook of Clinical Neurology, Vol 121 (3rd Series). San Diego: Elsevier; 2014.Google Scholar
Betjemann, J, Lowenstein, D. Status epilepticus in adults. Lancet Neurol. 2015; 14(6): 615–24.Google Scholar
Helmstaedter, C. Cognitive outcome of status epilepticus in adults. Epilepsia. 2007; 48(8): 85–90.Google Scholar
Hocker, S. Systemic complications of status epilepticus: an update. Epilepsy Behav. 2015; 49: 83–7.Google Scholar
Ciccotto, G, Blaya, M, Kelley, R. Stiff person syndrome. Neurol Clin. 2013; 31(1): 319–28.Google Scholar
Hadavi, S, Noyce, AJ, Leslie, RD, Giovannoni, G. Stiff person syndrome. Pract Neurol. 2011; 11(5): 272–82.Google Scholar
Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. 5th ed. London, UK: Elsevier; 2014.Google Scholar
Biller, J, Ferro, JM, ed. Neurologic aspects of systemic disease, Part III. Handbook of Clinical Neurology, Vol 121 (3rd Series). San Diego: Elsevier; 2014.Google Scholar
Rahal, JJ, Anderson, J, Rosenberg, C, Reagan, T, Thompson, LL. Effect of interferon-alpha2b therapy on St. Louis viral meningoencephalitis: clinical and laboratory results of a pilot study. J Infect Dis. 2004; 190(6): 1084.Google Scholar
Harbison, J, Newton, JL, Seifer, C, Kenny, RA. Stoke Adams attacks and cardiovascular syncope. Lancet. 2002; 359(9301): 158–60.Google Scholar
O'Rourke, RA. Clinical cardiology: the Stoke-Adams syndrome definition and etiology: mechanisms and treatment. Calif Med. 1972; 117(1): 96–9.Google Scholar
Bever, C, Aquino, AV, Penn, AS, et al. Prognosis of ocular myasthenia gravis. Ann Neurol. 1983; 14: 516–19.Google Scholar
Sudarshan, A, Goldie, WD. The spectrum of congenital facial diplegia (Moebius syndrome). Pediatr Neurol. 1985; 1: 180–4.Google Scholar
Thomke, F. Brainstem diseases causing isolated ocular motor nerve palsies. Neuroophthalmology. 2002; 28: 53–67.Google Scholar
Zee, DS. Internuclear ophthalmoplegia: pathophysiology and diagnosis. Bailliere's Clin Neurol. 1992; 1: 455–70.Google Scholar
Phares, CR, Lynfield, R, Farley, MM, et al. Active Bacterial Core Surveillance/Emerging Infections Program Network. Epidemiology of invasive group B streptococcal disease in the United States, 1999–2005. JAMA. 2008; 299(17): 2056.Google Scholar
Schrag, SJ, Zywicki, S, Farley, MM, et al. Group B streptococcal disease in the era of intrapartum antibiotic prophylaxis. N Engl J Med. 2000; 342(1): 15.Google Scholar
Skoff, TH, Farley, MM, Petit, S, et al. Increasing burden of invasive group B streptococcal disease in nonpregnant adults, 1990–2007. Clin Infect Dis. 2009; 49: 85.Google Scholar
Nishimura, RA, Otto, CM, Bonow, RO, et al. 2014 AHA/ACC guideline for the management of patients with valvular heart disease: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol. 2014; 63(22): e57.Google Scholar
No authors listed. Antibacterial prophylaxis for dental, GI, and GU procedures. Med Lett Drugs Ther. 2005; 47(1213): 59.Google Scholar
Wilson, W, Taubert, KA, Gewitz, M, et al., American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee, American Heart Association Council on Cardiovascular Disease in the Young, American Heart Association Council on Clinical Cardiology, American Heart Association Council on Cardiovascular Surgery and Anesthesia, Quality of Care and Outcomes Research Interdisciplinary Working Group. Prevention of infective endocarditis: guidelines from the American Heart Association: a guideline from the American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee, Council on Cardiovascular Disease in the Young, and the Council on Clinical Cardiology, Council on Cardiovascular Surgery and Anesthesia, and the Quality of Care and Outcomes Research Interdisciplinary Working Group. Circulation. 2007; 116(15): 1736.Google Scholar
Centers for Disease Control and Prevention (CDC). Active Bacterial Core Surveillance (ABCs) report. Emerging Infections Program Network Streptococcus pneumoniae; 2014. https://www.cdc.gov/abcs/reports-findings/pubs-strep-pneumo.html. Accessed Jan 29, 2017.Google Scholar
Centers for Disease Control and Prevention (CDC). Vaccines and preventable diseases. Updated Nov 22, 2016. https://www.cdc.gov/vaccines/vpd/index.html. Accessed Jan 29, 2017.Google Scholar
Thigpen, MC, Whitney, CG, Messonnier, NE, et al. Emerging Infections Programs Network. Bacterial meningitis in the United States, 1998–2007. N Engl J Med. 2011; 364(21): 2016.Google Scholar
Lazarus, R. From psychological stress to the emotions: a history of changing outlooks. Annu Rev Psychol. 1993; 44: 1–21.Google Scholar
Montero-Marin, J, Prado-Abril, J, Piva Demarzo, MM, Gascon, S, García-Campayo, J. Coping with stress and types of burnout: explanatory power of different coping strategies. PLoS One. 2014; 9(2): e89090.Google Scholar
Montero-Marín, J, García-Campayo, J, Mosquera, D, López, Y. A new definition of burnout syndrome based on Farbers's proposal. J Occup Med Toxicol. 2009; 4: 31.Google Scholar
Sapolsky, RM. Stress, glucocorticoids, and damage to the nervous system: the current state of confusion. Stress. 1996; 1(1): 1–19.Google Scholar
Benjamin, EJ, Blaha, MJ, Chiuve, SE, et al.; on behalf of the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Heart Disease and Stroke Statistics – 2017 Update: A Report from the American Heart Association. Circulation. 2017; 135: e146–e603.Google Scholar
Puthiyakunnon, S, Boddu, S, Li, Y, et al. Strongyloidiasis: an insight into its global prevalence and management. PLoS Negl Trop Dis. 2014; 8(8): e3018. DOI: 10.1371/journal.pntd.0003018.Google Scholar
Salvana, EMT, Salata, RA, King, CH. Parasitic infections of the central nervous system. In Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. 5th ed. London: Academic Press; 2014. pp. 947–68.Google Scholar
Schär, F, Trostdorf, U, Giardina, F, et al. Strongyloides stercoralis: global distribution and risk factors. PLoS Negl Trop Dis. 2013; 7(>7): e2288.Google Scholar
Comi, A. Current therapeutic options in Sturge-Weber syndrome. Semin Pediatr Neurol. 2015; 22(4): 295–301.Google Scholar
Sudarsanam, A, Ardorn-Holmes, SL. Sturge-Weber syndrome: from the past to the present. Eur J Paediatr Neurol. 2014; 18(3): 257–66.Google Scholar
Connolly, ES, Rabinstein, AA, Carhuapoma, JR, et al.; on behalf of the American Heart Association Stroke Council, Council on Cardiovascular Radiology and Intervention, Council on Cardiovascular Nursing, Council on Cardiovascular Surgery and Anesthesia, and Council on Clinical Cardiology. Guidelines for the Management of Aneurysmal Subarachnoid Hemorrhage. A Guideline for Healthcare Professionals from the American Heart Association/American Stroke Association. Stroke. 2012; 43(6): 1711–37.Google Scholar
Ochoa, VM, Yeghiazarians, Y. Subclavian artery stenosis: a review for the vascular medicine practitioner. Vasc Med. 2011; 16(1): 29–34.Google Scholar
Osiro, S, Zurada, A, Gielecki, J, et al. A review of subclavian steal syndrome with clinical correlation. Med Sci Monit. 2012; 18(5): RA57–63.Google Scholar
Coombs, JB, Coombs, BL, Chin, EJ. Acute spontaneous subdural hematoma in a middle-aged adult: case report and review of the literature. J Emerg Med. 2014; 47(3): e63–8.Google Scholar
Miller, JD, Nader, R. Acute subdural hematoma from bridging vein rupture: a potential mechanism for growth. J Neurosurg. 2014; 120(6): 1378–84.Google Scholar
Almenawer, SA, Farrokhyar, F, Hong, C, et al. Chronic subdural hematoma management: a systematic review and meta-analysis of 34,829 patients. Ann Surg. 2014; 259(3): 449–57.Google Scholar
de Beer, MH, Eysink Smeets, MM, Koppen, H. Spontaneous spinal subdural hematoma. Neurologist. 2017; 22(1): 34–9.Google Scholar
Gordon, WE, Kimball, BY, Arthur, AS. Traumatic lumbar spinal subdural hematoma. Interdiscip Neurosurg. 2014; 4(1): 123–7.Google Scholar
Kim, H-J, Cho, Y-J, Cho, J-Y, Lee, D-H, Hong, K-S. Acute subdural hematoma following spinal cerebrospinal fluid drainage in a patient with freezing of gait. J Clin Neurol. 2009; 5(2): 95–6.Google Scholar
Maddali, P, Walker, B, Fisahn, C, et al. Subdural thoracolumbar spine hematoma after spinal anesthesia: a rare occurrence and literature review of spinal hematomas after spinal anesthesia. Cureus. 2017; 9(2): e1032.Google Scholar
Cohen, AS, Matharu, MS, Goadsby, PJ. Suggested guidelines for treating SUNCT and SUNA. Cephalalgia. 2005; 25: 1200.Google Scholar
Cohen, AS, Matharu, MS, Goadsby, PJ. Short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing (SUNCT) or cranial autonomic features (SUNA) – a prospective clinical study of SUNCT and SUNA. Brain. 2006; 129(Pt 10): 2746–60.Google Scholar
Goadsby, PJ, Cittadini, E, Cohen, AS. Trigeminal autonomic cephalalgias: paroxysmal hemicrania, SUNCT/SUNA, and hemicrania continua. Semin Neurol. 2010; 30: 186–91.Google Scholar
Sjaastad, O. Chronic paroxysmal hemicrania, hemicrania continua and SUNCT: the fate of the three first described cases. J Headache Pain. 2006; 7(3): 151–6.Google Scholar
Charidimou, A, Linn, J, Vernooij, MW, et al. Cortical superficial siderosis: detection and clinical significance in cerebral amyloid angiopathy and related conditions. Brain. 2015; 138(Pt 8): 2126–39.Google Scholar
Fearnley, JM, Stevems, JM, Rudge, P. Superficial siderosis of the central nervous system. Brain. 1995; 118(Pt 4): 1051–66.Google Scholar
Belden, CJ, Weg, N, Minor, LB, Zinreich, SJ. CT evaluation of bone dehiscence of the superior semicircular canal as a cause of sound- and/or pressure-induced vertigo. Radiology. 2003; 226: 337–43.Google Scholar
Beyea, JA, Agrawal, SK, Parnes, LS. Transmastoid semicircular canal occlusion: a safe and highly effective treatment for benign paroxysmal positional vertigo and superior canal dehiscence. Laryngoscope. 2012; 122: 1862–6.Google Scholar
Merchant, SN, Rosowski, JJ. Conductive hearing loss caused by third-window lesions of the inner ear. Otol Neurotol. 2008; 29: 282–9.Google Scholar
Welgampola, MS. Evoked potential testing in neuro-otology. Curr Opin Neurol. 2008; 21: 29–35.Google Scholar
Gray, JE. Nerve injury associated with pelvic surgery. UpToDate. Updated Apr 21, 2017. https://www.uptodate.com/contents/nerve-injury-associated-with-pelvic-surgery. Accessed Sep 20, 2018.Google Scholar
Ihab, K, Rodger, B. Positioning patients for spine surgery: avoiding uncommon position-related complications. World J Orthop. 2014; 5(4): 425–43. Published online Sep 18, 2014. DOI: 10.5312/wjo.v5.i4.425.Google Scholar
Nazari, F, Azimi, A, Abdi, S. What is Susac syndrome? A brief review of articles. Iran J Neurol. 2014; 13(4): 209–14.Google Scholar
Susac, JO, Egan, RA, Rennebohm, RM, Lubow, M. Susac's syndrome: 1975–2005 microangiopathy/autoimmune endotheliopathy. J Neurol Sci. 2007; 257(1-2): 270–2.Google Scholar
Marques-Dias, MJ, Mercadante, MT, Tucker, D, Lombroso, P. Sydenham's chorea. Psychiatr Clin North Am. 1997; 20(4): 809–20.Google Scholar
Cardoso, F, Vargas, A, Oliveira, L, et al. Persistent Sydenham's chorea. Mov. Disord. 1999; 14: 805–7.Google Scholar
Church, AJ, Dale, RC, Cardoso, F, et al. CSF and serum immune parameters in Sydenham's chorea: evidence of an autoimmune syndrome? J Neuroimmunol. 2003; 136(1-2): 149–53.Google Scholar
Giedd, JN, Rapoport, JL, Kruesi, MJ, et al. Sydenham's chorea: Magnetic resonance imaging of the basal ganglia. Neurology. 1995; 45: 2199–203.Google Scholar
Swedo, SE, Leonard, HL, Schapiro, MB, et al. Sydenham's chorea: physical and psychological symptoms of St Vitus dance. Pediatrics. 1993; 91(4): 706–13.Google Scholar
Swedo, SE, Leckman, JF, Rose, NR. From research subgroup to clinical syndrome: modifying the PANDAS criteria to describe PANS (pediatric acute-onset neuropsychiatric syndrome). Pediatr Therapeut. 2012; 2: 113.Google Scholar
Brigo, F, Nardone, R, Bongiovanni, LG. Value of tongue biting in the differential diagnosis between epileptic seizure and syncope. Seizure. 2012; 21(8): 568–72.Google Scholar
Brigo, F, Nardone, R, Ausserer, H, et al. The value of urinary incontinence in the differential diagnosis of seizure. Seizure. 2013; 22(2): 85–90.Google Scholar
Da Silva, RM. Syncope: epidemiology, etiology, and prognosis. Front Physiol. 2014; 5: 471.Google Scholar
Webb, J, Long, B, Koyfman, A. An emergency medicine-focused review of seizure mimics. J Emerg Med. 2017; 52(5): 645–53.Google Scholar
Chawla, J. Neurocardiogenic syncope. Medlink Neurology. Updated November 20, 2015. San Diego: Medlink Corporation. Available from www.medlink.com/article/neurocardiogenic_syncope. Accessed Sep 20, 2018.Google Scholar
Centers for Disease Control and Prevention. Syphilis. Updated Sep 25, 2017. https://www.cdc.gov/std/stats16/Syphilis.htm. Accessed Sep 25, 2018.Google Scholar
Ho, EL, Lukehart, SA. Syphilis: using modern approaches to understand an old disease. J Clin Invest. 2011; 121(12): 4584–92. https://doi.org/10.1172/JCI57173.Google Scholar
Tuddenham, S, Ghanem, KG. Neurosyphilis: knowledge gaps and controversies. Sex Transmit Dis. 2018; 45(3): 147–51. DOI: 10.1097/OLQ.0000000000000723.Google Scholar
Menezes, AH, Greenlee, JDW, Longmuir, RA, Hansen, DR, Abode-Lyamah, K. Syringohydromyelia in association with syringobulbia and syringocephaly: case report. J Neurosurg Pediatr. 2015; 15(6): 657–61.Google Scholar
National Organization for Rare Disorders. Syringobulbia. https://rarediseases.org/rare-diseases/syringobulbia/. Accessed Sep 20, 2018.Google Scholar
Sarikaya, S, Acikgoz, B, Tekkok, IH, Gungen, YY. Conus ependymoma with holocord syringohydromyelia and syringobulbia. J Clin Neurosci. 2007; 14(9): 901–4.Google Scholar
Tubbs, RS, Bailey, M, Barrow, WC, et al. Morphometric analysis of the craniocervical juncture in children with Chiari I malformation and concomitant syringobulbia. Childs Nerv Syst. 2009; 25: 689–92.Google Scholar
Lisnevskaia, L, Murphy, G, Isenberg, D. Systemic lupus erythematosus. Lancet. 2014; 384(9957): 1878–88.Google Scholar
Vu Lam, N, Ghetu, M, Bieniek, M. Systemic lupus erythematosus: primary care approach to diagnosis and management. Am Fam Physician. 2016; 94(4): 284–94.Google Scholar
de Souza, AW, de Carvalho, JF. Diagnostic and classification criteria of Takayasu arteritis. J Autoimmun. 2014; 48–49: 79–83.Google Scholar
Keser, G, Direskeneli, H, Aksu, K. Management of Takayasu arteritis: a systematic review. Rheumatology (Oxford). 2014; 53(5): 793–801.Google Scholar
Woerner, M, Alvir, J, Saltz, B, Lieberman, J, et al. Prospective study of tardive dyskinesia in the elderly: rates and risk factors. Am J Psychiatry. 1998; 155(11): 1521–8.Google Scholar
Gardner, D, Baldessarini, R, Waraich, P. Modern antipsychotic drugs: a critical overview. CMAJ. 2005; 172(13): 1703–11.Google Scholar
Seeman, P. Atypical antipsychotics: mechanism of action. Can J Psychiatry. 2002; 47(1): 27–38.Google Scholar
Yassa, R, Jones, B. Complications of tardive dyskinesia: A review. Psychosomatics. 1985; 26(4): 305–13.Google Scholar
Bhidayasiri, R, Boonyawairoj, S. Spectrum of tardive syndromes: clinical recognition and management. Postgrad Med J. 2011; 87: 132e141. DOI: 10.1136/pgmj.2010.103234.Google Scholar
Haddad, PM, Dursun, SM. Neurological complications of psychiatric drugs: clinical features and management. Hum Psychopharmacol Clin Exp. 2008; 23: 15–26.Google Scholar
Waln, O, Jankovic, J. An update on tardive dyskinesia: from phenomenology to treatment. Tremor Other Hyperkinet Mov (NY). 2013; 3: pii: tre-03-161-4138-1. DOI: 10.7916/D88P5Z71.Google Scholar
Hazari, N, Kate, N, Grover, S. Clozapine and tardive movement disorders: A review. Asian J Psychiatry. 2013; 6: 439–51.Google Scholar
Hamosh, A. OMIM: Tay–Sachs Disease, TSD. Updated May 30, 2013. Johns Hopkins University. Available from www.omim.org/entry/272800. Accessed Jun 8, 2016.Google Scholar
Kaback, MM. Hexosaminidase A deficiency. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2016.Google Scholar
Waldman, CW, Waldman, SD, Waldman, RA. Giant cell arteritis. Med Clin North Am. 2013; 97(2): 329–35.Google Scholar
Brodie, HA, Thompson, TC. Management of complications from 820 temporal bone fractures. Am J Otol. 1997; 18: 188–97.Google Scholar
Johnson, FI, Semaan, MT, Megerian, CA. Temporal bone fracture: evaluation and management in the modern era. Otolaryngol Clin North Am. 2008; 41(3): 597–618.Google Scholar
Bora, E, Meletti, S. Social cognition in temporal lobe epilepsy: A systematic review and meta-analysis. Epilepsy Behav. 2016; 60: 50–7.Google Scholar
Garcia, CS. Depression in temporal lobe epilepsy: a review of prevalence, clinical features, and management considerations. Epilepsy Res Treat. 2012; 2012: 809843.Google Scholar
Zhao, F, et al. Neuropsychological deficits in temporal lobe epilepsy: A comprehensive review. Ann Indian Acad Neurol. 2014; 17(4): 374–82.Google Scholar
American Academy of Family Physicians. Temporomandibular joint (TMJ) pain. Am Fam Physician. 2007; 76(10): 1483–4.Google Scholar
Yule, PL, Durham, J, Wassell, RW. Pain Part 6: Temporomandibular disorders. Dent Update. 2016; 43(1): 39–42, 45–8.Google Scholar
Anttila, P. Tension-type headache in childhood and adolescence. Lancet Neurol. 2006; 5(3): 268–74.Google Scholar
Kaniecki, RG. Migraine and tension-type headache: an assessment of challenges in diagnosis. Neurology. 2002; 58(9 Suppl 6): S15–S20.Google Scholar
Sacco, S, Ricci, S, Carolei, A. Tension-type headache and systemic medical disorders. Curr Pain Headache Rep. 2011; 15(6): 438–43.Google Scholar
Schwartz, BS, Stewart, WF, Simon, D, Lipton, RB. Epidemiology of tension-type headache. JAMA. 1998; 279(5): 381–3.Google Scholar
Albers, P, Albrecht, W, Algaba, F, et al.; European Association of Urology. EAU guidelines on testicular cancer: 2011 update. Eur Urol. 2011; 60(2): 304–19.Google Scholar
Brydøy, M, Storstein, A, Dahl, O. Transient neurological adverse effects following low dose radiation therapy for early stage testicular seminoma. Radiother Oncol. 2007; 82(2): 137–44.Google Scholar
Fung, C, Vaughn, DJ. Complications associated with chemotherapy in testicular cancer management. Nat Rev Urol. 2011; 8(4): 213–22.Google Scholar
Höftberger, R, Rosenfeld, MR, Dalmau, J. Update on neurological paraneoplastic syndromes. Curr Opin Oncol. 2015; 27(6): 489–95.Google Scholar
Nichols, CR. Testicular cancer. Curr Probl Cancer. 1998; 22(4): 187–274. Review. PubMed PMID: 9743088.Google Scholar
Brook, I. Current concepts in the management of Clostridium tetani infection Expert Rev Anti Infect Ther. 2008; 6(3): 327–36. DOI: 10.1586/14787210.6.3.327.Google Scholar
Sexton, DJ. Tetanus. UpToDate. Updated Aug 3, 2018. https://www.uptodate.com/contents/tetanus. Accessed Sep 20, 2018.Google Scholar
Jalai, CM. Trends in the presentation, surgical treatment, and outcomes of tethered cord syndrome: A nationwide study from 2001 to 2010. J Clin Neurosci. 2017; 41: 92–7. DOI: 10.1016/j.jocn.2017.03.034. Epub Mar 22, 2017.Google Scholar
Khoury, C. Closed spinal dysraphism: clinical manifestations, diagnosis, and management UpToDate. Updated Sep 27, 2017. https://www.uptodate.com/contents/closed-spinal-dysraphism-clinical-manifestations-diagnosis-and-management. Accessed Sep 20, 2018.Google Scholar
O'Neill, BR. Use of magnetic resonance imaging to detect occult spinal dysraphism in infants. J Neurosurg Pediatr. 2017; 19(2): 217–26.Google Scholar
White, JT. Systematic review of urologic outcomes from tethered cord release in occult spinal dysraphism in children. Curr Urol Rep. 2015; 16(11): 78. DOI: 10.1007/s11934-015-0550-6.Google Scholar
Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
Chaitiraphan, S, Tanphaichitr, V, Cheng, TO. Nutritional heart disease. In Cheng, TO, ed. The international textbook of cardiology. New York: Pergamon Press; 1986. p. 864.Google Scholar
Tanphaichitr, V. Epidemiology and clinical assessment of vitamin deficiencies in Thai children. In Eeckels, RE, Ransome-Kuti, O, Kroonenberg, CC, eds. Child health in the tropics. Dordrecht: Martinus Nijhoff; 1985. p. 157.Google Scholar
Fattal-Valevski, A, Bloch-Mimouni, A, Kivity, S, et al. Epilepsy in children with infantile thiamine deficiency. Neurology. 2009; 73: 828.Google Scholar
Mimouni-Bloch, A, Goldberg-Stern, H, Strausberg, R, et al. Thiamine deficiency in infancy: long-term follow-up. Pediatr Neurol. 2014; 51: 311.Google Scholar
Galvin, R, Bråthen, G, Ivashynka, A, et al. EFNS guidelines for diagnosis, therapy and prevention of Wernicke encephalopathy. Eur J Neurol. 2010; 17: 1408.Google Scholar
Malamud, N, Skillicorn, SA. Relationship between the Wernicke and the Korsakoff syndrome: a clinicopathologic study of seventy cases. Arch Neurol Psychiat. 1956; 76: 586.Google Scholar
Diebler, C, Dulac, O. Pediatric neurology and neuroradiology: cerebral and cranial diseases. Berlin/Heidelberg: Springer Berlin Heidelberg; 1987.Google Scholar
Glastonbury, CM, Osborn, AG, Salzman, KL. Masses and malformations of the third ventricle: normal anatomic relationships and differential diagnoses. Radiographics. 2011; 31(7): 1889–905.Google Scholar
Horn, EM, Feiz-Erfan, I, Bristol, RE, et al. Treatment options for third ventricular colloid cysts: comparison of open microsurgical versus endoscopic resection. Neurosurgery. 2007; 60(4): 613–8; discussion 618–20.Google Scholar
Schiff, D, Hsu, L, Wen, PY. Uncommon brain tumors, skull base tumors, and intracranial cysts. In Samuels, M, Feske, S, eds. Office practice of neurology, 2nd ed. New York: Churchill Livingstone; 2003. p. 1092.Google Scholar
Brazis, PW, et al., eds. Peripheral nerves. In Localization in clinical neurology. 6th ed. Philadelphia, PA: Lippincott Williams and Wilkins; 2011. Chapter 2.Google Scholar
Klaassen, Z, Sorenson, E, Tubbs, RS, et al. Thoracic outlet syndrome: A neurological and vascular disorder. Clin Anat. 2014; 27: 724–32. DOI: 10.1002/ca.22271.Google Scholar
Makhoul, RG, Machleder, HI. Developmental anomalies at the thoracic outlet: an analysis of 200 consecutive cases. J Vasc Surg. 1992: 16(4): 534.Google Scholar
Slichter, SJ. Relationship between platelet count and bleeding risk in thrombocytopenic patients. Transfus Med Rev. 2004; 18: 153–67.Google Scholar
González-Duarte, A, García-Ramos, GS, Valdés-Ferrer, SI, Cantú-Brito, C. Clinical description of intracranial haemorrhage associated with bleeding disorders. J Stroke Cerebrovasc Dis Off J Natl Stroke Assoc. 2008; 17: 204–7.Google Scholar
Slichter, SJ, Kaufman, RM, Assmann, SF, et al. Dose of prophylactic platelet transfusions and prevention of haemorrhage. N Engl J Med. 2010; 362: 600–13.Google Scholar
Martinelli, I, Passamonti, SM, Bucciarelli, P. Thrombophilic states. Handb Clin Neurol. 2014; 120: 1061–71.Google Scholar
Pahus, SH, Hansen, AT, Hvas, A-M. Thrombophilia testing in young patients with ischemic stroke. Thromb Res. 2016; 137: 108–12.Google Scholar
Veyradier, A, Meyer, D. Thrombotic thrombocytopenic purpura and its diagnosis. J Thromb Haemost JTH. 2005; 3: 2420–7.Google Scholar
Bakshi, R, Shaikh, ZA, Bates, VE, Kinkel, PR. Thrombotic thrombocytopenic purpura: brain CT and MRI findings in 12 patients. Neurology. 1999; 52: 1285–8.Google Scholar
Adams, RD, Cammermeyer, J, Fitzgerald, PJ. The neuropathological aspects of thrombocytic acroangiothrombosis; a clinico-anatomical study of generalized platelet thrombosis. J Neurol Neurosurg Psychiatry. 1948; 11: 27–43.Google Scholar
Kessler, CS, Khan, BA, Lai-Miller, K. Thrombotic thrombocytopenic purpura: a hematological emergency. J Emerg Med. 2012; 43(3): 538–44.Google Scholar
Osborn, JD, Rodgers, GM. Update on thrombotic thrombocytopenic purpura. Clin Adv Hematol Oncol. 2011; 9(7): 531–6.Google Scholar
Landtblom, AM, et al. Sudden onset headache: a prospective study of features, incidence and causes. Cephalalgia. 2002; 22(5): 354–60.Google Scholar
Burch, HB, Wartofsky, L. Graves’ ophthalmopathy: current concepts regarding pathogenesis and management. Endocr Rev. 1993; 14: 747.Google Scholar
Prummel, MF, Wiersinga, WM. Smoking and risk of Graves’ disease. JAMA. 1993; 269: 479.Google Scholar
Lam, L, Nair, RJ, Tingle, L. Thyrotoxic periodic paralysis. Proc (Bayl Univ Med Cent). 2006; 19(2): 126–9.Google Scholar
Lin, S-H, Huang, C-L. Mechanism of thyrotoxic periodic paralysis. J Am Soc Nephrol. 2012; 23(6): 985–8. DOI: 10.1681/ASN.2012010046.Google Scholar
Hsieh, MJ, Lyu, RK, Chang, WN, et al. Hypokalemic thyrotoxic periodic paralysis: clinical characteristics and predictors of recurrent paralytic attacks. Eur J Neurol. 2008; 15: 559.Google Scholar
Manoukian, MA, Foote, JA, Crapo, LM. Clinical and metabolic features of thyrotoxic periodic paralysis in 24 episodes. Arch Intern Med. 1999; 159: 601.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Berg, D, Steinberger, JD, Olanow, CW, Naidich, TP, Yousry, TA. Milestones in magnetic resonance imaging and transcranial sonography of movement disorders. Mov Disord. 2011; 26(6): 979–92.Google Scholar
Chouinard, S, Ford, B. Adult onset tic disorders. J Neurol Neurosurg Psychiatry. 2000; 68(6): 738–43.Google Scholar
Knight, T, Steeves, T, Day, L, et al. Prevalence of tic disorders: a systematic review and meta-analysis. Pediatr Neurol. 2012; 47(2): 77–90.Google Scholar
Kwak, C, Dat Vuong, K, Jankovic, J. Premonitory sensory phenomenon in Tourette's syndrome. Mov Disord. 2003; 18: 1530–33.Google Scholar
Lehman, LL, Gilbert, DL, Leach, JL, Wu, SW, Standridge, SM. Vertebral artery dissection leading to stroke caused by violent neck tics of Tourette syndrome. Neurology. 2011; 77(18): 1706–8.Google Scholar
Plessen, KJ, Bansal, R, Peterson, BS. Imaging evidence for anatomical disturbances and neuroplastic compensation in persons with Tourette syndrome. J Psychosomat Res. 2009; 67: 559–73.Google Scholar
Robertson, MM. A personal 35 year perspective on Gilles de la Tourette syndrome: prevalence, phenomenology, comorbidities, and coexistent psychopathologies. Lancet Psychiatr. 2015: 2: 68–87.Google Scholar
Robertson, MM. A personal 35 year perspective on Gilles de la Tourette syndrome: assessment, investigations, and management. Lancet Psychiatry. 2015; 2: 88–104.Google Scholar
Suppa, A, Marsili, L, Di Stasio, F, et al. Cortical and brainstem plasticity in Tourette syndrome and obsessive-compulsive disorder. Mov Disord. 2014; 29(12): 1523–31.Google Scholar
Swedo, SE, Leckman, JF, Rose, NR. From research subgroup to clinical syndrome: modifying the PANDAS criteria to describe PANS (pediatric acute-onset neuropsychiatric syndrome). Pediatr Therapeut. 2012; 2: 113.Google Scholar
Wang, Z, Maia, TV, Marsh, R, et al. The neural circuits that generate tics in Tourette's syndrome. Am J Psychiatry. 2011; 168(12): 1326–37.Google Scholar
Diaz, JH. A comparative meta-analysis of tick paralysis in the United States and Australia. ClinToxicol. 2015; 53(9): 874–83.Google Scholar
Patterson, SK, et al. Myasthenia gravis and other disorders of the neuromuscular junction. In Brust, JCM, ed. Current diagnosis and treatment: neurology. 2nd ed. New York: McGraw-Hill; 2002. Chapter 22.Google Scholar
Ropper, A, Samuels, M. Disorders of the nervous system caused by drugs, toxins, and other chemical agents. In Adams and Victor's principles of neurology. 9th ed. New York: McGraw-Hill Education/Medical; 2009. Chapter 43.Google Scholar
Healthline. What is nicotine withdrawal? www.healthline.com/health/smoking/nicotine-withdrawal#Symptoms2. Accessed Sep 21, 2018.Google Scholar
Rettner, R. Your brain on nicotine: smoking may thin its outer layer. Live Science. Dec 3, 2010. Available at www.livescience.com/35222-smoking-thin-brain-cerebral-cortex-101202.html. Accessed Sep 21, 2018.Google Scholar
Tweed, JO, Hsia, SH, Lutfy, K, Friedman, TC. The endocrine effects of nicotine and cigarette smoke. Trend Endocrinol Metab. 2012; 23(7): 334–42. DOI: 10.1016/j.tem.2012.03.006.Google Scholar
Kline, LB, Hoyt, WF. The Tolosa-Hunt syndrome. J Neurol Neurosurg Psychiatry 2001; 71: 577.Google Scholar
La Mantia, L, Curone, M, Rapoport, AM, Bussone, G, International Headache Society. Tolosa-Hunt syndrome: critical literature review based on IHS 2004 criteria. Cephalalgia. 2006; 26(7): 772–81.Google Scholar
Moeller, JJ, Maxner, CE. The dilated pupil: an update. Curr Neurol Neurosci Rep. 2007; 7(5): 417–22.Google Scholar
Devuyst, G, Bogousslavsky, J, Meuli, R, et al. Stroke or transient ischemic attack with basilar artery stenosis or occlusion, clinical patterns and outcome. Arch Neurol. 2002; 59(4): 567–73.Google Scholar
Behse, F, et al. Histology and ultrasound of alterations in neuropathy. Muscle Nerve. 1978; 1(5): 368.Google Scholar
London, Z, et al. Toxic neuropathies associated with pharmaceutic and industrial agents. Neurol Clin. 2007; 25(1): 257–76.Google Scholar
Arena, JE, Rabinstein, AA. Transient global amnesia. Mayo Clin Proc. 2015; 90(2): 264–72.Google Scholar
Ranta, A, Barber, PA. Transient ischemic attack service provision: A review of available service models. Neurology. 2016; 86: 1–7.Google Scholar
Rothwell, PM, Giles, MF, Chandratheva, A, et al.; Early use of Existing Preventive Strategies for Stroke (EXPRESS) study. Effect of urgent treatment of transient ischaemic attack and minor stroke on early recurrent stroke (EXPRESS study): a prospective population-based sequential comparison. Lancet. 2007; 370(9596): 1432–42.Google Scholar
Sehatzadeh, S. Is transient ischemic attack a medical emergency? An evidence-based analysis. Ont Health Technol Assess Ser. 2015; 15(3): 1–45.Google Scholar
Finsterer, J, Auer, H. Parasitoses of the human central nervous system. J Helminthol. 2013; 87(3): 257–70.Google Scholar
Gottstein, B, Pozio, E, Nöckler, K. Epidemiology, diagnosis, treatment, and control of trichinellosis. Clin Microbiol Rev. 2009; 22(1): 127–45.Google Scholar
Smith, DS. Trichinosis (Trichinellosis). Medscape. Updated May 1, 2018. https://emedicine.medscape.com/article/230490-overview. Accessed Oct 11, 2018.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Chamberlain, SR, Fineberg, NA, Blackwell, AD, Robbins, TW, Sahakian, BJ. Motor inhibition and cognitive flexibility in obsessive-compulsive disorder and trichotillomania. Am J Psychiatry. 2006; 63(7): 1282–4.Google Scholar
Flessner, CA, Woods, DW, Franklin, ME, et al. The Milwaukee inventory for subtypes of trichotillomania-adult version (MIST-A): development of an instrument for the assessment of “focused” and “automatic” hair pulling. J Psychopathol Behav Assess. 2008; 30(1): 20–30.Google Scholar
Franklin, ME, Flessner, CA, Woods, DW, et al. The child and adolescent trichotillomania impact project: descriptive psychopathology, comorbidity, functional impairment, and treatment utilization. J Dev Behav Pediatr. 2008; 29(6): 493–500.Google Scholar
O'Sullivan, RL, Rauch, SL, Breiter, HC, et al. Reduced basal ganglia volumes in trichotillomania measured via morphometric magnetic resonance imaging. Biol Psychiatry. 1997; 42(1): 39–45.Google Scholar
Stein, DJ, Coetzer, R, Lee, M, Davids, B, Bouwer, C. Magnetic resonance brain imaging in women with obsessive-compulsive disorder and trichotillomania. Psychiatry Res. 1997; 74(3): 177–82.Google Scholar
Baad-Hansen, L, Benoliel, R. Neuropathic orofacial pain: facts and fiction. Cephalalgia. 2017; 37(7): 670–9. DOI: 10.1177/0333102417706310. Epub Apr 12, 2017.Google Scholar
Katusic, S, Williams, DB, Beard, CM. Epidemiology and clinical features of idiopathic trigeminal neuralgia and glossopharyngeal neuralgia: similarities and differences, Rochester, Minnesota, 1945–1984. Neuroepidemiology. 1991: 10: 276.Google Scholar
MacDonald, BK, Cockerell, OC, Sander, JW, Shorvon, SD. The incidence and lifetime prevalence of neurological disorders in a prospective community-based study in the UK. Brain. 2000; 123(Pt 4): 665.Google Scholar
Arul Selvan, VL. A case of tropical ataxic neuropathy. Apollo Med. 2013; 10(3): 223–5.Google Scholar
Netto, AB, Netto, CM, Mahadevan, A, Taly, AB, Agadi, JB. Tropical ataxic neuropathy – a century old enigma. Neurol India. 2016; 64: 1151–9.Google Scholar
Oluwole, O, Onabolu, A, Link, H, Rosling, H. Persistence of tropical ataxic neuropathy in a Nigerian community. J Neurol Neurosurg Psychiatry. 2000; 69(1): 96–101. DOI: 10.1136/jnnp.69.1.96.Google Scholar
Finsterer, J, Auer, H. Parasitoses of the human central nervous system. J Helminthol. 2013; 87(3): 257–70.Google Scholar
Salvana, EMT, Salata, RA, King, CH. Parasitic infections of the central nervous system. In Aminoff, MJ, Josephson, SA, eds. Aminoff's neurology and general medicine. 5th ed. London: Academic Press; 2014: pp. 947–68.Google Scholar
World Health Organization. Trypanosomiasis, human African (sleeping sickness). Feb 16, 2018. www.who.int/news-room/fact-sheets/detail/trypanosomiasis-human-african-(sleeping-sickness). Accessed Oct 11, 2018.Google Scholar
Centers for Disease Control and Prevention. Tuberculosis. Updated Jun 5, 2018. https://www.cdc.gov/tb/statistics/default.htm. Accessed Sep 25, 2018.Google Scholar
Changal, KH, Raina, AH. Central nervous system manifestations of tuberculosis: a review article. J Mycobac Dis. 2014; 4: 146. DOI: 10.4172/2161-1068.1000146.Google Scholar
Rock, RB, Olin, M, Baker, CA, Molitor, TW, Peterson, PK. Central nervous system tuberculosis: pathogenesis and clinical aspects. Clin Microbiol Rev. 2008; 21(2): 243–61. DOI: 10.1128/CMR.00042-07.Google Scholar
de Vries, PJ. Neurodevelopmental, psychiatric, and cognitive aspects of tuberous sclerosis complex. In Kwiatkowski, DJ, Whittemore, VH, Thiele, EA, eds. Tuberous sclerosis complex: genes, clinical features, and therapeutics. Weinheim, Germany: Wiley-Blackwell; 2010. pp. 229–67.Google Scholar
de Vries, PJ. Targeted treatments for cognitive and neurodevelopmental disorders in tuberous sclerosis complex. Neurotherapeutics. 2010; 7: 275–82.Google Scholar
Lewis, WW, Sahin, M, Scherrer, B, et al. Impaired language pathways in tuberous sclerosis complex patients with autism spectrum disorders. Cereb Cortex. 2013; 23: 1526–32.Google Scholar
Spurling Jeste, S, Wu, JY, Senturk, D, et al. Early developmental trajectories associated with ASD in infants with tuberous sclerosis complex. Neurology. 2014; 83: 160–8.Google Scholar
Jeste, SS, Sahin, M, Bolton, P, Ploubidis, GB, Humphrey, A. Characterization of autism in young children with tuberous sclerosis complex. J Child Neurol. 2008; 23: 520–5.Google Scholar
Northrup, H, Koenig, MK, Pearson, DA, et al. Tuberous sclerosis complex. Jul 13, 1999. Updated Sep 3, 2015. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2016. Available from www.ncbi.nlm.nih.gov/books/NBK1220/ www.omim.org/entry/191100.Google Scholar
Butler, T. Treatment of typhoid fever in the 21st century: promises and shortcomings. Clin Microbiol Infect. 2011; 17(7): 959–63.Google Scholar
Johnson, R, Mylona, E, Frankel, G. Typhoidal Salmonella: Distinctive virulence factors and pathogenesis. Cell Microbiol. 2018; 20(9): e12939.Google Scholar
Tomé, AM, Filipe, A. Quinolones: review of psychiatric and neurological adverse reactions. Drug Saf. 2011; 34(6): 465–88.Google Scholar
World Health Organization. Typhoid. Updated Sep 11, 2018. www.who.int/immunization/diseases/typhoid/en/. Accessed Oct 11, 2018.Google Scholar
Casella, G, Tontini, GE, Bassotti, G, et al. Neurological disorders and inflammatory bowel diseases. World J Gastroenterol. 2014; 20(27): 8764–82.Google Scholar
Ferro, JM, Oliveira, SN, Correia, L. Neurologic manifestations of inflammatory bowel diseases. Handb Clin Neurol. 2014; 120: 595–605.Google Scholar
Guinet-Charpentier, C, Bilbault, C, Kennel, A, et al. Unusual association of myasthenia gravis and ulcerative colitis in a 14-year-old boy. Arch Pediatr. 2015; 22(1): 81–3.Google Scholar
Morís, G. Inflammatory bowel disease: an increased risk factor for neurologic complications. World J Gastroenterol. 2014; 20(5): 1228–37.Google Scholar
Brazis, PW, et al., eds. Peripheral nerves. In Localization in clinical neurology. 6th ed. Philadelphia, PA: Lippincott Williams and Wilkins; 2011. Chapter 2.Google Scholar
Fadel, M. Occupational prognosis factors for ulnar nerve entrapment at the elbow: A systematic review. Hand Surg Rehabil. 2017; 36(4): 244–9.Google Scholar
Brejt, N, Berry, J, Nisbet, A, Bloomfield, D, Burkill, G. Pelvic radiculopathies, lumbosacral plexopathies, and neuropathies in oncologic disease: a multidisciplinary approach to a diagnostic challenge. Cancer Imaging. 2013; 13(4): 591–601.Google Scholar
Brock, S, Ellison, D, Frankel, J, Davis, C, Illidge, T. Anti-Yo antibody-positive cerebellar degeneration associated with endometrial carcinoma: case report and review of the literature. Clin Oncol (R Coll Radiol). 2001; 13(6): 476–9.Google Scholar
Cormio, G, Lissoni, A, Losa, G, et al. Brain metastases from endometrial carcinoma. Gynecol Oncol. 1996; 61(1): 40–3.Google Scholar
Miller, DS, Filiaci, G, Mannel, R, et al. Randomized Phase III Noninferiority Trial of First Line Chemotherapy for Metastatic or Recurrent Endometrial Carcinoma: A Gynecologic Oncology Group Study. LBA2. Presented at the 2012 Society of Gynecologic Oncology Annual Meeting, Austin, TX.Google Scholar
Torre, LA, Bray, F, Siegel, RL, et al. Global cancer statistics, 2012. CA Cancer J Clin. 2015; 65: 87.Google Scholar
Uccella, S, Morris, JM, Bakkum-Gamez, JN, et al. Bone metastasis in endometrial cancer: report on 19 patients and review of the medical literature. Gynecol Oncol. 2013; 130(3): 474–82.Google Scholar
Vasku, M, Papathemelis, T, Maass, N, Meinhold-Heerlein, I, Bauerschlag, D. Endometrial carcinoma presenting as vasculitic sensorimotor polyneuropathy. Case Rep Obstet Gynecol. 2011; 2011: 968756.Google Scholar
Adams, R, Victor, M. Principles of neurology. 5th ed. New York, NY: McGraw-Hill; 1993.Google Scholar
Bodack, M. Sciatic neuropathy secondary to a uterine fibroid: a case report. Am J Phys Med Rehab. 1999; 78(2): 157–9.Google Scholar
Brazis, PW, et al., eds. Peripheral nerves. In Localization in clinical neurology. 6th ed. Philadelphia, PA: Lippincott Williams and Wilkins; 2011. Chapter 2.Google Scholar
Jabs, DA, Nussenblatt, RB, Rosenbaum, JT; Standardization of Uveitis Nomenclature (SUN) Working Group. Standardization of uveitis nomenclature for reporting clinical data. Results of the first international workshop. Am J Ophthalmol. 2005; 140(3): 509–16.Google Scholar
Ben-Dor, I, Pichard, AD, Satler, LF, et al. Complications and outcome of balloon aortic valvuloplasty in high-risk or inoperable patients. JACC Cardiovasc Interv. 2010; 3(11): 1150–6.Google Scholar
Hui, DS, Shavelle, DM, Cunningham, MJ, et al. Contemporary use of balloon aortic valvuloplasty. Tex Heart Inst J. 2014; 41(5): 469–76.Google Scholar
Johns Hopkins Medicine Health Library. Valvuloplasty. Available from www.hopkinsmedicine.org/healthlibrary/test_procedures/cardiovascular/valvuloplasty_92,P07990/. Accessed Sep 24, 2018.Google Scholar
Preston-Maher, GL, Torii, R, Burriesci, G. A technical review of minimally invasive mitral valve replacements. Cardiovasc Eng Technol. 2015; 6(2): 174–84.Google Scholar
Dua, A, Lee, C. Epidemiology of peripheral artery disease and critical limb ischemia. Tech Vasc Interv Radiol. 2016; 19(2): 91–5.Google Scholar
Haig, AJ, Park, P, Henke, PK, et al. Reliability of the clinical examination in the diagnosis of neurogenic versus vascular claudication. Spine J. 2013; 13(12): 1826–34.Google Scholar
McKay, E, Counts, S. Multi-infarct dementia: a historical perspective. Dement Geriatr Cogn Dis Extra. 2017; 7: 160–71.Google Scholar
Smith, EE. Clinical presentation and epidemiology of vascular dementia. Clin Sci (Lond). 2017; 131(11): 1059–68.Google Scholar
Higgins, JP, McClinton, MA. Vascular insufficiency of the upper extremity. J Hand Surg. 2010; 35(9): 1545–57.Google Scholar
Gwathmey, KG, Burns, TM, Collins, MP, Dyck, PJ. Vasculitic neuropathies. Lancet Neurol. 2014; 13(1): 67–82.Google Scholar
Katirji, B, Kaminski, HJ, Ruff, RL. Neuromuscular disorders in clinical practice. 2nd ed. New York: Springer-Verlag New York; 2014.Google Scholar
Amuluru, K, Al-Mufti, F, Hannaford, S, et al. Symptomatic infratentorial thrombosed developmental venous anomaly: case report and review of the literature. Interv Neurol. 2016; 4(3–4): 130–7.Google Scholar
Baumgartner, H, Bonhoeffer, P, De Groot, NM, et al.; Task Force on the Management of Grown-up Congenital Heart Disease of the European Society of Cardiology (ESC); Association for European Paediatric Cardiology (AEPC); ESC Committee for Practice Guidelines (CPG). ESC Guidelines for the management of grown-up congenital heart disease (new version 2010). Eur Heart J. 2010; 31(23): 2915–51.Google Scholar
Cinteza, EE, Butera, G. Complex ventricular septal defects. Update on percutaneous closure. Rom J Morphol Embryol. 2016; 57(4): 1195–205.Google Scholar
De Bruin, G, Pereira da Silva, R. Stroke complicating traumatic ventricular septal defect. J Emerg Med. 2012; 43(6): 987–8.Google Scholar
Pineda, AM, Mihos, CG, Singla, S, et al. Percutaneous closure of intracardiac defects in adults: state of the art. J Invasive Cardiol. 2015; 27(12): 561–72.Google Scholar
Ortiz, J, Ruland, S. Cervicocerebral artery dissection. Curr Opin Cardiol. 2015; 30(6): 603–10.Google Scholar
Tiu, C, Terecoasa, E, Grecu, N, et al. Vertebral artery dissection: a contemporary perspective. Maedica (Buchar). 2016; 11(2): 144–9.Google Scholar
Jenkins, JS, Stewart, M. Endovascular treatment of vertebral artery stenosis. Prog Cardiovasc Dis. 2017; 59(6): 619–25.Google Scholar
Lima Neto, AC, Bittar, R, Gattas, GS, et al. Pathophysiology and diagnosis of vertebrobasilar insufficiency: a review of the literature. Int Arch Otorhinolaryngol. 2017; 21(3): 302–7.Google Scholar
Anson, E, Jeka, J. Perspectives on aging vestibular function. Front Neurol. 2016; 6: 269.Google Scholar
Ishiyama, G. Imbalance and vertigo: the aging human vestibular periphery. Semin Neurol. 2009; 29(5): 491–9.Google Scholar
Lalwani, AK. Vertigo, dysequilibrium, and imbalance with aging. In Jackler, RK, Brackmann, DE, eds. Neurotology. 2nd ed. Philadelphia: Mosby; 2005. pp. 533–9.Google Scholar
Kincaid, O, Lipton, HL. Viral myelitis: An update. Curr Neurol Neurosci Rep. 2006; 6: 469–75.Google Scholar
Crum-Cianflone, NF. Bacterial, fungal, parasitic, and viral myositis. Clin Microbiol Rev. 2008; 21(3): 473–94.Google Scholar
Moskowitz, Y, Leibowitz, E, Ronen, M, Aviel, E. Pseudotumor cerebri induced by vitamin A combined with minocycline. Ann Ophthalmol. 1993; 25: 306.Google Scholar
Bello, S, Meremikwu, MM, Ejemot-Nwadiaro, RI, Oduwole, O. Routine vitamin A supplementation for the prevention of blindness due to measles infection in children. Cochrane Database Syst Rev. 2014; 1: CD007719.Google Scholar
Friedman, DI. Medication-induced intracranial hypertension in dermatology. Am J Clin Dermatol. 2005; 6: 29.Google Scholar
Fraunfelder, FW, Fraunfelder, FT, Corbett, JJ. Isotretinoin-associated intracranial hypertension. Ophthalmology. 2004; 111: 1248.Google Scholar
Selhorst, JB, Kulkantrakorn, K, Corbett, JJ, et al. Retinol-binding protein in idiopathic intracranial hypertension (IIH). J Neuroophthalmol. 2000; 20: 250.Google Scholar
Warner, JE, Bernstein, PS, Yemelyanov, A, et al. Vitamin A in the cerebrospinal fluid of patients with and without idiopathic intracranial hypertension. Ann Neurol. 2002; 52: 647.Google Scholar
Tabassi, A, Salmasi, AH, Jalali, M. Serum and CSF vitamin A concentrations in idiopathic intracranial hypertension. Neurology. 2005; 64: 1893.Google Scholar
Warner, JE, Larson, AJ, Bhosale, P, et al. Retinol-binding protein and retinol analysis in cerebrospinal fluid and serum of patients with and without idiopathic intracranial hypertension. J Neuroophthalmol. 2007; 27: 258.Google Scholar
Biesalski, HK. Comparative assessment of the toxicology of vitamin A and retinoids in man. Toxicology. 1989; 57: 117.Google Scholar
Geubel, AP, De Galocsy, C, Alves, N, et al. Liver damage caused by therapeutic vitamin A administration: estimate of dose-related toxicity in 41 cases. Gastroenterology. 1991; 100: 1701.Google Scholar
Alemayehu, W. Pseudotumor cerebri (toxic effect of the “magic bullet”). Ethiop Med J. 1995; 33: 265.Google Scholar
Colucciello, M. Pseudotumor cerebri induced by all-trans retinoic acid treatment of acute promyelocytic leukemia. Arch Ophthalmol. 2003; 121: 1064.Google Scholar
Huiming, Y, Chaomin, W, Meng, M. Vitamin A for treating measles in children. Cochrane Database Syst Rev. 2005; 4: CD001479.Google Scholar
Sharieff, GQ, Hanten, K. Pseudotumor cerebri and hypercalcemia resulting from vitamin A toxicity. Ann Emerg Med. 1996; 27: 518.Google Scholar
Yeh, YC, Tang, HF, Fang, IM. Pseudotumor cerebri caused by all-trans-retinoic acid treatment for acute promyelocytic leukemia. Jpn J Ophthalmol. 2006; 50: 295.Google Scholar
Kasper, D, Fauci, A, Hauser, S, et al. Vitamin and trace mineral deficiency and excess. In Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
Ropper, A, Samuels, M, Klein, J. Diseases of the nervous system caused by nutritional deficiency. In Adams and Victor's principles of neurology. 10th ed. New York: McGraw-Hill Education/Medical; 2014. Chapter 41.Google Scholar
Zhao-Wei Ting, R, Szeto, C, Ho-Ming Chan, M, Ma, K, Chow, K. Risk factors of vitamin B12 deficiency in patients receiving metformin. Arch Intern Med. 2006; 166(18).Google Scholar
Doran, M, Rassam, SS, Jones, LM, Underhill, S. Toxicity after intermittent inhalation of nitrous oxide for analgesia. BMJ. 2004; 328: 1364.Google Scholar
Hadzic, A, Glab, K, Sanborn, KV, Thys, DM. Severe neurologic deficit after nitrous oxide anesthesia. Anesthesiology. 1995; 83: 863.Google Scholar
Lindenbaum, J, Healton, EB, Savage, DG, et al. Neuropsychiatric disorders caused by cobalamin deficiency in the absence of anemia or macrocytosis. N Engl J Med. 1988; 318: 1720.Google Scholar
Allen, RH, Stabler, SP, Savage, DG, Lindenbaum, J. Diagnosis of cobalamin deficiencies: I. Usefulness of serum methylmalonic acid and total homocysteine concentrations. Am J Hematol. 1990; 34: 90.Google Scholar
Flippo, TS, Holder, WD Jr. Neurologic degeneration associated with nitrous oxide anesthesia in patients with vitamin B12 deficiency. Arch Surg. 1993; 128: 1391.Google Scholar
Schilling, RF. Is nitrous oxide a dangerous anesthetic for vitamin B12-deficient subjects? JAMA. 1986; 255: 1605.Google Scholar
Weisberg, P, Scanlon, KS, Li, R, Cogswell, ME. Nutritional rickets among children in the United States: review of cases reported between 1986 and 2003. Am J Clin Nutr. 2004; 80: 1697S.Google Scholar
McAllister, JC, Lane, AT, Buckingham, BA. Vitamin D deficiency in the San Francisco Bay Area. J Pediatr Endocrinol Metab. 2006; 19: 205.Google Scholar
Mylott, BM, Kump, T, Bolton, ML, Greenbaum, LA. Rickets in the Dairy State. WMJ. 2004; 103: 84.Google Scholar
Shah, M, Salhab, N, Patterson, D, Seikaly, MG. Nutritional rickets still afflicts children in north Texas. Tex Med. 2000; 96: 64.Google Scholar
Mansbach, JM, Ginde, AA, Camargo, CA Jr. Serum 25-hydroxyvitamin D levels among US children aged 1 to 11 years: do children need more vitamin D? Pediatrics. 2009; 124: 1404.Google Scholar
Saintonge, S, Bang, H, Gerber, LM. Implications of a new definition of vitamin D deficiency in a multiracial US adolescent population: the National Health and Nutrition Examination Survey III. Pediatrics. 2009; 123: 797.Google Scholar
Gordon, CM, Feldman, HA, Sinclair, L, et al. Prevalence of vitamin D deficiency among healthy infants and toddlers. Arch Pediatr Adolesc Med. 2008; 162: 505.Google Scholar
Thomas, MK, Lloyd-Jones, DM, Thadhani, RI, et al. Hypovitaminosis D in medical inpatients. N Engl J Med. 1998; 338: 777.Google Scholar
Van der Meer, IM, Karamali, NS, Boeke, AJ, et al. High prevalence of vitamin D deficiency in pregnant non-Western women in The Hague, Netherlands. Am J Clin Nutr. 2006; 84: 350.Google Scholar
Yu, CK, Sykes, L, Sethi, M, et al. Vitamin D deficiency and supplementation during pregnancy. Clin Endocrinol (Oxf). 2009; 70: 685.Google Scholar
Compher, CW, Badellino, KO, Boullata, JI. Vitamin D and the bariatric surgical patient: a review. Obes Surg. 2008; 18: 220.Google Scholar
Annweiler, C, Schott, A, Berrut, G, et al. Vitamin D and ageing: neurological issues. Neuropsychobiology. 2010; 62: 139–50.Google Scholar
Ali, FE, Al-Bustan, MA, Al-Busairi, WA, Al-Mulla, F. Loss of seizure control due to anticonvulsant-induced hypocalcemia. Ann Pharmacother. 2004; 38: 1002–5.Google Scholar
Christiansen, C, Rodbro, P, Sjo, O. ‘Anticonvulsant action’ of vitamin D in epileptic patients? A controlled pilot study. Br Med J. 1974; 2: 258–9.Google Scholar
Rondanelli, M, Trotti, R, Opizzi, A, Solerte, SB. Relationship among nutritional status, pro/antioxidant balance and cognitive performance in a group of free-living healthy elderly. Minerva Med. 2007; 98: 639–45.Google Scholar
Torkildsen, O, Knappskog, PM, Nyland, HI, Myhr, KM. Vitamin D-dependent rickets as a possible risk factor for multiple sclerosis. Arch Neurol. 2008; 65: 809–11.Google Scholar
Kampman, MT, Wilsgaard, T, Mellgren, SI. Outdoor activities and diet in childhood and adolescence relate to MS risk above the Arctic Circle. J Neurol. 2007; 254: 471–7.Google Scholar
Munger, KL, Zhang, SM, O'Reilly, E, et al. Vitamin D intake and incidence of multiple sclerosis. Neurology. 2004; 62: 60–5.Google Scholar
McGrath, J, Saari, K, Hakko, H, et al. Vitamin D supplementation during the first year of life and risk of schizophrenia: a Finnish birth cohort study. Schizophr Res. 2004; 67: 237–45.Google Scholar
Gloth, FM 3rd, Alam, W, Hollis, B. Vitamin D versus broad spectrum phototherapy in the treatment of seasonal affective disorder. J Nutr Health Aging. 1999; 3: 5–7.Google Scholar
Skaria, J, Katiyar, BC, Srivastava, TP, Dube, B. Myopathy and neuropathy associated with osteomalacia. Acta Neurol Scand. 1975; 51: 37–58.Google Scholar
Pack, A. Bone health in people with epilepsy: is it impaired and what are the risk factors? Seizure. 2008; 17: 181–6.Google Scholar
Ropper, A, Samuels, M, Klein, J. Adams and Victor's principles of neurology. 10th ed. New York: McGraw-Hill Education/Medical; 2014.Google Scholar
Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
Ouahchi, K, Arita, M, Kayden, H, et al. Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein. Nat Genet. 1995; 9: 141.Google Scholar
Gotoda, T, Arita, M, Arai, H, et al. Adult-onset spinocerebellar dysfunction caused by a mutation in the gene for the alpha-tocopherol-transfer protein. N Engl J Med. 1995; 333: 1313.Google Scholar
Kono, N, Ohto, U, Hiramatsu, T, et al. Impaired α-TTP-PIPs interaction underlies familial vitamin E deficiency. Science. 2013; 340: 1106.Google Scholar
Yokota, T, Shiojiri, T, Gotoda, T, et al. Friedreich-like ataxia with retinitis pigmentosa caused by the His101Gln mutation of the alpha-tocopherol transfer protein gene. Ann Neurol. 1997; 41: 826.Google Scholar
Mariotti, C, Gellera, C, Rimoldi, M, et al. Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families. Neurol Sci. 2004; 25: 130.Google Scholar
Schuelke, M, Mayatepek, E, Inter, M, et al. Treatment of ataxia in isolated vitamin E deficiency caused by alpha-tocopherol transfer protein deficiency. J Pediatr. 1999; 134: 240.Google Scholar
Wetterau, JR, Aggerbeck, LP, Bouma, ME, et al. Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia. Science. 1992; 258: 999.Google Scholar
Sharp, D, Blinderman, L, Combs, KA, et al. Cloning and gene defects in microsomal triglyceride transfer protein associated with abetalipoproteinaemia. Nature. 1993; 365: 65.Google Scholar
Shoulders, CC, Brett, DJ, Bayliss, JD, et al. Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein. Hum Mol Genet. 1993; 2: 2109.Google Scholar
Rampoldi, L, Danek, A, Monaco, AP. Clinical features and molecular bases of neuroacanthocytosis. J Mol Med (Berl). 2002; 80: 475.Google Scholar
Sokol, RJ. Vitamin E deficiency and neurological disorders. In Packer, L, Fuchs, J, eds. Vitamin E in health and disease. New York: Marcel Dekker; 1993. p. 815.Google Scholar
Lohr, JB, Caligiuri, MP. A double-blind placebo-controlled study of vitamin E treatment of tardive dyskinesia. J Clin Psychiatry. 1996; 57: 167.Google Scholar
Soares, KV, McGrath, JJ. Vitamin E for neuroleptic-induced tardive dyskinesia. Cochrane Database Syst Rev. 2001; 4: CD000209.Google Scholar
Oski, FA, Barness, LA. Vitamin E deficiency: a previously unrecognized cause of hemolytic anemia in the premature infant. J Pediatr. 1967; 70: 211.Google Scholar
Ray, D, Deshmukh, P, Goswami, K, Garg, N. Antioxidant vitamin levels in sickle cell disorders. Natl Med J India. 2007; 20: 11.Google Scholar
Rachmilewitz, EA, Shifter, A, Kahane, I. Vitamin E deficiency in beta-thalassemia major: changes in hematological and biochemical parameters after a therapeutic trial with alpha-tocopherol. Am J Clin Nutr. 1979; 32: 1850.Google Scholar
Jaja, SI, Aigbe, PE, Gbenebitse, S, Temiye, EO. Changes in erythrocytes following supplementation with alpha-tocopherol in children suffering from sickle cell anaemia. Niger Postgrad Med J. 2005; 12: 110.Google Scholar
Miller, ER 3rd, Pastor-Barriuso, R, Dalal, D, et al. Meta-analysis: high-dosage vitamin E supplementation may increase all-cause mortality. Ann Intern Med. 2005; 142: 37.Google Scholar
Ropper, A, Samuels, M, Klein, J. Adams and Victor's principles of neurology. 10th ed. New York: McGraw-Hill Education/Medical; 2014.Google Scholar
Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
Volpe, JJ. Intracranial hemorrhage in early infancy: renewed importance of vitamin K deficiency. Pediatr Neurol. 2014; 50: 545.Google Scholar
Centers for Disease Control and Prevention. Notes from the field: Late vitamin K deficiency bleeding in infants whose parents declined vitamin K prophylaxis – Tennessee, 2013. MMWR Morb Mortal Wkly Rep. 2013; 62: 901.Google Scholar
Schulte, R, Jordan, LC, Morad, A, et al. Rise in late onset vitamin K deficiency bleeding in young infants because of omission or refusal of prophylaxis at birth. Pediatr Neurol. 2014; 50: 564.Google Scholar
Morandi, X, Riffaud, L, Chabert, E, Brassier, G. Acute nontraumatic spinal subdural hematomas in three patients. Spine. 2001; 26(23): E547–1.Google Scholar
Mattle, H, Sieb, JP, Rohner, M, Mumenthaler, M. Nontraumatic spinal epidural and subdural hematomas. Neurology. 1987; 37(8): 1351.Google Scholar
Schurgers, LJ, Shearer, MJ, Hamulyák, K, et al. Effect of vitamin K intake on the stability of oral anticoagulant treatment: dose-response relationships in healthy subjects. Blood. 2004; 104: 2682.Google Scholar
Garweg, JG, Koerner, F. Outcome indicators for vitrectomy in Terson syndrome. Acta Ophthalmol. 2009; 87(2): 222–26. DOI: 10.1111/j.1755–3768.2008.01200.x.Google Scholar
Kim, DY, Soo Geun, J, Seunghee, B, et al. Acute-onset vitreous hemorrhage of unknown origin before vitrectomy: causes and prognosis. J Ophthalmol. 2015; 2015: Article ID 429251. DOI: 10.1155/2015/429251.Google Scholar
Lee, GI, Choi, KS, Han, MH, et al. Practical incidence and risk factors of Terson's syndrome: a retrospective analysis in 322 consecutive patients with aneurysmal subarachnoid hemorrhage. J Cerebrovasc Endovas Neurosurg. 2015; 17(3): 203–8. DOI: 10.7461/jcen.2015.17.3.203.Google Scholar
Spraul, CW, Grossniklaus, HE. Vitreous hemorrhage. Surv Ophthalmol. 1997; 42(1): 3–39.Google Scholar
Andreoli, CM, Foster, CS. Vogt-Koyanagi-Harada disease. Int Ophthalmol Clin. 2006; 46(2): 111–22.Google Scholar
Rajendram, R, Evans, M, Rao, NA. Vogt-Koyanagi-Harada disease. Int Ophthalmol Clin. 2005; 45(2): 115–34.Google Scholar
Day, B, Eisenman, L, Black, J, Maccotta, L, Hogan, R. A case study of voltage-gated potassium channel antibody-related limbic encephalitis with PET/MRI findings. Epilepsy Behav Case Rep. 2015; 4: 23–6.Google Scholar
Merchut, MP. Management of voltage-gated potassium channel antibody disorders. Neurol Clin. 2010; 28(4): 941–59.Google Scholar
Vincent, A, Buckley, C, Schott, JM, et al. Potassium channel antibody-associated encephalopathy: A potentially immunotherapy-responsive form of limbic encephalitis. Brain. 2004; 127: 701–12.Google Scholar
Ntusi, NA, Coccia, CB, Cupido, BJ, Chin, A. An approach to the clinical assessment and management of syncope in adults. S Afr Med J. 2015; 105(8): 690–3.Google Scholar
Ricci, F, De Caterina, R, Fedorowski, A. Orthostatic hypotension: epidemiology, prognosis, and treatment. J Am Coll Cardiol. 2015; 66(7): 848–60.Google Scholar
Butman, JA, Linehan, WM, Lonser, RR. Neurologic manifestations of von Hippel-Lindau disease. JAMA. 2008; 300(11): 1334–42.Google Scholar
Lonser, RR, Glenn, GM, Walther, M, et al. von Hippel-Lindau disease. Lancet. 2003; 361(9374): 2059–67.Google Scholar
Megerian, CA, Semaan, MT. Evaluation and management of endolymphatic sac and duct tumors. Otolaryngol Clin North Am. 2007; 40(3): 463–78.Google Scholar
Baehring, JM, Hochberg, EP, Raje, N, Ulrickson, M, Hochberg, FH. Neurological manifestations of Waldenström macroglobulinemia. Nat Clin Pract Neurol. 2008; 4(10): 547–56.Google Scholar
Ropper, A, Samuels, M, Klein, J. Adams and Victor's principles of neurology. 10th ed. New York: McGraw-Hill Education/Medical; 2014.Google Scholar
Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
Victor, M, Adams, RA, Collins, GH. The Wernicke-Korsakoff syndrome and related disorders due to alcoholism and malnutrition. Philadelphia: FA Davis; 1989.Google Scholar
Harper, C. The incidence of Wernicke's encephalopathy in Australia: a neuropathological study of 131 cases. J Neurol Neurosurg Psychiatry. 1983; 46: 593.Google Scholar
Galvin, R, Bråthen, G, Ivashynka, A, et al. EFNS guidelines for diagnosis, therapy and prevention of Wernicke encephalopathy. Eur J Neurol. 2010; 17: 1408.Google Scholar
Malamud, N, Skillicorn, SA. Relationship between the Wernicke and the Korsakoff syndrome: a clinicopathologic study of seventy cases. Arch Neurol Psychiat. 1956; 76: 586.Google Scholar
Torvik, A. Two types of brain lesions in Wernicke's encephalopathy. Neuropathol Appl Neurobiol. 1985; 11: 179.Google Scholar
Park, SH, Kim, M, Na, DL, Jeon, BS. Magnetic resonance reflects the pathological evolution of Wernicke encephalopathy. J Neuroimaging. 2001; 11: 406.Google Scholar
Wrenn, KD, Murphy, F, Slovis, CM. A toxicity study of parenteral thiamine hydrochloride. Ann Emerg Med. 1989; 18: 867.Google Scholar
Agabio, R. Thiamine administration in alcohol-dependent patients. Alcohol Alcohol. 2005; 40: 155.Google Scholar
Anderson, M. Neurology of Whipple's disease. J Neurol Neurosurg Psychiatry. 2000; 68: 2–5.Google Scholar
Compain, C, Sacre, K, Puéchal, X, et al. Central nervous system involvement in Whipple disease: clinical study of 18 patients and long-term follow-up. Medicine (Baltimore). 2013; 92: 324–30.Google Scholar
Fenollar, F, Lagier, JC, Raoult, D. Tropheryma whipplei and Whipple's disease. J Infect. 2014; 69(2): 103–12.Google Scholar
Lynch, T, Fahn, S, Louis, ED, Odel, JG. Oculofacial-skeletal myorhythmia in Whipple's disease. Mov Disord. 1997; 12: 625–6.Google Scholar
Panegyres, PK, Edis, R, Beaman, M, Fallon, M. Primary Whipple's disease of the brain: characterization of the clinical syndrome and molecular diagnosis. QJM. 2006; 99: 609–23.Google Scholar
Rosales, RL. X-linked dystonia parkinsonism: clinical phenotype, genetics and therapeutics. J Mov Disord. 2010; 3(2): 32–8.Google Scholar
1.World Health Organization. Regional Zika Epidemiological update (Americas). Available from www.paho.org/hq/index.php?option=com_content&view=article&id=11599&Itemid=41691&lang=en. Accessed May 27, 2017.Google Scholar
De Fatima Vasco Aragao, M, van der Linden, V, Brainer-Lima, AM, et al. Clinical features and neuroimaging (CT and MRI) findings in presumed Zika virus related congenital infection and microcephaly: retrospective case series study. BMJ. 2016; 353: i1901. DOI: 10.1136/bmj.i1901.Google Scholar
Kasper, DL, Fauci, AS, Hauser, SL, et al., eds. Harrison's principles of internal medicine. 19th ed. New York: McGraw-Hill Education/Medical; 2015.Google Scholar
Hambidge, KM, Krebs, NF. Zinc deficiency: a special challenge. J Nutr. 2007; 137: 1101.Google Scholar
Vallee, BL, Wacker, WE, Bartholomay, AF, Hoch, FL. Zinc metabolism in hepatic dysfunction. II. Correlation of metabolic patterns with biochemical findings. N Engl J Med. 1957; 257: 1055.Google Scholar
King, JC. Assessment of techniques for determining human zinc requirements. J Am Diet Assoc. 1986; 86: 1523.Google Scholar
Ruz, M, Carrasco, F, Rojas, P, et al. Zinc absorption and zinc status are reduced after Roux-en-Y gastric bypass: a randomized study using 2 supplements. Am J Clin Nutr. 2011; 94: 1004.Google Scholar
Jakubovic, BD, Zipursky, JS, Wong, N, et al. Zinc deficiency presenting with necrolytic acral erythema and coma. Am J Med. 2015; 128: e3.Google Scholar
Walter, RM Jr, Uriu-Hare, JY, Olin, KL, et al. Copper, zinc, manganese, and magnesium status and complications of diabetes mellitus. Diabet Care. 1991; 14: 1050.Google Scholar
Küry, S, Dréno, B, Bézieau, S, et al. Identification of SLC39A4, a gene involved in acrodermatitis enteropathica. Nat Genet. 2002; 31: 239.Google Scholar
Wang, K, Pugh, EW, Griffen, S, et al. Homozygosity mapping places the acrodermatitis enteropathica gene on chromosomal region 8q24.3. Am J Hum Genet. 2001; 68: 1055.Google Scholar
Phebus, CK, Maciak, BJ, Gloninger, MF, Paul, HS. Zinc status of children with sickle cell disease: relationship to poor growth. Am J Hematol. 1988; 29: 67.Google Scholar
Yuzbasiyan-Gurkan, VA, Brewer, GJ, Vander, AJ, et al. Net renal tubular reabsorption of zinc in healthy man and impaired handling in sickle cell anemia. Am J Hematol. 1989; 31: 87.Google Scholar
Kumar, N, Gross, JB Jr, Ahlskog, JE. Copper deficiency myelopathy produces a clinical picture like subacute combined degeneration. Neurology. 2004; 63: 33.Google Scholar
Kumar, N. Copper deficiency myelopathy (human swayback). Mayo Clin Proc. 2006; 81: 1371.Google Scholar