Skip to main content Accessibility help
×
Hostname: page-component-788cddb947-jbkpb Total loading time: 0 Render date: 2024-10-12T22:22:04.334Z Has data issue: false hasContentIssue false

Section 1 - Diagnostics

Entries A–Z

Published online by Cambridge University Press:  30 May 2019

Alan B. Ettinger
Affiliation:
Safe Passage Diagnostics, New York
Deborah M. Weisbrot
Affiliation:
State University of New York, Stony Brook
Casey E. Gallimore
Affiliation:
University of Wisconsin
Get access
Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2019

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

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: S210.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
Ferrante, M. Brachial plexopathies. CONTINUUM 2014; 20(5): 1323–42.Google ScholarPubMed
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): 491510.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
Arlt, W, Allolio, B. Adrenal insufficiency. Lancet. 2003; 361: 1881–93.CrossRefGoogle 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: 693706.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: 4760.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: 416.CrossRefGoogle ScholarPubMed
Becker, HC. Kindling in alcohol withdrawal. Alcohol Health Res World. 1998; 22(1): 2533. 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
Apostolova, LG. Alzheimer disease. Continuum (Minneap Minn). 2016; 22: 419–34.Google 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
Bacigalupi, M. Amaurosis fugax: a clinical review. IJAHSP. 2006; 4: 16.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
Shin, SC, Robinson-Papp, J. Amyloid neuropathies. Mt Sinai J Med. 2012; 79: 733–48.Google Scholar
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: 713.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: 577600.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: 93104.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: 3540.Google Scholar
American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed. Washington, DC: American Psychiatric Association; 2013.Google Scholar
Attia, E, Walsh, BT. Anorexia nervosa. Am J Psychiatry. 2007; 164(12): 1805–10.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): 617.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: 94103.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): 299303.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: 897903.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: 6771.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
Gelabert-Gonzalez, M. Intracranial arachnoid cyst. Rev Neurol. 2004; 39(12): 1161–6.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
Postacchini, F. Lumbar disc herniation. New York: Springer; 1999.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: 494503.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. 798811.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): 5260.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): 95104.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: 199203.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
Ngan, C, Tan, A. Bacteroides fragilis meningitis. Singapore Med J. 1994; 35: 283–5.Google Scholar
Wexler, H. Bacteroides: the good, the bad, and the nitty-gritty. Clin Microbiol Rev. 2007; 20(4): 593621.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
Finney, GR. Perceptual-motor dysfunction. Continuum (Minneap Minn). 2015; 21: 678–89.Google Scholar
O'Reilly, RC, Munakata, Y, Frank, MJ, et al. Computational cognitive neuroscience. Wiki Book. Available from http:/ccnbook.colorado.eduGoogle Scholar
Moreaud, O. Balint syndrome. Arch Neurol. 2003; 60: 1329.Google 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: e9596.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: e7111.Google Scholar
Smith, JS, Shaffrey, CI, Abel, MF, Menezes, AH. Basilar invagination. Neurosurgery. 2010; 66: A39A47.Google Scholar
Bushby, K. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. Lancet Neurol. 2010; 9: 7793.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
Alam, S, Lux, AL. Epilepsies in infancy. Arch Dis Child. 2012; 97(11): 985–92.Google Scholar
Nabbout, R, Dulac, O. Epileptic syndromes in infancy and childhood. Curr Opin Neurol. 2008; 21(2): 161–6.Google Scholar
Cilio, MR. Neonatal seizures. Paediatr Child Health. 2009; 19: S28S31.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, 14621464.Google Scholar
Epley, JM. The canalith repositioning procedure: for treatment of benign paroxysmal positional vertigo. Otolaryngol Head Neck Surg. 1992; 107: 399404.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
Caplan, LR. Binswanger's disease – revisited. Neurology. 1995; 45: 626–33.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): 2734. 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): 1932.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): 797804.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): 525530.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): 8291.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): 197205.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
Geschwind, M. Prion diseases. Continuum (Minneap Minn). 2015; 21: 1612–38.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
Bromberg, MB. Brachial plexus syndrome. In Post, TW, ed. UpToDate. Waltham, MA; 2016.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
Bromberg, MB. Brachial plexus syndrome. In Post, TW, ed. UpToDate. Waltham, MA; 2016.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): 199209.Google Scholar
Susser, E, Wanderling, J. Epidemiology of nonaffective acute remitting psychosis vs schizophrenia: sex and sociocultural setting. Arch Gen Psychiatry. 1994; 51(4): 294301.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: 6971.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: 113.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): 7984.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): 8198.Google Scholar
Steinherz, K, Vissing, T. The medical effects of marijuana on the brain. 21st Century. 1997–1998(Winter): 5969.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
Fontaine, B. CANOMAD syndrome. Orphanet. March 2007.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): 797805.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): 9851018.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): 5961. Available from http://doi.org/10.1016/j.ijscr.2011.10.014Google Scholar
Miller, JK. Carcinoid syndrome and the APUD concept. Semin Anesth. 1987; 3: 228–37.Google 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): S813.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
Zoom, M, Smith, KS. The aetiology of complete heart-block. Br Med J. 1963; 2: 1149.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
Chen-Scarabelli, C. Neurocardiogenic syncope. BMJ. 2004; 329(7461): 336–41.Google Scholar
Grubb, BP. Neurocardiogenic syncope and related disorders of orthostatic intolerance. Circulation. 2005; 111(22): 29973006.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: 8592.Google Scholar
Amin, V, Pavri, BB. Carotid sinus syndrome. Cardiol Rev. 2015; 23: 130–4.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: 1620.Google Scholar
Sutton, R. Carotid sinus syndrome: Progress in understanding and management. Glob Cardiol Sci Pract. 2014; 2014: 18.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: 115.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: 198205.Google Scholar
Maraire, JN, Awad, IA. Intracranial cavernous malformations: lesion behavior and management strategies. Neurosurgery. 1995; 37: 591605.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. 483501.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: 392447.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): 91102.Google Scholar
Musana, A, Yale, SH. Central pontine myelinolysis: case series and review. WMJ. 2005; 104(6): 5660.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): 296302.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: 595607.Google Scholar
Jahaveri, S. Central sleep apnea. Clin Chest Med. 2010; 31: 235–48.Google Scholar
Jahaveri, S, Dempsey, JA. Central sleep apnea. Compr Physiol. 2013; 3: 141–63.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
Jahaveri, S, Dempsey, JA. Central sleep apnea. Compr Physiol. 2013; 3: 141–63.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: 111.Google Scholar
Eckert, DJ, Jordan, AS, Merchia, P, et al. Central sleep apnea: pathophysiology and treatment. Chest. 2007; 131: 595607.Google Scholar
Jahaveri, S, Dempsey, JA. Central sleep apnea. Compr Physiol. 2013; 3: 141–63Google 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): 294301.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): 1730.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): 24.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.e1723.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
Trafton, PG. Spinal cord injuries. Surg Clin North Am. 1982; 62(1): 6172.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): 4352. 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
Kirkland, L. Cholesterol embolism clinical presentation. Medscape. Oct 5, 2017.Google Scholar
Kronzon, I. Cholesterol embolization syndrome. Circulation. 2010; 122: 631–41. DOI: 10.1161/CIRCULATIONAHA.109.886465Google Scholar
Cardoso, F. Chorea gravidarum. Arch Neurol. 2002; 59(5): 868–70.Google 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
Robottom, BJ, Weiner, WJ. Chorea gravidarum. Handb Clin Neurol. 2011; 100: 231–5.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, EE, Bojrab, DI. Cholesteatoma. New York: Thieme; 2011. Chapter 1.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): 396405.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): 199207.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
Howell, MJ. Parasomnias: an updated review. Neurotherapeutics. 2012; 9: 753–75.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
Danks, DM. Copper deficiency in humans. Annu Rev Nutr. 1988; 8: 235.Google Scholar
Jaiser, SR, Winston, GP. Copper deficiency myelopathy. J Neurol. 2010; 257: 869.Google Scholar
Kumar, N, Gross, JB Jr, Ahlskog,