Hostname: page-component-5c6d5d7d68-ckgrl Total loading time: 0 Render date: 2024-08-20T04:04:33.321Z Has data issue: false hasContentIssue false
  • English
  • Français

A 44-Year-Old Man with Profound Behavioural Changes

Published online by Cambridge University Press:  02 December 2014

R. Laforce Jr ,
G.A. Kerchner ,
G.D. Rabinovici ,
J.C. Fong ,
B.L. Miller ,
W.W. Seeley  and
L.T. Grinberg
R. Laforce Jr*
Affiliation:
Memory and Aging Center & Department of Neurology, University of California San Francisco
G.A. Kerchner
Affiliation:
Stanford Center for Memory Disorders, Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA
G.D. Rabinovici
Affiliation:
Memory and Aging Center & Department of Neurology, University of California San Francisco
J.C. Fong
Affiliation:
Memory and Aging Center & Department of Neurology, University of California San Francisco
B.L. Miller
Affiliation:
Memory and Aging Center & Department of Neurology, University of California San Francisco
W.W. Seeley
Affiliation:
Memory and Aging Center & Department of Neurology, University of California San Francisco
L.T. Grinberg
Affiliation:
Memory and Aging Center & Department of Neurology, University of California San Francisco
*
UCSF Memory and Aging Center, 350 parnassus Avenue, Suite 905, San Francisco, California, 94143, USA. email: rlaforce@memory.ucsf.edu
Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content so a preview has been provided. As you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Brief Communications
Information
Canadian Journal of Neurological Sciences , Volume 39 , Issue 4 , July 2012 , pp. 527 - 530
Copyright
Copyright © The Canadian Journal of Neurological 2012

References

1.Rascovsky, K, Hodges, JR, Knopman, D, et al.Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain. 2011;134:2456–77.CrossRefGoogle ScholarPubMed
2.Neumann, M, Rademakers, R, Roeber, S, Baker, M, Kretzschmar, HA, Mackenzie, IR.A new subtype of frontotemporal lobar degeneration with FUS pathology. Brain. 2009;132:2922–31.Google Scholar
3.Snowden, JS, Hu, Q, Rollinson, S, et al.The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene. Acta Neuropathol. 2011;122:99–110.Google Scholar
4.Urwin, H, Josephs, KA, Rohrer, JD, et al.FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration. Acta Neuropathol. 2010;120:33–41.Google Scholar
5.Rabinovici, GD, Miller, BL.Frontotemporal lobar degeneration: epidemiology, pathophysiology, diagnosis and management. CNS Drugs. 2010;24:375–98.CrossRefGoogle ScholarPubMed