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Neurology
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Gait disorders/ataxia

Citations 111-120 of 142 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Prevalence of antigliadin antibodies in ataxia patients
M. Abele, L. Schöls, S. Schwartz, and T. Klockgether
Neurology 2003; 60: 1674-1675. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Idebenone treatment in Friedreich’s ataxia: Neurological, cardiac, and biochemical monitoring
G. Buyse, L. Mertens, G. Di Salvo, I. Matthijs, F. Weidemann, B. Eyskens, W. Goossens, N. Goemans, G. R. Sutherland, and J. L.K. Van Hove
Neurology 2003; 60: 1679-1681. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Nodulus infarction mimicking acute peripheral vestibulopathy
H. Lee, H. A. Yi, Y. W. Cho, C. H. Sohn, G. T. Whitman, S. Ying, and R. W. Baloh
Neurology 2003; 60: 1700-1702. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Cerebellar ataxia and coenzyme Q10 deficiency
C. Lamperti, A. Naini, M. Hirano, D.C. De Vivo, E. Bertini, S. Servidei, M. Valeriani, D. Lynch, B. Banwell, M. Berg, T. Dubrovsky, C. Chiriboga, C. Angelini, E. Pegoraro, and S. DiMauro
Neurology 2003; 60: 1206-1208. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Phenotypic variability of aprataxin gene mutations
C. Tranchant, M. Fleury, M. C. Moreira, M. Koenig, and J. M. Warter
Neurology 2003; 60: 868-870. [Abstract] [Full text] [PDF]  

ARTICLES
Anti-Tr antibodies as markers of paraneoplastic cerebellar degeneration and Hodgkin’s disease
F. Bernal, S. Shams’ili, I. Rojas, R. Sanchez-Valle, A. Saiz, J. Dalmau, J. Honnorat, P. Sillevis Smitt, and F. Graus
Neurology 2003; 60: 230-234. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
REM sleep behavior disorder and SCA-3 (Machado-Joseph disease)
Badar H. Syed, David B. Rye, and Gurwant Singh
Neurology 2003; 60: 148. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Cerebellar degeneration and autoimmunity to zinc-finger proteins of the cerebellum
L. Bataller, D.F. Wade, G.N. Fuller, M.R. Rosenfeld, and J. Dalmau
Neurology 2002; 59: 1985-1987. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
SCA-2 presenting as parkinsonism in an Alberta family: Clinical, genetic, and PET findings
S. Furtado, M. Farrer, Y. Tsuboi, M. L. Klimek, R. de la Fuente-Fernández, J. Hussey, P. Lockhart, D. B. Calne, O. Suchowersky, A. J. Stoessl, and Z. K. Wszolek
Neurology 2002; 59: 1625-1627. [Abstract] [Full text] [PDF]  

ARTICLES
Presymptomatic testing in Huntington’s disease and autosomal dominant cerebellar ataxias
C. Goizet, G. Lesca, and A. Dürr
Neurology 2002; 59: 1330-1336. [Abstract] [Full text] [PDF]  

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* Collected Resources Home

* Related collections:
 Movement Disorders
 All Movement Disorders
 Dystonia
 Blepharospasm
 Gait disorders/ataxia
 Cerebellum
 Huntington's disease
 Basal ganglia
 Parkinson's disease/Parkinsonism
 Motor Control
 Progressive supranuclear palsy
 Motor cortex
 Stiff person syndrome
 Surgery/Stimulation
 Tourette syndrome
 Tremor
 Tics
 Chorea
 Botulinum toxin
 Multiple system atrophy
 Rett Syndrome
 Myoclonus
 Spastic paraplegia


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