Gait disorders/ataxia

Citations 131-140 of 142 total displayed.

Past content (since Jan 2001):

ARTICLES
Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission

J. Jen, J. Wan, M. Graves, H. Yu, A. F. Mock, C. J. Coulin, G. Kim, Q. Yue, D. M. Papazian, and R. W. Baloh
Neurology 2001; 57: 1843-1848. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
A new autosomal dominant pure cerebellar ataxia

E. Storey, R. J.M. Gardner, M. A. Knight, M. L. Kennerson, R. R. Tuck, S. M. Forrest, and G. A. Nicholson
Neurology 2001; 57: 1913-1915. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus

J. L. Steckley, G. C. Ebers, M. Z. Cader, and R. S. McLachlan
Neurology 2001; 57: 1499-1502. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Pathogenic effect of an intermediate-size SCA-6 allele (CAG)₁₉ in a homozygous patient

C. Mariotti, C. Gellera, M. Grisoli, R. Mineri, A. Castucci, and S. Di Donato
Neurology 2001; 57: 1502-1504. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
SCA8 repeat expansions in ataxia: A controversial association

M.-J. Sobrido, J. A. Cholfin, S. Perlman, S. M. Pulst, and D. H. Geschwind
Neurology 2001; 57: 1310-1312. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Acute sensory ataxic neuropathy associated with monospecific anti-GD1b IgG antibody

C.-L. Pan, N. Yuki, M. Koga, M.-C. Chiang, and S.-T. Hsieh
Neurology 2001; 57: 1316-1318. [Abstract] [Full text] [PDF]  

ARTICLES
A prospective study of cerebral white matter abnormalities in older people with gait dysfunction

G. T. Whitman, T. Tang, A. Lin, and R. W. Baloh
Neurology 2001; 57: 990-994. [Abstract] [Full text] [PDF]  

ARTICLES
Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish family

M. Rantamäki, R. Krahe, A. Paetau, B. Cormand, I. Mononen, and B. Udd
Neurology 2001; 57: 1043-1049. [Abstract] [Full text] [PDF]  

ARTICLES
A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1

Y. Miyoshi, T. Yamada, M. Tanimura, T. Taniwaki, K. Arakawa, Y. Ohyagi, H. Furuya, K. Yamamoto, K. Sakai, T. Sasazuki, and J. Kira
Neurology 2001; 57: 96-100. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Serum transferrin receptor levels in Friedreich’s and other degenerative ataxias

V. Scarano, T. de Cristofaro, G. De Michele, E. Salvatore, I. De Biase, A. Monticelli, A. Filla, and S. Cocozza
Neurology 2001; 57: 159-160. [Abstract] [Full text] [PDF]  

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