Gait disorders/ataxia

Citations 131-140 of 144 total displayed.

Past content (since Jan 2001):

ARTICLES
Older people with impaired mobility have specific loci of periventricular abnormality on MRI

R. R. Benson, C. R.G. Guttmann, X. Wei, S. K. Warfield, C. Hall, J. A. Schmidt, R. Kikinis, and L. I. Wolfson
Neurology 2002; 58: 48-55. [Abstract] [Full text] [PDF]  

ARTICLES
Cerebellar ataxia associated with heteroallelic ceruloplasmin gene mutation

H. Miyajima, S. Kono, Y. Takahashi, M. Sugimoto, M. Sakamoto, and N. Sakai
Neurology 2001; 57: 2205-2210. [Abstract] [Full text] [PDF]  

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]  

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