Gait disorders/ataxia

Citations 71-80 of 142 total displayed.

Past content (since Jan 2001):

EDITORIALS
Familial hemiplegic migraine: More than just a headache

Michael Benatar and Corey M. Ford
Neurology 2005; 64: 592-593. [Full text] [PDF]  

ARTICLES
¹H-MRS alterations in the cerebellum of patients with familial hemiplegic migraine type 1

M. Dichgans, J. Herzog, T. Freilinger, M. Wilke, and D. P. Auer
Neurology 2005; 64: 608-613. [Abstract] [Full text] [PDF]  

ARTICLES
"Off" gait freezing and temporal discrimination threshold in patients with Parkinson disease

Myung-Sik Lee, Hyun-Sook Kim, and Chul-Hyoung Lyoo
Neurology 2005; 64: 670-674. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
A topodiagnostic investigation on body lateropulsion in medullary infarcts

F. Thömke, J. J. Marx, G. D. Iannetti, G. Cruccu, S. Fitzek, P. P. Urban, P. Stoeter, M. Dieterich, and H. C. Hopf
Neurology 2005; 64: 716-718. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Interlimb coordination deficits during cyclic movements in cerebellar hemiataxia

R. Martyn Bracewell, Ramesh Balasubramaniam, and Alan M. Wing
Neurology 2005; 64: 751-752. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Coenzyme Q deficiency and cerebellar ataxia associated with an aprataxin mutation

C. M. Quinzii, A. G. Kattah, A. Naini, H. O. Akman, V. K. Mootha, S. DiMauro, and M. Hirano
Neurology 2005; 64: 539-541. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Decreased cerebellar total creatine in episodic ataxia type 2: A ¹H MRS study

H. Harno, S. Heikkinen, M. A. Kaunisto, M. Kallela, A-M. Häkkinen, M. Wessman, M. Färkkilä, and N. Lundbom
Neurology 2005; 64: 542-544. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicism

G. Hudson, M. Deschauer, K. Busse, S. Zierz, and P. F. Chinnery
Neurology 2005; 64: 371-373. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures

R. Straussberg, L. Basel-Vanagaite, S. Kivity, R. Dabby, S. Cirak, P. Nurnberg, T. Voit, M. Mahajnah, D. Inbar, G. M. Saifi, J. R. Lupski, V. Delague, A. Megarbane, A. Richter, E. Leshinsky, and S. F. Berkovic
Neurology 2005; 64: 142-144. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia

A. Brussino, C. Gellera, A. Saluto, C. Mariotti, C. Arduino, B. Castellotti, M. Camerlingo, V. de Angelis, L. Orsi, P. Tosca, N. Migone, F. Taroni, and A. Brusco
Neurology 2005; 64: 145-147. [Abstract] [Full text] [PDF]  

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