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Neurology
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Gait disorders/ataxia

Citations 51-60 of 144 total displayed.

Past content (since Jan 2001):

ARTICLES
Ataxia with oculomotor apraxia type 2: A clinical, pathologic, and genetic study
C. Criscuolo, L. Chessa, S. Di Giandomenico, P. Mancini, F. Saccà, G. S. Grieco, M. Piane, F. Barbieri, G. De Michele, S. Banfi, F. Pierelli, N. Rizzuto, F. M. Santorelli, L. Gallosti, A. Filla, and C. Casali
Neurology 2006; 66: 1207-1210. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Sacsin-related ataxia (ARSACS): Expanding the genotype upstream from the gigantic exon
Y. Ouyang, Y. Takiyama, K. Sakoe, H. Shimazaki, T. Ogawa, S. Nagano, Y. Yamamoto, and I. Nakano
Neurology 2006; 66: 1103-1104. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Electrophysiologic characterization in spinocerebellar ataxia 17
F. Manganelli, A. Perretti, M. Nolano, B. Lanzillo, A. C. Bruni, G. De Michele, A. Filla, and L. Santoro
Neurology 2006; 66: 932-934. [Abstract] [Full text] [PDF]  

ARTICLES
Autoantibody targeting of brain and intestinal transglutaminase in gluten ataxia
M. Hadjivassiliou, M. Mäki, D. S. Sanders, C. A. Williamson, R. A. Grünewald, N. M. Woodroofe, and I. R. Korponay-Szabó
Neurology 2006; 66: 373-377. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Pontine and cerebellar atrophy correlate with clinical disability in SCA2
S. H. Ying, S. I. Choi, S. L. Perlman, R. W. Baloh, D. S. Zee, and A. W. Toga
Neurology 2006; 66: 424-426. [Abstract] [Full text] [PDF]  

NEUROIMAGES
Paroxysmal vertigo as the presenting symptom of Fabry disease
H. Prüss, G. Bohner, and R. Zschenderlein
Neurology 2006; 66: 249. [Full text] [PDF]  

BRIEF COMMUNICATIONS
An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
M. F. Waters, D. Fee, K. P. Figueroa, D. Nolte, U. Müller, J. Advincula, H. Coon, V. G. Evidente, and S. M. Pulst
Neurology 2005; 65: 1111-1113. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Autoantibodies in postinfectious acute cerebellar ataxia
Ayumi Uchibori, Manabu Sakuta, Susumu Kusunoki, and Atsuro Chiba
Neurology 2005; 65: 1114-1116. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III
K. Owada, K. Ishikawa, S. Toru, G. Ishida, M. Gomyoda, O. Tao, Y. Noguchi, K. Kitamura, I. Kondo, E. Noguchi, T. Arinami, and H. Mizusawa
Neurology 2005; 65: 629-632. [Abstract] [Full text] [PDF]  

VIEWS & REVIEWS
Camptocormia: Pathogenesis, classification, and response to therapy
Shaheda N. Azher and Joseph Jankovic
Neurology 2005; 65: 355-359. [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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