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Neurology
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Gait disorders/ataxia

Citations 121-130 of 144 total displayed.

Past content (since Jan 2001):

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]  

CLINICAL/SCIENTIFIC NOTES
Sensory ataxia in myelopathy with chronic hepatitis C virus infection
C. H. Nolte, A. S. Endres, and H. Meisel
Neurology 2002; 59: 958-959. [Full text] [PDF]  

BRIEF COMMUNICATIONS
P/Q type calcium-channel antibodies in paraneoplastic cerebellar degeneration with lung cancer
F. Graus, B. Lang, P. Pozo-Rosich, A. Saiz, R. Casamitjana, and A. Vincent
Neurology 2002; 59: 764-766. [Abstract] [Full text] [PDF]  

ARTICLES
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: The aprataxin gene mutations
H. Shimazaki, Y. Takiyama, K. Sakoe, K. Ikeguchi, K. Niijima, J. Kaneko, M. Namekawa, T. Ogawa, H. Date, S. Tsuji, I. Nakano, and M. Nishizawa
Neurology 2002; 59: 590-595. [Abstract] [Full text] [PDF]  

ARTICLES
Progression of gait disorder and rigidity and risk of death in older persons
R. S. Wilson, J. A. Schneider, L. A. Beckett, D. A. Evans, and D. A. Bennett
Neurology 2002; 58: 1815-1819. [Abstract] [Full text] [PDF]  

ARTICLES
The humoral response in the pathogenesis of gluten ataxia
M. Hadjivassiliou, S. Boscolo, G. A.B. Davies–Jones, R. A. Grünewald, T. Not, D. S. Sanders, J. E. Simpson, E. Tongiorgi, C. A. Williamson, and N. M. Woodroofe
Neurology 2002; 58: 1221-1226. [Abstract] [Full text] [PDF]  

ARTICLES
Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy
A. Filla, G. De Michele, S. Cocozza, A. Patrignani, G. Volpe, I. Castaldo, G. Ruggiero, V. Bonavita, C. Masters, G. Casari, and A. Bruni
Neurology 2002; 58: 922-928. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Spinocerebellar ataxia type 10 is rare in populations other than Mexicans
T. Matsuura, L. P.W. Ranum, V. Volpini, M. Pandolfo, H. Sasaki, K. Tashiro, K. Watase, H. Y. Zoghbi, and T. Ashizawa
Neurology 2002; 58: 983. [Full text] [PDF]  

ARTICLES
Spinocerebellar ataxias in the Netherlands: Prevalence and age at onset variance analysis
B.P.C. van de Warrenburg, R.J. Sinke, C.C. Verschuuren–Bemelmans, H. Scheffer, E.R. Brunt, P.F. Ippel, J.A. Maat–Kievit, D. Dooijes, N.C. Notermans, D. Lindhout, N.V.A.M. Knoers, and H.P.H. Kremer
Neurology 2002; 58: 702-708. [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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