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Neurology
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Gait disorders/ataxia

Citations 61-70 of 144 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Initial diagnoses given to persons with the fragile X associated tremor/ataxia syndrome (FXTAS)
D. A. Hall, E. Berry-Kravis, S. Jacquemont, C. D. Rice, J. Cogswell, L. Zhang, R. J. Hagerman, P. J. Hagerman, and M. A. Leehey
Neurology 2005; 65: 299-301. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
New calcium channel mutations predict aberrant RNA splicing in episodic ataxia
Louise H. Eunson, Tracey D. Graves, and Michael G. Hanna
Neurology 2005; 65: 308-310. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Fragile X-associated tremor/ataxia syndrome presenting in a woman after chemotherapy
J. P. O’Dwyer, C. Clabby, J. Crown, D. E. Barton, and M. Hutchinson
Neurology 2005; 65: 331-332. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Systemic mastocytosis: A potential neurologic emergency
G. B. Boncoraglio, A. Brucato, M. R. Carriero, E. Maccagnano, L. Robbiolo, L. O. Scappatura, D. Soligo, and E. A. Parati
Neurology 2005; 65: 332-333. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Ipsidirectional impairment of prism adaptation after unilateral lesion of anterior cerebellum
L. Pisella, Y. Rossetti, C. Michel, G. Rode, D. Boisson, D. Pélisson, and C. Tilikete
Neurology 2005; 65: 150-152. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia
M. Z. Cader, J. L. Steckley, D. A. Dyment, R. S. McLachlan, and G. C. Ebers
Neurology 2005; 65: 156-158. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
A phenotype without spasticity in sacsin-related ataxia
H. Shimazaki, Y. Takiyama, K. Sakoe, Y. Ando, and I. Nakano
Neurology 2005; 64: 2129-2131. [Abstract] [Full text] [PDF]  

EDITORIALS
Spinocerebellar ataxia type 14: Opening a new door in dominant ataxia research?
Massimo Pandolfo and Bart P.C. van de Warrenburg
Neurology 2005; 64: 1113-1114. [Full text] [PDF]  

ARTICLES
Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase {gamma} mutations
S. Winterthun, G. Ferrari, L. He, R. W. Taylor, M. Zeviani, D. M. Turnbull, B. A. Engelsen, G. Moen, and L. A. Bindoff
Neurology 2005; 64: 1204-1208. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
The clinical and genetic spectrum of spinocerebellar ataxia 14
D. -H. Chen, P. J. Cimino, L. P.W. Ranum, H. Y. Zoghbi, I. Yabe, L. Schut, R. L. Margolis, H. P. Lipe, A. Feleke, M. Matsushita, J. Wolff, C. Morgan, D. Lau, M. Fernandez, H. Sasaki, W. H. Raskind, and T. D. Bird
Neurology 2005; 64: 1258-1260. [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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