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Showing articles 0 to 17 of 17

Filter Applied: spinocerebellar degeneration (Click to remove)

Copper Deficiency
BMJ 348:g3691, Chhetri, S.K.,et al, 2014

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Spinocerebellar Ataxia Type 8
Neurol 55:649-657, Day,J.W. et al, 2000

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
Neurol 49:1598-1604, Brandmann,O.,et al, 1997

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Spinocerebellar Degeneration:Qualitative & Quantitative MR Analysis of Atrophy
J Comput Assist Tomogr 12:298-303, Nabatame,H.,et al, 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Cranial Computerized Tomography & Marie's Ataxia
Arch Neurol 35:55, Aita,J.F., 1978

Computerized Tomography & Auditory-evoked Potentials:Use in the Diagnosis of Olivopontocerebellar Degeneration
Arch Neurol 35:143, Gilroy,J.,et al, 1978

Physostigmine in Familial Ataxias
Neurol 27:70, Kark,R.A.,et al, 1977

Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
NEJM 296:1138, Jackson,J.F.,et al, 1977

A Case of Cerebellar Ataxia, with a Discussion of Classification
Arch Neurol 3:71, Locke,S.,et al, 1960



Showing articles 0 to 17 of 17