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Journal of Medical Genetics
|
August 1, 1988
Mitochondrial myopathy: a genetic study of 71 cases
A E Harding, R K Petty, J A Morgan-Hughes
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 1, 1994
Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom
T T Warner, G G Lennox, I Janota, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 1, 1989
Ataxia telangiectasia: a reappraisal of the ocular motor features and their value in the diagnosis of atypical cases
R Stell, A M Bronstein, G T Plant, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 1, 1995
Sequence of the superoxide dismutase 1 (SOD 1) gene in familial Parkinson's disease
O Bandmann, M B Davis, C D Marsden, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1995
Arg296 to Cys296 polymorphism in exon 6 of cytochrome P-450-2D6 (CYP2D6) is not associated with multiple system atrophy
O Bandmann, G K Wenning, N P Quinn, et al.
Clinical Genetics
|
December 1, 1981
Intrafamilial correlation in Friedreich's ataxia
R M Winter, A E Harding, M Baraitser, et al.
Somatic Cell and Molecular Genetics
|
July 1, 1997
Depletion of mitochondrial DNA by ddC in untransformed human cell lines
I Nelson, M G Hanna, N W Wood, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 1, 1989
Lumbar extradural arachnoid cyst presenting as a conus lesion in a man aged 77 years
J B Winer, A E Harding, L Symon, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 1, 1988
Degenerative cerebellar ataxia and focal dystonia
N A Fletcher, R Stell, A E Harding, et al.
Annals of Neurology
|
July 1, 1996
Striatal D1 and D2 dopamine receptor loss in asymptomatic mutation carriers of Huntington's disease
R A Weeks, P Piccini, A E Harding, et al.
Page
of 25
Search research articles
Search
Showing results (91-100 of 241) with videos related to
Sort By:
Page
of 25
Journal of Medical Genetics
|
August 1, 1988
Mitochondrial myopathy: a genetic study of 71 cases
A E Harding, R K Petty, J A Morgan-Hughes
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 1, 1994
Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom
T T Warner, G G Lennox, I Janota, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 1, 1989
Ataxia telangiectasia: a reappraisal of the ocular motor features and their value in the diagnosis of atypical cases
R Stell, A M Bronstein, G T Plant, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 1, 1995
Sequence of the superoxide dismutase 1 (SOD 1) gene in familial Parkinson's disease
O Bandmann, M B Davis, C D Marsden, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1995
Arg296 to Cys296 polymorphism in exon 6 of cytochrome P-450-2D6 (CYP2D6) is not associated with multiple system atrophy
O Bandmann, G K Wenning, N P Quinn, et al.
Clinical Genetics
|
December 1, 1981
Intrafamilial correlation in Friedreich's ataxia
R M Winter, A E Harding, M Baraitser, et al.
Somatic Cell and Molecular Genetics
|
July 1, 1997
Depletion of mitochondrial DNA by ddC in untransformed human cell lines
I Nelson, M G Hanna, N W Wood, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 1, 1989
Lumbar extradural arachnoid cyst presenting as a conus lesion in a man aged 77 years
J B Winer, A E Harding, L Symon, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 1, 1988
Degenerative cerebellar ataxia and focal dystonia
N A Fletcher, R Stell, A E Harding, et al.
Annals of Neurology
|
July 1, 1996
Striatal D1 and D2 dopamine receptor loss in asymptomatic mutation carriers of Huntington's disease
R A Weeks, P Piccini, A E Harding, et al.
Page
of 25