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Movement Disorders : Official Journal of the Movement Disorder Society
|
May 1, 1994
Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease
V Planté-Bordeneuve, M B Davis, D M Maraganore, et al.
Journal of the Neurological Sciences
|
March 1, 1994
Platelet mitochondrial function in Leber's hereditary optic neuropathy
P R Smith, J M Cooper, G G Govan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 1, 1988
The diverse neurological features of Niemann-Pick disease type C: a report of two cases
R J Coleman, S A Robb, B D Lake, et al.
The Quarterly Journal of Medicine
|
July 1, 1993
Mitochondrial DNA transfer RNA mutation Leu(UUR)A-->G 3260: a second family with myopathy and cardiomyopathy
M G Sweeney, M Brockington, M J Weston, et al.
Brain : a Journal of Neurology
|
December 1, 1991
Irish (Donegal) amyloidosis is associated with the transthyretinALA60 (Appalachian) variant
H Staunton, M B Davis, R J Guiloff, et al.
American Journal of Human Genetics
|
July 1, 1996
Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy
R M Chalmers, M B Davis, M G Sweeney, et al.
Annals of Neurology
|
May 1, 1996
A novel point mutation in the McLeod syndrome gene in neuroacanthocytosis
M F Ho, R M Chalmers, M B Davis, et al.
The Quarterly Journal of Medicine
|
October 1, 1993
Smoking and mitochondrial function: a model for environmental toxins
P R Smith, J M Cooper, G G Govan, et al.
Brain : a Journal of Neurology
|
June 1, 1990
Familial cerebral amyloid angiopathy with nonneuritic amyloid plaque formation
G T Plant, T Révész, R O Barnard, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 1, 1993
A familial disorder associated with palatal myoclonus, other brainstem signs, tetraparesis, ataxia and Rosenthal fibre formation
R S Howard, R Greenwood, J Gawler, et al.
Page
of 25
Search research articles
Search
Showing results (141-150 of 241) with videos related to
Sort By:
Page
of 25
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 1, 1994
Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease
V Planté-Bordeneuve, M B Davis, D M Maraganore, et al.
Journal of the Neurological Sciences
|
March 1, 1994
Platelet mitochondrial function in Leber's hereditary optic neuropathy
P R Smith, J M Cooper, G G Govan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 1, 1988
The diverse neurological features of Niemann-Pick disease type C: a report of two cases
R J Coleman, S A Robb, B D Lake, et al.
The Quarterly Journal of Medicine
|
July 1, 1993
Mitochondrial DNA transfer RNA mutation Leu(UUR)A-->G 3260: a second family with myopathy and cardiomyopathy
M G Sweeney, M Brockington, M J Weston, et al.
Brain : a Journal of Neurology
|
December 1, 1991
Irish (Donegal) amyloidosis is associated with the transthyretinALA60 (Appalachian) variant
H Staunton, M B Davis, R J Guiloff, et al.
American Journal of Human Genetics
|
July 1, 1996
Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy
R M Chalmers, M B Davis, M G Sweeney, et al.
Annals of Neurology
|
May 1, 1996
A novel point mutation in the McLeod syndrome gene in neuroacanthocytosis
M F Ho, R M Chalmers, M B Davis, et al.
The Quarterly Journal of Medicine
|
October 1, 1993
Smoking and mitochondrial function: a model for environmental toxins
P R Smith, J M Cooper, G G Govan, et al.
Brain : a Journal of Neurology
|
June 1, 1990
Familial cerebral amyloid angiopathy with nonneuritic amyloid plaque formation
G T Plant, T Révész, R O Barnard, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 1, 1993
A familial disorder associated with palatal myoclonus, other brainstem signs, tetraparesis, ataxia and Rosenthal fibre formation
R S Howard, R Greenwood, J Gawler, et al.
Page
of 25