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Muscle & Nerve. Supplement
|
January 1, 1995
Mitochondrial DNA diseases: genotype and phenotype in Leber's hereditary optic neuropathy
A E Harding, P Riordan-Eva, G G Govan
Journal of Medical Genetics
|
December 1, 1989
Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy
I J Holt, D H Miller, A E Harding
Revue Neurologique
|
January 1, 1992
[Demonstration of genetic mutation in most of the amyloid neuropathies with sporadic occurrence]
D Adams, M Reilly, A E Harding, et al.
Journal of Medical Genetics
|
March 1, 1990
Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance
S A Hawkins, N C Nevin, A E Harding
Brain : a Journal of Neurology
|
June 1, 1994
Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy. A clinical and genetic study of eight families
T P Enevoldson, M D Sanders, A E Harding
Brain : a Journal of Neurology
|
April 1, 1990
A genetic study of idiopathic torsion dystonia in the United Kingdom
N A Fletcher, A E Harding, C D Marsden
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 1, 1996
Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy
R M Chalmers, A C Bird, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 1, 1984
Autosomal recessive late onset multisystem disorder with cerebellar cortical atrophy at necropsy: report of a family
A E Harding, J V Diengdoh, A J Lees
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 1, 1988
Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy
I J Holt, D H Miller, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 1, 1991
The relationship between trauma and idiopathic torsion dystonia
N A Fletcher, A E Harding, C D Marsden
Page
of 25
Search research articles
Search
Showing results (61-70 of 241) with videos related to
Sort By:
Page
of 25
Muscle & Nerve. Supplement
|
January 1, 1995
Mitochondrial DNA diseases: genotype and phenotype in Leber's hereditary optic neuropathy
A E Harding, P Riordan-Eva, G G Govan
Journal of Medical Genetics
|
December 1, 1989
Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy
I J Holt, D H Miller, A E Harding
Revue Neurologique
|
January 1, 1992
[Demonstration of genetic mutation in most of the amyloid neuropathies with sporadic occurrence]
D Adams, M Reilly, A E Harding, et al.
Journal of Medical Genetics
|
March 1, 1990
Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance
S A Hawkins, N C Nevin, A E Harding
Brain : a Journal of Neurology
|
June 1, 1994
Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy. A clinical and genetic study of eight families
T P Enevoldson, M D Sanders, A E Harding
Brain : a Journal of Neurology
|
April 1, 1990
A genetic study of idiopathic torsion dystonia in the United Kingdom
N A Fletcher, A E Harding, C D Marsden
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 1, 1996
Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy
R M Chalmers, A C Bird, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 1, 1984
Autosomal recessive late onset multisystem disorder with cerebellar cortical atrophy at necropsy: report of a family
A E Harding, J V Diengdoh, A J Lees
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 1, 1988
Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy
I J Holt, D H Miller, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 1, 1991
The relationship between trauma and idiopathic torsion dystonia
N A Fletcher, A E Harding, C D Marsden
Page
of 25