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A E Harding

Showing results (61-70 of 241) with videos related to

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Muscle & Nerve. Supplement|January 1, 1995
Mitochondrial DNA diseases: genotype and phenotype in Leber's hereditary optic neuropathyA 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 neuropathyI 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 inheritanceS 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 familiesT 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 KingdomN A Fletcher, A E Harding, C D Marsden
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1996
Autosomal dominant optic atrophy with asymptomatic peripheral neuropathyR 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 familyA 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 atrophyI J Holt, D H Miller, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1991
The relationship between trauma and idiopathic torsion dystoniaN A Fletcher, A E Harding, C D Marsden
Pageof 25

Showing results (61-70 of 241) with videos related to

Sort By:
Pageof 25
Muscle & Nerve. Supplement|January 1, 1995
Mitochondrial DNA diseases: genotype and phenotype in Leber's hereditary optic neuropathyA 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 neuropathyI 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 inheritanceS 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 familiesT 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 KingdomN A Fletcher, A E Harding, C D Marsden
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1996
Autosomal dominant optic atrophy with asymptomatic peripheral neuropathyR 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 familyA 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 atrophyI J Holt, D H Miller, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1991
The relationship between trauma and idiopathic torsion dystoniaN A Fletcher, A E Harding, C D Marsden
Pageof 25