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A E Harding

Showing results (231-240 of 241) with videos related to

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American Journal of Human Genetics|August 1, 1996
Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathyD A Mackey, R J Oostra, T Rosenberg, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1994
Magnetic resonance imaging in degenerative ataxic disordersI E Ormerod, A E Harding, D H Miller, et al.
Neurology|October 11, 1992
Parkinson's disease in twins studied with 18F-dopa and positron emission tomographyD J Burn, M H Mark, E D Playford, et al.
Brain : a Journal of Neurology|March 1, 1997
The phenotypic manifestations of chromosome 17p11.2 duplicationP K Thomas, W Marques, M B Davis, et al.
Brain : a Journal of Neurology|February 1, 1991
Neuroacanthocytosis. A clinical, haematological and pathological study of 19 casesR J Hardie, H W Pullon, A E Harding, et al.
American Journal of Human Genetics|December 1, 1996
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locusG David, P Giunti, N Abbas, et al.
Lancet (London, England)|June 6, 1992
Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's diseaseC A Smith, A C Gough, P N Leigh, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1995
Bilateral simultaneous optic neuropathy in adults: clinical, imaging, serological, and genetic studiesS P Morrissey, F X Borruat, D H Miller, et al.
Journal of the Neurological Sciences|January 1, 1994
Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsyM G Sweeney, S R Hammans, L W Duchen, et al.
Annals of Neurology|July 1, 1996
Deficiency of respiratory chain complex I is a common cause of Leigh diseaseA A Morris, J V Leonard, G K Brown, et al.
Pageof 25

Showing results (231-240 of 241) with videos related to

Sort By:
Pageof 25
American Journal of Human Genetics|August 1, 1996
Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathyD A Mackey, R J Oostra, T Rosenberg, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1994
Magnetic resonance imaging in degenerative ataxic disordersI E Ormerod, A E Harding, D H Miller, et al.
Neurology|October 11, 1992
Parkinson's disease in twins studied with 18F-dopa and positron emission tomographyD J Burn, M H Mark, E D Playford, et al.
Brain : a Journal of Neurology|March 1, 1997
The phenotypic manifestations of chromosome 17p11.2 duplicationP K Thomas, W Marques, M B Davis, et al.
Brain : a Journal of Neurology|February 1, 1991
Neuroacanthocytosis. A clinical, haematological and pathological study of 19 casesR J Hardie, H W Pullon, A E Harding, et al.
American Journal of Human Genetics|December 1, 1996
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locusG David, P Giunti, N Abbas, et al.
Lancet (London, England)|June 6, 1992
Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's diseaseC A Smith, A C Gough, P N Leigh, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1995
Bilateral simultaneous optic neuropathy in adults: clinical, imaging, serological, and genetic studiesS P Morrissey, F X Borruat, D H Miller, et al.
Journal of the Neurological Sciences|January 1, 1994
Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsyM G Sweeney, S R Hammans, L W Duchen, et al.
Annals of Neurology|July 1, 1996
Deficiency of respiratory chain complex I is a common cause of Leigh diseaseA A Morris, J V Leonard, G K Brown, et al.
Pageof 25