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A E Harding

Showing results (51-60 of 241) with videos related to

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Brain : a Journal of Neurology|October 1, 1995
Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotide repeat expansion in families with autosomal dominant motor disorders, including the Drew family of WalworthP Giunti, M G Sweeney, A E Harding
Nature Genetics|March 1, 1994
DRPLA in EuropeT T Warner, L Williams, A E Harding
American Journal of Ophthalmology|April 15, 1986
Congenital trichomegaly, pigmentary retinal degeneration, and short statureM A Patton, A E Harding, M Baraitser
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1995
Familial amyloid polyneuropathy (TTR ala 60) in north west Ireland: a clinical, genetic, and epidemiological studyM M Reilly, H Staunton, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1987
Adult onset supranuclear ophthalmoplegia, cerebellar ataxia, and neurogenic proximal muscle weakness in a brother and sister: another hexosaminidase A deficiency syndromeA E Harding, E P Young, F Schon
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1987
Serum vitamin E concentrations are normal in Friedreich's ataxiaD P Muller, S Matthews, A E Harding
Journal of Medical Genetics|April 1, 1982
Autosomal dominant asymmetrical radial dysplasia, dysmorphic facies, and conductive hearing loss (facioauriculoradial dysplasia)A E Harding, C M Hall, M Baraitser
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
Genetic prediction in Huntington's disease: what are the limitations imposed by pedigree structure?V P Misra, M Baraitser, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1996
Debrisoquine hydroxylase polymorphism in Leber's hereditary optic neuropathyR M Chalmers, O Bandmann, A E Harding
Brain : a Journal of Neurology|June 1, 1993
Dementia associated with a 216 base pair insertion in the prion protein gene. Clinical and neuropathological featuresL W Duchen, M Poulter, A E Harding
Pageof 25

Showing results (51-60 of 241) with videos related to

Sort By:
Pageof 25
Brain : a Journal of Neurology|October 1, 1995
Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotide repeat expansion in families with autosomal dominant motor disorders, including the Drew family of WalworthP Giunti, M G Sweeney, A E Harding
Nature Genetics|March 1, 1994
DRPLA in EuropeT T Warner, L Williams, A E Harding
American Journal of Ophthalmology|April 15, 1986
Congenital trichomegaly, pigmentary retinal degeneration, and short statureM A Patton, A E Harding, M Baraitser
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1995
Familial amyloid polyneuropathy (TTR ala 60) in north west Ireland: a clinical, genetic, and epidemiological studyM M Reilly, H Staunton, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1987
Adult onset supranuclear ophthalmoplegia, cerebellar ataxia, and neurogenic proximal muscle weakness in a brother and sister: another hexosaminidase A deficiency syndromeA E Harding, E P Young, F Schon
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1987
Serum vitamin E concentrations are normal in Friedreich's ataxiaD P Muller, S Matthews, A E Harding
Journal of Medical Genetics|April 1, 1982
Autosomal dominant asymmetrical radial dysplasia, dysmorphic facies, and conductive hearing loss (facioauriculoradial dysplasia)A E Harding, C M Hall, M Baraitser
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
Genetic prediction in Huntington's disease: what are the limitations imposed by pedigree structure?V P Misra, M Baraitser, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1996
Debrisoquine hydroxylase polymorphism in Leber's hereditary optic neuropathyR M Chalmers, O Bandmann, A E Harding
Brain : a Journal of Neurology|June 1, 1993
Dementia associated with a 216 base pair insertion in the prion protein gene. Clinical and neuropathological featuresL W Duchen, M Poulter, A E Harding
Pageof 25