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Brain : a Journal of Neurology|October 1, 1996
A case-control study of Leber's hereditary optic neuropathyR M Charlmers, A E HardingJournal of Neurology|June 1, 1993
EEG and evoked potential findings in mitochondrial myopathiesS J Smith, A E HardingJournal of Neurology, Neurosurgery, and Psychiatry|August 1, 1980
Autosomal recessive forms of hereditary motor and sensory neuropathyA E Harding, P K ThomasJournal of Medical Genetics|August 1, 1981
'Pseudo-dominant' inheritance in Friedreich's ataxiaA E Harding, K J ZilkhaThe Quarterly Journal of Medicine|January 1, 1983
The heart disease of Friedreich's ataxia: a clinical and electrocardiographic study of 115 patients, with an analysis of serial electrocardiographic changes in 30 casesA E Harding, R L HewerBrain : 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 HardingJournal 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 HardingJournal 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 SchonJournal of Neurology, Neurosurgery, and Psychiatry|May 1, 1987
Serum vitamin E concentrations are normal in Friedreich's ataxiaD P Muller, S Matthews, A E HardingMovement 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 HardingPageof 21