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American Journal of Human Genetics|May 1, 1995
Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutationM G Hanna, I Nelson, M G Sweeney, et al.American Journal of Human Genetics|January 1, 1993
Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9qS Chamberlain, M Farrall, J Shaw, et al.Brain : a Journal of Neurology|August 1, 1994
A study of hereditary essential tremorP G Bain, L J Findley, P D Thompson, et al.American Journal of Human Genetics|June 1, 1994
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia IC Jodice, P Malaspina, F Persichetti, et al.Annals of Neurology|December 1, 1989
Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNAI J Holt, A E Harding, J M Cooper, et al.Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1995
Progressive neuronal degeneration of childhood with liver disease (Alpers' disease) presenting in young adultsB N Harding, N Alsanjari, S J Smith, et al.Revue Neurologique|January 1, 1991
The molecular pathology of human respiratory chain defectsJ A Morgan-Hughes, J M Cooper, A H Schapira, et al.Behavioral Neuroscience|December 1, 1996
Associative learning in patients with cerebellar ataxiaJ Tucker, A E Harding, M Jahanshahi, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1985
A study of the relationship between neurological function and serum vitamin E concentrations in patients with cystic fibrosisH J Willison, D P Muller, S Matthews, et al.Annals of Neurology|April 1, 1995
A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European familiesT T Warner, L D Williams, R W Walker, et al.Pageof 21