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Biochimica Et Biophysica Acta|July 25, 1990
The molecular pathology of respiratory-chain dysfunction in human mitochondrial myopathiesJ A Morgan-Hughes, A H Schapira, J M Cooper, et al.Annals of Neurology|June 1, 1993
Coexistence of hereditary motor and sensory neuropathy type Ia and IgM paraproteinemic neuropathyR Gregory, P K Thomas, R H King, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1993
Transthyretin gene mutations in British and French patients with amyloid neuropathyK Bhatia, M Reilly, D Adams, et al.Neuroreport|September 8, 1994
Nigral dopaminergic cell loss in vitamin E deficient ratsD T Dexter, I Nanayakkara, M A Goss-Sampson, et al.Neurology|August 1, 1997
A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndromeR M Chalmers, P J Lamont, I Nelson, et al.American Journal of Human Genetics|January 1, 1991
Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNAM A McShane, S R Hammans, M Sweeney, et al.Diabetologia|April 1, 1994
Mitochondrial gene defects in patients with NIDDMJ C Alcolado, A Majid, M Brockington, et al.Lancet (London, England)|December 5, 1992
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNAW Reardon, R J Ross, M G Sweeney, et al.Brain : a Journal of Neurology|January 1, 1997
Hereditary demyelinating neuropathy of infancy. A genetically complex syndromeJ Tyson, D Ellis, U Fairbrother, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 1996
Proton magnetic resonance spectroscopy in Huntington's disease: evidence in favour of the glutamate excitotoxic theoryS D Taylor-Robinson, R A Weeks, D J Bryant, et al.Pageof 21