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Brain : a Journal of Neurology|April 1, 1995
Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patientsM J Jackson, J A Schaefer, M A Johnson, et al.Diabetes Care|July 1, 1994
Biochemical and molecular studies of mitochondrial function in diabetes insipidus, diabetes mellitus, optic atrophy, and deafnessM J Jackson, L A Bindoff, K Weber, et al.American Journal of Human Genetics|November 1, 1991
Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigreesN Howell, L A Bindoff, D A McCullough, et al.Gut|December 15, 2000
Mitochondrial enteropathy: the primary pathology may not be within the gastrointestinal tractP F Chinnery, S Jones, L Sviland, et al.Annals of Neurology|September 1, 1996
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNAR W Taylor, P F Chinnery, F Haldane, et al.The Journal of Clinical Investigation|October 1, 1992
Combined enzyme defect of mitochondrial fatty acid oxidationS Jackson, R S Kler, K Bartlett, et al.The Journal of Biological Chemistry|September 15, 1993
Abnormal RNA processing associated with a novel tRNA mutation in mitochondrial DNA. A potential disease mechanismL A Bindoff, N Howell, J Poulton, et al.Diabetic Medicine : a Journal of the British Diabetic Association|June 1, 1997
Maternally inherited diabetes and deafness: prevalence in a hospital diabetic populationJ E Newkirk, R W Taylor, N Howell, et al.Neurology|April 13, 2005
Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutationsS Winterthun, G Ferrari, L He, et al.Journal of the Neurological Sciences|March 1, 1991
Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): a clinical, biochemical and molecular studyL A Bindoff, C Desnuelle, M A Birch-Machin, et al.Pageof 22