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American Journal of Medical Genetics|October 2, 2001
Epidemiology and treatment of mitochondrial disordersP F Chinnery, D M TurnbullMolecular Medicine Today|November 14, 2000
Mitochondrial DNA mutations in the pathogenesis of human diseaseP F Chinnery, D M TurnbullAnnals of Clinical Biochemistry|July 27, 2001
The ischaemic lactate-ammonia testC Livingstone, P F Chinnery, D M TurnbullJournal of Medical Genetics|March 19, 2002
Leber hereditary optic neuropathyP Yu-Wai-Man, D M Turnbull, P F ChinneryJournal of the Neurological Sciences|May 28, 2003
Clinical progression of mitochondrial myopathy is associated with the random accumulation of cytochrome c oxidase negative skeletal muscle fibresP F Chinnery, D Howel, D M Turnbull, et al.Trends in Genetics : TIG|January 10, 1998
Mammalian mitochondrial genetics: heredity, heteroplasmy and diseaseR N Lightowlers, P F Chinnery, D M Turnbull, et al.Journal of Medical Genetics|July 29, 1999
Mitochondrial DNA analysis: polymorphisms and pathogenicityP F Chinnery, N Howell, R M Andrews, et al.Brain : a Journal of Neurology|November 20, 1997
Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypesP F Chinnery, N Howell, R N Lightowlers, et al.Brain : a Journal of Neurology|November 3, 1998
MELAS and MERRF. The relationship between maternal mutation load and the frequency of clinically affected offspringP F Chinnery, N Howell, R N Lightowlers, et al.Human Reproduction (Oxford, England)|October 21, 2000
In-vitro genetic modification of mitochondrial functionR W Taylor, P F Chinnery, D M Turnbull, et al.Pageof 27