Showing results (71-80 of 220) with videos related to

Sort By:
Pageof 22
Journal of Medical Genetics|March 19, 2002
Leber hereditary optic neuropathyP Yu-Wai-Man, D M Turnbull, P F Chinnery
Analytical Biochemistry|October 1, 1993
A microtiter plate assay for cytochrome c oxidase in permeabilized whole cellsZ M Chrzanowska-Lightowlers, D M Turnbull, R N Lightowlers
Medical Hypotheses|February 8, 2005
Mitochondrial dysfunction plays a key role in progressive axonal loss in Multiple SclerosisH E Andrews, P P Nichols, D Bates, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1997
Characterisation of carnitine palmitoyltransferases in patients with a carnitine palmitoyltransferase deficiency: implications for diagnosis and therapyJ Schaefer, S Jackson, F Taroni, 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.
Annals of Neurology|July 1, 1983
Plasma concentrations of sodium valproate: their clinical valueD M Turnbull, M D Rawlins, D Weightman, et al.
British Medical Journal (Clinical Research Ed.)|March 16, 1985
Which drug for the adult epileptic patient: phenytoin or valproate?D M Turnbull, D Howel, M D Rawlins, et al.
Pageof 22