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Neurology|March 1, 1992
Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178R Medori, P Montagna, H J Tritschler, et al.
Biochemical Pharmacology|July 17, 1995
Reduction and transport of lipoic acid by human erythrocytesA Constantinescu, U Pick, G J Handelman, et al.
Neurology|April 1, 1991
Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndromeA Lombes, H Nakase, H J Tritschler, et al.
Biofactors (Oxford, England)|January 1, 1997
Lipoic acid increases de novo synthesis of cellular glutathione by improving cystine utilizationD Han, G Handelman, L Marcocci, et al.
American Journal of Human Genetics|March 1, 1991
mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseasesC T Moraes, S Shanske, H J Tritschler, et al.
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