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The Journal of Biological Chemistry|June 21, 1996
Fluxes of nicotinamide adenine dinucleotides through mitochondrial membranes in human cultured cellsP Rustin, B Parfait, D Chretien, et al.Journal of Inherited Metabolic Disease|November 20, 1998
Diffuse leukodystrophy in an infant with cytochrome-c oxidase deficiencyJ P Harpey, D Heron, M Prudent, et al.Genes, Brain, and Behavior|December 17, 2009
MitoPark mice mirror the slow progression of key symptoms and L-DOPA response in Parkinson's diseaseD Galter, K Pernold, T Yoshitake, et al.The Journal of Pediatrics|February 1, 1994
Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathiesP Rustin, J Lebidois, D Chretien, et al.Nature Genetics|November 5, 1997
Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxiaA Rötig, P de Lonlay, D Chretien, et al.Biochemical and Biophysical Research Communications|March 7, 1996
Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chainM A Birch-Machin, C Marsac, G Ponsot, et al.Biochemical and Biophysical Research Communications|July 30, 1997
The consequences of a mild respiratory chain deficiency on substrate competitive oxidation in human mitochondriaV Geromel, B Parfait, J C von Kleist-Retzow, et al.Cellular and Molecular Life Sciences : CMLS|September 7, 2005
Succinate dehydrogenase deficiency in humanJ-J Brière, J Favier, V El Ghouzzi, et al.Human Molecular Genetics|May 24, 2001
Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNAV Geromel, N Kadhom, I Cebalos-Picot, et al.Pediatric Radiology|November 3, 1998
Presentation of six cases of Stüve-Wiedemann syndromeV Cormier-Daire, A Munnich, S Lyonnet, et al.Pageof 18