M. Brivet

A Mitochondrial Pyruvate Carrier Required for Pyruvate Uptake in Yeast, <i>Drosophila</i> , and Humans

Daniel K. Bricker, Eric B. Taylor, John C. Schell et al. · Science · 2012 · 863 citations · Full text

Genetics, Molecular Genetics, Mitochondrial Biology +17

Arrhythmias and Conduction Defects as Presenting Symptoms of Fatty Acid Oxidation Disorders in Children

Damien Bonnet, Delphine Martin, Pascale de Lonlay et al. · Circulation · 1999 · 305 citations · Full text

Pyruvate dehydrogenase complex deficiency: four neurological phenotypes with differing pathogenesis

Christine Barnérias, Jean‐Marie Saudubray, Guy Touati et al. · Developmental Medicine & Child Neurology · 2009 · 171 citations · Full text

Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients

Christine Vianey‐Saban, P. Divry, M. Brivet et al. · Clinica Chimica Acta · 1998 · 156 citations

Aldehyde Dehydrogenase, Mitochondrial Function, Biochemistry +8

Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation

Ronald J. A. Wanders, Lodewijk IJlst, F Poggi et al. · Biochemical and Biophysical Research Communications · 1992 · 153 citations

Metabolic Syndrome, Metabolic Disorder, Mitochondrial Function +8