P. Divry

Clinical and Biochemical Phenotype in 11 Patients With Mevalonic Aciduria

G.F. Hoffmann, C. Charpentier, Ertan Mayatepek et al. · PEDIATRICS · 1993 · 290 citations

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

Novel<i>OCTN2</i>mutations: No genotype–phenotype correlations: Early carnitine therapy prevents cardiomyopathy

Anne‐Marie Lamhonwah, S. E. Olpin, R. J. Pollitt et al. · American Journal of Medical Genetics · 2002 · 119 citations

General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases

N. Gregersen, S. Kelvraa, K. Rasmussen et al. · Clinica Chimica Acta · 1983 · 94 citations

Non-ketotic Dicarboxylic Aciduria, Urology, Significant Organic Acids +5

DICARBOXYLIC ACIDURIA DUE TO MEDIUM CHAIN ACYL CoA DEHYDROGENASE DEFECT

P. Divry, Manuel Gomes David, N. Gregersen et al. · Acta Paediatrica · 1983 · 52 citations