C. Bertrand

Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblasts.

P. Divry, C. Vianey‐Saban, M. Mathieu, 1992, Clinica chimica acta; international journal of clinical chemistry.

Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts.

C. Vianey‐Saban, M. Zabot, C. Largillière, 1993, Biochimica et biophysica acta.

Mitochondrial very long chain acyl-CoA dehydrogenase deficiency--a new disorder of fatty acid oxidation.

N. Kacet, M. Fontaine, C. Largillière, 1995, Archives of disease in childhood. Fetal and neonatal edition.

Carnitine palmitoyl transferase I deficiency presenting as a Reye-like syndrome without hypoglycaemia

P. Divry, D. Floret, M. Mathieu, 1993, European Journal of Pediatrics.