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Clinical Chemistry|May 1, 1981
Laser nephelometry of orosomucoid in serum of newborns: reference intervals and relation to bacterial infectionsJ Bienvenu, L Sann, F Bienvenu, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|August 15, 1983
General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three casesN Gregersen, S Kølvraa, K Rasmussen, et al.Annales Pharmaceutiques Francaises|October 16, 1999
[Prenatal diagnosis of genetic diseases in France]M MathieuComparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1985
Partial characterisation of aspartate transcarbamylase from the mantle of the mussel Mytilus edulisM MathieuArchives Francaises De Pediatrie|June 1, 1993
[Generalized epilepsy disclosing medium-chain-acyl-CoA dehydrogenase deficiency]B Chabrol, J Mancini, C Bertrand, et al.Pediatrie|January 1, 1993
[Multiple acyl-CoA dehydrogenase deficiency. Report of 2 siblings]N Guffon, C Vianey-Saban, J C Berthier, et al.Acta Paediatrica Scandinavica|November 1, 1983
Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhoodP Divry, M David, N Gregersen, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1996
Acylcarnitine removal in a patient with acyl-CoA beta-oxidation deficiency disorder: effect of L-carnitine therapy and starvationM Fontaine, G Briand, L Vallée, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|July 10, 1998
Metabolic studies in a patient with severe carnitine palmitoyltransferase type II deficiencyM Fontaine, G Briand, C Largillière, et al.Pediatrie|December 1, 1984
[Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency]J P Collet, P Divry, J F Blanc, et al.Pageof 37