SYSTEME PEPTIDASIQUE DE STREPTOCOCCUS THERMOPHILUS 160. ETUDE D'UNE DIPEPTIDASE ET D'UNE AMINOPEPTIDASERABIER D.1972; ; S.L.; DA. 1972; PP. 1-37; H.T. 36; BIBL. 2 P.; (THESE DOCT. 3EME CYCLE, SPEC. BIOCHIM.; PARIS-SUD)Thesis

INVENTAIRE DES DIFFERENTES ACTIVITES PEPTIDASIQUES INTRACELLULAIRES DE STREPTOCOCCUS THERMOPHILUS. PURIFICATION ET PROPRIETES D'UNE DIPEPTIDE-HYDROLASE ET D'UNE AMINOPEPTIDASERABIER D; DESMAZEAUD MJ.1973; BIOCHIMIE; FR.; DA. 1973; VOL. 55; NO 4; PP. 389-404; ABS. ANGL.; BIBL. 31REF.Serial Issue

PREPARATION RAPIDE D'ORNITHINE-CARBAMYL TRANSFERASE DEPOURVUE D'ACTIVITE CARBAMYLPHOSPHATE SYNTHETASERABIER D; CATHELINEAU L; KAMOUN P et al.1978; ANN. BIOL. CLIN.; FRA; DA. 1978; VOL. 36; NO 5; PP. 449-451; ABS. ENG; BIBL. 8 REF.Article

INDUCTION OF UREA CYCLE ENZYMES BY GLUCAGON AND DESCAMETHASONE IN MONOLAYER CULTURES OF ADULT RAT HEPATOCYTESLIN RC; SNODGRASS PJ; RABIER D et al.1982; JOURNAL OF BIOLOGICAL CHEMISTRY; ISSN 0021-9258; USA; DA. 1982; VOL. 257; NO 9; PP. 5061-5067; BIBL. 34 REF.Article

BIOCHIMIE CELLULAIRE. ROLE DE L'ACETYLGLUTAMATE DANS LA STIMULATION DE LA CITRULLINOGENESE PAR LE GLUCAGONCATHELINEAU L; RABIER D; PETIT F et al.1980; C.R. HEBD. SEANCES ACAD. SCI., D; ISSN 0567-655X; FRA; DA. 1980; VOL. 291; NO 7; PP. 625-627; ABS. ENG; BIBL. 14 REF.Article

Hyperammoniémie et déficit héréditaires du cycle de l'uréeRABIER, D; CATHELINEAU, L.Le Pédiatre. 1990, Vol 26, Num 124, pp 205-215, issn 0397-9180, 10 p.Article

LA MALADIE FIBRO-KYSTIQUE DU PANCREAS: ACCUMULATION DE PEPTIDES A ACTIVITE PHLOGISTIQUE.LESEC G; NEZELOF C; RABIER D et al.1976; NOUV. PRESSE MED.; FR.; DA. 1976; VOL. 5; NO 37; PP. 2470; BIBL. 6 REF.Article

ORNITHINE TRANSCARBAMYLASE DEFICIENCIES IN HUMAN MALES. KINETIC AND IMMUNOCHEMICAL CLASSIFICATIONBRIAND P; FRANCOIS B; RABIER D et al.1982; BIOCHIM. BIOPHYS. ACTA; ISSN 0006-3002; NLD; DA. 1982; VOL. 704; NO 1; PP. 100-106; BIBL. 27 REF.Article

PROPIONATE AND SUCCINATE EFFECTS ON ACETYL GLUTAMATE BIOSYNTHESIS BY RAT LIVER MITOCHONDRIARABIER D; CATHELINEAU L; BRIAND P et al.1979; BIOCHEM. BIOPHYS. RES. COMMUNIC.; USA; DA. 1979; VOL. 91; NO 2; PP. 456-460; BIBL. 18 REF.Article

Early amniocentesis and amniotic fluid organic acid levels in the prenatal diagnosis of organic acidemiasCOUDE, M; CHADEFAUX, B; RABIER, D et al.Clinica chimica acta. 1990, Vol 187, Num 3, pp 329-332, issn 0009-8981Article

A scheme for the interpretation of primary and secondary disturbances of plasma and urinary amino acid profiles. A possible way to an expert systemPARVY, P; BARDET, J; RABIER, D et al.Clinica chimica acta. 1995, Vol 235, Num 1, pp 1-10, issn 0009-8981Article

Ornithine transcarbamylase and disaccharidase activities in damaged intestinal mucosa of children ― diagnosis of hereditary ornithine transcarbamylase deficiency in mucosaCATHELINEAU, L; BRIAND, P; RABIER, D et al.Journal of pediatric gastroenterology and nutrition. 1985, Vol 4, Num 6, pp 960-964, issn 0277-2116Article

Prenatal diagnosis of ornithine transcarbamylase deficiency : results in SPF^ASH miceMONASTIRI, K; RABIER, D; KAMOUN, P et al.Prenatal diagnosis. 1993, Vol 13, Num 6, pp 441-447, issn 0197-3851Article

Hyperlysinémie et hyperammoniémie = Hyperlysinemia and hyperammonemiaRABIER, D; PARVY, P; BERDET, J et al.Annales de biologie clinique (Paris). 1991, Vol 49, Num 1, pp 45-48, issn 0003-3898Conference Paper

Diagnostic prénatal des enzymopathies du cycle de l'urée = Prenatal diagnosis of enzymopathies of the urea cycleCHADEFAUX, B; RABIER, D; KAMOUN, P et al.Annales de biologie clinique (Paris). 1988, Vol 46, Num 7, pp 471-476, issn 0003-3898Conference Paper

Hypocarnitinaemia in Menkes diseaseKAMOUN, P; MAYER, M; RABIER, D et al.European journal of pediatrics. 1989, Vol 148, Num 8, issn 0340-6199, 788 [1 p.]Article

Contribution of fetal MR imaging in the prenatal diagnosis of zellweger syndromeMOCHEL, F; GREBILLE, A.-G; BENACHI, A et al.American journal of neuroradiology. 2006, Vol 27, Num 2, pp 333-336, issn 0195-6108, 4 p.Article

Trends in serum citrulline and acute rejection among recipients of small bowel transplantsPAPPAS, P. A; TZAKIS, A. G; NISHIDA, S et al.Transplantation proceedings. 2004, Vol 36, Num 2, pp 345-347, issn 0041-1345, 3 p.Conference Paper

Response of nitric oxide pathway to L-arginine infusion at the altitude of 4,350 mSCHNEIDER, J-C; BLAZY, I; DECHAUX, M et al.The European respiratory journal. 2001, Vol 18, Num 2, pp 286-292, issn 0903-1936Article

Genetic hypoglycaemia in infancy and childhood : Pathophysiology and diagnosisSAUDUBRAY, J. M; DE LONLAY, P; VASSAULT, A et al.Journal of inherited metabolic disease. 2000, Vol 23, Num 3, pp 197-214, issn 0141-8955Conference Paper

Tolerance to starvation in children on long-term total parenteral nutritionFRANCOIS, B; COLOMB, V; BONNEFONT, J. P et al.Clinical nutrition (Edinburgh). 1997, Vol 16, Num 3, pp 113-117, issn 0261-5614Article

Differing clinical presentation of succinic semialdehyde dehydrogenase deficiency in adolescent siblings from Lifu Island, New CaledoniaGIBSON, K. M; DOSKEY, A. E; RABIER, D et al.Journal of inherited metabolic disease. 1997, Vol 20, Num 3, pp 370-374, issn 0141-8955Conference Paper

Hypopigmentation in hemodialysis : acquired hair and skin fairness in a uremic patient undergoing maintenance hemodialysis : case report and review of the literatureBEN HMIDA, M; TURKI, H; HACHICHA, J et al.Dermatology (Basel). 1996, Vol 192, Num 2, pp 148-152, issn 1018-8665Article

Most cases of medium-chain acyl-CoA dehydrogenase deficiency escape detection in FranceFROMENTY, B; MANSOURI, A; BONNEFONT, J.-P et al.Human genetics. 1996, Vol 97, Num 3, pp 367-368, issn 0340-6717Article

Abnormal α-aminoadipic acid excretion in a newborn with a defect in platelet aggregation and antenatal cerebral haemorrhageCANDITO, M; RICHELME, C; PARVY, P et al.Journal of inherited metabolic disease. 1995, Vol 18, Num 1, pp 56-60, issn 0141-8955Article