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Prenatal Diagnosis|February 1, 1988
Prenatal diagnosis of propionic acidemia in chorionic villi by direct assay of propionyl CoA carboxylaseB Chadefaux, C Augereau, D Rabier, et al.Biochimie|January 1, 1983
Developmental changes of citrullinogenesis, mitochondrial N-acetylglutamate content and N-acetylglutamate synthetase in fetal and neonatal ratsD Rabier, P Briand, F X Coude, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|December 29, 1989
Ornithine carbamoyltransferase deficiency. A new variant with subnormal enzyme activityD Rabier, A Benoit, F Petit, et al.Annales De Biologie Clinique|January 1, 1988
[Genetic counseling in ornithine carbamoyltransferase deficiency]A Pelet, E Toumas, D Rabier, et al.Chirurgie; Memoires De L'Academie De Chirurgie|January 1, 1993
[Intrasplenic transplantation of hepatocytes in spf-ash mice with congenital ornithine transcarbamylase deficiency]J L Michel, D Rabier, C Rambaud, et al.Annales De Genetique|January 1, 1990
[Cri-du-chat disease: plasma and urinary amino acids]J Lejeune, M O Rethoré, M Peeters, et al.Prenatal Diagnosis|July 1, 1996
Gestational age-related reference values for amniotic fluid amino acids: a useful tool for prenatal diagnosis of aminoacidopathiesD Rabier, B Chadefaux-Vekemans, J F Oury, et al.Journal of Inherited Metabolic Disease|January 1, 1995
Abnormal alpha-aminoadipic acid excretion in a newborn with a defect in platelet aggregation and antenatal cerebral haemorrhageM Candito, C Richelme, P Parvy, et al.European Journal of Pediatrics|December 22, 1999
Liver transplantation in urea cycle disordersJ M Saudubray, G Touati, P Delonlay, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 1, 1994
[Diagnosis of metabolic coma in children]F Poggi-Travert, B Héron, T Billette de Villemeur, et al.Pageof 144