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Journal of Inherited Metabolic Disease|May 10, 2002
Plasma lysine concentration and availability of 2-ketoglutarate in liver mitochondriaP Kamoun, V Richard, D Rabier, et al.Prenatal Diagnosis|May 1, 1990
Glycine/serine ratio and the prenatal diagnosis of non-ketotic hyperglycinaemiaP Parvy, D Rabier, J Boue, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 1, 1994
[Protocol of metabolic investigations in hereditary metabolic diseases]F Poggi, D Rabier, A Vassault, 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.Annales De Biologie Clinique|January 1, 1988
[Prenatal diagnosis of enzymopathies of the urea cycle]B Chadefaux, D Rabier, P KamounPrenatal Diagnosis|June 1, 1993
Prenatal diagnosis of ornithine transcarbamylase deficiency: results in Spfash miceK Monastiri, D Rabier, P KamounAnnales De Biologie Clinique|January 1, 1978
[Rapid preparation of ornithine carbamyl transferase without carbamyl phosphate synthetase activity (author's transl)]D Rabier, L Cathelineau, P KamounBulletin De L'Academie Nationale De Medecine|June 12, 1998
[A new inherited metabolic disease: delta1-pyrroline 5-carboxylate synthetase deficiency]P Kamoun, B Aral, J M SaudubrayPageof 39