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Annales De Biologie Clinique|January 1, 1991
[Lysine metabolism in man]C Vianey-Liaud, P Divry, C Poinas, et al.Human Mutation|June 22, 2000
Identification of 5 novel mutations in the AGXT geneO Basmaison, M O Rolland, P Cochat, et al.Annals of Neurology|January 1, 1993
3-Methylglutaconic aciduria in "optic atrophy plus"H Costeff, O Elpeleg, N Apter, et al.Journal of Inherited Metabolic Disease|January 1, 1996
Stable-isotope selected-ion monitoring quantification of methylmalonic acid in dried filter-paper urine samplesJ M Parnet, P Divry, C Vianey-Saban, et al.Journal of Neurology|February 14, 1978
Erythrocyte ghost (Na+ + K+) ATPase activity in mice with hereditary muscular dystrophy (strain C57 BL/64J/dy)G Souweine, M O Rolland, I Maire, et al.Journal of Inherited Metabolic Disease|February 22, 2000
Effect of sodium benzoate in the treatment of atypical nonketotic hyperglycinaemiaJ M Neuberger, S Schweitzer, M O Rolland, et al.Biology of the Neonate|January 1, 1987
Ketogenesis in hypoglycemic neonates. Carnitine and dicarboxylic acids in neonatal hypoglycemiaL Sann, P Divry, B Cartier, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1992
Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblastsC Bertrand, R Dumoulin, P Divry, et al.European Journal of Pediatrics|September 1, 1984
Defective succinic semialdehyde dehydrogenase activity in 4-hydroxybutyric aciduriaK M Gibson, L Sweetman, W L Nyhan, et al.La Revue Du Praticien|November 20, 1997
[Hereditary diseases causing kidney calculi]P Cochat, M Jouvenet, H Pellet, et al.Pageof 14