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European Journal of Pediatrics|December 22, 1999
Liver transplantation in propionic acidaemiaJ M Saudubray, G Touati, P Delonlay, et al.Human Molecular Genetics|November 25, 2000
Hyperammonemia with reduced ornithine, citrulline, arginine and proline: a new inborn error caused by a mutation in the gene encoding delta(1)-pyrroline-5-carboxylate synthaseM R Baumgartner, C A Hu, S Almashanu, et al.Medical Hypotheses|August 23, 2001
Mental retardation in Down syndrome: a hydrogen sulfide hpothesisP KamounJournal of Inherited Metabolic Disease|January 1, 1995
Liver transplantation in two cases of propionic acidaemiaJ S Schlenzig, F Poggi-Travert, J Laurent, et al.Neuromuscular Disorders : NMD|March 29, 2000
Genotype/phenotype correlation in carnitine palmitoyl transferase II deficiency: lessons from a compound heterozygous patientL Thuillier, C Sevin, F Demaugre, et al.Journal of Inherited Metabolic Disease|January 1, 1996
Metabolic intermediates in lactic acidosis: compounds, samples and interpretationF Poggi-Travert, D Martin, T Billette de Villemeur, et al.Medical Hypotheses|April 1, 2014
Gene therapy: a novel way to treat respiratory failure?Pierre P KamounMedical Hypotheses|November 1, 1980
Is type 1b glycogenosis related to an anomeric preference for glucose-6-phosphate uptake by hepatic microsomes?P P KamounPageof 144