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40A new family affected by the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuria, Journal of Inherited Metabolic Disease Pyroglutamic acid as a marker of increased orotic acid, Journal of Inherited Metabolic Disease Hyperexcretion of homocitrulline in a Malaysian patient with lysinuric protein intolerance, European Journal of Pediatrics Inhibitory effect of intravenous lysine infusion on urea cycle metabolism, European Journal of Pediatrics Ornithine transcarbamylase deficiency combined with type 1 diabetes mellitus - a challenge in clinical and dietary management, Journal of Diabetes & Metabolic Disorders Effect of ammonium chloride on homocitrulline and homoarginine synthesis from lysine, Journal of Inherited Metabolic Disease D??nnschichtchromatographie von s??ure- und ??therl??slichen DNP-Aminos??uren im Urin, Klinische Wochenschrift Fructose 1,6-bisphosphatase: Dissociation of AMP cooperativity and AMP inhibition by carbamylation, Journal of Protein Chemistry Disorders of Ornithine Metabolism, Inborn Metabolic Diseases Hyperornithinemias, Inborn Metabolic Diseases