Organic acidurias : proceedings of the ninth symposium of the Society for the Study of Inborn Errors of Metabolism / edited by J. Stern and C. Toothill.

  • Society for the Study of Inborn Errors of Metabolism.
Date:
1972
Catalogue details

Licence: Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)

Credit: Organic acidurias : proceedings of the ninth symposium of the Society for the Study of Inborn Errors of Metabolism / edited by J. Stern and C. Toothill. Source: Wellcome Collection.

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    CONTENTS Page Active Participants v Preface viii Ketotic Hyperglycinaemia, W. L. Nyhan, Toshiyuki Ando and Karsten Rasmussen 1 Methylmalonic Aciduria Methylmalonyl CoA Mutase Activity in Leucocytes, В. Levin, V. G. Oberholzer and E. Ann Burgess 9 Discussion 16 Propionic Acidaemia, D. Gompertz 21 Discussion 25 A New Metabolic Error in the Leucine Degradation Pathway: j8-Hydroxyisovaleric Aciduria and /S-Methylcrotonyl Glycinuria, O. Stokke, E. Jellum and L. Eldjarn 27 Tiglyl Glycine Excretion in a Child with ^-Methylcrotonyl Gly¬ cinuria, D. Gompertz and G. H. Draffan 35 Discussion 37 Further Studies on Leigh's Encephalomyelopathy, C. J. de Groot, J. H. P. Jonxis and F. A. Hommes 40 Congenital Lactic Acidosis, K. Schärer 46 Discussion 51 Further Studies on a Family with Hepatic Glycogen Synthetase Deficiency, J. R. W. Dykes and J. Spencer-Peet 54 Discussion 60 p-Hydroxyphenylpyruvic Acid Metabolism in Hereditary Tyro- sinaemia, B. N. LaDu 62 Metabolism of p-Hydroxyphenylpyruvate in Hereditary Tyro- sinaemia, B. Lindblad, G. Lindstedt, S. Lindstedt and Marianne Rundgren 63 Discussion 81 A Variant of Branched-Chain Ketoaciduria, Selma E. Snyderman 87 Discussion 97 Benzoic Aciduria in Chronic Psychoses, T. L. Perry, Shirley Hansen and Donna Lesk 99 Discussion 111 ¡X