Literature DB >> 6775141

Enzyme inhibition as a possible cause of secondary increases in metabolite levels in patients with inborn errors of metabolism.

T Palmer, M Ameen.   

Abstract

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Year:  1980        PMID： 6775141     DOI： 10.1007/bf02312530

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  7 in total

1.  Purification and properties of L-lysine-alpha-ketoglutarate reductase from human placenta.

Authors:  T A Fjellstedt; J C Robinson
Journal:  Arch Biochem Biophys       Date:  1975-06       Impact factor: 4.013

2.  Letter: The presence of the homoanalogues of substrates of the urea cycle in the presence of argininosuccinate synthetase deficiency.

Authors:  L Cathelineau; J M Saudubray; C Charpentier; C Polonovski
Journal:  Pediatr Res       Date:  1974-10       Impact factor: 3.756

3.  Citrullinemia and an alternative urea cycle.

Authors:  B Levin; V G Oberholzer; T Palmer
Journal:  Pediatr Res       Date:  1973-08       Impact factor: 3.756

4.  Citrullinemia: a new case, with implications concerning adaptation to defective urea synthesis.

Authors:  A Scott-Emuakpor; J V Higgins; A F Kohrman
Journal:  Pediatr Res       Date:  1972-07       Impact factor: 3.756

5.  Saccharopinuria: a new inborn error of lysine metabolism.

Authors:  N A Carson; B G Scally; D W Neill; L J Carré
Journal:  Nature       Date:  1968-05-18       Impact factor: 49.962

6.  Biosynthesis and degradation of saccharopine, an intermediate of lysine metabolism.

Authors:  F C Fellows
Journal:  Biochem J       Date:  1973-10       Impact factor: 3.857

Review 7.  Hereditary metabolic disorders of the urea cycle.

Authors:  B Levin
Journal:  Adv Clin Chem       Date:  1971       Impact factor: 5.394
  7 in total

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