Literature DB >> 4522834

Urinary excretion of C6-C10 dicarboxylic acids in glycogen storage disease types I and 3.

J Dosman, J C Crawhall, G A Klassen, O A Mamer, P Neumann.   

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Year:  1974        PMID： 4522834     DOI： 10.1016/0009-8981(74)90065-5

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN： 0009-8981            Impact factor:   3.786


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  4 in total

1.  Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease.

Authors:  C E Mize; L J Waber; T Anderson; M J Bennett
Journal:  J Inherit Metab Dis       Date:  1997-07       Impact factor: 4.982

2.  Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency.

Authors:  J Bergoffen; P Kaplan; D E Hale; M J Bennett; G T Berry
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

3.  Catalytic defect of medium-chain acyl-coenzyme A dehydrogenase deficiency. Lack of both cofactor responsiveness and biochemical heterogeneity in eight patients.

Authors:  B A Amendt; W J Rhead
Journal:  J Clin Invest       Date:  1985-09       Impact factor: 14.808

4.  Intermittent non-ketotic dicarboxylic aciduria in two siblings with hypoglycaemia: an apparent defect in beta-oxidation of fatty acids.

Authors:  E W Naylor; L L Mosovich; R Guthrie; J E Evans; H Tieckelmann
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982
  4 in total

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