Literature DB >> 3813638

Inherited disorders of straight chain fatty acid oxidation.

R J Pollitt.   

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Year:  1987        PMID: 3813638      PMCID: PMC1778136          DOI: 10.1136/adc.62.1.6

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


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  7 in total

1.  Defects of metabolism of fatty acids in the sudden infant death syndrome.

Authors:  A J Howat; M J Bennett; S Variend; L Shaw; P C Engel
Journal:  Br Med J (Clin Res Ed)       Date:  1985-06-15

2.  Fluorometric assay of acyl-CoA dehydrogenases in normal and mutant human fibroblasts.

Authors:  F E Frerman; S I Goodman
Journal:  Biochem Med       Date:  1985-02

3.  General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases.

Authors:  N Gregersen; S Kølvraa; K Rasmussen; P B Mortensen; P Divry; M David; N Hobolth
Journal:  Clin Chim Acta       Date:  1983-08-15       Impact factor: 3.786

4.  Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes.

Authors:  C R Roe; D S Millington; D A Maltby; P Kinnebrew
Journal:  J Pediatr       Date:  1986-01       Impact factor: 4.406

5.  Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia.

Authors:  D E Hale; M L Batshaw; P M Coates; F E Frerman; S I Goodman; I Singh; C A Stanley
Journal:  Pediatr Res       Date:  1985-07       Impact factor: 3.756

6.  Dicarboxylic aciduria and medium chain triglyceride supplemented milk.

Authors:  M J Henderson; P R Dear
Journal:  Arch Dis Child       Date:  1986-06       Impact factor: 3.791

7.  Riboflavin-responsive ethylmalonic-adipic aciduria.

Authors:  A Green; T G Marshall; M J Bennett; R G Gray; R J Pollitt
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

  7 in total
  3 in total

Review 1.  Interrelationships of liver and brain with special reference to Reye syndrome.

Authors:  J K Brown; H Imam
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

2.  Acylcoenzyme A dehydrogenase deficiency in heart tissue from infants who died unexpectedly with fatty change in the liver.

Authors:  F Allison; M J Bennett; S Variend; P C Engel
Journal:  Br Med J (Clin Res Ed)       Date:  1988-01-02

3.  The phenylpropionic acid load test: experience with 72 children at-risk for beta-oxidation disorders.

Authors:  J F Glasgow; R Moore; P H Robinson; P J McKiernan
Journal:  Ir J Med Sci       Date:  1992-10       Impact factor: 1.568

  3 in total

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