Literature DB >> 6712135

The routine investigation of urinary organic acids in selected paediatric patients: results over a 2 1/2-year period.

M J Bennett, A Green, R J Pollitt, E Worthy.   

Abstract

Over a 2 1/2-year period 13 patients with inborn errors of organic acid metabolism, excluding undifferentiated lactic acidosis, have been diagnosed in our laboratories. The diagnostic yield in patients who had not previously been investigated by organic acid chromatography was 1 in 25, the majority of cases having presented with metabolic acidosis. A larger number of non-specific abnormalities were also detected. This type of investigation is beset with pitfalls and is extremely labour intensive.

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Year:  1984        PMID: 6712135     DOI: 10.1177/000456328402100108

Source DB:  PubMed          Journal:  Ann Clin Biochem        ISSN: 0004-5632            Impact factor:   2.057


  4 in total

1.  The incidence and presentation of dicarboxylic aciduria.

Authors:  M J Bennett; E Worthy; R J Pollitt
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

2.  Azelaic and pimelic acids: metabolic intermediates or artefacts?

Authors:  M J Bennett; M C Ragni; I Hood; D E Hale
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

3.  Biochemical investigations on a patient with a defect in cytosolic acetoacetyl-CoA thiolase, associated with mental retardation.

Authors:  M J Bennett; G P Hosking; M F Smith; R G Gray; B Middleton
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

4.  Urinary organic acids in succinic semialdehyde dehydrogenase deficiency: evidence of alpha-oxidation of 4-hydroxybutyric acid, interaction of succinic semialdehyde with pyruvate dehydrogenase and possible secondary inhibition of mitochondrial beta-oxidation.

Authors:  G K Brown; C H Cromby; N J Manning; R J Pollitt
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

  4 in total

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