Detection of inborn errors of fatty acid oxidation from acylcarnitine analysis of plasma and blood spots with the radioisotopic exchange-high-performance liquid chromatographic method-Reference-Cited by-同舟云学术

Detection of inborn errors of fatty acid oxidation from acylcarnitine analysis of plasma and blood spots with the radioisotopic exchange-high-performance liquid chromatographic method

Published:1993-05 Issue:5 Volume:122 Page:708-714
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Schmidt-Sommerfeld Eberhard,Penn Duna,Duran Marinus,Bennett Michael J.,Santer Rene,Stanley Charles A.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference16 articles.

1. Acyl-CoA dehydrogenase deficiencies;Roe,1989

2. Medium-chain acyl-CoA dehydrogenase deficiency: diagnosis by stable isotope dilution measurement of urinary n-hexanoylglycine and 3-phenyl propionylglycine;Rinaldo;N Engl J Med,1989

3. Application of high resolution fast atom bombardment and constant B/E ratio linked scanning to the identification and analysis of acylcarnitines in metabolic disease;Millington;Biomedical and Environmental Mass Spectrometry,1984

4. Quantitation of urinary carnitine esters in a patient with medium-chain acyl-coenzyme A dehydrogenase deficiency: effect of metabolic state and l-carnitine therapy;Schmidt-Sommerfeld;J Pediatr,1989

5. Urinary medium-chain acylcarnitines in medium-chain acyl-CoA dehydrogensase deficiency, medium-chain triglyceride feeding and valproic acid therapy: sensitivity and specificity of the radioisotopic exchange/HPLC method;Schmidt-Sommerfeld;Pediatr Res,1992

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