These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
181 related articles for article (PubMed ID: 4032135)
1. Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids. Duran M; Mitchell G; de Klerk JB; de Jager JP; Hofkamp M; Bruinvis L; Ketting D; Saudubray JM; Wadman SK J Pediatr; 1985 Sep; 107(3):397-404. PubMed ID: 4032135 [TBL] [Abstract][Full Text] [Related]
2. Oxidation of fatty acids in cultured fibroblasts: a model system for the detection and study of defects in oxidation. Saudubray JM; Coudé FX; Demaugre F; Johnson C; Gibson KM; Nyhan WL Pediatr Res; 1982 Oct; 16(10):877-81. PubMed ID: 7145511 [TBL] [Abstract][Full Text] [Related]
4. Abnormal urinary excretion of unsaturated dicarboxylic acids in patients with medium-chain acyl-CoA dehydrogenase deficiency. Tserng KY; Jin SJ; Kerr DS; Hoppel CL J Lipid Res; 1990 May; 31(5):763-71. PubMed ID: 2380628 [TBL] [Abstract][Full Text] [Related]
5. Octanoylglucuronide excretion in patients with a defective oxidation of medium-chain fatty acids. Duran M; Ketting D; van Vossen R; Beckeringh TE; Dorland L; Bruinvis L; Wadman SK Clin Chim Acta; 1985 Nov; 152(3):253-60. PubMed ID: 4064333 [TBL] [Abstract][Full Text] [Related]
6. Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency. Duran M; Hofkamp M; Rhead WJ; Saudubray JM; Wadman SK Pediatrics; 1986 Dec; 78(6):1052-7. PubMed ID: 3786030 [TBL] [Abstract][Full Text] [Related]
7. The differential diagnosis of dicarboxylic aciduria. Duran M; De Klerk JB; Wadman SK; Bruinvis L; Ketting D J Inherit Metab Dis; 1984; 7 Suppl 1():48-51. PubMed ID: 6434845 [TBL] [Abstract][Full Text] [Related]
8. A new patient with dicarboxylic aciduria suggestive of medium-chain Acyl-CoA dehydrogenase deficiency presenting as Reye's syndrome. Del Valle JA; Garcia MJ; Merinero B; Pérez-Cerdá C; Roman F; Jimenez A; Ugarte M; Martínez-Pardo M; Ludeña C; Camarero C J Inherit Metab Dis; 1984; 7(2):62-4. PubMed ID: 6434827 [TBL] [Abstract][Full Text] [Related]
9. General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases. Gregersen N; Kølvraa S; Rasmussen K; Mortensen PB; Divry P; David M; Hobolth N Clin Chim Acta; 1983 Aug; 132(2):181-91. PubMed ID: 6616873 [TBL] [Abstract][Full Text] [Related]
10. Diagnostic and therapeutic implications of medium-chain acylcarnitines in the medium-chain acyl-coA dehydrogenase deficiency. Roe CR; Millington DS; Maltby DA; Bohan TP; Kahler SG; Chalmers RA Pediatr Res; 1985 May; 19(5):459-66. PubMed ID: 4000772 [TBL] [Abstract][Full Text] [Related]
11. Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhood. Divry P; David M; Gregersen N; Kølvraa S; Christensen E; Collet JP; Dellamonica C; Cotte J Acta Paediatr Scand; 1983 Nov; 72(6):943-9. PubMed ID: 6673498 [TBL] [Abstract][Full Text] [Related]
12. [Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency]. Collet JP; Divry P; Blanc JF; Guibaud P; David M; Macabeo V; Vibert J; Hermier M Pediatrie; 1984 Dec; 39(8):661-8. PubMed ID: 6535973 [TBL] [Abstract][Full Text] [Related]
13. Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiency. Duran M; Bruinvis L; Ketting D; de Klerk JB; Wadman SK Clin Chem; 1988 Mar; 34(3):548-51. PubMed ID: 3349606 [TBL] [Abstract][Full Text] [Related]
14. A comparison of [9,10-3H]palmitic and [9,10-3H]myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblasts. Manning NJ; Olpin SE; Pollitt RJ; Webley J J Inherit Metab Dis; 1990; 13(1):58-68. PubMed ID: 2109149 [TBL] [Abstract][Full Text] [Related]
15. Medium-chain acyl-CoA dehydrogenase deficiency: metabolic effects and therapeutic efficacy of long-term L-carnitine supplementation. Treem WR; Stanley CA; Goodman SI J Inherit Metab Dis; 1989; 12(2):112-9. PubMed ID: 2502671 [TBL] [Abstract][Full Text] [Related]
16. Identification and quantification of intermediates of unsaturated fatty acid metabolism in plasma of patients with fatty acid oxidation disorders. Onkenhout W; Venizelos V; van der Poel PF; van den Heuvel MP; Poorthuis BJ Clin Chem; 1995 Oct; 41(10):1467-74. PubMed ID: 7586519 [TBL] [Abstract][Full Text] [Related]
17. C6-C10-dicarboxylic aciduria: biochemical considerations in relation to diagnosis of beta-oxidation defects. Gregersen N; Kølvraa S; Mortensen PB; Rasmussen K Scand J Clin Lab Invest Suppl; 1982; 161():15-27. PubMed ID: 6959231 [TBL] [Abstract][Full Text] [Related]
18. C6-C10-dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defects. Gregersen N; Wintzensen H; Christensen SK; Christensen MF; Brandt NJ; Rasmussen K Pediatr Res; 1982 Oct; 16(10):861-8. PubMed ID: 7145508 [TBL] [Abstract][Full Text] [Related]
19. Gas chromatography--mass spectrometry (GC--MS) diagnosis of two cases of medium chain acyl-CoA dehydrogenase deficiency. Divry P; Vianey-Liaud C; Cotte J J Inherit Metab Dis; 1984; 7 Suppl 1():44-7. PubMed ID: 6434844 [TBL] [Abstract][Full Text] [Related]
20. Production and disposal of medium-chain fatty acids in children with medium-chain acyl-CoA dehydrogenase deficiency. Heales SJ; Thompson GN; Massoud AF; Rahman S; Halliday D; Leonard JV J Inherit Metab Dis; 1994; 17(1):74-80. PubMed ID: 8051939 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]