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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]
3. 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]
5. Very long chain acyl-coenzyme A dehydrogenase deficiency in two siblings: evolution after prenatal diagnosis and prompt management. Sluysmans T; Tuerlinckx D; Hubinont C; Verellen-Dumoulin C; Brivet M; Vianey-Saban C J Pediatr; 1997 Sep; 131(3):444-6. PubMed ID: 9329424 [TBL] [Abstract][Full Text] [Related]
6. Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes. Coates PM; Hale DE; Stanley CA; Corkey BE; Cortner JA Pediatr Res; 1985 Jul; 19(7):671-6. PubMed ID: 4022673 [TBL] [Abstract][Full Text] [Related]
7. [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]
8. The oxidation of octanoic acid by cultured amniotic fluid cells: the effect of cell type and passage number. Allison F; Barnes IC; Bennett MJ Prenat Diagn; 1988 Jun; 8(5):383-6. PubMed ID: 3405975 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
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. 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]
13. 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]
14. Transient organic aciduria and persistent lacticacidemia in a patient with short-chain acyl-coenzyme A dehydrogenase deficiency. Dawson DB; Waber L; Hale DE; Bennett MJ J Pediatr; 1995 Jan; 126(1):69-71. PubMed ID: 7815229 [TBL] [Abstract][Full Text] [Related]
15. The incidence and presentation of dicarboxylic aciduria. Bennett MJ; Worthy E; Pollitt RJ J Inherit Metab Dis; 1987; 10(3):241-2. PubMed ID: 3123781 [No Abstract] [Full Text] [Related]
16. Neonatal onset of medium-chain acyl-coenzyme A dehydrogenase deficiency with confusing biochemical features. Christodoulou J; Hoare J; Hammond J; Ip WC; Wilcken B J Pediatr; 1995 Jan; 126(1):65-8. PubMed ID: 7815228 [TBL] [Abstract][Full Text] [Related]
17. Clinical and biochemical presentations in 20 cases of hydroxydicarboxylic aciduria. Pollitt RJ Prog Clin Biol Res; 1990; 321():495-502. PubMed ID: 2326308 [No Abstract] [Full Text] [Related]