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68. [Multiple acyl-CoA dehydrogenase deficiency. Report of 2 siblings]. Guffon N; Vianey-Saban C; Berthier JC; Till M; Bertrand C; Divry P; Guibaud P Pediatrie; 1993; 48(5):365-71. PubMed ID: 7777389 [TBL] [Abstract][Full Text] [Related]
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70. Effect of treatment with glycine and L-carnitine in medium-chain acyl-coenzyme A dehydrogenase deficiency. Rinaldo P; Schmidt-Sommerfeld E; Posca AP; Heales SJ; Woolf DA; Leonard JV J Pediatr; 1993 Apr; 122(4):580-4. PubMed ID: 8463904 [TBL] [Abstract][Full Text] [Related]
71. A method for quantitative acylcarnitine profiling in human skin fibroblasts using unlabelled palmitic acid: diagnosis of fatty acid oxidation disorders and differentiation between biochemical phenotypes of MCAD deficiency. Okun JG; Kölker S; Schulze A; Kohlmüller D; Olgemöller K; Lindner M; Hoffmann GF; Wanders RJ; Mayatepek E Biochim Biophys Acta; 2002 Oct; 1584(2-3):91-8. PubMed ID: 12385891 [TBL] [Abstract][Full Text] [Related]
72. Hypoglycaemia and elevated urine ethylmalonic acid in a child homozygous for the short-chain acyl-CoA dehydrogenase 625G > A gene variation. Birkebaek NH; Simonsen H; Gregersen N Acta Paediatr; 2002; 91(4):480-2. PubMed ID: 12061367 [TBL] [Abstract][Full Text] [Related]
73. 3-Hydroxyoctanoic aciduria: identification of a new organic acid in the urine of a patient with non-ketotic hypoglycemia. Kelley RI; Morton DH Clin Chim Acta; 1988 Jun; 175(1):19-26. PubMed ID: 3168281 [TBL] [Abstract][Full Text] [Related]
74. Ethylmalonic/adipic aciduria: effects of oral medium-chain triglycerides, carnitine, and glycine on urinary excretion of organic acids, acylcarnitines, and acylglycines. Rinaldo P; Welch RD; Previs SF; Schmidt-Sommerfeld E; Gargus JJ; O'Shea JJ; Zinn AB Pediatr Res; 1991 Sep; 30(3):216-21. PubMed ID: 1945558 [TBL] [Abstract][Full Text] [Related]
75. Medium-chain triglyceride medication as a pitfall in the diagnosis of non-ketotic C6-C10-dicarboxylic acidurias. Mortensen PB; Gregersen N Clin Chim Acta; 1980 Apr; 103(1):33-7. PubMed ID: 7389114 [TBL] [Abstract][Full Text] [Related]
76. Medium- and long-chain dicarboxylic aciduria in patients with Zellweger syndrome and neonatal adrenoleukodystrophy. Rocchiccioli F; Aubourg P; Bougnères PF Pediatr Res; 1986 Jan; 20(1):62-6. PubMed ID: 3945517 [TBL] [Abstract][Full Text] [Related]
77. The possible antiketogenic and gluconeogenic effect of the omega-oxidation of fatty acids in rats. Mortensen PB Biochim Biophys Acta; 1980 Nov; 620(2):177-85. PubMed ID: 7437451 [TBL] [Abstract][Full Text] [Related]
78. 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]
79. The oxidation of dicarboxylic acid CoA esters via peroxisomal fatty acyl-CoA oxidase. Poosch MS; Yamazaki RK Biochim Biophys Acta; 1989 Dec; 1006(3):291-8. PubMed ID: 2688746 [TBL] [Abstract][Full Text] [Related]
80. Glutaric aciduria Type II. Sweetman L; Nyhan WL; Tauner DA; Merritt TA; Singh M J Pediatr; 1980 Jun; 96(6):1020-6. PubMed ID: 7373461 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]