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22. Evaluation of liver fatty acid oxidation in the leptin-deficient obese mouse. Brix AE; Elgavish A; Nagy TR; Gower BA; Rhead WJ; Wood PA Mol Genet Metab; 2002 Mar; 75(3):219-26. PubMed ID: 11914033 [TBL] [Abstract][Full Text] [Related]
23. Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy. Westermann CM; Dorland L; Votion DM; de Sain-van der Velden MG; Wijnberg ID; Wanders RJ; Spliet WG; Testerink N; Berger R; Ruiter JP; van der Kolk JH Neuromuscul Disord; 2008 May; 18(5):355-64. PubMed ID: 18406615 [TBL] [Abstract][Full Text] [Related]
24. Is autism a disorder of fatty acid metabolism? Possible dysfunction of mitochondrial beta-oxidation by long chain acyl-CoA dehydrogenase. Clark-Taylor T; Clark-Taylor BE Med Hypotheses; 2004; 62(6):970-5. PubMed ID: 15142659 [TBL] [Abstract][Full Text] [Related]
25. Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: report of two siblings. Catzeflis C; Bachmann C; Hale DE; Coates PM; Wiesmann U; Colombo JP; Joris F; Délèze G Eur J Pediatr; 1990 May; 149(8):577-81. PubMed ID: 2347356 [TBL] [Abstract][Full Text] [Related]
27. Molecular analysis of medium chain acyl-CoA dehydrogenase deficiency. Strauss AW; Duran M; Zhang ZF; Alpers R; Kelly DP Prog Clin Biol Res; 1990; 321():609-23. PubMed ID: 2326315 [No Abstract] [Full Text] [Related]
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29. Molecular cloning and nucleotide sequence of cDNAs encoding human short chain acyl-CoA dehydrogenase and study of the molecular basis of human short chain acyl-CoA dehydrogenase deficiency. Naito E; Ozasa H; Ikeda Y; Tanaka K Prog Clin Biol Res; 1990; 321():625-32. PubMed ID: 2326316 [No Abstract] [Full Text] [Related]
30. Short-chain acyl-CoA dehydrogenase deficiency associated with a lipid-storage myopathy and secondary carnitine deficiency. Turnbull DM; Bartlett K; Stevens DL; Alberti KG; Gibson GJ; Johnson MA; McCulloch AJ; Sherratt HS N Engl J Med; 1984 Nov; 311(19):1232-6. PubMed ID: 6493275 [No Abstract] [Full Text] [Related]
31. Pathologic characterization of short-chain acyl-CoA dehydrogenase deficiency in BALB/cByJ mice. Armstrong DL; Masiowski ML; Wood PA Am J Med Genet; 1993 Nov; 47(6):884-92. PubMed ID: 8279487 [TBL] [Abstract][Full Text] [Related]
32. Functional correction of short-chain acyl-CoA dehydrogenase deficiency in transgenic mice: implications for gene therapy of human mitochondrial enzyme deficiencies. Kelly CL; Rhead WJ; Kutschke WK; Brix AE; Hamm DA; Pinkert CA; Lindsey JR; Wood PA Hum Mol Genet; 1997 Sep; 6(9):1451-5. PubMed ID: 9285781 [TBL] [Abstract][Full Text] [Related]
34. Screening of the most common medium-chain acyl CoA dehydrogenase (MCAD) deficiency mutation (K329E) in the Czech newborn population. Kozàk L; Hrabincovà E; Rudolfoà J; Vràbelovà S; Freiberger T Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():49-50. PubMed ID: 11400780 [TBL] [Abstract][Full Text] [Related]
35. The tissue-specific and developmental regulation of expression of rat medium-chain acyl-CoA dehydrogenase mRNA. Kelly DP; Strauss AW Prog Clin Biol Res; 1990; 321():599-608. PubMed ID: 2326314 [No Abstract] [Full Text] [Related]
36. [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]
37. Medium chain acyl-CoA dehydrogenase deficiency in the United Kingdom. Curtis D; Blakemore AI; Engel PC; Kolvraa S; Gregersen N; Pollitt RJ Prog Clin Biol Res; 1992; 375():489-94. PubMed ID: 1438392 [No Abstract] [Full Text] [Related]