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Journal Abstract Search
153 related items for PubMed ID: 8145917
1. Very long-chain acyl coenzyme A dehydrogenase deficiency presenting with exercise-induced myoglobinuria. Ogilvie I, Pourfarzam M, Jackson S, Stockdale C, Bartlett K, Turnbull DM. Neurology; 1994 Mar; 44(3 Pt 1):467-73. PubMed ID: 8145917 [Abstract] [Full Text] [Related]
2. A heterozygous missense mutation in adolescent-onset very long-chain acyl-CoA dehydrogenase deficiency with exercise-induced rhabdomyolysis. Hisahara S, Matsushita T, Furuyama H, Tajima G, Shigematsu Y, Imai T, Shimohama S. Tohoku J Exp Med; 2015 Apr; 235(4):305-10. PubMed ID: 25843429 [Abstract] [Full Text] [Related]
3. Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndrome. Treem WR, Witzleben CA, Piccoli DA, Stanley CA, Hale DE, Coates PM, Watkins JB. Hepatology; 1986 Apr; 6(6):1270-8. PubMed ID: 3793003 [Abstract] [Full Text] [Related]
4. A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase. Aoyama T, Uchida Y, Kelley RI, Marble M, Hofman K, Tonsgard JH, Rhead WJ, Hashimoto T. Biochem Biophys Res Commun; 1993 Mar 31; 191(3):1369-72. PubMed ID: 8466512 [Abstract] [Full Text] [Related]
5. Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse. Cox KB, Hamm DA, Millington DS, Matern D, Vockley J, Rinaldo P, Pinkert CA, Rhead WJ, Lindsey JR, Wood PA. Hum Mol Genet; 2001 Sep 15; 10(19):2069-77. PubMed ID: 11590124 [Abstract] [Full Text] [Related]
6. Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients. Vianey-Saban C, Divry P, Brivet M, Nada M, Zabot MT, Mathieu M, Roe C. Clin Chim Acta; 1998 Jan 12; 269(1):43-62. PubMed ID: 9498103 [Abstract] [Full Text] [Related]
7. The acyl-CoA dehydrogenation deficiencies. Recent advances in the enzymic characterization and understanding of the metabolic and pathophysiological disturbances in patients with acyl-CoA dehydrogenation deficiencies. Gregersen N. Scand J Clin Lab Invest Suppl; 1985 Jan 12; 174():1-60. PubMed ID: 3892650 [Abstract] [Full Text] [Related]
8. Complementation analysis of fatty acid oxidation disorders. Moon A, Rhead WJ. J Clin Invest; 1987 Jan 12; 79(1):59-64. PubMed ID: 3793932 [Abstract] [Full Text] [Related]
9. Immunochemical characterization of variant long-chain acyl-CoA dehydrogenase in cultured fibroblasts from nine patients with long-chain acyl-CoA dehydrogenase deficiency. Indo Y, Coates PM, Hale DE, Tanaka K. Pediatr Res; 1991 Sep 12; 30(3):211-5. PubMed ID: 1945557 [Abstract] [Full Text] [Related]
10. Very long-chain acyl-CoA dehydrogenase deficiency presenting as acute hypercapnic respiratory failure. Tong MK, Lam CS, Mak TW, Fu MY, Ng SH, Wanders RJ, Tang NL. Eur Respir J; 2006 Aug 12; 28(2):447-50. PubMed ID: 16880373 [Abstract] [Full Text] [Related]
11. Immunochemical characterization of variant medium-chain acyl-CoA dehydrogenase in fibroblasts from patients with medium-chain acyl-CoA dehydrogenase deficiency. Coates PM, Indo Y, Young D, Hale DE, Tanaka K. Pediatr Res; 1992 Jan 12; 31(1):34-8. PubMed ID: 1594327 [Abstract] [Full Text] [Related]
12. Combined enzyme defect of mitochondrial fatty acid oxidation. Jackson S, Kler RS, Bartlett K, Briggs H, Bindoff LA, Pourfarzam M, Gardner-Medwin D, Turnbull DM. J Clin Invest; 1992 Oct 12; 90(4):1219-25. PubMed ID: 1401059 [Abstract] [Full Text] [Related]
14. Altered Energetics of Exercise Explain Risk of Rhabdomyolysis in Very Long-Chain Acyl-CoA Dehydrogenase Deficiency. Diekman EF, Visser G, Schmitz JP, Nievelstein RA, de Sain-van der Velden M, Wardrop M, Van der Pol WL, Houten SM, van Riel NA, Takken T, Jeneson JA. PLoS One; 2016 Oct 12; 11(2):e0147818. PubMed ID: 26881790 [Abstract] [Full Text] [Related]
16. The effect of dantrolene sodium in Very Long Chain Acyl-CoA Dehydrogenase Deficiency. Voermans NC, Poels PJ, Kluijtmans LA, van Engelen BG. Neuromuscul Disord; 2005 Dec 12; 15(12):844-6. PubMed ID: 16288870 [Abstract] [Full Text] [Related]
17. Rhabdomyolysis caused by an inherited metabolic disease: very long-chain acyl-CoA dehydrogenase deficiency. Voermans NC, van Engelen BG, Kluijtmans LA, Stikkelbroeck NM, Hermus AR. Am J Med; 2006 Feb 12; 119(2):176-9. PubMed ID: 16443431 [No Abstract] [Full Text] [Related]