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22. A skeletal-muscle disorder associated with intermittent symptoms and a possible defect of lipid metabolism. Engel WK; Vick NA; Glueck CJ; Levy RI N Engl J Med; 1970 Mar; 282(13):697-704. PubMed ID: 5416202 [No Abstract] [Full Text] [Related]
23. [Clinical aspects of disorders of lipid metabolism in humans. II. Carnitine palmitoyltransferase deficiency]. Czyzewski K Neurol Neurochir Pol; 1988; 22(6):548-52. PubMed ID: 3077435 [No Abstract] [Full Text] [Related]
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25. Myoglobinuric acute renal failure associated with major urological surgery--an avoidable problem? Nimmo GR; Stewart SM; English PJ Intensive Care Med; 1988; 14(3):244-5. PubMed ID: 3379187 [TBL] [Abstract][Full Text] [Related]
26. Rhabdomyolysis and myoglobinuria as manifestations of child abuse. Schwengel D; Ludwig S Pediatr Emerg Care; 1985 Dec; 1(4):194-7. PubMed ID: 3842165 [TBL] [Abstract][Full Text] [Related]
27. [Acute rhabdomyolysis, myoglobinuria and renal insufficiency caused by ethanol: review of the literature and description of a clinical case with fatal outcome]. Piazza I; Girardi A G Clin Med; 1989 Nov; 70(11):661-9. PubMed ID: 2599288 [TBL] [Abstract][Full Text] [Related]
28. Rhabdomyolysis and renal failure following a wolf attack: case report. Smith CD; Moir CR; Mucha P J Trauma; 1991 Mar; 31(3):423-5. PubMed ID: 2002534 [TBL] [Abstract][Full Text] [Related]
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30. [Rhabdomyolysis and myoglobinuria]. Lindner A; Zierz S Nervenarzt; 2003 Jun; 74(6):505-15. PubMed ID: 12799789 [TBL] [Abstract][Full Text] [Related]
31. 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 [TBL] [Abstract][Full Text] [Related]
34. Acute renal failure from myoglobinuria secondary to myositis from severe falciparum malaria. Sinniah R; Lye W Am J Nephrol; 2000; 20(4):339-43. PubMed ID: 10970990 [TBL] [Abstract][Full Text] [Related]
35. A disorder of muscle lipid metabolism and myoglobinuria. Absence of carnitine palmityl transferase. Bank WJ; DiMauro S; Bonilla E; Capuzzi DM; Rowland LP N Engl J Med; 1975 Feb; 292(9):443-9. PubMed ID: 123038 [TBL] [Abstract][Full Text] [Related]