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2. Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency. Herman J, Nadler HL. J Pediatr; 1977 Aug 20; 91(2):247-50. PubMed ID: 874682 [Abstract] [Full Text] [Related]
3. The role of acyltransferases in fatty acid utilization. Borrebaek B, Christiansen R, Christophersen BO, Bremer J. Circ Res; 1976 May 20; 38(5 Suppl 1):I16-21. PubMed ID: 1269090 [Abstract] [Full Text] [Related]
4. Myoglobinuria and carnitine palmityltransferase (CPT) deficiency: studies with malonyl-CoA suggest absence of only CPT-II. Trevisan CP, Angelini C, Freddo L, Isaya G, Martinuzzi A. Neurology; 1984 Mar 20; 34(3):353-6. PubMed ID: 6538275 [Abstract] [Full Text] [Related]
5. 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 27; 292(9):443-9. PubMed ID: 123038 [Abstract] [Full Text] [Related]
6. Adaptation of muscle to exercise. Increase in levels of palmityl Coa synthetase, carnitine palmityltransferase, and palmityl Coa dehydrogenase, and in the capacity to oxidize fatty acids. Molé PA, Oscai LB, Holloszy JO. J Clin Invest; 1971 Nov 27; 50(11):2323-30. PubMed ID: 5096516 [Abstract] [Full Text] [Related]
7. Myoglobinuria in carnitine palmityltransferase deficiency. Rowett D. Int Urol Nephrol; 1982 Nov 27; 14(3):285-91. PubMed ID: 7161012 [Abstract] [Full Text] [Related]
8. Carnitine palmityl transferase deficiency: myoglobinuria and respiratory failure. Bertorini T, Yeh YY, Trevisan C, Stadlan E, Sabesin S, DiMauro S. Neurology; 1980 Mar 27; 30(3):263-71. PubMed ID: 7189025 [Abstract] [Full Text] [Related]
9. Familial recurrent rhabdomyolysis due to carnitine palmityl transferase deficiency. Patten BM, Wood JM, Harati Y, Hefferan P, Howell RR. Am J Med; 1979 Jul 27; 67(1):167-71. PubMed ID: 463910 [Abstract] [Full Text] [Related]
10. Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: a new syndrome. Engel AG, Angelini C. Science; 1973 Mar 02; 179(4076):899-902. PubMed ID: 4687787 [Abstract] [Full Text] [Related]
11. Disorders of lipid metabolism in muscle. Di Mauro S, Trevisan C, Hays A. Muscle Nerve; 1980 Mar 02; 3(5):369-88. PubMed ID: 7421873 [Abstract] [Full Text] [Related]
12. Carnitine palmityltransferase activity during myocardial ischemmia and at low ionic strengths. McMillin Wood J. Recent Adv Stud Cardiac Struct Metab; 1975 Mar 02; 7():335-9. PubMed ID: 1226448 [Abstract] [Full Text] [Related]
13. Partial deficiency of carnitine palmityltransferase: physiologic and biochemical consequences. Layzer RB, Havel RJ, McIlroy MB. Neurology; 1980 Jun 02; 30(6):627-33. PubMed ID: 7189839 [Abstract] [Full Text] [Related]
14. Effect of ionic strength on the activity of carnitine palmityltransferase I. Wood JM. Biochemistry; 1973 Dec 18; 12(26):5268-73. PubMed ID: 4760490 [No Abstract] [Full Text] [Related]
15. Carnitine palmityltransferase and its relation to palmityl-CoA synthetase in blood platelets from fasting, healthy subjects. Sander J, Farstad M. Scand J Clin Lab Invest; 1973 Oct 18; 32(2):183-8. PubMed ID: 4768304 [No Abstract] [Full Text] [Related]
16. Recurrent myoglobinuria due to muscle carnitine palmityl transferase deficiency. Reza MJ, Kar NC, Pearson CM, Kark RA. Ann Intern Med; 1978 May 18; 88(5):610-5. PubMed ID: 646243 [Abstract] [Full Text] [Related]
17. Carnitine palymityltransferase in neonatal and adult heart and liver mitochondria. Effect of phospholipase C treatment. McMillin Wood J. J Biol Chem; 1975 Apr 25; 250(8):3062-6. PubMed ID: 1123334 [Abstract] [Full Text] [Related]
18. The relationship between palmitoyl-coenzyme A synthetase activity and esterification of sn-glycerol 3-phosphate in rat liver mitochondria. Sánchez M, Nicholls DG, Brindley DN. Biochem J; 1973 Apr 25; 132(4):697-706. PubMed ID: 4721605 [Abstract] [Full Text] [Related]
19. Beta-oxidation enzymes in normal human muscle and in muscle from a patient with an unusual form of myopathic carnitine deficiency. Trevisan CP, Reichmann H, DeVivo DC, DiMauro S. Muscle Nerve; 1985 Oct 25; 8(8):672-5. PubMed ID: 2932640 [Abstract] [Full Text] [Related]
20. [Lipid metabolism disorder in skeletal musculature (carnitine palmitoyltransferase deficiency) and paroxysmal myoglobinuria]. Aver'ianov IuN, Aleksandrovskaia TN, Kal'nova LI, Morozova EA, Shaldaeva VV. Zh Nevropatol Psikhiatr Im S S Korsakova; 1980 Oct 25; 80(11):1623-8. PubMed ID: 6935889 [Abstract] [Full Text] [Related] Page: [Next] [New Search]