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Journal Abstract Search

185 related items for PubMed ID: 463910

  • 1. Familial recurrent rhabdomyolysis due to carnitine palmityl transferase deficiency.
    Patten BM, Wood JM, Harati Y, Hefferan P, Howell RR.
    Am J Med; 1979 Jul; 67(1):167-71. PubMed ID: 463910
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  • 2. Exercise-induced recurrent myoglobinuria: defective activity of inner carnitine palmitoyltransferase in muscle mitochondria of two patients.
    Trevisan CP, Isaya G, Angelini C.
    Neurology; 1987 Jul; 37(7):1184-8. PubMed ID: 3601082
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  • 3. 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; 34(3):353-6. PubMed ID: 6538275
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  • 4. [Recurrent rhabdomyolysis and deficiency of carnitine palmityl transferase. Evidence of the responsibility of a mutant in 2 brothers].
    Dupond JL, Mousson B, Guerber F, Humbert P, Maire I, Gibey R.
    Presse Med; 1988 Nov 19; 17(41):2187-90. PubMed ID: 2974578
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  • 5. [Muscular carnitine-palmityl-transferase deficiency].
    Rumpf KW, Kaiser H, Goebel HH, Wagner HA, Ullmann B, DiMauro S, Scheler F.
    Dtsch Med Wochenschr; 1983 Jul 08; 108(27):1058-61. PubMed ID: 6861647
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  • 6. Partial deficiency of carnitine palmityltransferase: physiologic and biochemical consequences.
    Layzer RB, Havel RJ, McIlroy MB.
    Neurology; 1980 Jun 08; 30(6):627-33. PubMed ID: 7189839
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  • 12. Myoglobinuria in carnitine palmityltransferase deficiency.
    Rowett D.
    Int Urol Nephrol; 1982 Jun 08; 14(3):285-91. PubMed ID: 7161012
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  • 13. Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency.
    Herman J, Nadler HL.
    J Pediatr; 1977 Aug 08; 91(2):247-50. PubMed ID: 874682
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  • 14. Familial combined deficiency of muscle carnitine and carnitine palmityl transferase (CPT).
    Skard Heier M, Dietrichson P, Landaas S.
    Acta Neurol Scand; 1986 Dec 08; 74(6):479-85. PubMed ID: 3825503
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  • 15. Myoglobinuria and carnitine palmityl transferase deficiency in father and son.
    Mongini T, Doriguzzi C, Palmucci L, Chiadò-Piat L, Maniscalco M, Schiffer D.
    J Neurol; 1991 Sep 08; 238(6):323-4. PubMed ID: 1940982
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  • 16. Carnitine palmitoyltransferase II deficiency with normal carnitine palmitoyltransferase I in skeletal muscle and leucocytes.
    Scholte HR, Jennekens FG, Bouvy JJ.
    J Neurol Sci; 1979 Jan 08; 40(1):39-51. PubMed ID: 762593
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  • 17. [Recurrent paroxysmal myoglobinuria with acute renal insufficiency caused by muscular carnitine (palmitoyltransferase deficiency. A case].
    Meunier J, Perrot D, Bret M, Pissere-Meunier J, Bouletreau P, Pasquier J, Carrier H, Berthillier G.
    Nouv Presse Med; 1982 Sep 25; 11(37):2767-71. PubMed ID: 7145668
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