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Journal Abstract Search

156 related items for PubMed ID: 874682

  • 1. Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency.
    Herman J, Nadler HL.
    J Pediatr; 1977 Aug; 91(2):247-50. PubMed ID: 874682
    [Abstract] [Full Text] [Related]

  • 2. Myoglobinuria in carnitine palmityltransferase deficiency.
    Rowett D.
    Int Urol Nephrol; 1982 Aug; 14(3):285-91. PubMed ID: 7161012
    [Abstract] [Full Text] [Related]

  • 3. Carnitine palmityl transferase deficiency: myoglobinuria and respiratory failure.
    Bertorini T, Yeh YY, Trevisan C, Stadlan E, Sabesin S, DiMauro S.
    Neurology; 1980 Mar; 30(3):263-71. PubMed ID: 7189025
    [Abstract] [Full Text] [Related]

  • 4. Recurrent myoglobinuria due to muscle carnitine palmityl transferase deficiency.
    Reza MJ, Kar NC, Pearson CM, Kark RA.
    Ann Intern Med; 1978 May; 88(5):610-5. PubMed ID: 646243
    [Abstract] [Full Text] [Related]

  • 5. [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
    [Abstract] [Full Text] [Related]

  • 6. Combined partial deficiency of muscle carnitine palmitoyltransferase and carnitine with autosomal dominant inheritance.
    Ionasescu V, Hug G, Hoppel C.
    J Neurol Neurosurg Psychiatry; 1980 Aug 25; 43(8):679-82. PubMed ID: 7431028
    [Abstract] [Full Text] [Related]

  • 7. Carnitine palmityltransferase deficiency with permanent weakness.
    Gieron MA, Korthals JK.
    Pediatr Neurol; 1987 Aug 25; 3(1):51-3. PubMed ID: 3508048
    [Abstract] [Full Text] [Related]

  • 8. Muscle carnitine palmityltransferase deficiency and myoglobinuria.
    DiMauro S, DiMauro PM.
    Science; 1973 Nov 20; 182(4115):929-31. PubMed ID: 4745596
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. [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
    [Abstract] [Full Text] [Related]

  • 11. Partial deficiency of muscle carnitine palmitoyltransferase with normal ketone production.
    Hostetler KY, Hoppel CL, Romine JS, Sipe JC, Gross SR, Higginbottom PA.
    N Engl J Med; 1978 Mar 09; 298(10):553-7. PubMed ID: 272487
    [No Abstract] [Full Text] [Related]

  • 12. Carnitine palmityl transferase deficiency: clinical variability, carrier detection, and autosomal-recessive inheritance.
    Angelini C, Freddo L, Battistella P, Bresolin N, Pierobon-Bormioli S, Armani M, Vergani L.
    Neurology; 1981 Jul 09; 31(7):883-6. PubMed ID: 7195512
    [Abstract] [Full Text] [Related]

  • 13. Partial deficiency of carnitine palmityltransferase: physiologic and biochemical consequences.
    Layzer RB, Havel RJ, McIlroy MB.
    Neurology; 1980 Jun 09; 30(6):627-33. PubMed ID: 7189839
    [Abstract] [Full Text] [Related]

  • 14. Familial combined deficiency of muscle carnitine and carnitine palmityl transferase (CPT).
    Skard Heier M, Dietrichson P, Landaas S.
    Acta Neurol Scand; 1986 Dec 09; 74(6):479-85. PubMed ID: 3825503
    [Abstract] [Full Text] [Related]

  • 15. Recurrent exertional myalgia and myoglobinuria due to carnitine palmityltransferase deficiency.
    Argov Z, DiMauro S.
    Isr J Med Sci; 1983 Jun 09; 19(6):552-4. PubMed ID: 6862863
    [No Abstract] [Full Text] [Related]

  • 16. Familial recurrent rhabdomyolysis due to carnitine palmityl transferase deficiency.
    Patten BM, Wood JM, Harati Y, Hefferan P, Howell RR.
    Am J Med; 1979 Jul 09; 67(1):167-71. PubMed ID: 463910
    [Abstract] [Full Text] [Related]

  • 17. Metabolic causes of myoglobinuria.
    Tonin P, Lewis P, Servidei S, DiMauro S.
    Ann Neurol; 1990 Feb 09; 27(2):181-5. PubMed ID: 2156480
    [Abstract] [Full Text] [Related]

  • 18. [Myopathy due to carnitine palmitoyltransferase deficiency. Report of 2 cases with enzymatic analyses on muscle tissue].
    Werneck LC, Boer CA, Papadimitriou A, Di Mauro S.
    Arq Neuropsiquiatr; 1983 Dec 09; 41(4):377-84. PubMed ID: 6661102
    [Abstract] [Full Text] [Related]

  • 19. [A female case of carnitine palmitoyltransferase deficiency].
    Taniwaki T, Kira J, Kitaguchi T, Goto I, Sugiyama N.
    Rinsho Shinkeigaku; 1989 Mar 09; 29(3):382-4. PubMed ID: 2752669
    [Abstract] [Full Text] [Related]

  • 20. 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]

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