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Journal Abstract Search

149 related items for PubMed ID: 6861647

  • 1. [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]

  • 2. [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]

  • 3. [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 Sep 25; 80(11):1623-8. PubMed ID: 6935889
    [Abstract] [Full Text] [Related]

  • 4. [Recurrent myoglobinuria caused by carnitine-palmityl-transferase deficiency].
    Pamies-Andreu E, Sánchez-Román J, Bautista J, Segura DI.
    Rev Clin Esp; 1987 May 25; 180(8):462-3. PubMed ID: 3616029
    [No Abstract] [Full Text] [Related]

  • 5. Recurrent myoglobinuria due to muscle carnitine palmityl transferase deficiency.
    Reza MJ, Kar NC, Pearson CM, Kark RA.
    Ann Intern Med; 1978 May 25; 88(5):610-5. PubMed ID: 646243
    [Abstract] [Full Text] [Related]

  • 6. Selective carnitine palmitoyltransferase deficiency in fibroblasts from a patient with muscle CPT deficiency.
    Pula TP, Max SR, Zielke HR, Chacon M, Baab P, Gumbinas M, Reed WD.
    Ann Neurol; 1981 Aug 25; 10(2):196-8. PubMed ID: 7283405
    [Abstract] [Full Text] [Related]

  • 7. Metabolic causes of myoglobinuria.
    Tonin P, Lewis P, Servidei S, DiMauro S.
    Ann Neurol; 1990 Feb 25; 27(2):181-5. PubMed ID: 2156480
    [Abstract] [Full Text] [Related]

  • 8. [A female case of carnitine palmitoyltransferase deficiency].
    Taniwaki T, Kira J, Kitaguchi T, Goto I, Sugiyama N.
    Rinsho Shinkeigaku; 1989 Mar 25; 29(3):382-4. PubMed ID: 2752669
    [Abstract] [Full Text] [Related]

  • 9. Carnitine palmityl transferase deficiency: myoglobinuria and respiratory failure.
    Bertorini T, Yeh YY, Trevisan C, Stadlan E, Sabesin S, DiMauro S.
    Neurology; 1980 Mar 25; 30(3):263-71. PubMed ID: 7189025
    [Abstract] [Full Text] [Related]

  • 10. [Primary cardiomyopathy in children with lipid infiltration of the myocardium and skeletal muscles and demonstration of a palmityl-carnitine transferase deficiency. Apropos of 4 cases].
    Normand J, Carrier H, Berthillier G, Bozio A, Jocteur-Monrozier D, André M, Joffre B.
    Arch Mal Coeur Vaiss; 1979 May 25; 72(5):529-35. PubMed ID: 115406
    [Abstract] [Full Text] [Related]

  • 11. Carnitine palmitoyltransferase deficiency: a common cause of recurrent myoglobinuria.
    Sadeh M, Gutman A.
    Isr J Med Sci; 1990 Sep 25; 26(9):510-5. PubMed ID: 2228562
    [Abstract] [Full Text] [Related]

  • 12. [Acute recurrent renal insufficiency in a patient with atraumatic rhabdomyolysis caused by carnitine-palmitoyltransferase deficiency].
    Castiglione A, Cornelio F, Vendemia F, Rimoldi M, Sinico R, Baroni M, D'Amico G.
    Minerva Nefrol; 1981 Sep 25; 28(3):229-34. PubMed ID: 7329599
    [No Abstract] [Full Text] [Related]

  • 13. Familial recurrent rhabdomyolysis due to carnitine palmityl transferase deficiency.
    Patten BM, Wood JM, Harati Y, Hefferan P, Howell RR.
    Am J Med; 1979 Jul 25; 67(1):167-71. PubMed ID: 463910
    [Abstract] [Full Text] [Related]

  • 14. Muscle carnitine palmityltransferase deficiency: a case with enzyme deficiency in cultured fibroblasts.
    DiDonato S, Cornelio F, Pacini L, Peluchetti D, Rimoldi M, Spreafico S.
    Ann Neurol; 1978 Nov 25; 4(5):465-7. PubMed ID: 736528
    [Abstract] [Full Text] [Related]

  • 15. [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
    [Abstract] [Full Text] [Related]

  • 16. 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 19; 31(7):883-6. PubMed ID: 7195512
    [Abstract] [Full Text] [Related]

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

  • 18. [Heterogeneity of carnitine palmitoyltransferase deficiencies. Deficiency of CPT I in the hepatic form and CPT II in the muscular form].
    Bonnefont JP, Ogier H, Mitchell G, Demaugre F, Pelet A, Saudubray JM, Frezal J.
    Arch Fr Pediatr; 1985 Jun 19; 42 Suppl 1():613-7. PubMed ID: 4083994
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency.
    Herman J, Nadler HL.
    J Pediatr; 1977 Aug 09; 91(2):247-50. PubMed ID: 874682
    [Abstract] [Full Text] [Related]

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