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Journal Abstract Search

157 related items for PubMed ID: 7189839

  • 1. Partial deficiency of carnitine palmityltransferase: physiologic and biochemical consequences.
    Layzer RB, Havel RJ, McIlroy MB.
    Neurology; 1980 Jun; 30(6):627-33. PubMed ID: 7189839
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  • 2. 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; 4(5):465-7. PubMed ID: 736528
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  • 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
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  • 4. Disorders of lipid metabolism in muscle.
    Di Mauro S, Trevisan C, Hays A.
    Muscle Nerve; 1980 Mar; 3(5):369-88. PubMed ID: 7421873
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  • 6. 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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  • 9. Biochemical and physiologic consequences of carnitine palmityltransferase deficiency.
    Carroll JE, Brooke MH, DeVivo DC, Kaiser KK, Hagberg JM.
    Muscle Nerve; 1978 Jul; 1(2):103-10. PubMed ID: 750917
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  • 11. 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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  • 12. Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency.
    Herman J, Nadler HL.
    J Pediatr; 1977 Aug; 91(2):247-50. PubMed ID: 874682
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  • 13. [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 Aug; 80(11):1623-8. PubMed ID: 6935889
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  • 14. Heterogeneity of carnitine-palmitoyltransferase deficiency.
    Di Donato S, Castiglione A, Rimoldi M, Cornelio F, Vendemia F, Cardace G, Bertagnolio B.
    J Neurol Sci; 1981 May; 50(2):207-15. PubMed ID: 7229666
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  • 15. 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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  • 16. 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
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  • 17. 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; 40(1):39-51. PubMed ID: 762593
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  • 18. 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; 31(7):883-6. PubMed ID: 7195512
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