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Journal Abstract Search

151 related items for PubMed ID: 736528

  • 1. 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. [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 Nov; 42 Suppl 1():613-7. PubMed ID: 4083994
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  • 8. Immunoquantitative analysis of human carnitine palmitoyltransferase I and II defects.
    Demaugre F, Bonnefont JP, Cepanec C, Scholte J, Saudubray JM, Leroux JP.
    Pediatr Res; 1990 May; 27(5):497-500. PubMed ID: 2345677
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  • 13. A case of carnitine palmitoyltransferase II deficiency in human skeletal muscle.
    Singh R, Shepherd IM, Derrick JP, Ramsay RR, Sherratt HS, Turnbull DM.
    FEBS Lett; 1988 Dec 05; 241(1-2):126-30. PubMed ID: 3197828
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  • 14. Disorders of lipid metabolism in muscle.
    Di Mauro S, Trevisan C, Hays A.
    Muscle Nerve; 1980 Dec 05; 3(5):369-88. PubMed ID: 7421873
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  • 18. [Alterations of mitochondria in metabolic diseases. Carnitine deficiency, carnitine palmitoyltransferase deficiency and beta oxidation].
    Angelini C.
    Acta Neurol (Napoli); 1989 Oct 05; 11(5):330-4. PubMed ID: 2603779
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