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Journal Abstract Search

165 related items for PubMed ID: 6425943

  • 1. [Carnitine deficiency myopathy].
    Ziegan J, Kühn HJ, Lössner J, Künnert B, Lehmann J.
    Acta Histochem Suppl; 1984; 30():251-5. PubMed ID: 6425943
    [No Abstract] [Full Text] [Related]

  • 2. [A case of myopathy with carnitine deficiency].
    Martin P, Carrier H, Renaud JF, Kullmann B, Delpont E, Romey G, Cartier B, Bedoucha P.
    Rev Neurol (Paris); 1986; 142(6-7):625-34. PubMed ID: 3797933
    [Abstract] [Full Text] [Related]

  • 3. Mitochondria-lipid-glycogen myopathy, hyperlactacidemia, and carnitine deficiency.
    Di Donato S, Cornelio F, Balestrini MR, Bertagnolio B, Peluchetti D.
    Neurology; 1978 Nov; 28(11):1110-6. PubMed ID: 568729
    [Abstract] [Full Text] [Related]

  • 4. [Secondary muscular carnitine deficiency following immunosuppressive treatment].
    Lössner J, Kühn HJ, Lehmann J, Ziegan J.
    Psychiatr Neurol Med Psychol (Leipz); 1989 Oct; 41(10):614-20. PubMed ID: 2608761
    [Abstract] [Full Text] [Related]

  • 5. Mitochondrial myopathies.
    DiMauro S, Bonilla E, Zeviani M, Nakagawa M, DeVivo DC.
    Ann Neurol; 1985 Jun; 17(6):521-38. PubMed ID: 3927817
    [Abstract] [Full Text] [Related]

  • 6. [Carnitine deficiency myopathy (author's transl)].
    Jerusalem F, Engel AG, Sengupta C, Imbach P, Lämmli J.
    Dtsch Med Wochenschr; 1980 Apr 04; 105(14):469-73. PubMed ID: 7363806
    [Abstract] [Full Text] [Related]

  • 7. Mitochondrial myopathy with diffuse activation and focal deficiency of mitochondrial ATPase and carnitine deficiency.
    Müller-Höcker J, Paetzke I, Pongratz D, Hübner G.
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1985 Apr 04; 48(2):185-96. PubMed ID: 2859691
    [Abstract] [Full Text] [Related]

  • 8. [Myopathy with carnitine deficiency and lactic acidosis. A contribution to differential diagnosis of carnitine deficiency myopathies and mitochondrial myopathies].
    Cammann R, Dunker H, Schumacher H, Ruitenbeek W, Sperner J.
    Z Arztl Fortbild (Jena); 1992 Jul 10; 86(13):667-71. PubMed ID: 1642019
    [No Abstract] [Full Text] [Related]

  • 9. Primary systemic carnitine deficiency under successful therapy: clinical, biochemical, ultrahistochemical and renal clearance studies.
    von Petrykowski W, Ketelsen UP, Schmidt-Sommerfield E, Penn D, Sawicka E, Struck E, Lehnert W, Haap K, Strassburg HM.
    Clin Neuropathol; 1985 Jul 10; 4(2):63-71. PubMed ID: 3995808
    [Abstract] [Full Text] [Related]

  • 10. [A case of mitochondrial myopathy with nemaline rods accompanied by a partial deficiency of cytochrome c oxidase].
    Kitagawa Y, Ishihara T, Koga Y, Hanada T, Irimajiri S.
    Rinsho Shinkeigaku; 1988 Apr 10; 28(4):388-95. PubMed ID: 2850881
    [No Abstract] [Full Text] [Related]

  • 11. [Histoenzymatic and ultrastructural aspects of mitochondrial myopathy (mitochondriopathy)].
    Antoci B, Pizzolitto S.
    Pathologica; 1984 Apr 10; 76(1046):655-68. PubMed ID: 6537477
    [No Abstract] [Full Text] [Related]

  • 12. Primary carnitine deficiency: adult onset lipid storage myopathy with a mild clinical course.
    Vielhaber S, Feistner H, Weis J, Kreuder J, Sailer M, Schröder JM, Kunz WS.
    J Clin Neurosci; 2004 Nov 10; 11(8):919-24. PubMed ID: 15519880
    [Abstract] [Full Text] [Related]

  • 13. Pathology of inflammatory and metabolic myopathies.
    Armbrustmacher VW, Griffin JL.
    Pathol Annu; 1981 Nov 10; 16 Pt 1():15-60. PubMed ID: 6949130
    [No Abstract] [Full Text] [Related]

  • 14. Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle.
    Müller-Höcker J, Pongratz D, Deufel T, Trijbels JM, Endres W, Hübner G.
    Virchows Arch A Pathol Anat Histopathol; 1983 Nov 10; 399(1):11-23. PubMed ID: 6298999
    [Abstract] [Full Text] [Related]

  • 15. [Congenital oculoskeletal myopathy with abnormal muscle and liver mitochondria (author's transl)].
    Okamura K, Nagae K, Omae T, Mita T.
    Rinsho Shinkeigaku; 1975 Apr 10; 15(4):177-83. PubMed ID: 1170056
    [No Abstract] [Full Text] [Related]

  • 16. [Carnitine deficiency myopathy: a case of late diagnosis].
    Rico Corral MA, de la Vega Vázquez JM, Holgado Silva C, Aznar Martín A, Zamora Madaría E.
    An Med Interna; 2002 Aug 10; 19(8):415-8. PubMed ID: 12244790
    [Abstract] [Full Text] [Related]

  • 17. [Carnitine deficiency myopathy (author's transl)].
    Jerusalem F.
    Nervenarzt; 1980 May 10; 51(5):266-71. PubMed ID: 7007897
    [No Abstract] [Full Text] [Related]

  • 18. [Hereditary myopathy with succinate dehydrogenase deficiency--a rare life-threatening disease].
    Linderholm H, Almay BG, Bäcklund U, Stegmayr B, Thornell LE.
    Lakartidningen; 1992 Apr 08; 89(15):1283-8. PubMed ID: 1578996
    [No Abstract] [Full Text] [Related]

  • 19. "Lipid storage myopathy" with muscle carnitine deficiency only.
    Buscaino GA, Marolda M, Borgia A, Cocchiararo M, Scarafile P.
    Acta Neurol (Napoli); 1982 Feb 08; 4(1):1-13. PubMed ID: 7090864
    [No Abstract] [Full Text] [Related]

  • 20. Carnitine deficiency of skeletal muscle: report of a treated case.
    Angelini C, Lücke S, Cantarutti F.
    Neurology; 1976 Jul 08; 26(7):633-7. PubMed ID: 945511
    [Abstract] [Full Text] [Related]

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