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Journal Abstract Search


145 related items for PubMed ID: 2493147

  • 21. [A case of mitochondrial encephalomyopathy--Mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes (MELAS)].
    Ihara Y, Namba R, Demiya M, Matsumoto T, Shirabe T.
    Rinsho Shinkeigaku; 1987 Aug; 27(8):969-75. PubMed ID: 3690923
    [No Abstract] [Full Text] [Related]

  • 22. [Mitochondrial abnormalities and diseases].
    Goto Y, Sugita H.
    Nihon Naika Gakkai Zasshi; 1991 May 10; 80(5):775-80. PubMed ID: 1651974
    [No Abstract] [Full Text] [Related]

  • 23. Characterization of iron-sulfur clusters in rat liver submitochondrial particles by electron paramagnetic resonance spectroscopy. Alterations produced by chronic ethanol consumption.
    Thayer WS, Ohnishi T, Rubin E.
    Biochim Biophys Acta; 1980 Jun 10; 591(1):22-36. PubMed ID: 6248107
    [Abstract] [Full Text] [Related]

  • 24. Iron-sulfur N-1 clusters studied in NADH-ubiquinone oxidoreductase and in soluble NADH dehydrogenase.
    Ohnishi T, Blum H, Galante YM, Hatefi Y.
    J Biol Chem; 1981 Sep 10; 256(17):9216-20. PubMed ID: 6267066
    [Abstract] [Full Text] [Related]

  • 25. Studies on the structure of NADH:ubiquinone oxidoreductase complex: topography of the subunits of the iron-sulfur flavoprotein component.
    Han AL, Yagi T, Hatefi Y.
    Arch Biochem Biophys; 1988 Dec 10; 267(2):490-6. PubMed ID: 2463782
    [Abstract] [Full Text] [Related]

  • 26. [Mitochondrial angiopathy in the cerebral blood vessels of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes)].
    Ohama E, Ohara S, Ikuta F, Tanaka K, Nishizawa M, Miyatake T.
    No To Shinkei; 1988 Feb 10; 40(2):109-18. PubMed ID: 3370163
    [Abstract] [Full Text] [Related]

  • 27. [Mitochondrial encephalomyopathy--MERRF and MELAS are clinicopathologically distinctive entities].
    Tanaka K, Nishizawa M, Miyatake T, Takeda S, Ohama E.
    Rinsho Shinkeigaku; 1987 Nov 10; 27(11):1468-73. PubMed ID: 3129227
    [No Abstract] [Full Text] [Related]

  • 28. Studies on the structure of NADH: ubiquinone oxidoreductase complex: topography of the subunits of the iron-sulfur protein component.
    Han AL, Yagi T, Hatefi Y.
    Arch Biochem Biophys; 1989 Nov 15; 275(1):166-73. PubMed ID: 2510601
    [Abstract] [Full Text] [Related]

  • 29. Generalized mitochondrial microangiopathy and vascular cytochrome c oxidase deficiency. Occurrence in a case of MELAS syndrome with mitochondrial cardiomyopathy-myopathy and combined complex I/IV deficiency.
    Müller-Höcker J, Hübner G, Bise K, Förster C, Hauck S, Paetzke I, Pongratz D, Kadenbach B.
    Arch Pathol Lab Med; 1993 Feb 15; 117(2):202-10. PubMed ID: 8381271
    [Abstract] [Full Text] [Related]

  • 30. A reductase/isomerase subunit of mitochondrial NADH:ubiquinone oxidoreductase (complex I) carries an NADPH and is involved in the biogenesis of the complex.
    Schulte U, Haupt V, Abelmann A, Fecke W, Brors B, Rasmussen T, Friedrich T, Weiss H.
    J Mol Biol; 1999 Sep 24; 292(3):569-80. PubMed ID: 10497022
    [Abstract] [Full Text] [Related]

  • 31. EPR studies of iron-sulfur clusters in isolated subunits and subfractions of NADH-ubiquinone oxidoreductase.
    Ohnishi T, Ragan CI, Hatefi Y.
    J Biol Chem; 1985 Mar 10; 260(5):2782-8. PubMed ID: 2982836
    [Abstract] [Full Text] [Related]

  • 32. Vascular involvement in mitochondrial myopathy.
    Sakuta R, Nonaka I.
    Ann Neurol; 1989 Jun 10; 25(6):594-601. PubMed ID: 2500889
    [Abstract] [Full Text] [Related]

  • 33. Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS).
    Yoneda M, Tanaka M, Nishikimi M, Suzuki H, Tanaka K, Nishizawa M, Atsumi T, Ohama E, Horai S, Ikuta F.
    J Neurol Sci; 1989 Sep 10; 92(2-3):143-58. PubMed ID: 2809615
    [Abstract] [Full Text] [Related]

  • 34. Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies.
    Tanaka M, Nishikimi M, Suzuki H, Ozawa T, Koga Y, Nonaka I.
    Biochem Int; 1987 Mar 10; 14(3):525-30. PubMed ID: 2884999
    [Abstract] [Full Text] [Related]

  • 35. A mitochondrial encephalomyopathy with cardiomyopathy. A case revealing a defect of complex I in the respiratory chain.
    Nishizawa M, Tanaka K, Shinozawa K, Kuwabara T, Atsumi T, Miyatake T, Ohama E.
    J Neurol Sci; 1987 Apr 10; 78(2):189-201. PubMed ID: 3106581
    [Abstract] [Full Text] [Related]

  • 36. Mitochondrial encephalomyopathy (MELAS): pathological study and successful therapy with coenzyme Q10 and idebenone.
    Ihara Y, Namba R, Kuroda S, Sato T, Shirabe T.
    J Neurol Sci; 1989 May 10; 90(3):263-71. PubMed ID: 2738608
    [Abstract] [Full Text] [Related]

  • 37. Mitochondrial myopathy with a defect of mitochondrial-protein transport.
    Schapira AH, Cooper JM, Morgan-Hughes JA, Landon DN, Clark JB.
    N Engl J Med; 1990 Jul 05; 323(1):37-42. PubMed ID: 2113185
    [No Abstract] [Full Text] [Related]

  • 38. [Kearns-Sayre syndrome: mitochondrial encephalomyopathy caused by deficiency of the respiratory chain].
    Desnuelle C, Pellissier JF, Serratrice G, Pouget J, Turnbull DM.
    Rev Neurol (Paris); 1989 Jul 05; 145(12):842-50. PubMed ID: 2559448
    [Abstract] [Full Text] [Related]

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