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Journal Abstract Search

103 related items for PubMed ID: 2163788

  • 1. [Mitochondrial encephalomyopathy (focal cytochrome c oxidase deficiency) with transient episodes of muscle weakness and elevation of serum creatine kinase activity].
    Ohno M, Kobayashi T, Tanaka K, Goto I, Nonaka I.
    Rinsho Shinkeigaku; 1990 Mar; 30(3):317-9. PubMed ID: 2163788
    [Abstract] [Full Text] [Related]

  • 2. [A case of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes) with progressive cytochrome c oxidase deficiency].
    Sumi K, Nagaura T, Itagaki Y, Inui K, Abe J.
    Rinsho Shinkeigaku; 1989 Jul; 29(7):901-8. PubMed ID: 2553313
    [Abstract] [Full Text] [Related]

  • 3. [A mitochondrial encephalomyopathy due to partial cytochrome c oxidase deficiency with giant evoked potentials--a case report].
    Higashi Y, Higashi S, Terao A, Yasuda T, Shirabe T.
    Rinsho Shinkeigaku; 1990 Oct; 30(10):1084-9. PubMed ID: 2177689
    [Abstract] [Full Text] [Related]

  • 4. Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency.
    Lalani SR, Vladutiu GD, Plunkett K, Lotze TE, Adesina AM, Scaglia F.
    Arch Neurol; 2005 Feb; 62(2):317-20. PubMed ID: 15710863
    [Abstract] [Full Text] [Related]

  • 5. Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency.
    DiMauro S, Nicholson JF, Hays AP, Eastwood AB, Papadimitriou A, Koenigsberger R, DeVivo DC.
    Ann Neurol; 1983 Aug; 14(2):226-34. PubMed ID: 6312869
    [Abstract] [Full Text] [Related]

  • 6. [MELAS-like episodes in an adult case with cytochrome c oxidase deficiency].
    Kihira T, Kohmoto J, Yoshida S, Hironishi M, Kondo T, Nakao N, Goto Y, Nishino K, Nonaka I.
    Rinsho Shinkeigaku; 2004 Mar; 44(3):187-92. PubMed ID: 15233272
    [Abstract] [Full Text] [Related]

  • 7. Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin.
    Boustany RN, Aprille JR, Halperin J, Levy H, DeLong GR.
    Ann Neurol; 1983 Oct; 14(4):462-70. PubMed ID: 6314875
    [Abstract] [Full Text] [Related]

  • 8. [Mitochondrial neurogastrointestinal encephalomyopathy presenting with protein-losing gastroenteropathy and serum copper deficiency: a case report].
    Hamano H, Ohta T, Takekawa Y, Kouda K, Shinohara Y.
    Rinsho Shinkeigaku; 1997 Oct; 37(10):917-22. PubMed ID: 9490904
    [Abstract] [Full Text] [Related]

  • 9. [31P-NMR spectroscopy of mitochondrial myopathies: the relation between abnormal energy metabolism and muscle biopsy findings].
    Kawai M, Itoh M, Okazawa H, Kamakura K.
    Rinsho Shinkeigaku; 1989 Feb; 29(2):167-71. PubMed ID: 2546706
    [Abstract] [Full Text] [Related]

  • 10. [A case of mitochondrial encephalomyopathy with decreased cytochrome c oxidase].
    Amitani H, Yamano T, Nakagawa M, Osame M, Igata A.
    Rinsho Shinkeigaku; 1987 Jun; 27(6):737-40. PubMed ID: 2822320
    [No Abstract] [Full Text] [Related]

  • 11. [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 Jun; 145(12):842-50. PubMed ID: 2559448
    [Abstract] [Full Text] [Related]

  • 12. [Peripheral neuropathy in two children with mitochondrial encephalomyopathy].
    Tanaka J, Taniike M, Inui K, Nagai T, Okada S.
    Rinsho Shinkeigaku; 1991 Jul; 31(7):772-4. PubMed ID: 1664789
    [Abstract] [Full Text] [Related]

  • 13. [A case of mitochondrial encephalomyopathy characterized by repeated stroke-like episodes].
    Mizuno Y, Ishiguro K, Okamoto K, Morimatsu M, Hirai S.
    Rinsho Shinkeigaku; 1989 Mar; 29(3):360-6. PubMed ID: 2502353
    [Abstract] [Full Text] [Related]

  • 14. [A female infant of mitochondrial myopathy with findings of active necrosis and regeneration of muscle fibers].
    Nagaura T, Sumi K, Nonaka I.
    Rinsho Shinkeigaku; 1990 Apr; 30(4):432-8. PubMed ID: 2387114
    [Abstract] [Full Text] [Related]

  • 15. [Delayed manifestation of mitochondrial myopathy--complex I and IV deficiency of the mitochondrial respiratory chain with progressive paresis].
    Beyenburg S, von Wersebe O, Zierz S.
    Nervenarzt; 1991 Aug; 62(8):506-11. PubMed ID: 1658669
    [Abstract] [Full Text] [Related]

  • 16. Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency.
    Koga Y, Nonaka I, Kobayashi M, Tojyo M, Nihei K.
    Ann Neurol; 1988 Dec; 24(6):749-56. PubMed ID: 3144939
    [Abstract] [Full Text] [Related]

  • 17. Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patient.
    Zeviani M, Nonaka I, Bonilla E, Okino E, Moggio M, Jones S, DiMauro S.
    Ann Neurol; 1985 Apr; 17(4):414-7. PubMed ID: 2988412
    [Abstract] [Full Text] [Related]

  • 18. [A case of mitochondrial encephalomyopathy with a defect in electron transport at complex I and IV in skeletal muscle showing peripheral neuropathy].
    Ohnishi A, Nakano S, Hashimoto T, Tsuji S, Murai Y.
    Rinsho Shinkeigaku; 1988 Jan; 28(1):107-11. PubMed ID: 2838209
    [No Abstract] [Full Text] [Related]

  • 19. Cytochrome c oxidase--deficient myogenic cell lines in mitochondrial myopathy.
    Shimoizumi H, Momoi MY, Ohta S, Kagawa Y, Momoi T, Yanagisawa M.
    Ann Neurol; 1989 Jun; 25(6):615-21. PubMed ID: 2545162
    [Abstract] [Full Text] [Related]

  • 20. [Congenital nemaline myopathy with mitochondrial abnormalities. An adult case report].
    Oya Y, Segawa M, Ogawa M, Goto Y, Nonaka I, Kawai M.
    Rinsho Shinkeigaku; 2000 May; 40(5):452-8. PubMed ID: 11002727
    [Abstract] [Full Text] [Related]

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