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Journal Abstract Search

144 related items for PubMed ID: 3152098

  • 1. [Mitochondrial myopathy and abnormal mitochondrial DNA].
    Takeshita K.
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):834-8. PubMed ID: 3152098
    [No Abstract] [Full Text] [Related]

  • 2.
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  • 3. [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]

  • 4. [Clinical aspects of mitochondrial encephalomyopathy--abnormality of mitochondrial respiratory chain].
    Nakagawa M, Osame M.
    No To Shinkei; 1990 Aug; 42(8):719-33. PubMed ID: 2121197
    [No Abstract] [Full Text] [Related]

  • 5. [Familial cases of mitochondrial cytopathy].
    Ishitsu T, Matsuda I, Kitano A, Shimoji A, Kimura H.
    Rinsho Shinkeigaku; 1987 Aug; 27(8):983-9. PubMed ID: 3121229
    [No Abstract] [Full Text] [Related]

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  • 7. [Mitochondrial encephalomyopathies. A comparison of Kearns-Sayre syndrome, MELAS and MERRF].
    Zenner K, Gold R, Meurers B, Reichmann H.
    Nervenarzt; 1990 Oct; 61(10):597-603. PubMed ID: 2177152
    [No Abstract] [Full Text] [Related]

  • 8.
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  • 9. [Biochemistry of mitochondrial encephalomyopathy].
    Ozawa T, Tanaka M.
    No To Shinkei; 1990 Aug; 42(8):707-17. PubMed ID: 2223265
    [No Abstract] [Full Text] [Related]

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

  • 12. Kearns-Sayre syndrome with reduced plasma and cerebrospinal fluid folate.
    Allen RJ, DiMauro S, Coulter DL, Papadimitriou A, Rothenberg SP.
    Ann Neurol; 1983 Jun; 13(6):679-82. PubMed ID: 6881930
    [Abstract] [Full Text] [Related]

  • 13. [Disorders of mitochondrial energy metabolism in patients with the Kearns-Sayre syndrome].
    Capková M, Tesarová M, Wenchich L, Cerná L, Hansíková H, Hůlková H, Hrubá E, Elleder M, Zeman J.
    Cas Lek Cesk; 2002 Feb 01; 141(2):51-4. PubMed ID: 11925663
    [Abstract] [Full Text] [Related]

  • 14. [Mitochondrial encephalomyopathy].
    Ozawa T, Tanaka M.
    Tanpakushitsu Kakusan Koso; 1990 May 01; 35(7 Suppl):1236-45. PubMed ID: 2162552
    [No Abstract] [Full Text] [Related]

  • 15. Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome.
    Shanske S, Moraes CT, Lombes A, Miranda AF, Bonilla E, Lewis P, Whelan MA, Ellsworth CA, DiMauro S.
    Neurology; 1990 Jan 01; 40(1):24-8. PubMed ID: 2296377
    [Abstract] [Full Text] [Related]

  • 16. Kearns-Sayre syndrome: biochemical studies of mitochondrial metabolism.
    Martens ME, Peterson PL, Lee CP, Nigro MA, Hart Z, Glasberg M, Hatfield JS, Chang CH.
    Ann Neurol; 1988 Nov 01; 24(5):630-7. PubMed ID: 2849368
    [Abstract] [Full Text] [Related]

  • 17. [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]

  • 18. Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscle.
    Romero NB, Lestienne P, Marsac C, Paturneau-Jouas M, Nelson I, François D, Eymard B, Fardeau M.
    J Neurol Sci; 1989 Nov 10; 93(2-3):297-309. PubMed ID: 2556504
    [Abstract] [Full Text] [Related]

  • 19. [Myopathy].
    Kinoshita M.
    Nihon Naika Gakkai Zasshi; 1990 Sep 10; 79(9):1329-34. PubMed ID: 2175342
    [No Abstract] [Full Text] [Related]

  • 20. [The mitochondrial genome and its relation to human pathology].
    López de Munain A, Martí-Massó JF.
    Neurologia; 1991 Sep 10; 6(7):251-5. PubMed ID: 1768444
    [No Abstract] [Full Text] [Related]

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