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138 related items for PubMed ID: 2883759

  • 1. Fatal mitochondrial cardiomyopathy in Kearns-Sayre syndrome with deficiency of cytochrome-c-oxidase in cardiac and skeletal muscle. An enzymehistochemical--ultra-immunocytochemical--fine structural study in longterm frozen autopsy tissue.
    Müller-Höcker J, Johannes A, Droste M, Kadenbach B, Pongratz D, Hübner G.
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1986; 52(4):353-67. PubMed ID: 2883759
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  • 2. Congestive heart failure due to mitochondrial cardiomyopathy in Kearns-Sayre syndrome.
    Kleber FX, Park JW, Hübner G, Johannes A, Pongratz D, König E.
    Klin Wochenschr; 1987 May 15; 65(10):480-6. PubMed ID: 3599796
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  • 6. Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres.
    Oldfors A, Larsson NG, Holme E, Tulinius M, Kadenbach B, Droste M.
    J Neurol Sci; 1992 Jul 15; 110(1-2):169-77. PubMed ID: 1324295
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  • 14. Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndrome.
    Goto Y, Itami N, Kajii N, Tochimaru H, Endo M, Horai S.
    J Pediatr; 1990 Jun 15; 116(6):904-10. PubMed ID: 2161456
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  • 15. 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
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  • 17. Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.
    Mita S, Schmidt B, Schon EA, DiMauro S, Bonilla E.
    Proc Natl Acad Sci U S A; 1989 Dec 15; 86(23):9509-13. PubMed ID: 2556715
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  • 18. Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.
    Degoul F, Nelson I, Lestienne P, Francois D, Romero N, Duboc D, Eymard B, Fardeau M, Ponsot G, Paturneau-Jouas M.
    J Neurol Sci; 1991 Feb 15; 101(2):168-77. PubMed ID: 1851820
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