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112 related items for PubMed ID: 3037990

  • 1. Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues.
    Bresolin N, Moggio M, Bet L, Gallanti A, Prelle A, Nobile-Orazio E, Adobbati L, Ferrante C, Pellegrini G, Scarlato G.
    Ann Neurol; 1987 Jun; 21(6):564-72. PubMed ID: 3037990
    [Abstract] [Full Text] [Related]

  • 2. Cytochrome c oxidase activity in single muscle fibers: assay techniques and diagnostic applications.
    Johnson MA, Bindoff LA, Turnbull DM.
    Ann Neurol; 1993 Jan; 33(1):28-35. PubMed ID: 8388186
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  • 3. [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 Jan; 145(12):842-50. PubMed ID: 2559448
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  • 4. 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; 24(5):630-7. PubMed ID: 2849368
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  • 8. [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
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  • 9. Coenzyme Q in serum and muscle of 5 patients with Kearns-Sayre syndrome and 12 patients with ophthalmoplegia plus.
    Zierz S, Jahns G, Jerusalem F.
    J Neurol; 1989 Feb; 236(2):97-101. PubMed ID: 2709060
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  • 10. Kearns-Sayre syndrome associated with de Toni-Debré-Fanconi syndrome due to cytochrome-c-oxidase (COX) deficiency.
    Berio A, Piazzi A.
    Panminerva Med; 2001 Sep; 43(3):211-4. PubMed ID: 11579332
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  • 11. Corneal endothelium in a case of mitochondrial encephalomyopathy (Kearns-Sayre syndrome).
    Ohkoshi K, Ishida N, Yamaguchi T, Kanki K.
    Cornea; 1989 Sep; 8(3):210-4. PubMed ID: 2743782
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  • 12. 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; 86(23):9509-13. PubMed ID: 2556715
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  • 13. 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 Dec; 52(4):353-67. PubMed ID: 2883759
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  • 14. [Progressive external ophthalmoplegia and the Kearns-Sayre syndrome: a clinical and molecular study of 6 cases].
    Barrientos A, Casademont J, Grau JM, Cardellach F, Montoya J, Estivill X, Urbano-Márquez A, Nunes V.
    Med Clin (Barc); 1995 Jul 01; 105(5):180-4. PubMed ID: 7630231
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  • 15. A case of Kearns-Sayre syndrome with autoimmune thyroiditis and possible Hashimoto encephalopathy.
    Berio A, Piazzi A.
    Panminerva Med; 2002 Sep 01; 44(3):265-9. PubMed ID: 12094144
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  • 16. A case of Kearns-Sayre sindrome with autoimmune thyroiditis and complete atrio-ventricular block.
    Berio A, Piazzi A.
    Minerva Cardioangiol; 2006 Jun 01; 54(3):387-91. PubMed ID: 16733514
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  • 17. Histological, enzymatic and mitochondrial DNA studies in patients with Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.
    Reichmann H, Degoul F, Gold R, Meurers B, Ketelsen UP, Hartmann J, Marsac C, Lestienne P.
    Eur Neurol; 1991 Jun 01; 31(2):108-13. PubMed ID: 1646110
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  • 18. Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile.
    Fassati A, Bordoni A, Amboni P, Fortunato F, Fagiolari G, Bresolin N, Prelle A, Comi G, Scarlato G.
    J Neurol Sci; 1994 May 01; 123(1-2):140-6. PubMed ID: 8064307
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  • 19. Decreased activities in mitochondrial inner membrane electron transport system in muscle from patients with Kearns-Sayre syndrome.
    Yorifuji S, Ogasahara S, Takahashi M, Tarui S.
    J Neurol Sci; 1985 Nov 01; 71(1):65-75. PubMed ID: 4087020
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  • 20. 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 01; 93(2-3):297-309. PubMed ID: 2556504
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