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Journal Abstract Search

126 related items for PubMed ID: 7067593

  • 21. [Ptosis as the leading symptom of Kearns-Sayre syndrome. A case report for differential diagnosis of external ophthalmoplegia].
    Vock K, Todt H, Fötzsch R, Fischer R.
    Kinderarztl Prax; 1990 Feb; 58(2):93-7. PubMed ID: 2332951
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  • 22. Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10.
    Bresolin N, Bet L, Binda A, Moggio M, Comi G, Nador F, Ferrante C, Carenzi A, Scarlato G.
    Neurology; 1988 Jun; 38(6):892-9. PubMed ID: 3368070
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  • 23. [Maternally inherited diabetes mellitus, deafness, chronic progressive external ophthalmoplegia and myopathy as the result of A3243G mutation of mtDNA].
    Gál A, Szabó A, Pentelényi K, Pál Z.
    Orv Hetil; 2008 Aug 24; 149(34):1593-8. PubMed ID: 18708313
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  • 24. Oculopharyngeal and distal myopathy: a case study from Papua New Guinea.
    Scrimgeour EM, Mastaglia FL.
    Am J Med Genet; 1984 Apr 24; 17(4):763-71. PubMed ID: 6720743
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  • 25. Kearns-Sayre syndrome -3 case reports and review of clinical feature.
    Park SB, Ma KT, Kook KH, Lee SY.
    Yonsei Med J; 2004 Aug 31; 45(4):727-35. PubMed ID: 15344217
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  • 26. [Kearns-Sayre syndrome: a case report].
    Gaboune L, Baha Ali T, Benfdil N, Khoumiri R, Ouaggag B, Sayouti A, Moutaouakil A.
    J Fr Ophtalmol; 2012 Nov 31; 35(9):718.e1-4. PubMed ID: 22981519
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  • 27. 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 31; 236(2):97-101. PubMed ID: 2709060
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  • 29. [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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  • 30. Oculopharyngeal muscular dystrophy in Norway. Survey of a large Norwegian family.
    Salvesen R, Brautaset NJ.
    Acta Neurol Scand; 1996 Apr 01; 93(4):281-5. PubMed ID: 8739439
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  • 31. The Kearns-Shy syndrome. A multisystem disease with mitochondrial abnormality demonstrated in skeletal muscle and skin.
    Karpati G, Carpenter S, Larbrisseau A, Lafontaine R.
    J Neurol Sci; 1973 Jun 01; 19(2):133-51. PubMed ID: 4712930
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  • 35. Familial Kearns-Sayre syndrome.
    Schnitzler ER, Robertson WC.
    Neurology; 1979 Aug 01; 29(8):1172-4. PubMed ID: 572507
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  • 37. Clinical features of mitochondrial myopathy.
    Byrne E, Blumbergs PC, Hallpike JF, Mukherjee TM.
    Aust N Z J Med; 1983 Aug 01; 13(4):353-8. PubMed ID: 6580859
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