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Journal Abstract Search

173 related items for PubMed ID: 7171761

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  • 7. Mitochondrial cytochrome b gene deletion in Kearns-Sayre syndrome associated with a subclinical type of peripheral neuropathy.
    Zanssen S, Molnar M, Buse G, Schröder JM.
    Clin Neuropathol; 1998; 17(6):291-6. PubMed ID: 9832255
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  • 9. Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritance.
    Passos-Bueno MR, Marie SK, Monteiro M, Neustein I, Whittle MR, Vainzof M, Zatz M.
    Am J Med Genet; 1994 Aug 15; 52(2):170-3. PubMed ID: 7802003
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  • 12. A case of Kearns-Sayre sindrome with autoimmune thyroiditis and complete atrio-ventricular block.
    Berio A, Piazzi A.
    Minerva Cardioangiol; 2006 Jun 15; 54(3):387-91. PubMed ID: 16733514
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  • 13. [Autosomal recessive chronic progressive external ophthalmoplegia].
    Inose M, Higuchi I.
    Nihon Rinsho; 2002 Apr 15; 60 Suppl 4():455-7. PubMed ID: 12013911
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  • 14. Conduction disturbances in the Kearns-Sayre syndrome.
    Rakovec P, Starc R, Butinar D, Janezic A.
    Cor Vasa; 1986 Apr 15; 28(4):294-7. PubMed ID: 3769490
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  • 15. Oculopharyngeal and distal myopathy: a case study from Papua New Guinea.
    Scrimgeour EM, Mastaglia FL.
    Am J Med Genet; 1984 Apr 15; 17(4):763-71. PubMed ID: 6720743
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  • 16. [Kearns-Sayre syndrome and mitral valve prolapse. Description of a clinical case].
    Calabrese G, Mezio MG, Scolozzi D, De Rinaldis G.
    G Ital Cardiol; 1985 Dec 15; 15(12):1196-9. PubMed ID: 3835101
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  • 18. Kearns-Sayre syndromes an absolute indication for prophylactic implantation of definitive pacemaker?
    Barragán-Campos HM, Barrera-Ramírez CF, Iturralde Torres P, Ilarraza-Lomelí H, Avila-Casado MC, Estañol B, Dorantes J, Oseguera J.
    Arch Inst Cardiol Mex; 1999 Dec 15; 69(6):559-65. PubMed ID: 10742853
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  • 20. [Kearns-Sayre syndrome].
    Hertelendy A, Szigeti Z, Reichard L, Marek P, Sápi Z.
    Orv Hetil; 1998 Aug 09; 139(32):1913-6. PubMed ID: 9731448
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