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Journal Abstract Search

343 related items for PubMed ID: 1892371

  • 1. Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromes.
    Zupanc ML, Moraes CT, Shanske S, Langman CB, Ciafaloni E, DiMauro S.
    Ann Neurol; 1991 Jun; 29(6):680-3. PubMed ID: 1892371
    [Abstract] [Full Text] [Related]

  • 2. [A case of incomplete Kearns-Sayre syndrome with a stroke like episode].
    Furuya H, Sugimura T, Yamada T, Hayashi K, Kobayashi T.
    Rinsho Shinkeigaku; 1997 Aug; 37(8):680-4. PubMed ID: 9404143
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  • 4. [MELAS associated with diabetes mellitus and point mutation in mitochondrial DNA].
    Onishi H, Inoue K, Osaka H, Nagatomo H, Ando N, Yamada Y, Suzuki K, Hanihara T, Kawamoto S, Okuda K.
    No To Shinkei; 1992 Mar; 44(3):259-64. PubMed ID: 1591103
    [Abstract] [Full Text] [Related]

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

  • 6. A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.
    Goto Y, Nonaka I, Horai S.
    Nature; 1990 Dec 13; 348(6302):651-3. PubMed ID: 2102678
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  • 7. A novel 7301-bp deletion in mitochondrial DNA in a patient with Kearns-Sayre syndrome, diabetes mellitus, and primary amenorrhoea.
    De Block CE, De Leeuw IH, Maassen JA, Ballaux D, Martin JJ.
    Exp Clin Endocrinol Diabetes; 2004 Feb 13; 112(2):80-3. PubMed ID: 15031771
    [Abstract] [Full Text] [Related]

  • 8. Kearns-Sayre syndrome. A case report.
    Altunbaşak S, Bingöl G, Ozbarlas N, Akçören Z, Hergüner O.
    Turk J Pediatr; 1998 Feb 13; 40(2):255-9. PubMed ID: 9677732
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  • 9. [Mitochondrial disease and complete heart block. Kearns-Sayre syndrome. Description of a case].
    Perocchio M, Tomassini B, Biasia R, Belli Valletta M, Cerutti A, Bobba F.
    Minerva Med; 1992 Dec 13; 83(12 Suppl 1):7-13. PubMed ID: 1300476
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  • 11. Mitochondrial genome analysis in Kearns-Sayre syndrome.
    Lertrit P, Atchaneeyasakul L, Devahastin V, Saechan V, Sangruchi T, Neungton N, Lekhakula S.
    Southeast Asian J Trop Med Public Health; 1995 Dec 13; 26 Suppl 1():162-5. PubMed ID: 8629098
    [Abstract] [Full Text] [Related]

  • 12. [Molecular biology of mitochondrial DNA and mutations in mitochondrial cytopathy].
    Ito T.
    Nihon Rinsho; 1993 Jun 13; 51(6):1425-8. PubMed ID: 8320824
    [Abstract] [Full Text] [Related]

  • 13. [Mitochondrial DNA deletions in Kearns-Sayre syndrome].
    Carod-Artal FJ, Lopez Gallardo E, Solano A, Dahmani Y, Herrero MD, Montoya J.
    Neurologia; 2006 Sep 13; 21(7):357-64. PubMed ID: 16977556
    [Abstract] [Full Text] [Related]

  • 14. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M, Mita S, Sakuta R, Nonaka I, Araki S.
    Ann Neurol; 1993 Mar 13; 33(3):275-80. PubMed ID: 7684581
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  • 15. [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
    [Abstract] [Full Text] [Related]

  • 16. Clinical syndromes associated with ragged red fibers.
    Rowland LP, Blake DM, Hirano M, Di Mauro S, Schon EA, Hays AP, Devivo DC.
    Rev Neurol (Paris); 1991 Jul 01; 147(6-7):467-73. PubMed ID: 1962052
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  • 18. Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.
    Moraes CT, DiMauro S, Zeviani M, Lombes A, Shanske S, Miranda AF, Nakase H, Bonilla E, Werneck LC, Servidei S.
    N Engl J Med; 1989 May 18; 320(20):1293-9. PubMed ID: 2541333
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  • 19. Chronic progressive external ophthalmoplegia with T9957C mitochondrial DNA mutation in a Taiwanese patient.
    Liu CH, Liou CW, Liu CH, Kuo HC, Chu CC, Huang CC.
    Acta Neurol Taiwan; 2011 Mar 18; 20(1):53-8. PubMed ID: 21249588
    [Abstract] [Full Text] [Related]

  • 20. [Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation].
    Zhang Y, Wang ZX, Niu SL, Xu YF, Pei P, Yuan Y, Yang YL, Qi Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Feb 18; 27(1):77-80. PubMed ID: 15782498
    [Abstract] [Full Text] [Related]

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