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191 related items for PubMed ID: 1769162

  • 1. [Chronic progressive external ophthalmoplegia (CPEO); mitochondrial DNA deletion, brain MRI and electrophysiological studies].
    Nakagawa M, Tokimura M, Kuriyama M, Higuchi I, Osame M.
    Rinsho Shinkeigaku; 1991 Sep; 31(9):981-6. PubMed ID: 1769162
    [Abstract] [Full Text] [Related]

  • 2. [Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome].
    Wang ZX, Yuan Y, Gao F, Qi Y, Shen DG, Chen QT.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):273-8. PubMed ID: 12903032
    [Abstract] [Full Text] [Related]

  • 3. Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement: can we predict progression?
    Auré K, Ogier de Baulny H, Laforêt P, Jardel C, Eymard B, Lombès A.
    Brain; 2007 Jun; 130(Pt 6):1516-24. PubMed ID: 17439982
    [Abstract] [Full Text] [Related]

  • 4. [Chronic progressive external ophthalmoplegia (CPEO) with deleted mitochondrial DNA].
    Tanno Y, Yoneda M, Ohnishi Y, Miyatake T, Ozawa T.
    Rinsho Shinkeigaku; 1989 Sep; 29(9):1176-9. PubMed ID: 2598547
    [Abstract] [Full Text] [Related]

  • 5.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Goldstein A, Falk MJ.
    ; 1993 Sep. PubMed ID: 20301382
    [Abstract] [Full Text] [Related]

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

  • 7. [Partial deletion of mitochondrial DNA in mitochondrial encephalomyopathies].
    Wang W, Zhang J, Guo Y, Guo Z, Ren H.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1997 Aug; 19(4):278-83. PubMed ID: 10453567
    [Abstract] [Full Text] [Related]

  • 8. [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]

  • 9. Unusual clinical presentation of a patient carrying a novel single 1.8 kb deletion of mitochondrial DNA.
    Zoccolella S, Torraco A, Amati A, Lamberti P, Serlenga L, Papa S, Petruzzella V.
    Funct Neurol; 2006 Jul 01; 21(1):39-41. PubMed ID: 16735000
    [Abstract] [Full Text] [Related]

  • 10. Patient with Kearns-Sayre syndrome exhibiting abnormal magnetic resonance image of the brain.
    Kamata Y, Mashima Y, Yokoyama M, Tanaka K, Goto Y, Oguchi Y.
    J Neuroophthalmol; 1998 Dec 01; 18(4):284-8. PubMed ID: 9858014
    [Abstract] [Full Text] [Related]

  • 11. Segmental cytochrome c-oxidase deficiency in CPEO: teased muscle fiber analysis.
    Matsuoka T, Goto Y, Hasegawa H, Nonaka I.
    Muscle Nerve; 1992 Feb 01; 15(2):209-13. PubMed ID: 1312676
    [Abstract] [Full Text] [Related]

  • 12. [A case of chronic progressive external ophthalmoplegia associated with familial hypercholesterolemia].
    Orimo S, Arai M, Hiyamuta E, Goto Y.
    Rinsho Shinkeigaku; 1992 Jan 01; 32(1):37-41. PubMed ID: 1628435
    [Abstract] [Full Text] [Related]

  • 13. CPEO and KSS differ in the percentage and location of the mtDNA deletion.
    López-Gallardo E, López-Pérez MJ, Montoya J, Ruiz-Pesini E.
    Mitochondrion; 2009 Sep 01; 9(5):314-7. PubMed ID: 19410662
    [Abstract] [Full Text] [Related]

  • 14. Ophthalmoplegia in Mitochondrial Disease.
    Lee SJ, Na JH, Han J, Lee YM.
    Yonsei Med J; 2018 Dec 01; 59(10):1190-1196. PubMed ID: 30450853
    [Abstract] [Full Text] [Related]

  • 15. [A case of Kearns-Sayre syndrome].
    Kokot W, Iwaszkiewicz-Bilikiewiczowa B, Lewczuk A, Sworczak K.
    Klin Oczna; 1996 Dec 01; 98(4):327-30. PubMed ID: 9463130
    [Abstract] [Full Text] [Related]

  • 16. Mitochondrial gene defect in patients with chronic progressive external ophthalmoplegia.
    Chen Q, Li X, Wu L, Qi Y, Wu X.
    Chin Med J (Engl); 1998 Jun 01; 111(6):500-3. PubMed ID: 11245066
    [Abstract] [Full Text] [Related]

  • 17. Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA.
    Kärppä M, Herva R, Moslemi AR, Oldfors A, Kakko S, Majamaa K.
    Brain; 2005 Aug 01; 128(Pt 8):1861-9. PubMed ID: 15857931
    [Abstract] [Full Text] [Related]

  • 18. The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions.
    Zhao Y, Hou Y, Zhao X, Liufu T, Yu M, Zhang W, Xie Z, Zhang VW, Yuan Y, Wang Z.
    Mol Genet Genomic Med; 2024 Jan 01; 12(1):e2328. PubMed ID: 38018320
    [Abstract] [Full Text] [Related]

  • 19. [Diagnostic value of mitochondrial DNA analysis in chronic progressive external ophthalmoplegia (CPEO)].
    Kornblum C, Kunz WS, Klockgether T, Roggenkämper P, Schröder R.
    Klin Monbl Augenheilkd; 2004 Dec 01; 221(12):1057-61. PubMed ID: 15599814
    [Abstract] [Full Text] [Related]

  • 20. [Ocular mitochondrial myopathies: a spectrum of clinical presentations].
    Glutz von Blotzheim S, Borruat FX, Hirt L.
    Klin Monbl Augenheilkd; 1998 May 01; 212(5):299-300. PubMed ID: 9677561
    [Abstract] [Full Text] [Related]

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