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220 related items for PubMed ID: 1346348

  • 1. Mitochondrial DNA mutation and heteroplasmy in type I Leber hereditary optic neuropathy.
    Zhu DP, Economou EP, Antonarakis SE, Maumenee IH.
    Am J Med Genet; 1992 Jan 15; 42(2):173-9. PubMed ID: 1346348
    [Abstract] [Full Text] [Related]

  • 2. Mitochondrial DNA mutation in Leber's hereditary optic neuropathy.
    Yen MY, Yen TC, Pang CY, Liu JH, Wei YH.
    Invest Ophthalmol Vis Sci; 1992 Jul 15; 33(8):2561-6. PubMed ID: 1634353
    [Abstract] [Full Text] [Related]

  • 3. Clinical correlation of mitochondrial DNA heteroplasmy and Leber's hereditary optic neuropathy.
    Isashiki Y, Nakagawa M.
    Jpn J Ophthalmol; 1991 Jul 15; 35(3):259-67. PubMed ID: 1770665
    [Abstract] [Full Text] [Related]

  • 4. High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy.
    Nakamura M, Ara F, Yamada M, Hotta Y, Hayakawa M, Fujiki K, Kanai A, Sakai J, Inoue M, Yamamoto M.
    Jpn J Ophthalmol; 1992 Jul 15; 36(1):56-61. PubMed ID: 1635296
    [Abstract] [Full Text] [Related]

  • 5. Quantitative determination of heteroplasmy in Leber's hereditary optic neuropathy by single-strand conformation polymorphism.
    Mashima Y, Saga M, Hiida Y, Oguchi Y, Wakakura M, Kudoh J, Shimizu N.
    Invest Ophthalmol Vis Sci; 1995 Jul 15; 36(8):1714-20. PubMed ID: 7601652
    [Abstract] [Full Text] [Related]

  • 6. Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy.
    Jacobi FK, Leo-Kottler B, Mittelviefhaus K, Zrenner E, Meyer J, Pusch CM, Wissinger B.
    Invest Ophthalmol Vis Sci; 2001 May 15; 42(6):1208-14. PubMed ID: 11328729
    [Abstract] [Full Text] [Related]

  • 7. [Analysis of mutations and heteroplasmy at mitochondrial DNA 11778 using non-RI single strand conformation polymorphisms in Leber's hereditary optic neuropathy].
    Toyo-Oka Y, Wada C, Yamabe H, Inoue M, Ishigaki M, Matsuyama N, Ohnuki Y, Ichibe Y, Wakakura M, Ohtani H.
    Rinsho Byori; 1996 Jul 15; 44(7):676-80. PubMed ID: 8741498
    [Abstract] [Full Text] [Related]

  • 8. Homoplasmic and exclusive ND4 gene mutation in Japanese pedigrees with Leber's disease.
    Nakamura M, Fujiwara Y, Yamamoto M.
    Invest Ophthalmol Vis Sci; 1993 Mar 15; 34(3):488-95. PubMed ID: 8449667
    [Abstract] [Full Text] [Related]

  • 9. Rapid quantification of the heteroplasmy of mutant mitochondrial DNAs in Leber's hereditary optic neuropathy using the Invader technology.
    Mashima Y, Nagano M, Funayama T, Zhang Q, Egashira T, Kudho J, Shimizu N, Oguchi Y.
    Clin Biochem; 2004 Apr 15; 37(4):268-76. PubMed ID: 15003728
    [Abstract] [Full Text] [Related]

  • 10. Mitochondrial DNA analysis of Leber's hereditary optic neuropathy.
    Hiida Y, Mashima Y, Oguchi Y, Uemura Y, Kudoh J, Sakai K, Shimizu N.
    Jpn J Ophthalmol; 1991 Apr 15; 35(1):102-6. PubMed ID: 1895564
    [Abstract] [Full Text] [Related]

  • 11. [Mitochondrial DNA mutation in Leber's hereditary optic neuropathy in China].
    Zhang LS, Huang Y, Li FY.
    Zhonghua Yi Xue Za Zhi; 1994 Jun 15; 74(6):349-51, 390. PubMed ID: 7994643
    [Abstract] [Full Text] [Related]

  • 12. Tissue distribution of the ND4/11778 mutation in heteroplasmic lineages with Leber hereditary optic neuropathy.
    Juvonen V, Nikoskelainen E, Lamminen T, Penttinen M, Aula P, Savontaus ML.
    Hum Mutat; 1997 Jun 15; 9(5):412-7. PubMed ID: 9143920
    [Abstract] [Full Text] [Related]

  • 13. [Leber's hereditary optic neuropathy].
    Konrádová V, Zeman J, Stratilová L, Hermanská J, Vseticka I, Misovicová N, Kurca E, Gerinec A, Houstĕk J.
    Cas Lek Cesk; 1999 Oct 20; 138(18):565-8. PubMed ID: 10596473
    [Abstract] [Full Text] [Related]

  • 14.
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  • 15. A family with Leber's hereditary optic neuropathy with mitochondrial DNA heteroplasmy related to disease expression.
    Tanaka A, Kiyosawa M, Mashima Y, Tokoro T.
    J Neuroophthalmol; 1998 Jun 20; 18(2):81-3. PubMed ID: 9621260
    [Abstract] [Full Text] [Related]

  • 16. Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA.
    Hotta Y, Fujiki K, Hayakawa M, Nakajima A, Kanai A, Mashima Y, Hiida Y, Shinoda K, Yamada K, Oguchi Y.
    Jpn J Ophthalmol; 1995 Jun 20; 39(1):96-108. PubMed ID: 7643491
    [Abstract] [Full Text] [Related]

  • 17. [Detection of mtDNA*LHON G11778A mutation by real-time polymerase chain reaction using TaqMan-MGB probe technology].
    Li YM, Wang JY, Chen Y, Shao JB, Wang J, Tong Y.
    Zhonghua Yan Ke Za Zhi; 2006 Aug 20; 42(8):728-32. PubMed ID: 17081446
    [Abstract] [Full Text] [Related]

  • 18. Leber hereditary optic neuropathy: mitochondrial mutations and degeneration of the optic nerve.
    Howell N.
    Vision Res; 1997 Dec 20; 37(24):3495-507. PubMed ID: 9425526
    [Abstract] [Full Text] [Related]

  • 19. A mutation of mitochondrial DNA in Japanese families with Leber's hereditary optic neuropathy.
    Fujiki K, Hotta Y, Hayakawa M, Saito K, Ara F, Ueda S, Goto T, Ishida M, Yanashima K, Shiono T.
    Jinrui Idengaku Zasshi; 1991 Jun 20; 36(2):143-7. PubMed ID: 1681125
    [Abstract] [Full Text] [Related]

  • 20. Detection of the G to A mitochondrial DNA mutation at position 11778 in German families with Leber's hereditary optic neuropathy.
    Kormann BA, Schuster H, Berninger TA, Leo-Kottler B.
    Hum Genet; 1991 Nov 20; 88(1):98-100. PubMed ID: 1959931
    [Abstract] [Full Text] [Related]

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