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373 related items for PubMed ID: 11328729

  • 1. 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; 42(6):1208-14. PubMed ID: 11328729
    [Abstract] [Full Text] [Related]

  • 2. 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; 36(8):1714-20. PubMed ID: 7601652
    [Abstract] [Full Text] [Related]

  • 3. 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; 18(2):81-3. PubMed ID: 9621260
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  • 4. 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; 37(4):268-76. PubMed ID: 15003728
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  • 5. Genetic analysis of Japanese pedigrees with Leber's hereditary optic neuropathy.
    Nakamura M.
    Kobe J Med Sci; 1993 Dec; 39(5-6):171-82. PubMed ID: 8182918
    [Abstract] [Full Text] [Related]

  • 6. [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; 44(7):676-80. PubMed ID: 8741498
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  • 7. 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 Jul; 39(1):96-108. PubMed ID: 7643491
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  • 8. Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
    Leo-Kottler B, Christ-Adler M, Baumann B, Zrenner E, Wissinger B.
    Ger J Ophthalmol; 1996 Jul; 5(4):233-40. PubMed ID: 8854108
    [Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. [Analysis on the effect of secondary mutations on Leber's hereditary optic neuropathy].
    Wang Y, Tong Y, Hu SX, Wang JY, Shao JB, Zhang HX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug 20; 24(4):397-400. PubMed ID: 17680528
    [Abstract] [Full Text] [Related]

  • 11. 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 20; 33(8):2561-6. PubMed ID: 1634353
    [Abstract] [Full Text] [Related]

  • 12. 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 20; 34(3):488-95. PubMed ID: 8449667
    [Abstract] [Full Text] [Related]

  • 13. Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population.
    Dogulu CF, Kansu T, Seyrantepe V, Ozguc M, Topaloglu H, Johns DR.
    Eye (Lond); 2001 Apr 20; 15(Pt 2):183-8. PubMed ID: 11339587
    [Abstract] [Full Text] [Related]

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  • 15. 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]

  • 16. Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans.
    Kim JY, Hwang JM, Chang BL, Park SS.
    J Neurol; 2003 Mar 15; 250(3):278-81. PubMed ID: 12638016
    [Abstract] [Full Text] [Related]

  • 17. Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family.
    Kaplanová V, Zeman J, Hansíková H, Cerná L, Houst'ková H, Misovicová N, Houstek J.
    J Neurol Sci; 2004 Aug 30; 223(2):149-55. PubMed ID: 15337616
    [Abstract] [Full Text] [Related]

  • 18. [Mitochondrial DNA mutation in Leber's hereditary optic neuropathy in China].
    Zhang LS, Huang Y, Li FY.
    Zhonghua Yi Xue Za Zhi; 1994 Jun 30; 74(6):349-51, 390. PubMed ID: 7994643
    [Abstract] [Full Text] [Related]

  • 19. Clinical correlation of mitochondrial DNA heteroplasmy and Leber's hereditary optic neuropathy.
    Isashiki Y, Nakagawa M.
    Jpn J Ophthalmol; 1991 Jun 30; 35(3):259-67. PubMed ID: 1770665
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