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Journal Abstract Search

222 related items for PubMed ID: 1770533

  • 1. Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy.
    Poulton J, Deadman ME, Bronte-Stewart J, Foulds WS, Gardiner RM.
    J Med Genet; 1991 Nov; 28(11):765-70. PubMed ID: 1770533
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  • 3. 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 Nov; 35(1):102-6. PubMed ID: 1895564
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  • 4. High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy.
    Mashima Y, Hiida Y, Oguchi Y, Kudoh J, Shimizu N.
    Hum Genet; 1993 Aug; 92(1):101-2. PubMed ID: 8103501
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  • 8. 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; 33(8):2561-6. PubMed ID: 1634353
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  • 9. 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
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  • 10. Mitochondrial DNA analysis in Leber's hereditary optic neuropathy.
    Barboni P, Mantovani V, Montagna P, Bragliani M, Cortelli P, Lugaresi E, Puddu P, Caramazza R.
    Ophthalmic Paediatr Genet; 1992 Dec; 13(4):219-26. PubMed ID: 1488222
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  • 11. [Molecular genetic analysis for Leber's hereditary optic neuropathy (LHON)].
    Tanno Y, Yoneda M, Tanaka K, Tsuji S.
    Nihon Rinsho; 1993 Sep; 51(9):2396-402. PubMed ID: 8411719
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  • 12. An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 gene.
    Howell N, McCullough D.
    Am J Hum Genet; 1990 Oct; 47(4):629-34. PubMed ID: 2121024
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  • 13. Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation.
    Murakami T, Mita S, Tokunaga M, Maeda H, Ueyama H, Kumamoto T, Uchino M, Ando M.
    J Neurol Sci; 1996 Oct; 142(1-2):111-3. PubMed ID: 8902729
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  • 14. Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy.
    Matsumoto M, Hayasaka S, Kadoi C, Hotta Y, Fujiki K, Fujimaki T, Takeda M, Ishida N, Endo S, Kanai A.
    Ophthalmic Genet; 1999 Sep; 20(3):153-60. PubMed ID: 10520236
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  • 15. No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON.
    Gerbitz KD, Paprotta A, Obermaier-Kusser B, Rietschel M, Zerres K.
    FEBS Lett; 1992 Dec 21; 314(3):251-5. PubMed ID: 1361456
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  • 16. 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 21; 36(2):143-7. PubMed ID: 1681125
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  • 17. Pre-excitation syndrome in Leber's hereditary optic neuropathy.
    Nikoskelainen EK, Savontaus ML, Huoponen K, Antila K, Hartiala J.
    Lancet; 1994 Sep 24; 344(8926):857-8. PubMed ID: 7916404
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  • 18. [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 24; 24(4):397-400. PubMed ID: 17680528
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  • 19. Exclusive homoplasmic 11778 mutation in mitochondrial DNA of Chinese patients with Leber's hereditary optic neuropathy.
    Yen MY, Lee HC, Wang AG, Chang WL, Liu JH, Wei YH.
    Jpn J Ophthalmol; 1999 Aug 24; 43(3):196-200. PubMed ID: 10413253
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  • 20. Leber's hereditary optic neuropathy mitochondrial DNA mutations at nucleotides 11778 and 3460 in multiple sclerosis.
    Mojon DS, Herbert J, Sadiq SA, Miller JR, Madonna M, Hirano M.
    Ophthalmologica; 1999 Aug 24; 213(3):171-5. PubMed ID: 10202290
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