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Journal Abstract Search

373 related items for PubMed ID: 11328729

  • 21. Clinical spectrum of Leber's hereditary optic neuropathy.
    Kerrison JB, Newman NJ.
    Clin Neurosci; 1997; 4(5):295-301. PubMed ID: 9292259
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  • 22. Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy.
    Ventura DF, Gualtieri M, Oliveira AG, Costa MF, Quiros P, Sadun F, de Negri AM, Salomão SR, Berezovsky A, Sherman J, Sadun AA, Carelli V.
    Invest Ophthalmol Vis Sci; 2007 May; 48(5):2362-70. PubMed ID: 17460303
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  • 25. 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 May; 35(1):102-6. PubMed ID: 1895564
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  • 26. Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation.
    Black GC, Craig IW, Oostra RJ, Norby S, Rosenberg T, Morten K, Laborde A, Poulton J.
    Eye (Lond); 1995 May; 9 ( Pt 4)():513-6. PubMed ID: 7498577
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  • 27. 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 May; 36(1):56-61. PubMed ID: 1635296
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  • 28. 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 May; 43(3):196-200. PubMed ID: 10413253
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  • 30. Leber's hereditary optic neuropathy: heteroplasmy is likely to be significant in the expression of LHON in families with the 3460 ND1 mutation.
    Black GC, Morten K, Laborde A, Poulton J.
    Br J Ophthalmol; 1996 Oct; 80(10):915-7. PubMed ID: 8976705
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  • 31. [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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  • 32. 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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  • 34. 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 Dec; 213(3):171-5. PubMed ID: 10202290
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  • 36. Heteroplasmy in Leber's hereditary optic neuropathy.
    Smith KH, Johns DR, Heher KL, Miller NR.
    Arch Ophthalmol; 1993 Nov; 111(11):1486-90. PubMed ID: 8240102
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  • 39. Genotypes of aldehyde dehydrogenase and alcohol dehydrogenase polymorphisms in patients with Leber's hereditary optic neuropathy.
    Isashiki Y, Tabata Y, Kamimura K, Ohba N.
    Jpn J Hum Genet; 1997 Mar; 42(1):187-91. PubMed ID: 9183998
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