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Journal Abstract Search

465 related items for PubMed ID: 16424523

  • 1. Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study.
    Quiros PA, Torres RJ, Salomao S, Berezovsky A, Carelli V, Sherman J, Sadun F, De Negri A, Belfort R, Sadun AA.
    Br J Ophthalmol; 2006 Feb; 90(2):150-3. PubMed ID: 16424523
    [Abstract] [Full Text] [Related]

  • 2. 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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  • 3. Subclinical carriers and conversions in Leber hereditary optic neuropathy: a prospective psychophysical study.
    Sadun AA, Salomao SR, Berezovsky A, Sadun F, Denegri AM, Quiros PA, Chicani F, Ventura D, Barboni P, Sherman J, Sutter E, Belfort R, Carelli V.
    Trans Am Ophthalmol Soc; 2006 May; 104():51-61. PubMed ID: 17471325
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  • 4. Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy.
    Ventura DF, Quiros P, Carelli V, Salomão SR, Gualtieri M, Oliveira AG, Costa MF, Berezovsky A, Sadun F, de Negri AM, Sadun AA.
    Invest Ophthalmol Vis Sci; 2005 Dec; 46(12):4809-14. PubMed ID: 16303983
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  • 7. Retinal nerve fiber layer evaluation by optical coherence tomography in unaffected carriers with Leber's hereditary optic neuropathy mutations.
    Savini G, Barboni P, Valentino ML, Montagna P, Cortelli P, De Negri AM, Sadun F, Bianchi S, Longanesi L, Zanini M, Carelli V.
    Ophthalmology; 2005 Jan; 112(1):127-31. PubMed ID: 15629832
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  • 8. [Sudden blindness: consider Leber's hereditary optic neuropathy].
    Schieving JH, de Vries BB, Hol F, Stroink H.
    Ned Tijdschr Geneeskd; 2008 Oct 25; 152(43):2313-6. PubMed ID: 19024058
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  • 9. Influence of mutation type on clinical expression of Leber hereditary optic neuropathy.
    Spruijt L, Kolbach DN, de Coo RF, Plomp AS, Bauer NJ, Smeets HJ, de Die-Smulders CE.
    Am J Ophthalmol; 2006 Apr 25; 141(4):676-82. PubMed ID: 16564802
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  • 11. 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 25; 42(6):1208-14. PubMed ID: 11328729
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  • 12. Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers.
    Bianco A, Valletti A, Longo G, Bisceglia L, Montoya J, Emperador S, Guerriero S, Petruzzella V.
    BMC Res Notes; 2018 Dec 20; 11(1):911. PubMed ID: 30572950
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  • 14. Leber's hereditary optic neuropathy is associated with the mitochondrial ND6 T14484C mutation in three Chinese families.
    Sun YH, Wei QP, Zhou X, Qian Y, Zhou J, Lu F, Qu J, Guan MX.
    Biochem Biophys Res Commun; 2006 Aug 18; 347(1):221-5. PubMed ID: 16806060
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  • 15. [A pedigree of Leber's hereditary optic neuropathy with mtDNA 14484 mutation].
    Tong Y, Wang Y, Jiang F, Liu B, Zhang S, Yang W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct 18; 25(5):531-3. PubMed ID: 18841565
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  • 17. Genetic analysis of Japanese pedigrees with Leber's hereditary optic neuropathy.
    Nakamura M.
    Kobe J Med Sci; 1993 Dec 18; 39(5-6):171-82. PubMed ID: 8182918
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  • 18. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
    Mao YJ, Qu J, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb 18; 25(1):45-9. PubMed ID: 18247303
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  • 20. Severe manifestation of Leber's hereditary optic neuropathy due to 11778G>A mtDNA mutation in a female with hypoestrogenism due to Perrault syndrome.
    Badura-Stronka M, Wawrocka A, Zawieja K, Silska S, Krawczyński MR.
    Mitochondrion; 2013 Nov 18; 13(6):831-4. PubMed ID: 23748049
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