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Journal Abstract Search

291 related items for PubMed ID: 17471325

  • 1. 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; 104():51-61. PubMed ID: 17471325
    [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
    [Abstract] [Full Text] [Related]

  • 3. 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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  • 4. Ophthalmologic findings in a large pedigree of 11778/Haplogroup J Leber hereditary optic neuropathy.
    Sadun F, De Negri AM, Carelli V, Salomao SR, Berezovsky A, Andrade R, Moraes M, Passos A, Belfort R, da Rosa AB, Quiros P, Sadun AA.
    Am J Ophthalmol; 2004 Feb; 137(2):271-7. PubMed ID: 14962416
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  • 5. Leber's hereditary optic neuropathy with childhood onset.
    Barboni P, Savini G, Valentino ML, La Morgia C, Bellusci C, De Negri AM, Sadun F, Carta A, Carbonelli M, Sadun AA, Carelli V.
    Invest Ophthalmol Vis Sci; 2006 Dec; 47(12):5303-9. PubMed ID: 17122117
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  • 6. A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy.
    Sadun AA, Carelli V, Salomao SR, Berezovsky A, Quiros P, Sadun F, DeNegri AM, Andrade R, Schein S, Belfort R.
    Trans Am Ophthalmol Soc; 2002 Dec; 100():169-78; discussion 178-9. PubMed ID: 12545691
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  • 11. [A study of clinical and genetic characteristics of a Leber hereditary optic neuropathy family with the heteroplasmic m.14484T>C mutation].
    Sun Y, Lei K, Xu ZL, Geng Y.
    Zhonghua Yan Ke Za Zhi; 2018 Jul 11; 54(7):526-534. PubMed ID: 29996615
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  • 12. Mitochondrial abnormalities in patients with LHON-like optic neuropathies.
    Abu-Amero KK, Bosley TM.
    Invest Ophthalmol Vis Sci; 2006 Oct 11; 47(10):4211-20. PubMed ID: 17003408
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  • 14. 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 11; 141(4):676-82. PubMed ID: 16564802
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  • 16. 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 11; 112(1):127-31. PubMed ID: 15629832
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  • 17. Association of optic disc size with development and prognosis of Leber's hereditary optic neuropathy.
    Ramos Cdo V, Bellusci C, Savini G, Carbonelli M, Berezovsky A, Tamaki C, Cinoto R, Sacai PY, Moraes-Filho MN, Miura HM, Valentino ML, Iommarini L, De Negri AM, Sadun F, Cortelli P, Montagna P, Salomao SR, Sadun AA, Carelli V, Barboni P.
    Invest Ophthalmol Vis Sci; 2009 Apr 11; 50(4):1666-74. PubMed ID: 19098324
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  • 18. Visual electrophysiologic findings in patients from an extensive Brazilian family with Leber's hereditary optic neuropathy.
    Salomão SR, Berezovsky A, Andrade RE, Belfort R, Carelli V, Sadun AA.
    Doc Ophthalmol; 2004 Mar 11; 108(2):147-55. PubMed ID: 15455797
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  • 19. [Clinical examination of Leber hereditary optic neuropathy in patients with the same gene mutation].
    Chelstowska J, Mroczek K, Niebudek D, Małecka-Idzikowska A, Bartnik E, Hanna Nizankowska M, Sasiadek M.
    Przegl Lek; 2002 Mar 11; 59(10):777-9. PubMed ID: 12632910
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  • 20. Mild Leber hereditary optic neuropathy (LHON) in a Western European family due to the rare Asian m.14502T>C variant in the MT-ND6 gene.
    Vandeputte J, Van Heetvelde M, Van Cauwenbergh C, Seneca S, De Baere E, Leroy BP, De Zaeytijd J.
    Ophthalmic Genet; 2021 Aug 11; 42(4):440-445. PubMed ID: 33858285
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