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Journal Abstract Search

370 related items for PubMed ID: 25342614

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  • 46. Mitochondrial Genetic Heterogeneity in Leber's Hereditary Optic Neuropathy: Original Study with Meta-Analysis.
    Jha RK, Dawar C, Hasan Q, Pujar A, Gupta G, Vishnu VY, Kekunnaya R, Thangaraj K.
    Genes (Basel); 2021 Aug 24; 12(9):. PubMed ID: 34573281
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  • 47. Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia.
    Korkiamäki P, Kervinen M, Karjalainen K, Majamaa K, Uusimaa J, Remes AM.
    Acta Ophthalmol; 2013 Nov 24; 91(7):630-4. PubMed ID: 22970697
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  • 48. Analysis of the entire mitochondrial genome reveals Leber's hereditary optic neuropathy mitochondrial DNA mutations in an Arab cohort with multiple sclerosis.
    Al-Kafaji G, Alharbi MA, Alkandari H, Salem AH, Bakhiet M.
    Sci Rep; 2022 Jun 30; 12(1):11099. PubMed ID: 35773337
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  • 51. m.3635G>A mutation as a cause of Leber hereditary optic neuropathy.
    Kodroń A, Krawczyński MR, Tońska K, Bartnik E.
    J Clin Pathol; 2014 Jul 30; 67(7):639-41. PubMed ID: 24747208
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  • 52. Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy.
    Ji Y, Zhang J, Lu Y, Yi Q, Chen M, Xie S, Mao X, Xiao Y, Meng F, Zhang M, Yang R, Guan MX.
    J Biol Chem; 2020 Sep 18; 295(38):13224-13238. PubMed ID: 32723871
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  • 53. Macular nerve fibers temporal to fovea may have a greater potential to recover function in patients with Leber's hereditary optic neuropathy.
    Mashima Y, Sato EA, Ohde H, Oguchi Y.
    Jpn J Ophthalmol; 2002 Sep 18; 46(6):660-7. PubMed ID: 12543194
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  • 56. High Mitochondrial DNA Copy Number Is a Protective Factor From Vision Loss in Heteroplasmic Leber's Hereditary Optic Neuropathy (LHON).
    Bianco A, Bisceglia L, Russo L, Palese LL, D'Agruma L, Emperador S, Montoya J, Guerriero S, Petruzzella V.
    Invest Ophthalmol Vis Sci; 2017 Apr 01; 58(4):2193-2197. PubMed ID: 28403426
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  • 57. Mitochondrial DNA variants in a cohort from Argentina with suspected Leber's hereditary optic neuropathy (LHON).
    Buonfiglio PI, Menazzi S, Francipane L, Lotersztein V, Ferreiro V, Elgoyhen AB, Dalamón V.
    PLoS One; 2023 Apr 01; 18(2):e0275703. PubMed ID: 36827238
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  • 59. Leber's hereditary optic neuropathy mutations in Korean patients with multiple sclerosis.
    Hwang JM, Chang BL, Park SS.
    Ophthalmologica; 2001 Apr 01; 215(6):398-400. PubMed ID: 11741103
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