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Journal Abstract Search

184 related items for PubMed ID: 35892476

  • 1. Leber Hereditary Optic Neuropathy in Southwestern Ontario: A Growing List of Mutations.
    McDonald HM, Sadikovic B, Sheldon CA, Bursztyn LLCD.
    Can J Neurol Sci; 2023 Sep; 50(5):738-744. PubMed ID: 35892476
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  • 4. Visual Outcomes in Leber Hereditary Optic Neuropathy Patients With the m.11778G>A (MTND4) Mitochondrial DNA Mutation.
    Newman NJ, Carelli V, Taiel M, Yu-Wai-Man P.
    J Neuroophthalmol; 2020 Dec; 40(4):547-557. PubMed ID: 32969847
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  • 9. 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; 91(7):630-4. PubMed ID: 22970697
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  • 10. Leber's Hereditary Optic Neuropathy as a Promising Disease for Gene Therapy Development.
    Karaarslan C.
    Adv Ther; 2019 Dec; 36(12):3299-3307. PubMed ID: 31605306
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  • 11. Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy.
    Amaral-Fernandes MS, Marcondes AM, do Amor Divino Miranda PM, Maciel-Guerra AT, Sartorato EL.
    Mol Vis; 2011 Dec; 17():3175-9. PubMed ID: 22194643
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  • 12. [Rare pathogenic nucleotide variants of mitochondrial DNA associated with Leber's hereditary optic neuropathy].
    Andreeva NA, Murakhovskaya YK, Krylova TD, Tsygankova PG, Sheremet NL.
    Vestn Oftalmol; 2023 Dec; 139(6):166-174. PubMed ID: 38235644
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  • 13. Leber hereditary optic neuropathy plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6.
    Berardo A, Emmanuele V, Vargas W, Tanji K, Naini A, Hirano M.
    J Neurol; 2020 Mar; 267(3):823-829. PubMed ID: 31776719
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  • 15. Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy.
    Jiang P, Liang M, Zhang J, Gao Y, He Z, Yu H, Zhao F, Ji Y, Liu X, Zhang M, Fu Q, Tong Y, Sun Y, Zhou X, Huang T, Qu J, Guan MX.
    Invest Ophthalmol Vis Sci; 2015 Jul; 56(8):4778-88. PubMed ID: 26218905
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  • 16. Digenic Leigh syndrome on the background of the m.11778G>A Leber hereditary optic neuropathy variant.
    Blickhäuser B, Stenton SL, Neuhofer CM, Floride E, Nesbitt V, Fratter C, Koch J, Kauffmann B, Catarino C, Schlieben LD, Kopajtich R, Carelli V, Sadun AA, McFarland R, Fang F, La Morgia C, Paquay S, Nassogne MC, Ghezzi D, Lamperti C, Wortmann S, Poulton J, Klopstock T, Prokisch H.
    Brain; 2024 Jun 03; 147(6):1967-1974. PubMed ID: 38478578
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  • 18. Childhood-onset Leber hereditary optic neuropathy.
    Majander A, Bowman R, Poulton J, Antcliff RJ, Reddy MA, Michaelides M, Webster AR, Chinnery PF, Votruba M, Moore AT, Yu-Wai-Man P.
    Br J Ophthalmol; 2017 Nov 03; 101(11):1505-1509. PubMed ID: 28314831
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  • 19. Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients.
    Zhang AM, Jia X, Guo X, Zhang Q, Yao YG.
    J Transl Med; 2012 Mar 09; 10():43. PubMed ID: 22400981
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