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Journal Abstract Search

299 related items for PubMed ID: 32969847

  • 21. 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; 101(11):1505-1509. PubMed ID: 28314831
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  • 22. 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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  • 27. Randomized trial of bilateral gene therapy injection for m.11778G>A MT-ND4 Leber optic neuropathy.
    Newman NJ, Yu-Wai-Man P, Subramanian PS, Moster ML, Wang AG, Donahue SP, Leroy BP, Carelli V, Biousse V, Vignal-Clermont C, Sergott RC, Sadun AA, Rebolleda Fernández G, Chwalisz BK, Banik R, Bazin F, Roux M, Cox ED, Taiel M, Sahel JA, LHON REFLECT Study Group .
    Brain; 2023 Apr 19; 146(4):1328-1341. PubMed ID: 36350566
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  • 29. Identification of an ND4 Mutation in Leber Hereditary Optic Neuropathy.
    Lu Q, Guo Y, Yi J, Deng X, Yang Z, Yuan X, Deng H.
    Optom Vis Sci; 2017 Dec 19; 94(12):1090-1094. PubMed ID: 29116953
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  • 34. Mitochondrial genome variation in male LHON patients with the m.11778G > A mutation.
    Piotrowska-Nowak A, Krawczyński MR, Kosior-Jarecka E, Ambroziak AM, Korwin M, Ołdak M, Tońska K, Bartnik E.
    Metab Brain Dis; 2020 Dec 19; 35(8):1317-1327. PubMed ID: 32740724
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  • 35. ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait.
    Behbehani R, Melhem M, Alghanim G, Behbehani K, Alsmadi O.
    Br J Ophthalmol; 2014 Jun 19; 98(6):826-31. PubMed ID: 24568867
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  • 39. Genotypic and phenotypic characteristics of Korean children with childhood-onset Leber's hereditary optic neuropathy.
    Ahn YJ, Park Y, Shin SY, Chae H, Kim M, Park SH.
    Graefes Arch Clin Exp Ophthalmol; 2020 Oct 19; 258(10):2283-2290. PubMed ID: 32506279
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