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Journal Abstract Search

124 related items for PubMed ID: 38346855

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  • 2. mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese population.
    Jia X, Li S, Wang P, Guo X, Zhang Q.
    Biochem Biophys Res Commun; 2010 Dec 10; 403(2):237-41. PubMed ID: 21074518
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  • 3. 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 10; 42(4):440-445. PubMed ID: 33858285
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  • 4. [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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  • 7. Leber's Hereditary Optic Neuropathy is Associated with Compound Primary Mutations of Mitochondrial ND1 m.3635G > A and ND6 m.14502 T > C.
    Jin X, Wang L, Gong Y, Chen B, Wang Y, Chen T, Wei S.
    Ophthalmic Genet; 2015 Jul 11; 36(4):291-8. PubMed ID: 24417559
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  • 8. Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India.
    Khan NA, Govindaraj P, Soumittra N, Sharma S, Srilekha S, Ambika S, Vanniarajan A, Meena AK, Uppin MS, Sundaram C, Bindu PS, Gayathri N, Taly AB, Thangaraj K.
    Invest Ophthalmol Vis Sci; 2017 Aug 01; 58(10):3923-3930. PubMed ID: 28768321
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  • 9. Pathogenic mitochondrial DNA mutations and associated clinical features in Korean patients with Leber's hereditary optic neuropathy.
    Yum HR, Chae H, Shin SY, Kim Y, Kim M, Park SH.
    Invest Ophthalmol Vis Sci; 2014 Oct 23; 55(12):8095-101. PubMed ID: 25342614
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  • 13. Visual prognosis better in eyes with less severe reduction of visual acuity one year after onset of Leber hereditary optic neuropathy caused by the 11,778 mutation.
    Mashima Y, Kigasawa K, Shinoda K, Wakakura M, Oguchi Y.
    BMC Ophthalmol; 2017 Oct 18; 17(1):192. PubMed ID: 29047345
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  • 14. [Long-term changes in morphological and functional parameters of the optic nerve in patients with various genetic variants of hereditary optic neuropathies].
    Murakhovskaya YK, Andreeva NA, Tsygankova PG, Krylova TD, Sheremet NL.
    Vestn Oftalmol; 2023 Oct 18; 139(6):77-86. PubMed ID: 38235633
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  • 18. Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families.
    Liu XL, Zhou X, Zhou J, Zhao F, Zhang J, Li C, Ji Y, Zhang Y, Wei QP, Sun YH, Yang L, Lin B, Yuan Y, Li Y, Qu J, Guan MX.
    Ophthalmology; 2011 May 18; 118(5):978-85. PubMed ID: 21131053
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