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Journal Abstract Search

387 related items for PubMed ID: 28761322

  • 1.
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  • 2. Multiplex MALDI-TOF MS detection of mitochondrial variants in Brazilian patients with hereditary optic neuropathy.
    Miranda PM, Matilde da Silva-Costa S, Balieiro JC, Fernandes MS, Alves RM, Guerra AT, Marcondes AM, Sartorato EL.
    Mol Vis; 2016; 22():1024-35. PubMed ID: 27582625
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  • 5. [Detection of mtDNA*LHON G11778A mutation by real-time polymerase chain reaction using TaqMan-MGB probe technology].
    Li YM, Wang JY, Chen Y, Shao JB, Wang J, Tong Y.
    Zhonghua Yan Ke Za Zhi; 2006 Aug; 42(8):728-32. PubMed ID: 17081446
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  • 6. 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 Aug; 17():3175-9. PubMed ID: 22194643
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  • 7. 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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  • 8. [Mutation analysis in a family of Leber hereditary optic neuropathy].
    She CY, Gu H, Xu J, Ma K, Liu NP.
    Zhonghua Yan Ke Za Zhi; 2011 Dec; 47(12):1080-3. PubMed ID: 22336116
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  • 9. TaqMan-MGB probe quantitative PCR assays to genotype and quantify three mtDNA mutations of Leber hereditary optic neuropathy.
    Xue B, Li Y, Wang X, Li R, Zeng X, Yang M, Xu X, Ye T, Bao L, Huang Y.
    Sci Rep; 2020 Jul 23; 10(1):12264. PubMed ID: 32704028
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  • 10. Leber's hereditary optic neuropathy: clinical and molecular profile of a Brazilian sample.
    Maciel-Guerra AT, Zanchetta LM, Amaral Fernandes MS, Andrade PB, do Amor Divino Miranda PM, Sartorato EL.
    Ophthalmic Genet; 2010 Sep 23; 31(3):126-8. PubMed ID: 20565249
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  • 11. [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 Sep 23; 59(10):777-9. PubMed ID: 12632910
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  • 12. Mitochondrial D-loop variation in leber hereditary neuropathy patients harboring primary G11778A, G3460A, T14484C mutations: J and W haplogroups as high-risk factors.
    Shafa Shariat Panahi M, Houshmand M, Tabassi AR.
    Arch Med Res; 2006 Nov 23; 37(8):1028-33. PubMed ID: 17045122
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  • 16. Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy.
    Jia X, Li S, Xiao X, Guo X, Zhang Q.
    J Hum Genet; 2006 Nov 23; 51(10):851-856. PubMed ID: 16972023
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  • 17. Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.
    Liang M, Jiang P, Li F, Zhang J, Ji Y, He Y, Xu M, Zhu J, Meng X, Zhao F, Tong Y, Liu X, Sun Y, Zhou X, Mo JQ, Qu J, Guan MX.
    Invest Ophthalmol Vis Sci; 2014 Mar 06; 55(3):1321-31. PubMed ID: 24398099
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  • 18. The epidemiology and mutation types of Leber's hereditary optic neuropathy in Thailand.
    Sathianvichitr K, Sigkaman B, Chirapapaisan N, Laowanapiban P, Padungkiatsagul T, Apinyawasisuk S, Witthayaweerasak J, Chuenkongkaew W.
    Ann Med; 2022 Dec 06; 54(1):1601-1607. PubMed ID: 35723074
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  • 20. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
    Chinnery PF, Brown DT, Andrews RM, Singh-Kler R, Riordan-Eva P, Lindley J, Applegarth DA, Turnbull DM, Howell N.
    Brain; 2001 Jan 06; 124(Pt 1):209-18. PubMed ID: 11133798
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