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123 related items for PubMed ID: 20565249

  • 1. 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; 31(3):126-8. PubMed ID: 20565249
    [Abstract] [Full Text] [Related]

  • 2. Rapid quantification of the heteroplasmy of mutant mitochondrial DNAs in Leber's hereditary optic neuropathy using the Invader technology.
    Mashima Y, Nagano M, Funayama T, Zhang Q, Egashira T, Kudho J, Shimizu N, Oguchi Y.
    Clin Biochem; 2004 Apr; 37(4):268-76. PubMed ID: 15003728
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  • 3. Reduced frequency of known mutations in a cohort of LHON patients from India.
    Sundaresan P, Kumar SM, Thompson S, Fingert JH.
    Ophthalmic Genet; 2010 Dec; 31(4):196-9. PubMed ID: 20809775
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  • 6. Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families.
    Martin-Kleiner I, Gabrilovac J, Bradvica M, Vidović T, Cerovski B, Fumić K, Boranić M.
    Coll Antropol; 2006 Mar; 30(1):171-4. PubMed ID: 16617593
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  • 7. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
    Mao YJ, Qu J, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb; 25(1):45-9. PubMed ID: 18247303
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  • 8. Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.
    Sudoyo H, Suryadi H, Lertrit P, Pramoonjago P, Lyrawati D, Marzuki S.
    J Hum Genet; 2002 Feb; 47(11):594-604. PubMed ID: 12436196
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  • 9. [Leber's hereditary optic neuropathy].
    Konrádová V, Zeman J, Stratilová L, Hermanská J, Vseticka I, Misovicová N, Kurca E, Gerinec A, Houstĕk J.
    Cas Lek Cesk; 1999 Oct 20; 138(18):565-8. PubMed ID: 10596473
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  • 10. Leber's hereditary optic neuropathy mutations in ethambutol-induced optic neuropathy.
    Hwang JM, Kim J, Park SS.
    J Neurol; 2003 Jan 20; 250(1):87-9. PubMed ID: 12527998
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  • 11. 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 20; 37(8):1028-33. PubMed ID: 17045122
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  • 12. [Rapid genetic screening of Leber's hereditary optic neuropathy with mtDNA G11778A mutation by AS-PCR with whole blood].
    Yang JH, Tong Y, Li BH, Chen YK.
    Zhonghua Yan Ke Za Zhi; 2005 Mar 20; 41(3):243-5. PubMed ID: 15840367
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  • 13. A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy.
    Sadun AA, Carelli V, Salomao SR, Berezovsky A, Quiros P, Sadun F, DeNegri AM, Andrade R, Schein S, Belfort R.
    Trans Am Ophthalmol Soc; 2002 Mar 20; 100():169-78; discussion 178-9. PubMed ID: 12545691
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  • 14. Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans.
    Kim JY, Hwang JM, Chang BL, Park SS.
    J Neurol; 2003 Mar 20; 250(3):278-81. PubMed ID: 12638016
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  • 15. 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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  • 16. [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 06; 47(12):1080-3. PubMed ID: 22336116
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  • 17. [Sudden blindness: consider Leber's hereditary optic neuropathy].
    Schieving JH, de Vries BB, Hol F, Stroink H.
    Ned Tijdschr Geneeskd; 2008 Oct 25; 152(43):2313-6. PubMed ID: 19024058
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  • 20. 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 25; 54(1):1601-1607. PubMed ID: 35723074
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