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Journal Abstract Search

177 related items for PubMed ID: 20021885

  • 21. [Penetrance of Leber hereditary optic neuropathy individuals with mitochondrial DNA 11778 mutation in the Shanxi area].
    Zheng ML, Zhang GL, Hua AL, Zhang YL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):166-7. PubMed ID: 15079802
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  • 22. [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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  • 23. A patient with two mitochondrial DNA mutations causing PEO and LHON.
    Melberg A, Moslemi AR, Palm O, Raininko R, Stålberg E, Oldfors A.
    Eur J Med Genet; 2009 Oct 25; 52(1):47-8. PubMed ID: 19015050
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  • 25. 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 25; 250(3):278-81. PubMed ID: 12638016
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  • 26. [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 25; 47(12):1080-3. PubMed ID: 22336116
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  • 29. [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 Dec 25; 59(10):777-9. PubMed ID: 12632910
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  • 30. Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy.
    Ventura DF, Gualtieri M, Oliveira AG, Costa MF, Quiros P, Sadun F, de Negri AM, Salomão SR, Berezovsky A, Sherman J, Sadun AA, Carelli V.
    Invest Ophthalmol Vis Sci; 2007 May 25; 48(5):2362-70. PubMed ID: 17460303
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  • 32. Brain stem lesion in mitochondrial DNA G11778A mutation of Leber's hereditary optic neuropathy.
    Chen YT, Chen WL, Chen SN, Liu CS.
    J Formos Med Assoc; 2015 Jul 25; 114(7):668-9. PubMed ID: 24560448
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  • 33. [LHON (Leber's hereditary optic neuropathy)].
    Mashima Y.
    Nihon Rinsho; 2002 Apr 25; 60 Suppl 4():282-6. PubMed ID: 12013866
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  • 34. [Leber's optic neuropathy: a case report].
    Pato-Pato A, Cimas-Hernando I, Lorenzo-González JR.
    Rev Neurol; 2002 Apr 25; 42(1):22-4. PubMed ID: 16402322
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  • 35. Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation--A case report.
    Grazina MM, Diogo LM, Garcia PC, Silva ED, Garcia TD, Robalo CB, Oliveira CR.
    Eur J Paediatr Neurol; 2007 Mar 25; 11(2):115-8. PubMed ID: 17254817
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  • 38. [Detection of mtDNA 11778 (G-->A) point mutation in a family with Leber's hereditary optic neuropathy by site-specific polymerase chain reaction].
    Niu SL, Zhang Y, Xu YF, Bu DF, Ren ZQ, Wang SY, Liu GH, Qi Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2003 Apr 25; 25(2):153-5. PubMed ID: 12905709
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  • 39. The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stress.
    Chao de la Barca JM, Simard G, Amati-Bonneau P, Safiedeen Z, Prunier-Mirebeau D, Chupin S, Gadras C, Tessier L, Gueguen N, Chevrollier A, Desquiret-Dumas V, Ferré M, Bris C, Kouassi Nzoughet J, Bocca C, Leruez S, Verny C, Miléa D, Bonneau D, Lenaers G, Martinez MC, Procaccio V, Reynier P.
    Brain; 2016 Nov 01; 139(11):2864-2876. PubMed ID: 27633772
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  • 40. Increase of mitochondrial DNA in blood cells of patients with Leber's hereditary optic neuropathy with 11778 mutation.
    Yen MY, Chen CS, Wang AG, Wei YH.
    Br J Ophthalmol; 2002 Sep 01; 86(9):1027-30. PubMed ID: 12185132
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