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Journal Abstract Search

529 related items for PubMed ID: 17254817

  • 21. Leber's hereditary optic neuropathy is associated with the mitochondrial ND6 T14484C mutation in three Chinese families.
    Sun YH, Wei QP, Zhou X, Qian Y, Zhou J, Lu F, Qu J, Guan MX.
    Biochem Biophys Res Commun; 2006 Aug 18; 347(1):221-5. PubMed ID: 16806060
    [Abstract] [Full Text] [Related]

  • 22. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.
    Kim JY, Hwang JM, Park SS.
    Ann Neurol; 2002 May 18; 51(5):630-4. PubMed ID: 12112111
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  • 23. 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 18; 48(5):2362-70. PubMed ID: 17460303
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  • 24. 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 May 18; 100():169-78; discussion 178-9. PubMed ID: 12545691
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  • 26. Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population.
    Dogulu CF, Kansu T, Seyrantepe V, Ozguc M, Topaloglu H, Johns DR.
    Eye (Lond); 2001 Apr 18; 15(Pt 2):183-8. PubMed ID: 11339587
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  • 27. A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystonia.
    Spruijt L, Smeets HJ, Hendrickx A, Bettink-Remeijer MW, Maat-Kievit A, Schoonderwoerd KC, Sluiter W, de Coo IF, Hintzen RQ.
    Arch Neurol; 2007 Jun 18; 64(6):890-3. PubMed ID: 17562939
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  • 28. 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 18; 37(4):268-76. PubMed ID: 15003728
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  • 29. Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patient.
    Lertrit P, Ruangvaravate N, Trongpanich Y, Imsumran A, Mungkornkarn C, Neungton N.
    J Med Assoc Thai; 1999 Jan 18; 82(1):59-64. PubMed ID: 10087740
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  • 30. [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 Jan 18; 59(10):777-9. PubMed ID: 12632910
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  • 31. Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese.
    Zhang AM, Zou Y, Guo X, Jia X, Zhang Q, Yao YG.
    Biochem Biophys Res Commun; 2009 Aug 21; 386(2):392-5. PubMed ID: 19527690
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  • 34. [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 21; 25(2):153-5. PubMed ID: 12905709
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  • 36. [Leber's optic neuropathy: a case report].
    Pato-Pato A, Cimas-Hernando I, Lorenzo-González JR.
    Rev Neurol; 2003 Apr 21; 42(1):22-4. PubMed ID: 16402322
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  • 39. Mitochondrial dysfunction due to Leber's hereditary optic neuropathy as a cause of visual loss during assessment for epilepsy surgery.
    Niehusmann P, Surges R, von Wrede RD, Elger CE, Wellmer J, Reimann J, Urbach H, Vielhaber S, Bien CG, Kunz WS.
    Epilepsy Behav; 2011 Jan 21; 20(1):38-43. PubMed ID: 21145289
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  • 40. Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran.
    Houshmand M, Sanati MH, Rashedi I, Sharifpanah F, Asghari E, Lotfi J.
    Eur Neurol; 2004 Jan 21; 51(2):68-71. PubMed ID: 14671420
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