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Journal Abstract Search

462 related items for PubMed ID: 12632910

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  • 3. [Diagnostic and differential diagnostic potential of mitochondrial DNA assessment in patients with Leber's hereditary optic neuropathy].
    Feng X, Pu W, Gao D.
    Zhonghua Yan Ke Za Zhi; 2001 May; 37(3):174-7. PubMed ID: 11864415
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  • 5. Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations.
    Brown MD, Allen JC, Van Stavern GP, Newman NJ, Wallace DC.
    Am J Med Genet; 2001 Dec 15; 104(4):331-8. PubMed ID: 11754070
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  • 6. 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 15; 250(3):278-81. PubMed ID: 12638016
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  • 7. Mitochondrial abnormalities in patients with LHON-like optic neuropathies.
    Abu-Amero KK, Bosley TM.
    Invest Ophthalmol Vis Sci; 2006 Oct 15; 47(10):4211-20. PubMed ID: 17003408
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  • 8. [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 15; 42(8):728-32. PubMed ID: 17081446
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  • 9. 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 15; 37(4):268-76. PubMed ID: 15003728
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  • 10. [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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  • 11. [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 25; 21(2):166-7. PubMed ID: 15079802
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  • 12. Leber's hereditary optic neuropathy with childhood onset.
    Barboni P, Savini G, Valentino ML, La Morgia C, Bellusci C, De Negri AM, Sadun F, Carta A, Carbonelli M, Sadun AA, Carelli V.
    Invest Ophthalmol Vis Sci; 2006 Dec 25; 47(12):5303-9. PubMed ID: 17122117
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  • 13. 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 25; 37(8):1028-33. PubMed ID: 17045122
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  • 15. 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 Nov 25; 100():169-78; discussion 178-9. PubMed ID: 12545691
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  • 17. 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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  • 18. Influence of mutation type on clinical expression of Leber hereditary optic neuropathy.
    Spruijt L, Kolbach DN, de Coo RF, Plomp AS, Bauer NJ, Smeets HJ, de Die-Smulders CE.
    Am J Ophthalmol; 2006 Apr 21; 141(4):676-82. PubMed ID: 16564802
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  • 19. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.
    Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T.
    Eur J Paediatr Neurol; 2002 Apr 21; 6(2):121-3. PubMed ID: 11995959
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  • 20. Retinal nerve fiber layer evaluation by optical coherence tomography in unaffected carriers with Leber's hereditary optic neuropathy mutations.
    Savini G, Barboni P, Valentino ML, Montagna P, Cortelli P, De Negri AM, Sadun F, Bianchi S, Longanesi L, Zanini M, Carelli V.
    Ophthalmology; 2005 Jan 21; 112(1):127-31. PubMed ID: 15629832
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