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Journal Abstract Search

552 related items for PubMed ID: 16617593

  • 21. 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; 54(1):1601-1607. PubMed ID: 35723074
    [Abstract] [Full Text] [Related]

  • 22. 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; 47(12):5303-9. PubMed ID: 17122117
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  • 23. Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.
    Qu J, Zhou X, Zhang J, Zhao F, Sun YH, Tong Y, Wei QP, Cai W, Yang L, West CE, Guan MX.
    Ophthalmology; 2009 Mar; 116(3):558-564.e3. PubMed ID: 19167085
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  • 24. 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; 20(1):38-43. PubMed ID: 21145289
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  • 25. 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 Jan; 6(2):121-3. PubMed ID: 11995959
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  • 26. Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA.
    Hotta Y, Fujiki K, Hayakawa M, Nakajima A, Kanai A, Mashima Y, Hiida Y, Shinoda K, Yamada K, Oguchi Y.
    Jpn J Ophthalmol; 1995 Jan; 39(1):96-108. PubMed ID: 7643491
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  • 30. [Evaluation of serum levels of SOD and MDA in patients with Leber's hereditary optic neuropathy carrying the mitochondrial DNA G11778A mutation].
    Liu Z, Sun CB, Tong Y, Qu J.
    Zhonghua Yan Ke Za Zhi; 2009 Aug; 45(8):719-23. PubMed ID: 20021885
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  • 34. [Hyperintense optic nerve lesion on T2-weighted MRI imaging in the acute stage of Leber's hereditary optic neuropathy: a case report].
    Honda H, Tsujihata M, Ochi M, Satoh A, Tomita I, Fujikawa A.
    Rinsho Shinkeigaku; 2006 Apr; 46(4):294-6. PubMed ID: 16768101
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  • 36. Alterations in multifocal visual evoked potentials during the acute phase of Leber's hereditary optic neuropathy.
    Gränse L.
    Acta Ophthalmol Scand; 2006 Aug; 84(4):549-51. PubMed ID: 16879580
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  • 37. A family with 3460G>A and 11778G>A mutations and haplogroup analysis of Polish Leber hereditary optic neuropathy patients.
    Tonska K, Kurzawa M, Ambroziak AM, Korwin-Rujna M, Szaflik JP, Grabowska E, Szaflik J, Bartnik E.
    Mitochondrion; 2008 Dec; 8(5-6):383-8. PubMed ID: 18801464
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  • 39. 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; 64(6):890-3. PubMed ID: 17562939
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  • 40. 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; 250(3):278-81. PubMed ID: 12638016
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