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Journal Abstract Search

323 related items for PubMed ID: 24263387

  • 21. Anti-aquaporin-4 antibody positivity in neuromyelitis optica is associated with lesion activity.
    Liu Y, Han Y, Duan Y, Huang J, Ren Z, Butzkueven H, Li K.
    Eur Neurol; 2013; 70(1-2):113-6. PubMed ID: 23860467
    [Abstract] [Full Text] [Related]

  • 22. [Leber's optic neuropathy: a case report].
    Pato-Pato A, Cimas-Hernando I, Lorenzo-González JR.
    Rev Neurol; 2013; 42(1):22-4. PubMed ID: 16402322
    [Abstract] [Full Text] [Related]

  • 23. Case report: A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation.
    Chuenkongkaew W, Lertrit P, Suphavilai R.
    Southeast Asian J Trop Med Public Health; 2004 Mar; 35(1):167-8. PubMed ID: 15272763
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  • 24. Phylogenetic assessment of the mitochondrial DNA displacement loop haplotype in Japanese patients with Leber's hereditary optic neuropathy harboring the mitochondrial DNA G11778A mutation.
    Isashiki Y, Sonoda S, Izumo S, Sakamoto T, Tachikui H, Inoue I.
    Ophthalmic Res; 2003 Mar; 35(4):224-31. PubMed ID: 12815198
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  • 25. 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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  • 27. A multiple sclerosis-like illness in a man harboring the mtDNA 14484 mutation.
    Bhatti MT, Newman NJ.
    J Neuroophthalmol; 1999 Mar; 19(1):28-33. PubMed ID: 10098545
    [Abstract] [Full Text] [Related]

  • 28. Heterogeneity of aquaporin-4 autoimmunity and spinal cord lesions in multiple sclerosis in Japanese.
    Matsuoka T, Matsushita T, Kawano Y, Osoegawa M, Ochi H, Ishizu T, Minohara M, Kikuchi H, Mihara F, Ohyagi Y, Kira J.
    Brain; 2007 May; 130(Pt 5):1206-23. PubMed ID: 17439988
    [Abstract] [Full Text] [Related]

  • 29. [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
    [Abstract] [Full Text] [Related]

  • 30. Posterior reversible encephalopathy syndrome in a leber hereditary optic neuropathy patient with mitochondrial DNA 11778G>A point mutation.
    Da Y, Zhang X, Li F, Yang X, Zhang X, Jia J.
    J Neuroophthalmol; 2013 Sep; 33(3):276-8. PubMed ID: 23782927
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  • 34. Leber's hereditary optic neuropathy with 3460 mitochondrial DNA mutation.
    Hwang JM, Chang BL, Koh HJ, Kim JY, Park SS.
    J Korean Med Sci; 2002 Apr; 17(2):283-6. PubMed ID: 11961321
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  • 35. [A pedigree of Leber's hereditary optic neuropathy with mtDNA 14484 mutation].
    Tong Y, Wang Y, Jiang F, Liu B, Zhang S, Yang W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):531-3. PubMed ID: 18841565
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  • 38. The prevalence of long spinal cord lesions and anti-aquaporin 4 antibodies in neuromyelitis optica patients in Taiwan.
    Wang KC, Tsai CP, Lee CL, Chen SY, Chen SJ.
    Eur Neurol; 2011 Oct; 65(2):99-104. PubMed ID: 21273778
    [Abstract] [Full Text] [Related]

  • 39. 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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