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Journal Abstract Search

665 related items for PubMed ID: 18841565

  • 41. 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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  • 42. 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; 48(5):2362-70. PubMed ID: 17460303
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  • 43. [Analysis on the effect of secondary mutations on Leber's hereditary optic neuropathy].
    Wang Y, Tong Y, Hu SX, Wang JY, Shao JB, Zhang HX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):397-400. PubMed ID: 17680528
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  • 44. [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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  • 51. Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study.
    Quiros PA, Torres RJ, Salomao S, Berezovsky A, Carelli V, Sherman J, Sadun F, De Negri A, Belfort R, Sadun AA.
    Br J Ophthalmol; 2006 Feb; 90(2):150-3. PubMed ID: 16424523
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  • 53. Leber hereditary optic neuropathy possibly triggered by exposure to tire fire.
    Sanchez RN, Smith AJ, Carelli V, Sadun AA, Keltner JL.
    J Neuroophthalmol; 2006 Dec; 26(4):268-72. PubMed ID: 17204920
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  • 54. High incidence of visual recovery among four Japanese patients with Leber's hereditary optic neuropathy with the 14484 mutation.
    Yamada K, Mashima Y, Kigasawa K, Miyashita K, Wakakura M, Oguchi Y.
    J Neuroophthalmol; 1997 Jun; 17(2):103-7. PubMed ID: 9176781
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  • 55. Difficulty differentiating Leber's from dominant optic neuropathy in a patient with remote visual loss.
    Jacobson DM, Stone EM.
    J Clin Neuroophthalmol; 1991 Sep; 11(3):152-7. PubMed ID: 1836796
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  • 56. Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family.
    Kaplanová V, Zeman J, Hansíková H, Cerná L, Houst'ková H, Misovicová N, Houstek J.
    J Neurol Sci; 2004 Aug 30; 223(2):149-55. PubMed ID: 15337616
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