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Journal Abstract Search

106 related items for PubMed ID: 15002319

  • 1. [Leber's hereditary optic atrophy: neurological and other non-optic appearances].
    Rudenskaia GE, Zakharova EIu, Adarcheva LS, Mikhaĭlova EN, Karlova IZ.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2004; 104(2):38-42. PubMed ID: 15002319
    [Abstract] [Full Text] [Related]

  • 2. [Past, present, and future in Leber's hereditary optic neuropathy].
    Oguchi Y.
    Nippon Ganka Gakkai Zasshi; 2001 Dec; 105(12):809-27. PubMed ID: 11802455
    [Abstract] [Full Text] [Related]

  • 3. Leber's hereditary optic neuropathy associated with multiple sclerosis: Harding's syndrome.
    Parry-Jones AR, Mitchell JD, Gunarwardena WJ, Shaunak S.
    Pract Neurol; 2008 Apr; 8(2):118-21. PubMed ID: 18344382
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. [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
    [Abstract] [Full Text] [Related]

  • 6. [Leber's hereditary optic neuropathy: DNA-diagnosis and clinico-genetic comparisons in 12 families].
    Zakharova EIu, Rudenskaia GE, Karlova IZ, Adarcheva LS, Mikhaĭlova EN.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2003 Oct; 103(7):44-50. PubMed ID: 12938654
    [Abstract] [Full Text] [Related]

  • 7. [Clinical features and the mutation of Leber's hereditary optic neuropathy in Chinese patients].
    Wang Y, Guo XM, Jia XY, Li SQ, Xiao XS, Guo L, Zhang QJ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):334-6. PubMed ID: 15952130
    [Abstract] [Full Text] [Related]

  • 8. Wolff-Parkinson-White syndrome and noncompaction in Leber's hereditary optic neuropathy due to the variant m.3460G>A.
    Finsterer J, Stollberger C, Gatterer E.
    J Int Med Res; 2018 May; 46(5):2054-2060. PubMed ID: 29562793
    [Abstract] [Full Text] [Related]

  • 9. [Leber's hereditary optic neuropathy (LHON) with mutation at G3460A and MS-like phenotype].
    Jamrozik Z, Tutaj A, Piechowski-Jóźwiak B, Mroczek-Tońska K, Bartnik E, Kwieciński H.
    Neurol Neurochir Pol; 2003 May; 37(3):713-20. PubMed ID: 14593764
    [Abstract] [Full Text] [Related]

  • 10. 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 May; 6(2):121-3. PubMed ID: 11995959
    [Abstract] [Full Text] [Related]

  • 11. Clinical features of Leber's hereditary optic neuropathy with the 11778 mitochondrial DNA mutation in Taiwanese patients.
    Hung HL, Kao LY, Huang CC.
    Chang Gung Med J; 2003 Jan; 26(1):41-7. PubMed ID: 12656308
    [Abstract] [Full Text] [Related]

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  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Ondine's curse in a woman with Leber's hereditary optic neuropathy.
    Sadler M, Wiles CM, Stoodley N, Linnane SJ, Smith AP.
    J Neurol Neurosurg Psychiatry; 2002 Sep; 73(3):347-8. PubMed ID: 12185183
    [No Abstract] [Full Text] [Related]

  • 15. Bilateral vision loss due to Leber's hereditary optic neuropathy after long-term alcohol, nicotine and drug abuse.
    Maass J, Matthé E.
    Doc Ophthalmol; 2018 Apr; 136(2):145-153. PubMed ID: 29372350
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  • 17. Retinal function and neural conduction along the visual pathways in affected and unaffected carriers with Leber's hereditary optic neuropathy.
    Ziccardi L, Sadun F, De Negri AM, Barboni P, Savini G, Borrelli E, La Morgia C, Carelli V, Parisi V.
    Invest Ophthalmol Vis Sci; 2013 Oct 21; 54(10):6893-901. PubMed ID: 24071953
    [Abstract] [Full Text] [Related]

  • 18. 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 21; 35(1):167-8. PubMed ID: 15272763
    [Abstract] [Full Text] [Related]

  • 19. A case of neuromyelitis optica harboring both anti-aquaporin-4 antibodies and a pathogenic mitochondrial DNA mutation for Leber's hereditary optic neuropathy.
    Shiraishi W, Hayashi S, Kamada T, Isobe N, Yamasaki R, Murai H, Ohyagi Y, Kira J.
    Mult Scler; 2014 Feb 21; 20(2):258-60. PubMed ID: 24263387
    [Abstract] [Full Text] [Related]

  • 20. Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy.
    Funalot B, Reynier P, Vighetto A, Ranoux D, Bonnefont JP, Godinot C, Malthièry Y, Mas JL.
    Ann Neurol; 2002 Sep 21; 52(3):374-7. PubMed ID: 12205655
    [Abstract] [Full Text] [Related]

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