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Journal Abstract Search

119 related items for PubMed ID: 2641110

  • 21. Magnetic resonance imaging findings in Leber's hereditary optic neuropathy.
    Dotti MT, Caputo N, Signorini E, Federico A.
    Eur Neurol; 1992; 32(1):17-9. PubMed ID: 1563448
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  • 22. Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.
    Holt IJ, Miller DH, Harding AE.
    J Med Genet; 1989 Dec; 26(12):739-43. PubMed ID: 2575667
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  • 23. BAEP changes in Leber's hereditary optic atrophy: further confirmation of multisystem involvement.
    Mondelli M, Rossi A, Scarpini C, Dotti MT, Federico A.
    Acta Neurol Scand; 1990 Apr; 81(4):349-53. PubMed ID: 2360403
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  • 24. [A molecular genetic study of Leber's disease].
    Zhang LS.
    Zhonghua Yan Ke Za Zhi; 1993 Mar; 29(2):103-4. PubMed ID: 8404350
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  • 26. Peripapillary fluorescein leakage in 11778 Leber's optic neuropathy.
    Yen MY, Wei YH, Liu JH.
    J Neuroophthalmol; 1996 Sep; 16(3):178-81. PubMed ID: 8865009
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  • 28. [Hereditary optic nerve atrophy. A clinical-genealogical status over Danish families with Leber disease].
    Rosenberg T, Kann E, Nørby S.
    Ugeskr Laeger; 1995 May 08; 157(19):2707-11. PubMed ID: 7770969
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  • 30. Cuban epidemic optic neuropathy and its relationship to toxic and hereditary optic neuropathy.
    Santiesteban-Freixas R, Mendoza-Santiesteban CE, Columbie-Garbey Y, Quevedo AG, Garcia AG, Rodríguez RC.
    Semin Ophthalmol; 2010 Jul 08; 25(4):112-22. PubMed ID: 20695731
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  • 31. [Positive diagnosis of Leber's hereditary optic neuropathy using molecular genetics].
    Souied E, Pisella PJ, Ossareh B, Brézin A, Junes P, Wild-Decrette C, Munnich A, Bonnefont JP, Mondon H.
    J Fr Ophtalmol; 1997 Jul 08; 20(1):65-70. PubMed ID: 9099286
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  • 33. Leber's hereditary optic atrophy: an atypical case with response to hydroxycobalamine therapy.
    Chew SJ.
    Singapore Med J; 1990 Jun 08; 31(3):293-4. PubMed ID: 2392710
    [Abstract] [Full Text] [Related]

  • 34. [Leber's hereditary optic neuropathy with onset at the age of 54 years].
    Nakamura N, Furukawa Y, Fujiki K, Hayakawa M, Mizuno Y.
    Rinsho Shinkeigaku; 1994 Mar 08; 34(3):258-60. PubMed ID: 8200145
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  • 37. A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy.
    Parker WD, Oley CA, Parks JK.
    N Engl J Med; 1989 May 18; 320(20):1331-3. PubMed ID: 2497346
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