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PUBMED FOR HANDHELDS

Journal Abstract Search


145 related items for PubMed ID: 11510171

  • 21.
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  • 22. 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
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  • 25. Leber's hereditary optic atrophy: an atypical case with response to hydroxycobalamine therapy.
    Chew SJ.
    Singapore Med J; 1990 Jun; 31(3):293-4. PubMed ID: 2392710
    [Abstract] [Full Text] [Related]

  • 26. Clinical Observation of Patients with Leber's Hereditary Optic Neuropathy Before Gene Therapy.
    Yuan J, Zhang Y, Liu H, Tian Z, Li X, Zheng Y, Gao Q, Song L, Xiao X, Sun J, Wang Z, Li B.
    Curr Gene Ther; 2018 Jun; 18(6):386-392. PubMed ID: 30394208
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  • 28. 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; 52(3):374-7. PubMed ID: 12205655
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  • 29. [Leber's idiopathic stellate neuroretinitis: about two cases].
    Manic H, Boissonnot M, Gicquel JJ, Rovira JC, Dighiero P.
    J Fr Ophtalmol; 2003 Jan; 26(1):59-63. PubMed ID: 12610411
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  • 32. 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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  • 33. [Leber's hereditary optic neuropathy].
    Takai Y, Yamagami A, Ishikawa H.
    Rinsho Shinkeigaku; 2024 May 24; 64(5):326-332. PubMed ID: 38644210
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  • 34. Latent, acute, and chronic Leber's hereditary optic neuropathy.
    Kerrison JB.
    Ophthalmology; 2005 Jan 24; 112(1):1-2. PubMed ID: 15629812
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  • 37. [Leber's hereditary optic neuropathy in malnutrition: a case report].
    Lachmund U, Mojon DS.
    Klin Monbl Augenheilkd; 2006 May 24; 223(5):393-6. PubMed ID: 16705513
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  • 38. 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 24; 30(1):171-4. PubMed ID: 16617593
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  • 39. [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 24; 37(3):174-7. PubMed ID: 11864415
    [Abstract] [Full Text] [Related]

  • 40.
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