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Journal Abstract Search

700 related items for PubMed ID: 11995959

  • 41. Mitochondrial dysfunction due to Leber's hereditary optic neuropathy as a cause of visual loss during assessment for epilepsy surgery.
    Niehusmann P, Surges R, von Wrede RD, Elger CE, Wellmer J, Reimann J, Urbach H, Vielhaber S, Bien CG, Kunz WS.
    Epilepsy Behav; 2011 Jan; 20(1):38-43. PubMed ID: 21145289
    [Abstract] [Full Text] [Related]

  • 42. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
    Pénisson-Besnier I, Moreau C, Jacques C, Roger JC, Dubas F, Reynier P.
    Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773
    [Abstract] [Full Text] [Related]

  • 43. 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
    [Abstract] [Full Text] [Related]

  • 44. [Mutations in mitochondrial DNA in ocular diseases--Leher's hereditary optic neuropathy and Kearns' syndrome].
    Rydzanicz M, Mrugacz M, Gajecka M.
    Klin Oczna; 2008 Apr; 110(7-9):321-4. PubMed ID: 19112871
    [Abstract] [Full Text] [Related]

  • 45. The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stress.
    Chao de la Barca JM, Simard G, Amati-Bonneau P, Safiedeen Z, Prunier-Mirebeau D, Chupin S, Gadras C, Tessier L, Gueguen N, Chevrollier A, Desquiret-Dumas V, Ferré M, Bris C, Kouassi Nzoughet J, Bocca C, Leruez S, Verny C, Miléa D, Bonneau D, Lenaers G, Martinez MC, Procaccio V, Reynier P.
    Brain; 2016 Nov 01; 139(11):2864-2876. PubMed ID: 27633772
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  • 46. [Atypical presentation of Leber's optic neuropathy].
    Borruat FX, Sanders MD.
    Klin Monbl Augenheilkd; 1994 May 01; 204(5):400-2. PubMed ID: 8051882
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  • 47. Brain white matter 1 H MRS in Leber optic neuropathy mutation carriers.
    Ostojic J, Jancic J, Kozic D, Semnic R, Koprivsek K, Prvulovic M, Kostic V.
    Acta Neurol Belg; 2009 Dec 01; 109(4):305-9. PubMed ID: 20120211
    [Abstract] [Full Text] [Related]

  • 48. [Leber's hereditary optic neuropathy].
    Hilo W, Jabaly-Habib H, Modi N, Briscoe D.
    Harefuah; 2013 Aug 01; 152(8):486-9, 498, 497. PubMed ID: 24167936
    [Abstract] [Full Text] [Related]

  • 49. [Optic neuropathy caused by alcoholism and smoking: a diagnostic pitfall of Leber's optic neuropathy].
    Borruat FX, Hirt L, Regli F.
    Rev Neurol (Paris); 1994 Nov 01; 150(11):799-801. PubMed ID: 7597375
    [Abstract] [Full Text] [Related]

  • 50. [Evaluation of serum levels of SOD and MDA in patients with Leber's hereditary optic neuropathy carrying the mitochondrial DNA G11778A mutation].
    Liu Z, Sun CB, Tong Y, Qu J.
    Zhonghua Yan Ke Za Zhi; 2009 Aug 01; 45(8):719-23. PubMed ID: 20021885
    [Abstract] [Full Text] [Related]

  • 51. [Rapid genetic screening of Leber's hereditary optic neuropathy with mtDNA G11778A mutation by AS-PCR with whole blood].
    Yang JH, Tong Y, Li BH, Chen YK.
    Zhonghua Yan Ke Za Zhi; 2005 Mar 01; 41(3):243-5. PubMed ID: 15840367
    [Abstract] [Full Text] [Related]

  • 52. 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 01; 47(12):5303-9. PubMed ID: 17122117
    [Abstract] [Full Text] [Related]

  • 53. [Mitochondrial DNA mutation in Leber's hereditary optic neuropathy in China].
    Zhang LS, Huang Y, Li FY.
    Zhonghua Yi Xue Za Zhi; 1994 Jun 01; 74(6):349-51, 390. PubMed ID: 7994643
    [Abstract] [Full Text] [Related]

  • 54. Mitochondrial D-loop variation in leber hereditary neuropathy patients harboring primary G11778A, G3460A, T14484C mutations: J and W haplogroups as high-risk factors.
    Shafa Shariat Panahi M, Houshmand M, Tabassi AR.
    Arch Med Res; 2006 Nov 01; 37(8):1028-33. PubMed ID: 17045122
    [Abstract] [Full Text] [Related]

  • 55. Optic nerve sheath distention in Leber's optic neuropathy and the significance of the "Wallace mutation".
    Smith JL, Tse DT, Byrne SF, Johns DR, Stone EM.
    J Clin Neuroophthalmol; 1990 Dec 01; 10(4):231-8. PubMed ID: 2150839
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  • 60. A multiple sclerosis-like illness in a man harboring the mtDNA 14484 mutation.
    Bhatti MT, Newman NJ.
    J Neuroophthalmol; 1999 Mar 01; 19(1):28-33. PubMed ID: 10098545
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