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189 related items for PubMed ID: 14593764

  • 1. [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; 37(3):713-20. PubMed ID: 14593764
    [Abstract] [Full Text] [Related]

  • 2. Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man.
    La Russa A, Cittadella R, Andreoli V, Valentino P, Trecroci F, Caracciolo M, Gallo O, Gambardella A, Quattrone A.
    Mult Scler; 2011 Jun; 17(6):763-6. PubMed ID: 21685233
    [Abstract] [Full Text] [Related]

  • 3. Leber's optic neuropathy associated with disseminated white matter disease: a case report and review.
    Perez F, Anne O, Debruxelles S, Menegon P, Lambrecq V, Lacombe D, Martin-Negrier ML, Brochet B, Goizet C.
    Clin Neurol Neurosurg; 2009 Jan; 111(1):83-6. PubMed ID: 18848389
    [Abstract] [Full Text] [Related]

  • 4. 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; 20(2):258-60. PubMed ID: 24263387
    [Abstract] [Full Text] [Related]

  • 5. Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran.
    Houshmand M, Sanati MH, Rashedi I, Sharifpanah F, Asghari E, Lotfi J.
    Eur Neurol; 2004 Feb; 51(2):68-71. PubMed ID: 14671420
    [Abstract] [Full Text] [Related]

  • 6. 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; 30(1):171-4. PubMed ID: 16617593
    [Abstract] [Full Text] [Related]

  • 7. Neuropathology of white matter disease in Leber's hereditary optic neuropathy.
    Kovács GG, Höftberger R, Majtényi K, Horváth R, Barsi P, Komoly S, Lassmann H, Budka H, Jakab G.
    Brain; 2005 Jan; 128(Pt 1):35-41. PubMed ID: 15483043
    [Abstract] [Full Text] [Related]

  • 8. [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
    [Abstract] [Full Text] [Related]

  • 9. Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation--A case report.
    Grazina MM, Diogo LM, Garcia PC, Silva ED, Garcia TD, Robalo CB, Oliveira CR.
    Eur J Paediatr Neurol; 2007 Mar; 11(2):115-8. PubMed ID: 17254817
    [Abstract] [Full Text] [Related]

  • 10. Multiple sclerosis associated with Leber's Hereditary Optic Neuropathy.
    Palace J.
    J Neurol Sci; 2009 Nov 15; 286(1-2):24-7. PubMed ID: 19800080
    [Abstract] [Full Text] [Related]

  • 11. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
    Mao YJ, Qu J, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb 15; 25(1):45-9. PubMed ID: 18247303
    [Abstract] [Full Text] [Related]

  • 12. Leber's hereditary optic neuropathy mutations in Korean patients with multiple sclerosis.
    Hwang JM, Chang BL, Park SS.
    Ophthalmologica; 2001 Feb 15; 215(6):398-400. PubMed ID: 11741103
    [Abstract] [Full Text] [Related]

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  • 14. 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 Feb 15; 6(2):121-3. PubMed ID: 11995959
    [Abstract] [Full Text] [Related]

  • 15. Leber's hereditary optic neuropathy masquerading as optic neuritis with spontaneous visual recovery.
    Hsu TK, Wang AG, Yen MY, Liu JH.
    Clin Exp Optom; 2014 Jan 15; 97(1):84-6. PubMed ID: 23905692
    [Abstract] [Full Text] [Related]

  • 16. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis.
    Kellar-Wood H, Robertson N, Govan GG, Compston DA, Harding AE.
    Ann Neurol; 1994 Jul 15; 36(1):109-12. PubMed ID: 8024249
    [Abstract] [Full Text] [Related]

  • 17. Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eye.
    Mauri E, Dilena R, Boccazzi A, Ronchi D, Piga D, Triulzi F, Gagliardi D, Brusa R, Faravelli I, Bresolin N, Magri F, Corti S, Comi GP.
    BMC Neurol; 2018 Dec 27; 18(1):220. PubMed ID: 30591017
    [Abstract] [Full Text] [Related]

  • 18. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.
    Kim JY, Hwang JM, Park SS.
    Ann Neurol; 2002 May 27; 51(5):630-4. PubMed ID: 12112111
    [Abstract] [Full Text] [Related]

  • 19. Leber hereditary optic neuropathy - historical report in comparison with the current knowledge.
    Piotrowska A, Korwin M, Bartnik E, Tońska K.
    Gene; 2015 Jan 15; 555(1):41-9. PubMed ID: 25261848
    [Abstract] [Full Text] [Related]

  • 20. [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 15; 37(3):174-7. PubMed ID: 11864415
    [Abstract] [Full Text] [Related]

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