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Journal Abstract Search

429 related items for PubMed ID: 19301602

  • 1. [Case of Leber's hereditary optic neuropathy with mitochondrial DNA 11778 mutation exhibiting cerebellar ataxia, dilated cardiomyopathy and peripheral neuropathy].
    Watanabe Y, Odaka M, Hirata K.
    Brain Nerve; 2009 Mar; 61(3):309-12. PubMed ID: 19301602
    [Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. 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; 35(1):167-8. PubMed ID: 15272763
    [Abstract] [Full Text] [Related]

  • 4. Leber's hereditary optic neuropathy mutations in ethambutol-induced optic neuropathy.
    Hwang JM, Kim J, Park SS.
    J Neurol; 2003 Jan; 250(1):87-9. PubMed ID: 12527998
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. [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; 37(3):174-7. PubMed ID: 11864415
    [Abstract] [Full Text] [Related]

  • 7. 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; 51(5):630-4. PubMed ID: 12112111
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. [Sudden blindness: consider Leber's hereditary optic neuropathy].
    Schieving JH, de Vries BB, Hol F, Stroink H.
    Ned Tijdschr Geneeskd; 2008 Oct 25; 152(43):2313-6. PubMed ID: 19024058
    [Abstract] [Full Text] [Related]

  • 10. [A case of mitochondrial myopathy with external ophthalmoplegia and ataxic neuropathy].
    Mano A, Kikukawa H, Tsuchiya T, Tanaka K, Tanaka M.
    Rinsho Shinkeigaku; 2003 Sep 25; 43(9):564-7. PubMed ID: 14727565
    [Abstract] [Full Text] [Related]

  • 11. 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 25; 111(1):83-6. PubMed ID: 18848389
    [Abstract] [Full Text] [Related]

  • 12. 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 25; 20(2):258-60. PubMed ID: 24263387
    [Abstract] [Full Text] [Related]

  • 13. 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 25; 47(12):5303-9. PubMed ID: 17122117
    [Abstract] [Full Text] [Related]

  • 14. 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 25; 52(3):374-7. PubMed ID: 12205655
    [Abstract] [Full Text] [Related]

  • 15. 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 25; 30(1):171-4. PubMed ID: 16617593
    [Abstract] [Full Text] [Related]

  • 16. 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 25; 128(Pt 1):35-41. PubMed ID: 15483043
    [Abstract] [Full Text] [Related]

  • 17. Successful chemotherapy in a male patient with malignant lymphoma and Leber's hereditary optic neuropathy (LHON).
    Zanssen S, Buse G.
    Am J Hematol; 2003 Apr 25; 72(4):263-6. PubMed ID: 12666138
    [Abstract] [Full Text] [Related]

  • 18. [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; 25(5):531-3. PubMed ID: 18841565
    [Abstract] [Full Text] [Related]

  • 19. [Leber's optic neuropathy: a case report].
    Pato-Pato A, Cimas-Hernando I, Lorenzo-González JR.
    Rev Neurol; 2008 Oct 25; 42(1):22-4. PubMed ID: 16402322
    [Abstract] [Full Text] [Related]

  • 20. Irreversible optic neuropathy in wernicke encephalopathy and leber hereditary optic neuropathy.
    Li JM, Rucker JC.
    J Neuroophthalmol; 2010 Mar 25; 30(1):49-53. PubMed ID: 20182208
    [Abstract] [Full Text] [Related]

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