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Journal Abstract Search

155 related items for PubMed ID: 12185183

  • 1. Ondine's curse in a woman with Leber's hereditary optic neuropathy.
    Sadler M, Wiles CM, Stoodley N, Linnane SJ, Smith AP.
    J Neurol Neurosurg Psychiatry; 2002 Sep; 73(3):347-8. PubMed ID: 12185183
    [No Abstract] [Full Text] [Related]

  • 2. A case of neuromyelitis optica harboring both anti-aquaporin-4 antibodies and a pathogenic mitochondrial DNA mutation for Leber's hereditary optic neuropathy: clinical commentary.
    Comabella M.
    Mult Scler; 2014 Feb; 20(2):261. PubMed ID: 24323818
    [No Abstract] [Full Text] [Related]

  • 3. 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; 6(2):121-3. PubMed ID: 11995959
    [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. [Past, present, and future in Leber's hereditary optic neuropathy].
    Oguchi Y.
    Nippon Ganka Gakkai Zasshi; 2001 Dec; 105(12):809-27. PubMed ID: 11802455
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. [New mitochondrial DNA mutation in Leber's hereditary optic neuropathy: A case report].
    Thulliez M, Laudier B, Vignal-Clermont C, Hardy G, Bonicel P.
    J Fr Ophtalmol; 2018 Jun; 41(6):e293-e299. PubMed ID: 29910133
    [No Abstract] [Full Text] [Related]

  • 8. Frequency of rare mitochondrial DNA mutations in patients with suspected Leber's hereditary optic neuropathy.
    Taylor RW, Jobling MS, Turnbull DM, Chinnery PF.
    J Med Genet; 2003 Jul; 40(7):e85. PubMed ID: 12843334
    [No Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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]

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

  • 12. Brain stem lesion in mitochondrial DNA G11778A mutation of Leber's hereditary optic neuropathy.
    Chen YT, Chen WL, Chen SN, Liu CS.
    J Formos Med Assoc; 2015 Jul; 114(7):668-9. PubMed ID: 24560448
    [No Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 35(1):167-8. PubMed ID: 15272763
    [Abstract] [Full Text] [Related]

  • 16. [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 01; 25(5):531-3. PubMed ID: 18841565
    [Abstract] [Full Text] [Related]

  • 17. A Rare Mutation Associated With Probable Late-Onset Leber's Hereditary Optic Neuropathy.
    Fondriest JJ, Golnik KC.
    J Neuroophthalmol; 2020 Sep 01; 40(3):411-413. PubMed ID: 32355048
    [No Abstract] [Full Text] [Related]

  • 18. 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 01; 111(1):83-6. PubMed ID: 18848389
    [Abstract] [Full Text] [Related]

  • 19. Postoperative amaurosis after ethmoidectomy revealing Leber's hereditary optic neuropathy.
    Perruisseau-Carrier J, Debry C, Riehm S, Djennaoui I.
    Eur Ann Otorhinolaryngol Head Neck Dis; 2019 Sep 01; 136(4):337-338. PubMed ID: 31387800
    [No Abstract] [Full Text] [Related]

  • 20. Mitochondrial DNA 13513G>A mutation presenting with Leber's hereditary optic neuropathy.
    Chen BS, Biousse V, Newman NJ.
    Clin Exp Ophthalmol; 2019 Dec 01; 47(9):1202-1204. PubMed ID: 31368143
    [No Abstract] [Full Text] [Related]

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