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Journal Abstract Search

173 related items for PubMed ID: 27756254

  • 1. Severe inflammatory disease activity 14 months after cessation of Natalizumab in a patient with Leber's optic neuropathy and multiple sclerosis - a case report.
    Holmøy T, Beiske AG, Zarnovicky S, Myro AZ, Røsjø E, Kerty E.
    BMC Neurol; 2016 Oct 18; 16(1):197. PubMed ID: 27756254
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  • 2. 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 18; 8(2):118-21. PubMed ID: 18344382
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  • 4. Optic nerve atrophy and whole and regional brain atrophy in Leber's hereditary optic neuropathy with multiple sclerosis-like disease with m.11778G>A mutation.
    Rościszewska-Żukowska I, Bartosik-Psujek H.
    Mult Scler Relat Disord; 2020 Jul 18; 42():102071. PubMed ID: 32387972
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  • 5. 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 18; 17(6):763-6. PubMed ID: 21685233
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  • 6. 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 18; 111(1):83-6. PubMed ID: 18848389
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  • 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 18; 128(Pt 1):35-41. PubMed ID: 15483043
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  • 8. Leber's hereditary optic neuropathy misdiagnosed as optic neuritis and Lyme disease in a patient with multiple sclerosis.
    Chang M.
    BMJ Case Rep; 2018 Dec 07; 11(1):. PubMed ID: 30567205
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  • 9. 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 07; 20(2):258-60. PubMed ID: 24263387
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  • 11. Mitochondria in neuroinflammation - Multiple sclerosis (MS), leber hereditary optic neuropathy (LHON) and LHON-MS.
    Bargiela D, Chinnery PF.
    Neurosci Lett; 2019 Sep 25; 710():132932. PubMed ID: 28668384
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  • 12. 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
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  • 14. Magnetic resonance imaging negative myelopathy in Leber's hereditary optic neuropathy: a case report.
    Martikainen MH, Suomela M, Majamaa K.
    BMC Neurol; 2022 Dec 15; 22(1):487. PubMed ID: 36522697
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  • 16. 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 15; 52(3):374-7. PubMed ID: 12205655
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  • 17. White matter changes in Leber's hereditary optic neuropathy: MRI findings.
    Küker W, Weir A, Quaghebeur G, Palace J.
    Eur J Neurol; 2007 May 15; 14(5):591-3. PubMed ID: 17437624
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  • 18. Magnetic resonance imaging, magnetisation transfer imaging, and diffusion weighted imaging correlates of optic nerve, brain, and cervical cord damage in Leber's hereditary optic neuropathy.
    Inglese M, Rovaris M, Bianchi S, La Mantia L, Mancardi GL, Ghezzi A, Montagna P, Salvi F, Filippi M.
    J Neurol Neurosurg Psychiatry; 2001 Apr 15; 70(4):444-9. PubMed ID: 11254765
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  • 19. Visual recovery in a man with the rare combination of mtDNA 11778 LHON mutation and a MS-like disease after mitoxantrone therapy.
    Buhmann C, Gbadamosi J, Heesen C.
    Acta Neurol Scand; 2002 Oct 15; 106(4):236-9. PubMed ID: 12225323
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  • 20. [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 Oct 15; 37(3):713-20. PubMed ID: 14593764
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