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Journal Abstract Search

323 related items for PubMed ID: 24263387

  • 1. 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]

  • 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. 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
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  • 4. Neuromyelitis optica antibody in Leber hereditary optic neuropathy: case report.
    Simão LM.
    Arq Bras Oftalmol; 2012 Apr; 75(4):280-2. PubMed ID: 23258662
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  • 6. [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
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  • 7. Leber hereditary optic neuropathy mimicking neuromyelitis optica.
    McClelland CM, Van Stavern GP, Tselis AC.
    J Neuroophthalmol; 2011 Sep; 31(3):265-8. PubMed ID: 21734595
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  • 9. [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 Sep; 37(3):713-20. PubMed ID: 14593764
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  • 10. [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
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  • 11. 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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  • 13. Devic's neuromyelitis optica and mitochondrial DNA mutation: a case report.
    Ghezzi A, Baldini S, Zaffaroni M, Leoni G, Koudriavtseva T, Casini AR, Zeviani M.
    Neurol Sci; 2004 Nov 27; 25 Suppl 4():S380-2. PubMed ID: 15727239
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  • 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 27; 52(3):374-7. PubMed ID: 12205655
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  • 15. 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 Sep 27; 6(2):121-3. PubMed ID: 11995959
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  • 17. [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 27; 41(3):243-5. PubMed ID: 15840367
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  • 18. 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 27; 97(1):84-6. PubMed ID: 23905692
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  • 20. [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
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