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Journal Abstract Search

160 related items for PubMed ID: 24560448

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  • 2. [Evaluation of serum levels of SOD and MDA in patients with Leber's hereditary optic neuropathy carrying the mitochondrial DNA G11778A mutation].
    Liu Z, Sun CB, Tong Y, Qu J.
    Zhonghua Yan Ke Za Zhi; 2009 Aug; 45(8):719-23. PubMed ID: 20021885
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  • 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
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  • 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
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  • 8. 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
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  • 9. 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
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  • 12. 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
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  • 13. 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
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  • 19. Comparison of retinal nerve fibre layers between 11778 and 14484 mutations in Leber's hereditary optic neuropathy.
    Seo JH, Hwang JM, Park SS.
    Eye (Lond); 2010 Jan; 24(1):107-11. PubMed ID: 19247386
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