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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

156 related items for PubMed ID: 21685233

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  • 26. Leber's hereditary optic neuropathy mutations in Korean patients with multiple sclerosis.
    Hwang JM, Chang BL, Park SS.
    Ophthalmologica; 2001; 215(6):398-400. PubMed ID: 11741103
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  • 28. 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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  • 31. Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genes.
    Wilichowski E, Ohlenbusch A, Hanefeld F.
    Neuropediatrics; 1998 Dec; 29(6):307-12. PubMed ID: 10029350
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