Spinocerebellar Ataxias
This graph shows the total number of publications written about "Spinocerebellar Ataxias" by people in the URMC Research Network by year, and whether "Spinocerebellar Ataxias" was a major or minor topic of these publication.
Below are the most recent publications written about "Spinocerebellar Ataxias" by people in Profiles.
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Osborne RJ, Thornton CA. RNA-dominant diseases. Hum Mol Genet. 2006 Oct 15; 15 Spec No 2:R162-9.
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Chung MY, Lu YC, Cheng NC, Soong BW. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23. Brain. 2003 Jun; 126(Pt 6):1293-9.
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Wiest G, Tian JR, Baloh RW, Crane BT, Demer JL. Initiation of the linear vestibulo-ocular reflex in cerebellar dysfunction. Ann N Y Acad Sci. 2001 Oct; 942:505-7.
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La Spada AR, Fu YH, Sopher BL, Libby RT, Wang X, Li LY, Einum DD, Huang J, Possin DE, Smith AC, Martinez RA, Koszdin KL, Treuting PM, Ware CB, Hurley JB, Ptácek LJ, Chen S. Polyglutamine-expanded ataxin-7 antagonizes CRX function and induces cone-rod dystrophy in a mouse model of SCA7. Neuron. 2001 Sep 27; 31(6):913-27.
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