يعرض 1 - 20 نتائج من 41 نتيجة بحث عن '"Hurtig, HI"', وقت الاستعلام: 0.50s تنقيح النتائج
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    Relation: pii: ncomms8247; Kouri, N., Ross, O. A., Dombroski, B., Younkin, C. S., Serie, D. J., Soto-Ortolaza, A., Baker, M., Finch, N. C. A., Yoon, H., Kim, J., Fujioka, S., McLean, C. A., Ghetti, B., Spina, S., Cantwell, L. B., Farlow, M. R., Grafman, J., Huey, E. D., Han, M. R. ,. Dickson, D. W. (2015). Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. NATURE COMMUNICATIONS, 6 (1), https://doi.org/10.1038/ncomms8247.; http://hdl.handle.net/11343/260448

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    المساهمون: Höglinger, Gu1, Melhem, Nm, Dickson, Dw, Sleiman, Pm, Wang, L, Klei, L, Rademakers, R, de Silva, R, Litvan, I, Riley, De, van Swieten, Jc, Heutink, P, Wszolek, Zk, Uitti, Rj, Vandrovcova, J, Hurtig, Hi, Gross, Rg, Maetzler, W, Goldwurm, S, Tolosa, E, Borroni, B, Pastor, P, PSP Genetics Study, Group, Cantwell, Lb, Han, Mr, Dillman, A, van der Brug, Mp, Gibbs, Jr, Cookson, Mr, Hernandez, Dg, Singleton, Ab, Farrer, Mj, Yu, Ce, Golbe, Li, Revesz, T, Hardy, J, Lees, Aj, Devlin, B, Antonini, A, Hakonarson, H, Müller, U, Schellenberg, G. D.

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000292184600017; volume:43; issue:7; firstpage:699; lastpage:705; numberofpages:7; journal:NATURE GENETICS; http://hdl.handle.net/11577/3252385; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-79959689333; https://www.scopus.com/inward/record.uri?eid=2-s2.0-79959689333&doi=10.1038%2fng.859&partnerID=40&md5=d5f5861d4d9fef7735d1f08967857bd1

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    المصدر: Kalia , LV , Lang , AE , Hazrati , LN , Fujioka , S , Wszolek , ZK , Dickson , DW , Ross , OA , Van Deerlin , VM , Trojanowski , JQ , Hurtig , HI , Alcalay , RN , Marder , KS , Clark , LN , Gaig , C , Tolosa , E , Ruiz-Martinez , J , Marti-Masso , JF , Ferrer , I , de Munain , AL , Goldman , SM , Schule , B , Langston , JW , Aasly , JO , Giordana , MT , Bonifati ....

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    المصدر: Höglinger, GU; Melhem, NM; Dickson, DW; Sleiman, PMA; Wang, LS; Klei, L; et al.(2011). Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. Nature Genetics, 43(7), 699-705. doi: 10.1038/ng.859. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/3z78h0m8

    مصطلحات موضوعية: eye diseases

    وصف الملف: application/pdf

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    المصدر: Annals of Neurology; Feb2006, Vol. 59 Issue 2, p315-322, 8p

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    Periodical
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