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Page 1
Clinical correlations with Lewy body pathology in LRRK2-related Parkinson disease.
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-Martínez J, Marti-Masso JF, Ferrer I, López de Munain A, Goldman SM, Schüle B, Langston JW, Aasly JO, Giordana MT, Bonifati V, Puschmann A, Canesi M, Pezzoli G, Maues De Paula A, Hasegawa K, Duyckaerts C, Brice A, Stoessl AJ, Marras C. Kalia LV, et al. Among authors: hazrati ln. JAMA Neurol. 2015 Jan;72(1):100-5. doi: 10.1001/jamaneurol.2014.2704. JAMA Neurol. 2015. PMID: 25401511 Free PMC article.
The prion hypothesis in Parkinson's disease: Braak to the future.
Visanji NP, Brooks PL, Hazrati LN, Lang AE. Visanji NP, et al. Among authors: hazrati ln. Acta Neuropathol Commun. 2013 May 8;1:2. doi: 10.1186/2051-5960-1-2. Acta Neuropathol Commun. 2013. PMID: 24252164 Free PMC article. Review.
Clinicopathological review of pallidonigroluysian atrophy.
Wong JC, Armstrong MJ, Lang AE, Hazrati LN. Wong JC, et al. Among authors: hazrati ln. Mov Disord. 2013 Mar;28(3):274-81. doi: 10.1002/mds.25232. Epub 2012 Oct 31. Mov Disord. 2013. PMID: 23114877 Review.
Reply to: Gray et al.
Visanji NP, Marras C, Liu LW, Hazrati LN, Lang AE. Visanji NP, et al. Among authors: hazrati ln. Mov Disord. 2014 Aug;29(9):1225-6. doi: 10.1002/mds.25941. Epub 2014 Jun 12. Mov Disord. 2014. PMID: 24925804 No abstract available.
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
Höglinger GU, Melhem NM, Dickson DW, Sleiman PM, Wang LS, 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, Hakonarson H, Müller U, Schellenberg GD. Höglinger GU, et al. Nat Genet. 2011 Jun 19;43(7):699-705. doi: 10.1038/ng.859. Nat Genet. 2011. PMID: 21685912 Free PMC article.
Minimal change multiple system atrophy: an aggressive variant?
Ling H, Asi YT, Petrovic IN, Ahmed Z, Prashanth LK, Hazrati LN, Nishizawa M, Ozawa T, Lang A, Lees AJ, Revesz T, Holton JL. Ling H, et al. Among authors: hazrati ln. Mov Disord. 2015 Jun;30(7):960-7. doi: 10.1002/mds.26220. Epub 2015 Apr 8. Mov Disord. 2015. PMID: 25854893
127 results