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Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease.
Shadrin AA, Mucha S, Ellinghaus D, Makarious MB, Blauwendraat C, Sreelatha AAK, Heras-Garvin A, Ding J, Hammer M, Foubert-Samier A, Meissner WG, Rascol O, Pavy-Le Traon A, Frei O, O'Connell KS, Bahrami S, Schreiber S, Lieb W, Müller-Nurasyid M, Schminke U, Homuth G, Schmidt CO, Nöthen MM, Hoffmann P, Gieger C, Wenning G; European Multiple System Atrophy Study Group; Gibbs JR, Franke A, Hardy J, Stefanova N, Gasser T, Singleton A, Houlden H, Scholz SW, Andreassen OA, Sharma M. Shadrin AA, et al. Among authors: hardy j. Mov Disord. 2021 Feb;36(2):449-459. doi: 10.1002/mds.28338. Epub 2020 Oct 27. Mov Disord. 2021. PMID: 33107653 Free PMC article.
Phenomenology of "Lubag" or X-linked dystonia-parkinsonism.
Evidente VG, Advincula J, Esteban R, Pasco P, Alfon JA, Natividad FF, Cuanang J, Luis AS, Gwinn-Hardy K, Hardy J, Hernandez D, Singleton A. Evidente VG, et al. Among authors: hardy j. Mov Disord. 2002 Nov;17(6):1271-7. doi: 10.1002/mds.10271. Mov Disord. 2002. PMID: 12465067
Ethnic differences and disease phenotypes.
Hardy J, Singleton A, Gwinn-Hardy K. Hardy J, et al. Science. 2003 May 2;300(5620):739-40. doi: 10.1126/science.300.5620.739. Science. 2003. PMID: 12730580 No abstract available.
Genes and parkinsonism.
Hardy J, Cookson MR, Singleton A. Hardy J, et al. Lancet Neurol. 2003 Apr;2(4):221-8. doi: 10.1016/s1474-4422(03)00350-8. Lancet Neurol. 2003. PMID: 12849210 Review.
The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval.
Zimprich A, Müller-Myhsok B, Farrer M, Leitner P, Sharma M, Hulihan M, Lockhart P, Strongosky A, Kachergus J, Calne DB, Stoessl J, Uitti RJ, Pfeiffer RF, Trenkwalder C, Homann N, Ott E, Wenzel K, Asmus F, Hardy J, Wszolek Z, Gasser T. Zimprich A, et al. Among authors: hardy j. Am J Hum Genet. 2004 Jan;74(1):11-9. doi: 10.1086/380647. Epub 2003 Dec 19. Am J Hum Genet. 2004. PMID: 14691730 Free PMC article.
3,443 results