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GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16.
Soto-Ortolaza AI, Heckman MG, Labbé C, Serie DJ, Puschmann A, Rayaprolu S, Strongosky A, Boczarska-Jedynak M, Opala G, Krygowska-Wajs A, Barcikowska M, Czyzewski K, Lynch T, Uitti RJ, Wszolek ZK, Ross OA. Soto-Ortolaza AI, et al. Among authors: uitti rj. Am J Neurodegener Dis. 2013 Nov 29;2(4):287-99. eCollection 2013. Am J Neurodegener Dis. 2013. PMID: 24319646 Free PMC article.
Hereditary tauopathies and parkinsonism.
Wszolek ZK, Tsuboi Y, Farrer M, Uitti RJ, Hutton ML. Wszolek ZK, et al. Among authors: uitti rj. Adv Neurol. 2003;91:153-63. Adv Neurol. 2003. PMID: 12442674 Review. No abstract available.
Magnetic resonance imaging and deep brain stimulation.
Uitti RJ, Tsuboi Y, Pooley RA, Putzke JD, Turk MF, Wszolek ZK, Witte RJ, Wharen RE Jr. Uitti RJ, et al. Neurosurgery. 2002 Dec;51(6):1423-28; discussion 1428-31. Neurosurgery. 2002. PMID: 12445347
Clinical and genetic studies of families with the tau N279K mutation (FTDP-17).
Tsuboi Y, Baker M, Hutton ML, Uitti RJ, Rascol O, Delisle MB, Soulages X, Murrell JR, Ghetti B, Yasuda M, Komure O, Kuno S, Arima K, Sunohara N, Kobayashi T, Mizuno Y, Wszolek ZK. Tsuboi Y, et al. Among authors: uitti rj. Neurology. 2002 Dec 10;59(11):1791-3. doi: 10.1212/01.wnl.0000038909.49164.4b. Neurology. 2002. PMID: 12473774
353 results