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Page 1
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: wszolek zk. Neurology. 2002 Dec 10;59(11):1791-3. doi: 10.1212/01.wnl.0000038909.49164.4b. Neurology. 2002. PMID: 12473774
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.
Kachergus J, Mata IF, Hulihan M, Taylor JP, Lincoln S, Aasly J, Gibson JM, Ross OA, Lynch T, Wiley J, Payami H, Nutt J, Maraganore DM, Czyzewski K, Styczynska M, Wszolek ZK, Farrer MJ, Toft M. Kachergus J, et al. Among authors: wszolek zk. Am J Hum Genet. 2005 Apr;76(4):672-80. doi: 10.1086/429256. Epub 2005 Feb 22. Am J Hum Genet. 2005. PMID: 15726496 Free PMC article.
Molecular pathogenesis of Parkinson disease.
Eriksen JL, Wszolek Z, Petrucelli L. Eriksen JL, et al. Arch Neurol. 2005 Mar;62(3):353-7. doi: 10.1001/archneur.62.3.353. Arch Neurol. 2005. PMID: 15767499 Review.
Parkinson disease: handedness predicts asymmetry.
Uitti RJ, Baba Y, Whaley NR, Wszolek ZK, Putzke JD. Uitti RJ, et al. Among authors: wszolek zk. Neurology. 2005 Jun 14;64(11):1925-30. doi: 10.1212/01.WNL.0000163993.82388.C8. Neurology. 2005. PMID: 15955945
Gender and the Parkinson's disease phenotype.
Baba Y, Putzke JD, Whaley NR, Wszolek ZK, Uitti RJ. Baba Y, et al. Among authors: wszolek zk. J Neurol. 2005 Oct;252(10):1201-5. doi: 10.1007/s00415-005-0835-7. Epub 2005 Sep 12. J Neurol. 2005. PMID: 16151602
Lrrk2 and Lewy body disease.
Ross OA, Toft M, Whittle AJ, Johnson JL, Papapetropoulos S, Mash DC, Litvan I, Gordon MF, Wszolek ZK, Farrer MJ, Dickson DW. Ross OA, et al. Among authors: wszolek zk. Ann Neurol. 2006 Feb;59(2):388-93. doi: 10.1002/ana.20731. Ann Neurol. 2006. PMID: 16437559
717 results