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Page 1
The effect of tau genotype on clinical features in FTDP-17.
Baba Y, Tsuboi Y, Baker MC, Uitti RJ, Hutton ML, Dickson DW, Farrer M, Putzke JD, Woodruff BK, Ghetti B, Murrell JR, Boeve BF, Petersen RC, Verpillat P, Brice A, Delisle MB, Rascol O, Arima K, Dysken MW, Yasuda M, Kobayashi T, Sunohara N, Komure O, Kuno S, Sperfeld AD, Stoppe G, Kohlhase J, Pickering-Brown S, Neary D, Bugiani O, Wszolek ZK. Baba Y, et al. Parkinsonism Relat Disord. 2005 Jun;11(4):205-8. doi: 10.1016/j.parkreldis.2005.01.003. Parkinsonism Relat Disord. 2005. PMID: 15878580
Atypical Parkinsonism and SCA8.
Baba Y, Uitti RJ, Farrer MJ, Wszolek ZK. Baba Y, et al. Parkinsonism Relat Disord. 2006 Sep;12(6):396. doi: 10.1016/j.parkreldis.2006.06.001. Epub 2006 Jul 18. Parkinsonism Relat Disord. 2006. PMID: 16846746 No abstract available.
Aprataxin (APTX) gene mutations resembling multiple system atrophy.
Baba Y, Uitti RJ, Boylan KB, Uehara Y, Yamada T, Farrer MJ, Couchon E, Batish SD, Wszolek ZK. Baba Y, et al. Parkinsonism Relat Disord. 2007 Apr;13(3):139-42. doi: 10.1016/j.parkreldis.2006.08.010. Epub 2006 Oct 27. Parkinsonism Relat Disord. 2007. PMID: 17049295
Essential tremor: phenotypic expression in a clinical cohort.
Whaley NR, Putzke JD, Baba Y, Wszolek ZK, Uitti RJ. Whaley NR, et al. Among authors: baba y. Parkinsonism Relat Disord. 2007 Aug;13(6):333-9. doi: 10.1016/j.parkreldis.2006.12.004. Epub 2007 Feb 8. Parkinsonism Relat Disord. 2007. PMID: 17291815
Heredofamilial brain calcinosis syndrome.
Baba Y, Broderick DF, Uitti RJ, Hutton ML, Wszolek ZK. Baba Y, et al. Mayo Clin Proc. 2005 May;80(5):641-51. doi: 10.4065/80.5.641. Mayo Clin Proc. 2005. PMID: 15887432 Review.
Gender and the Parkinson's disease phenotype.
Baba Y, Putzke JD, Whaley NR, Wszolek ZK, Uitti RJ. Baba Y, et al. J Neurol. 2005 Oct;252(10):1201-5. doi: 10.1007/s00415-005-0835-7. Epub 2005 Sep 12. J Neurol. 2005. PMID: 16151602
2,203 results