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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. Among authors: yamada t. 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
Alterations of T-lymphocyte populations in Parkinson disease.
Baba Y, Kuroiwa A, Uitti RJ, Wszolek ZK, Yamada T. Baba Y, et al. Among authors: yamada t. Parkinsonism Relat Disord. 2005 Dec;11(8):493-8. doi: 10.1016/j.parkreldis.2005.07.005. Epub 2005 Sep 9. Parkinsonism Relat Disord. 2005. PMID: 16154792
DCTN1 mutations in Perry syndrome.
Farrer MJ, Hulihan MM, Kachergus JM, Dächsel JC, Stoessl AJ, Grantier LL, Calne S, Calne DB, Lechevalier B, Chapon F, Tsuboi Y, Yamada T, Gutmann L, Elibol B, Bhatia KP, Wider C, Vilariño-Güell C, Ross OA, Brown LA, Castanedes-Casey M, Dickson DW, Wszolek ZK. Farrer MJ, et al. Among authors: yamada t. Nat Genet. 2009 Feb;41(2):163-5. doi: 10.1038/ng.293. Epub 2009 Jan 11. Nat Genet. 2009. PMID: 19136952 Free PMC article.
Acute measles encephalitis in adults.
Baba Y, Tsuboi Y, Inoue H, Yamada T, Wszolek ZK, Broderick DF. Baba Y, et al. Among authors: yamada t. J Neurol. 2006 Jan;253(1):121-4. doi: 10.1007/s00415-005-0923-8. Epub 2005 Aug 25. J Neurol. 2006. PMID: 16133728 No abstract available.
POPC/apoA-I discs as a potent lipoprotein modulator in Tangier disease.
Uehara Y, Tsuboi Y, Zhang B, Miura S, Baba Y, Higuchi MA, Yamada T, Rye KA, Saku K. Uehara Y, et al. Among authors: yamada t. Atherosclerosis. 2008 Mar;197(1):283-9. doi: 10.1016/j.atherosclerosis.2007.04.025. Epub 2007 Jun 8. Atherosclerosis. 2008. PMID: 17560579
12,034 results
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