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The UCHL1 S18Y polymorphism and Parkinson's disease in a Japanese population.
Snapinn KW, Larson EB, Kawakami H, Ujike H, Borenstein AR, Izumi Y, Kaji R, Maruyama H, Mata IF, Morino H, Oda M, Tsuang DW, Yearout D, Edwards KL, Zabetian CP. Snapinn KW, et al. Among authors: kaji r. Parkinsonism Relat Disord. 2011 Jul;17(6):473-5. doi: 10.1016/j.parkreldis.2011.01.019. Epub 2011 Feb 22. Parkinsonism Relat Disord. 2011. PMID: 21345711 Free PMC article.
LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease.
Zabetian CP, Yamamoto M, Lopez AN, Ujike H, Mata IF, Izumi Y, Kaji R, Maruyama H, Morino H, Oda M, Hutter CM, Edwards KL, Schellenberg GD, Tsuang DW, Yearout D, Larson EB, Kawakami H. Zabetian CP, et al. Among authors: kaji r. Mov Disord. 2009 May 15;24(7):1034-41. doi: 10.1002/mds.22514. Mov Disord. 2009. PMID: 19343804 Free PMC article.
Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis.
Kamada M, Maruyama H, Tanaka E, Morino H, Wate R, Ito H, Kusaka H, Kawano Y, Miki T, Nodera H, Izumi Y, Kaji R, Kawakami H. Kamada M, et al. Among authors: kaji r. J Neurol Sci. 2009 Sep 15;284(1-2):69-71. doi: 10.1016/j.jns.2009.04.017. Epub 2009 May 2. J Neurol Sci. 2009. PMID: 19411082 Free article.
654 results