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Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's disease.
Nishioka K, Hayashi S, Farrer MJ, Singleton AB, Yoshino H, Imai H, Kitami T, Sato K, Kuroda R, Tomiyama H, Mizoguchi K, Murata M, Toda T, Imoto I, Inazawa J, Mizuno Y, Hattori N. Nishioka K, et al. Among authors: mizuno y. Ann Neurol. 2006 Feb;59(2):298-309. doi: 10.1002/ana.20753. Ann Neurol. 2006. PMID: 16358335
Novel PINK1 mutations in early-onset parkinsonism.
Hatano Y, Li Y, Sato K, Asakawa S, Yamamura Y, Tomiyama H, Yoshino H, Asahina M, Kobayashi S, Hassin-Baer S, Lu CS, Ng AR, Rosales RL, Shimizu N, Toda T, Mizuno Y, Hattori N. Hatano Y, et al. Among authors: mizuno y. Ann Neurol. 2004 Sep;56(3):424-7. doi: 10.1002/ana.20251. Ann Neurol. 2004. PMID: 15349870
Progress in the pathogenesis and genetics of Parkinson's disease.
Mizuno Y, Hattori N, Kubo S, Sato S, Nishioka K, Hatano T, Tomiyama H, Funayama M, Machida Y, Mochizuki H. Mizuno Y, et al. Philos Trans R Soc Lond B Biol Sci. 2008 Jun 27;363(1500):2215-27. doi: 10.1098/rstb.2008.2273. Philos Trans R Soc Lond B Biol Sci. 2008. PMID: 18426756 Free PMC article. Review.
Mutation analysis of the PINK1 gene in 391 patients with Parkinson disease.
Kumazawa R, Tomiyama H, Li Y, Imamichi Y, Funayama M, Yoshino H, Yokochi F, Fukusako T, Takehisa Y, Kashihara K, Kondo T, Elibol B, Bostantjopoulou S, Toda T, Takahashi H, Yoshii F, Mizuno Y, Hattori N. Kumazawa R, et al. Among authors: mizuno y. Arch Neurol. 2008 Jun;65(6):802-8. doi: 10.1001/archneur.65.6.802. Arch Neurol. 2008. PMID: 18541801
Expanding the clinical phenotype of SNCA duplication carriers.
Nishioka K, Ross OA, Ishii K, Kachergus JM, Ishiwata K, Kitagawa M, Kono S, Obi T, Mizoguchi K, Inoue Y, Imai H, Takanashi M, Mizuno Y, Farrer MJ, Hattori N. Nishioka K, et al. Among authors: mizuno y. Mov Disord. 2009 Sep 15;24(12):1811-9. doi: 10.1002/mds.22682. Mov Disord. 2009. PMID: 19562770
2,576 results