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Page 1
Genetic and clinical study of PARK7 in Japanese Parkinson's disease.
Ishiguro M, Funayama M, Hatano T, Nishida H, Wada Y, Noda K, Tomiyama M, Yoshino H, Li Y, Ong S, Cioffi E, Nishioka K, Hattori N. Ishiguro M, et al. Among authors: funayama m. Heliyon. 2024 Jul 26;10(15):e35271. doi: 10.1016/j.heliyon.2024.e35271. eCollection 2024 Aug 15. Heliyon. 2024. PMID: 39170205 Free PMC article.
Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries.
Tomiyama H, Li Y, Funayama M, Hasegawa K, Yoshino H, Kubo S, Sato K, Hattori T, Lu CS, Inzelberg R, Djaldetti R, Melamed E, Amouri R, Gouider-Khouja N, Hentati F, Hatano Y, Wang M, Imamichi Y, Mizoguchi K, Miyajima H, Obata F, Toda T, Farrer MJ, Mizuno Y, Hattori N. Tomiyama H, et al. Among authors: funayama m. Mov Disord. 2006 Aug;21(8):1102-8. doi: 10.1002/mds.20886. Mov Disord. 2006. PMID: 16622854
[Molecular genetics of PINK1].
Funayama M, Hattori N. Funayama M, et al. Brain Nerve. 2007 Aug;59(8):831-8. Brain Nerve. 2007. PMID: 17713119 Review. Japanese.
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. Among authors: funayama m. 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: funayama m. Arch Neurol. 2008 Jun;65(6):802-8. doi: 10.1001/archneur.65.6.802. Arch Neurol. 2008. PMID: 18541801
Familial Parkinsonism with digenic parkin and PINK1 mutations.
Funayama M, Li Y, Tsoi TH, Lam CW, Ohi T, Yazawa S, Uyama E, Djaldetti R, Melamed E, Yoshino H, Imamichi Y, Takashima H, Nishioka K, Sato K, Tomiyama H, Kubo S, Mizuno Y, Hattori N. Funayama M, et al. Mov Disord. 2008 Jul 30;23(10):1461-5. doi: 10.1002/mds.22143. Mov Disord. 2008. PMID: 18546294
368 results