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Meta-iodobenzylguanidine myocardial scintigraphy in Perry disease.
Mishima T, Fujioka S, Nishioka K, Li Y, Sato K, Houzen H, Yabe I, Shiomi K, Eriguchi M, Hara H, Hattori N, Tsuboi Y. Mishima T, et al. Among authors: nishioka k. Parkinsonism Relat Disord. 2021 Feb;83:49-53. doi: 10.1016/j.parkreldis.2020.12.017. Epub 2021 Jan 12. Parkinsonism Relat Disord. 2021. PMID: 33476877
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: nishioka k. 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.
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. Among authors: nishioka k. Mov Disord. 2008 Jul 30;23(10):1461-5. doi: 10.1002/mds.22143. Mov Disord. 2008. PMID: 18546294
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. Mov Disord. 2009 Sep 15;24(12):1811-9. doi: 10.1002/mds.22682. Mov Disord. 2009. PMID: 19562770
Cerebral infarcts associated with adenomyosis among middle-aged women.
Yamashiro K, Tanaka R, Nishioka K, Ueno Y, Shimura H, Okuma Y, Hattori N, Urabe T. Yamashiro K, et al. Among authors: nishioka k. J Stroke Cerebrovasc Dis. 2012 Nov;21(8):910.e1-5. doi: 10.1016/j.jstrokecerebrovasdis.2011.10.017. Epub 2011 Dec 3. J Stroke Cerebrovasc Dis. 2012. PMID: 22142777
1,918 results