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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: hattori n. Mov Disord. 2009 Sep 15;24(12):1811-9. doi: 10.1002/mds.22682. Mov Disord. 2009. PMID: 19562770
Impaired in vivo dopamine release in parkin knockout mice.
Oyama G, Yoshimi K, Natori S, Chikaoka Y, Ren YR, Funayama M, Shimo Y, Takahashi R, Nakazato T, Kitazawa S, Hattori N. Oyama G, et al. Among authors: hattori n. Brain Res. 2010 Sep 17;1352:214-22. doi: 10.1016/j.brainres.2010.06.065. Epub 2010 Jul 8. Brain Res. 2010. PMID: 20620130
VPS35 mutation in Japanese patients with typical Parkinson's disease.
Ando M, Funayama M, Li Y, Kashihara K, Murakami Y, Ishizu N, Toyoda C, Noguchi K, Hashimoto T, Nakano N, Sasaki R, Kokubo Y, Kuzuhara S, Ogaki K, Yamashita C, Yoshino H, Hatano T, Tomiyama H, Hattori N. Ando M, et al. Among authors: hattori n. Mov Disord. 2012 Sep 15;27(11):1413-7. doi: 10.1002/mds.25145. Epub 2012 Sep 18. Mov Disord. 2012. PMID: 22991136
2,469 results