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Rhinorrhea in Parkinson's disease: a consecutive multicenter study in Japan.
Kano O, Yoshioka M, Nagayama H, Hamada S, Maeda T, Hasegawa T, Kadowaki T, Sengoku R, Terashi H, Hatano T, Nomoto N, Inoue M, Shimura H, Takahashi T, Uchiyama T, Watanabe H, Kaneko S, Takahashi T, Baba Y, Kubo S; Young Japanese Expert Group for Parkinson's Disease and Movement Disorders: YJ-EXPANDS. Kano O, et al. J Neurol Sci. 2014 Aug 15;343(1-2):88-90. doi: 10.1016/j.jns.2014.05.039. Epub 2014 May 27. J Neurol Sci. 2014. PMID: 24932941
A Japanese multicenter survey characterizing pain in Parkinson's disease.
Kubo S, Hamada S, Maeda T, Uchiyama T, Hashimoto M, Nomoto N, Kano O, Takahashi T, Terashi H, Takahashi T, Hatano T, Hasegawa T, Baba Y, Sengoku R, Watanabe H, Kadowaki T, Inoue M, Kaneko S, Shimura H, Nagayama H. Kubo S, et al. J Neurol Sci. 2016 Jun 15;365:162-6. doi: 10.1016/j.jns.2016.04.015. Epub 2016 Apr 14. J Neurol Sci. 2016. PMID: 27206899
Anhedonia and its correlation with clinical aspects in Parkinson's disease.
Nagayama H, Maeda T, Uchiyama T, Hashimoto M, Nomoto N, Kano O, Takahashi T, Terashi H, Hamada S, Hasegawa T, Hatano T, Takahashi T, Baba Y, Sengoku R, Watanabe H, Inoue M, Kadowaki T, Kaneko S, Shimura H, Kubo SI; Young Japanese Expert Group for Parkinson's Disease and Movement Disorders: YJ-EXPANDS. Nagayama H, et al. Among authors: kubo si. J Neurol Sci. 2017 Jan 15;372:403-407. doi: 10.1016/j.jns.2016.10.051. Epub 2016 Nov 3. J Neurol Sci. 2017. PMID: 27839720
Arylsulfatase A, a genetic modifier of Parkinson's disease, is an α-synuclein chaperone.
Lee JS, Kanai K, Suzuki M, Kim WS, Yoo HS, Fu Y, Kim DK, Jung BC, Choi M, Oh KW, Li Y, Nakatani M, Nakazato T, Sekimoto S, Funayama M, Yoshino H, Kubo SI, Nishioka K, Sakai R, Ueyama M, Mochizuki H, Lee HJ, Sardi SP, Halliday GM, Nagai Y, Lee PH, Hattori N, Lee SJ. Lee JS, et al. Among authors: kubo si. Brain. 2019 Sep 1;142(9):2845-2859. doi: 10.1093/brain/awz205. Brain. 2019. PMID: 31312839
Recessive Parkinson's disease.
Kubo S, Hattori N, Mizuno Y. Kubo S, et al. Mov Disord. 2006 Jul;21(7):885-93. doi: 10.1002/mds.20841. Mov Disord. 2006. PMID: 16615060 Review.
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. Mov Disord. 2006 Aug;21(8):1102-8. doi: 10.1002/mds.20886. Mov Disord. 2006. PMID: 16622854
81 results