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Dystonia: Still a Mysterious Syndrome.
Morigaki R, Miyamoto R. Morigaki R, et al. Among authors: miyamoto r. Life (Basel). 2022 Jul 4;12(7):989. doi: 10.3390/life12070989. Life (Basel). 2022. PMID: 35888079 Free PMC article.
Generalized dystonia in a patient with a novel mutation in the GLUD1 gene.
Miyamoto R, Goto S, Sako W, Miyashiro A, Kim I, Escande F, Harada M, Morigaki R, Asanuma K, Mizobuchi Y, Nagahiro S, Izumi Y, Kaji R. Miyamoto R, et al. Mov Disord. 2012 Aug;27(9):1198-9. doi: 10.1002/mds.25081. Epub 2012 Jun 21. Mov Disord. 2012. PMID: 22730017 No abstract available.
Phenotype variability and allelic heterogeneity in KMT2B-Associated disease.
Kawarai T, Miyamoto R, Nakagawa E, Koichihara R, Sakamoto T, Mure H, Morigaki R, Koizumi H, Oki R, Montecchiani C, Caltagirone C, Orlacchio A, Hattori A, Mashimo H, Izumi Y, Mezaki T, Kumada S, Taniguchi M, Yokochi F, Saitoh S, Goto S, Kaji R. Kawarai T, et al. Among authors: miyamoto r. Parkinsonism Relat Disord. 2018 Jul;52:55-61. doi: 10.1016/j.parkreldis.2018.03.022. Epub 2018 Apr 5. Parkinsonism Relat Disord. 2018. PMID: 29653907
Dystonia and Cerebellum: From Bench to Bedside.
Morigaki R, Miyamoto R, Matsuda T, Miyake K, Yamamoto N, Takagi Y. Morigaki R, et al. Among authors: miyamoto r. Life (Basel). 2021 Jul 31;11(8):776. doi: 10.3390/life11080776. Life (Basel). 2021. PMID: 34440520 Free PMC article. Review.
[Dystonia genes and elucidation of their roles in dystonia pathogenesis].
Kawarai T, Miyamoto R, Murakami N, Miyazaki Y, Koizumi H, Sako W, Mukai Y, Sato K, Matsumoto S, Sakamoto T, Izumi Y, Kaji R. Kawarai T, et al. Among authors: miyamoto r. Rinsho Shinkeigaku. 2013;53(6):419-29. doi: 10.5692/clinicalneurol.53.419. Rinsho Shinkeigaku. 2013. PMID: 23782819 Review. Japanese.
481 results