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Genetics and gene therapy in Dravet syndrome.
Higurashi N, Broccoli V, Hirose S. Higurashi N, et al. Among authors: hirose s. Epilepsy Behav. 2022 Jun;131(Pt B):108043. doi: 10.1016/j.yebeh.2021.108043. Epub 2021 May 28. Epilepsy Behav. 2022. PMID: 34053869 Review.
Clinical spectrum of SCN2A mutations.
Shi X, Yasumoto S, Kurahashi H, Nakagawa E, Fukasawa T, Uchiya S, Hirose S. Shi X, et al. Among authors: hirose s. Brain Dev. 2012 Aug;34(7):541-5. doi: 10.1016/j.braindev.2011.09.016. Epub 2011 Oct 24. Brain Dev. 2012. PMID: 22029951 Review.
PCDH19 mutation in Japanese females with epilepsy.
Higurashi N, Shi X, Yasumoto S, Oguni H, Sakauchi M, Itomi K, Miyamoto A, Shiraishi H, Kato T, Makita Y, Hirose S. Higurashi N, et al. Among authors: hirose s. Epilepsy Res. 2012 Mar;99(1-2):28-37. doi: 10.1016/j.eplepsyres.2011.10.014. Epub 2011 Nov 1. Epilepsy Res. 2012. PMID: 22050978
SCN1A testing for epilepsy: application in clinical practice.
Hirose S, Scheffer IE, Marini C, De Jonghe P, Andermann E, Goldman AM, Kauffman M, Tan NC, Lowenstein DH, Sisodiya SM, Ottman R, Berkovic SF; Genetics Commission of the International League Against Epilepsy. Hirose S, et al. Epilepsia. 2013 May;54(5):946-52. doi: 10.1111/epi.12168. Epub 2013 Apr 15. Epilepsia. 2013. PMID: 23586701 Free article.
A human Dravet syndrome model from patient induced pluripotent stem cells.
Higurashi N, Uchida T, Lossin C, Misumi Y, Okada Y, Akamatsu W, Imaizumi Y, Zhang B, Nabeshima K, Mori MX, Katsurabayashi S, Shirasaka Y, Okano H, Hirose S. Higurashi N, et al. Among authors: hirose s. Mol Brain. 2013 May 2;6:19. doi: 10.1186/1756-6606-6-19. Mol Brain. 2013. PMID: 23639079 Free PMC article.
2,057 results