Kurahashi H - Search Results

1

Autosomal dominant nocturnal frontal lobe epilepsy: a genotypic comparative study of Japanese and Korean families carrying the CHRNA4 Ser284Leu mutation.

Hwang SK, Makita Y, Kurahashi H, Cho YW, Hirose S. Hwang SK, et al. Among authors: kurahashi h. J Hum Genet. 2011 Aug;56(8):609-12. doi: 10.1038/jhg.2011.69. Epub 2011 Jul 14. J Hum Genet. 2011. PMID: 21753767

2

Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures.

Kurahashi H, Wang JW, Ishii A, Kojima T, Wakai S, Kizawa T, Fujimoto Y, Kikkawa K, Yoshimura K, Inoue T, Yasumoto S, Ogawa A, Kaneko S, Hirose S. Kurahashi H, et al. Neurology. 2009 Oct 13;73(15):1214-7. doi: 10.1212/WNL.0b013e3181bc0158. Neurology. 2009. PMID: 19822871

3

KCNQ2 abnormality in BECTS: benign childhood epilepsy with centrotemporal spikes following benign neonatal seizures resulting from a mutation of KCNQ2.

Ishii A, Miyajima T, Kurahashi H, Wang JW, Yasumoto S, Kaneko S, Hirose S. Ishii A, et al. Among authors: kurahashi h. Epilepsy Res. 2012 Nov;102(1-2):122-5. doi: 10.1016/j.eplepsyres.2012.07.011. Epub 2012 Aug 10. Epilepsy Res. 2012. PMID: 22884718

4

Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy.

Wang JW, Shi XY, Kurahashi H, Hwang SK, Ishii A, Higurashi N, Kaneko S, Hirose S; Epilepsy Genetic Study Group Japan. Wang JW, et al. Among authors: kurahashi h. Epilepsy Res. 2012 Dec;102(3):195-200. doi: 10.1016/j.eplepsyres.2012.06.006. Epub 2012 Jul 20. Epilepsy Res. 2012. PMID: 23195492

5

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: kurahashi h. 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.

6

On the likelihood of SCN1A microdeletions or duplications in Dravet syndrome with missense mutation.

Shi X, Wang J, Kurahashi H, Ishii A, Higurashi N, Kaneko S, Hirose S. Shi X, et al. Among authors: kurahashi h. Brain Dev. 2012 Sep;34(8):617-9. doi: 10.1016/j.braindev.2011.11.005. Epub 2011 Dec 27. Brain Dev. 2012. PMID: 22206733

7

Novel de novo splice-site mutation of SCN1A in a patient with partial epilepsy with febrile seizures plus.

Kumakura A, Ito M, Hata D, Oh N, Kurahashi H, Wang JW, Hirose S. Kumakura A, et al. Among authors: kurahashi h. Brain Dev. 2009 Feb;31(2):179-82. doi: 10.1016/j.braindev.2008.06.001. Epub 2008 Jul 15. Brain Dev. 2009. PMID: 18632234

8

PRRT2 mutations in Japanese patients with benign infantile epilepsy and paroxysmal kinesigenic dyskinesia.

Okumura A, Shimojima K, Kurahashi H, Numoto S, Shimada S, Ishii A, Ohmori I, Takahashi S, Awaya T, Kubota T, Sakakibara T, Ishihara N, Hattori A, Torisu H, Tohyama J, Inoue T, Haibara A, Nishida T, Yuhara Y, Miya K, Tanaka R, Hirose S, Yamamoto T. Okumura A, et al. Among authors: kurahashi h. Seizure. 2019 Oct;71:1-5. doi: 10.1016/j.seizure.2019.05.017. Epub 2019 May 20. Seizure. 2019. PMID: 31154286 Free article.

9

Phenotypes of children with 20q13.3 microdeletion affecting KCNQ2 and CHRNA4.

Okumura A, Atsushi Ishii, Shimojima K, Kurahashi H, Yoshitomi S, lmai K, Imamura M, Seki Y, Toshiaki Shimizu T, Hirose S, Yamamoto T. Okumura A, et al. Among authors: kurahashi h. Epileptic Disord. 2015 Jun;17(2):165-71. doi: 10.1684/epd.2015.0746. Epileptic Disord. 2015. PMID: 26030193 Free article.

10

Focal epilepsy resulting from a de novo SCN1A mutation.

Okumura A, Kurahashi H, Hirose S, Okawa N, Watanabe K. Okumura A, et al. Among authors: kurahashi h. Neuropediatrics. 2007 Oct;38(5):253-6. doi: 10.1055/s-2008-1062703. Neuropediatrics. 2007. PMID: 18330841

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