Kurahashi H - Search Results

1

Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy.

Wang JW, Kurahashi H, Ishii A, Kojima T, Ohfu M, Inoue T, Ogawa A, Yasumoto S, Oguni H, Kure S, Fujii T, Ito M, Okuno T, Shirasaka Y, Natsume J, Hasegawa A, Konagaya A, Kaneko S, Hirose S. Wang JW, et al. Among authors: kurahashi h. Epilepsia. 2008 Sep;49(9):1528-34. doi: 10.1111/j.1528-1167.2008.01609.x. Epub 2008 Apr 21. Epilepsia. 2008. PMID: 18479393 Free article.

2

Long-term follow-up of patients with benign partial epilepsy in infancy.

Okumura A, Watanabe K, Negoro T, Hayakawa F, Kato T, Maruyama K, Kubota T, Suzuki M, Kurahashi H, Azuma Y. Okumura A, et al. Among authors: kurahashi h. Epilepsia. 2006 Jan;47(1):181-5. doi: 10.1111/j.1528-1167.2006.00385.x. Epilepsia. 2006. PMID: 16417547 Free article.

3

Phenytoin desensitization monitored by antigen specific T cell response using carboxyfluorescein succinimidyl ester dilution assay.

Okumura A, Tsuge I, Kubota T, Kurahashi H, Natsume J, Negoro T, Watanabe K. Okumura A, et al. Among authors: kurahashi h. Eur J Paediatr Neurol. 2007 Nov;11(6):385-8. doi: 10.1016/j.ejpn.2007.03.001. Epub 2007 Apr 10. Eur J Paediatr Neurol. 2007. PMID: 17428709

4

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

5

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

6

Hemiconvulsion-hemiplegia syndrome in a patient with severe myoclonic epilepsy in infancy.

Sakakibara T, Nakagawa E, Saito Y, Sakuma H, Komaki H, Sugai K, Sasaki M, Kurahashi H, Hirose S. Sakakibara T, et al. Among authors: kurahashi h. Epilepsia. 2009 Sep;50(9):2158-62. doi: 10.1111/j.1528-1167.2009.02175.x. Epub 2009 Jun 26. Epilepsia. 2009. PMID: 19563349 Free article.

7

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

8

Spinocerebellar ataxias type 27 derived from a disruption of the fibroblast growth factor 14 gene with mimicking phenotype of paroxysmal non-kinesigenic dyskinesia.

Shimojima K, Okumura A, Natsume J, Aiba K, Kurahashi H, Kubota T, Yokochi K, Yamamoto T. Shimojima K, et al. Among authors: kurahashi h. Brain Dev. 2012 Mar;34(3):230-3. doi: 10.1016/j.braindev.2011.04.014. Epub 2011 May 19. Brain Dev. 2012. PMID: 21600715

9

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

10

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.

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