Ito M - Search Results

1

Seizure phenotypes of a family with missense mutations in SCN2A.

Ito M, Shirasaka Y, Hirose S, Sugawara T, Yamakawa K. Ito M, et al. Pediatr Neurol. 2004 Aug;31(2):150-2. doi: 10.1016/j.pediatrneurol.2004.02.013. Pediatr Neurol. 2004. PMID: 15301839

2

Genetic abnormalities underlying familial epilepsy syndromes.

Hirose S, Okada M, Yamakawa K, Sugawara T, Fukuma G, Ito M, Kaneko S, Mitsudome A. Hirose S, et al. Among authors: ito m. Brain Dev. 2002 Jun;24(4):211-22. doi: 10.1016/s0387-7604(02)00056-6. Brain Dev. 2002. PMID: 12015163 Review.

3

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: ito m. 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.

4

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: ito m. 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

5

Three Japanese patients with glucose transporter type 1 deficiency syndrome.

Fujii T, Ho YY, Wang D, De Vivo DC, Miyajima T, Wong HY, Tsang PT, Shirasaka Y, Kudo T, Ito M. Fujii T, et al. Among authors: ito m. Brain Dev. 2007 Mar;29(2):92-7. doi: 10.1016/j.braindev.2006.07.007. Epub 2006 Sep 1. Brain Dev. 2007. PMID: 16949238

6

Cloxazolam treatment for patients with intractable epilepsy.

Ito M, Miyajima T, Fujii T, Okuno T. Ito M, et al. Pediatr Neurol. 2004 Feb;30(2):111-4. doi: 10.1016/j.pediatrneurol.2003.07.004. Pediatr Neurol. 2004. PMID: 14984903 Clinical Trial.

7

Mutation screening of AP3M2 in Japanese epilepsy patients.

Huang MC, Okada M, Nakatsu F, Oguni H, Ito M, Morita K, Nagafuji H, Hirose S, Sakaki Y, Kaneko S, Ohno H, Kojima T. Huang MC, et al. Among authors: ito m. Brain Dev. 2007 Sep;29(8):462-7. doi: 10.1016/j.braindev.2006.12.004. Epub 2007 Feb 12. Brain Dev. 2007. PMID: 17293072

8

A novel missense mutation in the DKC1 gene in a Japanese family with X-linked dyskeratosis congenita.

Hiramatsu H, Fujii T, Kitoh T, Sawada M, Osaka M, Koami K, Irino T, Miyajima T, Ito M, Sugiyama T, Okuno T. Hiramatsu H, et al. Among authors: ito m. Pediatr Hematol Oncol. 2002 Sep;19(6):413-9. doi: 10.1080/08880010290097170. Pediatr Hematol Oncol. 2002. PMID: 12186364

9

Focal glucose hypermetabolism in interictal state of West syndrome.

Kumada T, Okazawa H, Yamauchi H, Kitoh T, Ito M. Kumada T, et al. Among authors: ito m. Pediatr Neurol. 2006 Jan;34(1):47-50. doi: 10.1016/j.pediatrneurol.2005.05.019. Pediatr Neurol. 2006. PMID: 16376279

10

Dichloroacetate therapy in Leigh syndrome with a mitochondrial T8993C mutation.

Fujii T, Ito M, Miyajima T, Okuno T. Fujii T, et al. Among authors: ito m. Pediatr Neurol. 2002 Jul;27(1):58-61. doi: 10.1016/s0887-8994(02)00378-8. Pediatr Neurol. 2002. PMID: 12160976

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