Kato M - Search Results

1

SPTAN1 encephalopathy: distinct phenotypes and genotypes.

Tohyama J, Nakashima M, Nabatame S, Gaik-Siew C, Miyata R, Rener-Primec Z, Kato M, Matsumoto N, Saitsu H. Tohyama J, et al. Among authors: kato m. J Hum Genet. 2015 Apr;60(4):167-73. doi: 10.1038/jhg.2015.5. Epub 2015 Jan 29. J Hum Genet. 2015. PMID: 25631096 Review.

2

Lissencephaly and the molecular basis of neuronal migration.

Kato M, Dobyns WB. Kato M, et al. Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R89-96. doi: 10.1093/hmg/ddg086. Hum Mol Genet. 2003. PMID: 12668601 Review.

3

BAC array CGH reveals genomic aberrations in idiopathic mental retardation.

Miyake N, Shimokawa O, Harada N, Sosonkina N, Okubo A, Kawara H, Okamoto N, Kurosawa K, Kawame H, Iwakoshi M, Kosho T, Fukushima Y, Makita Y, Yokoyama Y, Yamagata T, Kato M, Hiraki Y, Nomura M, Yoshiura K, Kishino T, Ohta T, Mizuguchi T, Niikawa N, Matsumoto N. Miyake N, et al. Among authors: kato m. Am J Med Genet A. 2006 Feb 1;140(3):205-11. doi: 10.1002/ajmg.a.31098. Am J Med Genet A. 2006. PMID: 16419101

4

Magnetoencephalography in patients with tuberous sclerosis and localization-related epilepsy.

Kamimura T, Tohyama J, Oishi M, Akasaka N, Kanazawa O, Sasagawa M, Kato M, Ohno K, Masuda H, Kameyama S, Uchiyama M. Kamimura T, et al. Among authors: kato m. Epilepsia. 2006 Jun;47(6):991-7. doi: 10.1111/j.1528-1167.2006.00511.x. Epilepsia. 2006. PMID: 16822245 Free article.

5

Acute encephalopathy with refractory status epilepticus: bilateral mesial temporal and claustral lesions, associated with a peripheral marker of oxidative DNA damage.

Shiihara T, Kato M, Ichiyama T, Takahashi Y, Tanuma N, Miyata R, Hayasaka K. Shiihara T, et al. Among authors: kato m. J Neurol Sci. 2006 Dec 1;250(1-2):159-61. doi: 10.1016/j.jns.2006.07.002. Epub 2006 Aug 28. J Neurol Sci. 2006. PMID: 16935306

6

A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome).

Kato M, Saitoh S, Kamei A, Shiraishi H, Ueda Y, Akasaka M, Tohyama J, Akasaka N, Hayasaka K. Kato M, et al. Am J Hum Genet. 2007 Aug;81(2):361-6. doi: 10.1086/518903. Epub 2007 Jun 11. Am J Hum Genet. 2007. PMID: 17668384 Free PMC article.

7

Megalencephaly and polymicrogyria with polydactyly syndrome.

Tohyama J, Akasaka N, Saito N, Yoshimura J, Nishiyama K, Kato M. Tohyama J, et al. Among authors: kato m. Pediatr Neurol. 2007 Aug;37(2):148-51. doi: 10.1016/j.pediatrneurol.2007.04.008. Pediatr Neurol. 2007. PMID: 17675034

8

Early onset West syndrome with cerebral hypomyelination and reduced cerebral white matter.

Tohyama J, Akasaka N, Osaka H, Maegaki Y, Kato M, Saito N, Yamashita S, Ohno K. Tohyama J, et al. Among authors: kato m. Brain Dev. 2008 May;30(5):349-55. doi: 10.1016/j.braindev.2007.10.006. Epub 2007 Dec 11. Brain Dev. 2008. PMID: 18065176

9

Two new cases of pure 1q terminal deletion presenting with brain malformations.

Hiraki Y, Okamoto N, Ida T, Nakata Y, Kamada M, Kanemura Y, Yamasaki M, Fujita H, Nishimura G, Kato M, Harada N, Matsumoto N. Hiraki Y, et al. Among authors: kato m. Am J Med Genet A. 2008 May 15;146A(10):1241-7. doi: 10.1002/ajmg.a.32275. Am J Med Genet A. 2008. PMID: 18384145

10

De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy.

Saitsu H, Kato M, Mizuguchi T, Hamada K, Osaka H, Tohyama J, Uruno K, Kumada S, Nishiyama K, Nishimura A, Okada I, Yoshimura Y, Hirai S, Kumada T, Hayasaka K, Fukuda A, Ogata K, Matsumoto N. Saitsu H, et al. Among authors: kato m. Nat Genet. 2008 Jun;40(6):782-8. doi: 10.1038/ng.150. Epub 2008 May 11. Nat Genet. 2008. PMID: 18469812

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