Kato M - Search Results

1

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.

2

Fluctuation of computed tomographic findings in white matter in Alexander's disease.

Shiihara T, Kato M, Honma T, Ohtaki S, Sawaishi Y, Hayasaka K. Shiihara T, et al. Among authors: kato m. J Child Neurol. 2002 Mar;17(3):227-30. doi: 10.1177/088307380201700316. J Child Neurol. 2002. PMID: 12026242

3

Progressive sliding hiatal hernia as a complication of Menkes' syndrome.

Shiihara T, Kato M, Honma T, Kimura T, Matsunaga A, Kodama H, Hayasaka K. Shiihara T, et al. Among authors: kato m. J Child Neurol. 2002 May;17(5):401-2. doi: 10.1177/088307380201700521. J Child Neurol. 2002. PMID: 12150594

4

Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans.

Kitamura K, Yanazawa M, Sugiyama N, Miura H, Iizuka-Kogo A, Kusaka M, Omichi K, Suzuki R, Kato-Fukui Y, Kamiirisa K, Matsuo M, Kamijo S, Kasahara M, Yoshioka H, Ogata T, Fukuda T, Kondo I, Kato M, Dobyns WB, Yokoyama M, Morohashi K. Kitamura K, et al. Among authors: kato fukui y, kato m. Nat Genet. 2002 Nov;32(3):359-69. doi: 10.1038/ng1009. Epub 2002 Oct 15. Nat Genet. 2002. PMID: 12379852

5

Microcephaly, cerebellar atrophy, and focal segmental glomerulosclerosis in two brothers: a possible mild form of Galloway-Mowat syndrome.

Shiihara T, Kato M, Kimura T, Matsunaga A, Joh K, Hayasaka K. Shiihara T, et al. Among authors: kato m. J Child Neurol. 2003 Feb;18(2):147-9. doi: 10.1177/08830738030180021801. J Child Neurol. 2003. PMID: 12693786

6

Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation.

Kato M, Das S, Petras K, Kitamura K, Morohashi KI, Abuelo DN, Barr M, Bonneau D, Brady AF, Carpenter NJ, Cipero KL, Frisone F, Fukuda T, Guerrini R, Iida E, Itoh M, Lewanda AF, Nanba Y, Oka A, Proud VK, Saugier-Veber P, Schelley SL, Selicorni A, Shaner R, Silengo M, Stewart F, Sugiyama N, Toyama J, Toutain A, Vargas AL, Yanazawa M, Zackai EH, Dobyns WB. Kato M, et al. Hum Mutat. 2004 Feb;23(2):147-159. doi: 10.1002/humu.10310. Hum Mutat. 2004. PMID: 14722918

7

Craniosynostosis with extra copy of MSX2 in a patient with partial 5q-trisomy.

Shiihara T, Kato M, Kimura T, Hayasaka K, Yamamori S, Ogata T. Shiihara T, et al. Among authors: kato m. Am J Med Genet A. 2004 Jul 15;128A(2):214-6. doi: 10.1002/ajmg.a.20552. Am J Med Genet A. 2004. PMID: 15214020 No abstract available.

8

Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAP.

Shiihara T, Sawaishi Y, Adachi M, Kato M, Hayasaka K. Shiihara T, et al. Among authors: kato m. J Neurol Sci. 2004 Oct 15;225(1-2):125-7. doi: 10.1016/j.jns.2004.07.008. J Neurol Sci. 2004. PMID: 15465095

9

Clinically mild encephalitis/encephalopathy with a reversible splenial lesion.

Shiihara T, Kato M, Hayasaka K. Shiihara T, et al. Among authors: kato m. Neurology. 2005 Apr 26;64(8):1487; author reply 1487. Neurology. 2005. PMID: 15858866 No abstract available.

10

Costello syndrome showing moyamoya-like vasculopathy.

Shiihara T, Kato M, Mitsuhashi Y, Hayasaka K. Shiihara T, et al. Among authors: kato m. Pediatr Neurol. 2005 May;32(5):361-3. doi: 10.1016/j.pediatrneurol.2004.12.010. Pediatr Neurol. 2005. PMID: 15866441

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