Sakauchi M - Search Results

1

Retrospective multiinstitutional study of the prevalence of early death in Dravet syndrome.

Sakauchi M, Oguni H, Kato I, Osawa M, Hirose S, Kaneko S, Takahashi Y, Takayama R, Fujiwara T. Sakauchi M, et al. Epilepsia. 2011 Jun;52(6):1144-9. doi: 10.1111/j.1528-1167.2011.03053.x. Epub 2011 Apr 11. Epilepsia. 2011. PMID: 21480880 Free article.

2

Mortality in Dravet syndrome: search for risk factors in Japanese patients.

Sakauchi M, Oguni H, Kato I, Osawa M, Hirose S, Kaneko S, Takahashi Y, Takayama R, Fujiwara T. Sakauchi M, et al. Epilepsia. 2011 Apr;52 Suppl 2:50-4. doi: 10.1111/j.1528-1167.2011.03002.x. Epilepsia. 2011. PMID: 21463280 Free article.

3

An electroclinical study of absence seizures in Dravet syndrome.

Tsuda Y, Oguni H, Sakauchi M, Osawa M. Tsuda Y, et al. Among authors: sakauchi m. Epilepsy Res. 2013 Jan;103(1):88-96. doi: 10.1016/j.eplepsyres.2012.07.010. Epub 2012 Jul 21. Epilepsy Res. 2013. PMID: 22824327

4

Idiopathic myoclonic-astatic epilepsy of early childhood--nosology based on electrophysiologic and long-term follow-up study of patients.

Oguni H, Hayashi K, Imai K, Funatsuka M, Sakauchi M, Shirakawa S, Osawa M. Oguni H, et al. Among authors: sakauchi m. Adv Neurol. 2005;95:157-74. Adv Neurol. 2005. PMID: 15508921 Review. No abstract available.

5

Higurashi N, Nakamura M, Sugai M, Ohfu M, Sakauchi M, Sugawara Y, Nakamura K, Kato M, Usui D, Mogami Y, Fujiwara Y, Ito T, Ikeda H, Imai K, Takahashi Y, Nukui M, Inoue T, Okazaki S, Kirino T, Tomonoh Y, Inoue T, Takano K, Shimakawa S, Hirose S. Higurashi N, et al. Among authors: sakauchi m. Epilepsy Res. 2013 Sep;106(1-2):191-9. doi: 10.1016/j.eplepsyres.2013.04.005. Epub 2013 May 24. Epilepsy Res. 2013. PMID: 23712037

6

A recurrent KCNT1 mutation in two sporadic cases with malignant migrating partial seizures in infancy.

Ishii A, Shioda M, Okumura A, Kidokoro H, Sakauchi M, Shimada S, Shimizu T, Osawa M, Hirose S, Yamamoto T. Ishii A, et al. Among authors: sakauchi m. Gene. 2013 Dec 1;531(2):467-71. doi: 10.1016/j.gene.2013.08.096. Epub 2013 Sep 10. Gene. 2013. PMID: 24029078

7

Myoclonic-astatic epilepsy of early childhood--clinical and EEG analysis of myoclonic-astatic seizures, and discussions on the nosology of the syndrome.

Oguni H, Fukuyama Y, Tanaka T, Hayashi K, Funatsuka M, Sakauchi M, Shirakawa S, Osawa M. Oguni H, et al. Among authors: sakauchi m. Brain Dev. 2001 Nov;23(7):757-64. doi: 10.1016/s0387-7604(01)00281-9. Brain Dev. 2001. PMID: 11701290 Review.

8

Treatment and long-term prognosis of myoclonic-astatic epilepsy of early childhood.

Oguni H, Tanaka T, Hayashi K, Funatsuka M, Sakauchi M, Shirakawa S, Osawa M. Oguni H, et al. Among authors: sakauchi m. Neuropediatrics. 2002 Jun;33(3):122-32. doi: 10.1055/s-2002-33675. Neuropediatrics. 2002. PMID: 12200741

9

PCDH19 mutation in Japanese females with epilepsy.

Higurashi N, Shi X, Yasumoto S, Oguni H, Sakauchi M, Itomi K, Miyamoto A, Shiraishi H, Kato T, Makita Y, Hirose S. Higurashi N, et al. Among authors: sakauchi m. Epilepsy Res. 2012 Mar;99(1-2):28-37. doi: 10.1016/j.eplepsyres.2011.10.014. Epub 2011 Nov 1. Epilepsy Res. 2012. PMID: 22050978

10

Cardiac involvement in Fukuyama-type congenital muscular dystrophy.

Nakanishi T, Sakauchi M, Kaneda Y, Tomimatsu H, Saito K, Nakazawa M, Osawa M. Nakanishi T, et al. Among authors: sakauchi m. Pediatrics. 2006 Jun;117(6):e1187-92. doi: 10.1542/peds.2005-2469. Epub 2006 May 22. Pediatrics. 2006. PMID: 16717122

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