Miyazaki S - Search Results

1

Prognostic factors for epileptic seizures in severe motor and intellectual disabilities syndrome (SMIDS)--a clinical and electroencephalographic study.

Matsumoto A, Miyazaki S, Hayakawa C, Komori T, Nakamura M, Oshio A. Matsumoto A, et al. Among authors: miyazaki s. Epilepsy Res. 2009 Oct;86(2-3):175-82. doi: 10.1016/j.eplepsyres.2009.06.005. Epub 2009 Aug 25. Epilepsy Res. 2009. PMID: 19709858

2

Epilepsy in severe motor and intellectual disabilities syndrome (SMIDS)--a clinical and electroencephalographic study of epileptic syndromes.

Matsumoto A, Miyazaki S, Hayakawa C, Komori T, Nakamura M. Matsumoto A, et al. Among authors: miyazaki s. Epilepsy Res. 2007 Dec;77(2-3):120-7. doi: 10.1016/j.eplepsyres.2007.09.006. Epub 2007 Nov 5. Epilepsy Res. 2007. PMID: 17983730

3

[Tracheostomy for home-care patients with severe motor and intellectual disabilities].

Miura K, Suzuki Y, Kumagai T, Hayakawa C, Matsumoto A, Miyazaki S, Mizuno S. Miura K, et al. Among authors: miyazaki s. No To Hattatsu. 2005 Jul;37(4):293-8. No To Hattatsu. 2005. PMID: 16026094 Japanese.

4

Epilepsy in Angelman syndrome associated with chromosome 15q deletion.

Matsumoto A, Kumagai T, Miura K, Miyazaki S, Hayakawa C, Yamanaka T. Matsumoto A, et al. Among authors: miyazaki s. Epilepsia. 1992 Nov-Dec;33(6):1083-90. doi: 10.1111/j.1528-1157.1992.tb01763.x. Epilepsia. 1992. PMID: 1464268

5

[Clinical symptoms of the Rett syndrome patients with MECP2 gene abnormalities].

Miura K, Kumagai T, Suzuki Y, Ohki T, Matsumoto A, Miyazaki S, Hayakawa C, Sonta S, Yamada Y, Wakamatsu N. Miura K, et al. Among authors: miyazaki s. No To Hattatsu. 2005 Jan;37(1):39-45. No To Hattatsu. 2005. PMID: 15675358 Japanese.

6

Difficulty in writing Japanese semantic characters in a 9-year-old boy with Williams syndrome.

Nakamura M, Hara K, Watamaki T, Nishimura B, Kumagai T, Matsumoto A, Miura K, Yamanaka T, Hayakawa C, Miyazaki S. Nakamura M, et al. Among authors: miyazaki s. J Intellect Disabil Res. 1999 Dec;43 ( Pt 6):562-7. doi: 10.1046/j.1365-2788.1999.00237.x. J Intellect Disabil Res. 1999. PMID: 10622373

7

Factors influencing effectiveness of thyrotropin-releasing hormone therapy for severe epilepsy in childhood: significance of serum prolactin levels.

Matsumoto A, Kumagai T, Takeuchi T, Miyazaki S, Watanabe K. Matsumoto A, et al. Among authors: miyazaki s. Epilepsia. 1989 Jan-Feb;30(1):45-9. doi: 10.1111/j.1528-1157.1989.tb05279.x. Epilepsia. 1989. PMID: 2492223

8

Williams syndrome and deficiency in visuospatial recognition.

Nakamura M, Watanabe K, Matsumoto A, Yamanaka T, Kumagai T, Miyazaki S, Matsushima M, Mita K. Nakamura M, et al. Among authors: miyazaki s. Dev Med Child Neurol. 2001 Sep;43(9):617-21. doi: 10.1017/s0012162201001128. Dev Med Child Neurol. 2001. PMID: 11570631 Free article. Clinical Trial.

9

Nonsense and frameshift mutations in ZFHX1B, encoding Smad-interacting protein 1, cause a complex developmental disorder with a great variety of clinical features.

Yamada K, Yamada Y, Nomura N, Miura K, Wakako R, Hayakawa C, Matsumoto A, Kumagai T, Yoshimura I, Miyazaki S, Kato K, Sonta S, Ono H, Yamanaka T, Nagaya M, Wakamatsu N. Yamada K, et al. Among authors: miyazaki s. Am J Hum Genet. 2001 Dec;69(6):1178-85. doi: 10.1086/324343. Epub 2001 Oct 2. Am J Hum Genet. 2001. PMID: 11592033 Free PMC article.

10

Molecular analysis of Japanese patients with Rett syndrome: Identification of five novel mutations and genotype-phenotype correlation.

Yamada Y, Miura K, Kumagai T, Hayakawa C, Miyazaki S, Matsumoto A, Kurosawa K, Nomura N, Taniguchi H, Sonta SI, Yamanaka T, Wakamatsu N. Yamada Y, et al. Among authors: miyazaki s. Hum Mutat. 2001 Sep;18(3):253. doi: 10.1002/humu.1186. Hum Mutat. 2001. PMID: 11524741

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