Nakamura M - Search Results

1

Evolution of seizures and electroencephalographical findings in 23 cases of deletion type Angelman syndrome.

Uemura N, Matsumoto A, Nakamura M, Watanabe K, Negoro T, Kumagai T, Miura K, Ohki T, Mizuno S, Okumura A, Aso K, Hayakawa F, Kondo Y. Uemura N, et al. Among authors: nakamura m. Brain Dev. 2005 Aug;27(5):383-8. doi: 10.1016/j.braindev.2004.01.009. Brain Dev. 2005. PMID: 15963670

2

Disparities in visuo-spatial constructive abilities in Williams syndrome patients with typical deletion on chromosome 7q11.23.

Muramatsu Y, Tokita Y, Mizuno S, Nakamura M. Muramatsu Y, et al. Among authors: nakamura m. Brain Dev. 2017 Feb;39(2):145-153. doi: 10.1016/j.braindev.2016.09.003. Epub 2016 Sep 29. Brain Dev. 2017. PMID: 27692871

3

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: nakamura m. 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

4

[Intervention to reduce the difficulty in kanji copying related to the visuo-spatial dysfunction in patients with Williams syndrome].

Nakamura M, Mizuno S, Kumagai T. Nakamura M, et al. No To Hattatsu. 2010 Sep;42(5):353-8. No To Hattatsu. 2010. PMID: 20845766 Japanese.

5

Characteristics of epilepsy in patients with Kabuki syndrome with KMT2D mutations.

Kurahashi N, Miyake N, Mizuno S, Koshimizu E, Kurahashi H, Yamada K, Natsume J, Aoki Y, Nakamura M, Taniai H, Maki Y, Abe-Hatano C, Matsumoto N, Maruyama K. Kurahashi N, et al. Among authors: nakamura m. Brain Dev. 2017 Sep;39(8):672-677. doi: 10.1016/j.braindev.2017.03.025. Epub 2017 Apr 9. Brain Dev. 2017. PMID: 28404210

6

[Central nervous system involvements in Duchenne/Becker muscular dystrophy].

Kumagai T, Miura K, Ohki T, Matsumoto A, Miyazaki S, Nakamura M, Ochi N, Takahashi O. Kumagai T, et al. Among authors: nakamura m. No To Hattatsu. 2001 Nov;33(6):480-6. No To Hattatsu. 2001. PMID: 11725514 Japanese.

7

Development of visuospatial ability and kanji copying in Williams Syndrome.

Nakamura M, Mizuno S, Douyuu S, Matsumoto A, Kumagai T, Watanabe S, Kakigi R. Nakamura M, et al. Pediatr Neurol. 2009 Aug;41(2):95-100. doi: 10.1016/j.pediatrneurol.2009.02.005. Pediatr Neurol. 2009. PMID: 19589456

8

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: nakamura m. 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

9

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. 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.

10

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. 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

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