Miura K - Search Results

1

Two cases of chromosome 4q35-linked early onset facioscapulohumeral muscular dystrophy with mental retardation and epilepsy.

Miura K, Kumagai T, Matsumoto A, Iriyama E, Watanabe K, Goto K, Arahata K. Miura K, et al. Neuropediatrics. 1998 Oct;29(5):239-41. doi: 10.1055/s-2007-973568. Neuropediatrics. 1998. PMID: 9810558

2

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: miura k. Epilepsia. 1992 Nov-Dec;33(6):1083-90. doi: 10.1111/j.1528-1157.1992.tb01763.x. Epilepsia. 1992. PMID: 1464268

3

Magnetic resonance imaging and positron emission tomography of band heterotopia.

Miura K, Watanabe K, Maeda N, Matsumoto A, Kumagai T, Ito K, Kato T. Miura K, et al. Brain Dev. 1993 Jul-Aug;15(4):288-90. doi: 10.1016/0387-7604(93)90025-4. Brain Dev. 1993. PMID: 8250151

4

Epilepsies of neonatal onset.

Miura K, Watanabe K, Aso K, Hayakawa F, Takeuchi T, Matsumoto A, Kumagai T, Negoro T, Haga Y, Kito M, et al. Miura K, et al. Jpn J Psychiatry Neurol. 1993 Jun;47(2):347-9. doi: 10.1111/j.1440-1819.1993.tb02099.x. Jpn J Psychiatry Neurol. 1993. PMID: 8271590 No abstract available.

5

[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: miura k. No To Hattatsu. 2001 Nov;33(6):480-6. No To Hattatsu. 2001. PMID: 11725514 Japanese.

6

Evolutional changes and outcome of West syndrome: correlation with magnetic resonance imaging findings.

Okumura A, Watanabe K, Negoro T, Aso K, Natsume J, Kubota T, Matsumoto A, Miura K, Furune J, Nomura K, Hayakawa F, Kato T. Okumura A, et al. Among authors: miura k. Epilepsia. 1998;39 Suppl 5:46-9. doi: 10.1111/j.1528-1157.1998.tb05150.x. Epilepsia. 1998. PMID: 9737445 Free article.

7

MRI findings in patients with symptomatic localization-related epilepsies beginning in infancy and early childhood.

Okumura A, Watanabe K, Negoro T, Ishiguro Y, Miura K, Matsumoto A, Hayakawa F, Kato T, Furune S, Maeda N, Nomura K, Takenaka J, Kubota T. Okumura A, et al. Among authors: miura k. Seizure. 2000 Dec;9(8):566-71. doi: 10.1053/seiz.2000.0452. Seizure. 2000. PMID: 11162754 Free article.

8

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: miura k. 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.

9

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: miura k. 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

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: miura k. Hum Mutat. 2001 Sep;18(3):253. doi: 10.1002/humu.1186. Hum Mutat. 2001. PMID: 11524741

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