Matsumoto A - Search Results

1

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

2

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. Epilepsia. 1989 Jan-Feb;30(1):45-9. doi: 10.1111/j.1528-1157.1989.tb05279.x. Epilepsia. 1989. PMID: 2492223

3

Clinical effects of thyrotropin-releasing hormone for severe epilepsy in childhood: a comparative study with ACTH therapy.

Matsumoto A, Kumagai T, Takeuchi T, Miyazaki S, Watanabe K. Matsumoto A, et al. Epilepsia. 1987 Jan-Feb;28(1):49-55. doi: 10.1111/j.1528-1157.1987.tb03622.x. Epilepsia. 1987. PMID: 3024959 Clinical Trial.

4

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. Among authors: matsumoto a. Neuropediatrics. 1998 Oct;29(5):239-41. doi: 10.1055/s-2007-973568. Neuropediatrics. 1998. PMID: 9810558

5

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: matsumoto a. Epilepsia. 1998;39 Suppl 5:46-9. doi: 10.1111/j.1528-1157.1998.tb05150.x. Epilepsia. 1998. PMID: 9737445 Free article.

6

Long-term prognosis of tuberous sclerosis with epilepsy in children.

Yamamoto N, Watanabe K, Negoro T, Matsumoto A, Miyazaki S, Kumagai T, Iwase K. Yamamoto N, et al. Among authors: matsumoto a. Brain Dev. 1987;9(3):292-5. doi: 10.1016/s0387-7604(87)80047-5. Brain Dev. 1987. PMID: 3116877

7

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. Among authors: matsumoto a. 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.

8

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. Among authors: matsumoto a. Brain Dev. 1993 Jul-Aug;15(4):288-90. doi: 10.1016/0387-7604(93)90025-4. Brain Dev. 1993. PMID: 8250151

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

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