Hirose S - Search Results

1

The effectiveness of clonazepam on the Rolandic discharges.

Mitsudome A, Ohfu M, Yasumoto S, Ogawa A, Hirose S, Ogata H, Yamada T. Mitsudome A, et al. Among authors: hirose s. Brain Dev. 1997 Jun;19(4):274-8. doi: 10.1016/s0387-7604(97)00575-5. Brain Dev. 1997. PMID: 9187478 Clinical Trial.

2

Valproate therapy does not deplete carnitine levels in otherwise healthy children.

Hirose S, Mitsudome A, Yasumoto S, Ogawa A, Muta Y, Tomoda Y. Hirose S, et al. Pediatrics. 1998 May;101(5):E9. doi: 10.1542/peds.101.5.e9. Pediatrics. 1998. PMID: 9565442

3

Are some idiopathic epilepsies disorders of ion channels?: A working hypothesis.

Hirose S, Okada M, Kaneko S, Mitsudome A. Hirose S, et al. Epilepsy Res. 2000 Oct;41(3):191-204. doi: 10.1016/s0920-1211(00)00141-8. Epilepsy Res. 2000. PMID: 10962210 Review.

4

Electroclinical picture of autosomal dominant nocturnal frontal lobe epilepsy in a Japanese family.

Ito M, Kobayashi K, Fujii T, Okuno T, Hirose S, Iwata H, Mitsudome A, Kaneko S. Ito M, et al. Among authors: hirose s. Epilepsia. 2000 Jan;41(1):52-8. doi: 10.1111/j.1528-1157.2000.tb01505.x. Epilepsia. 2000. PMID: 10643924 Free article. Review.

5

A novel intragenetic PvuII marker in the human neuronal nicotinic acetylcholine receptor a4 subunit gene (CHRNA4). Mutation and polymorphism report no. 62. Online.

Iwata H, Hirose S, Akiyoshi H, Kaneko S, Mitsudome A. Iwata H, et al. Among authors: hirose s. Hum Mutat. 1999;14(1):93. doi: 10.1002/(SICI)1098-1004(1999)14:1<93::AID-HUMU25>3.0.CO;2-U. Hum Mutat. 1999. PMID: 10447275 No abstract available.

6

Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures.

Kurahashi H, Wang JW, Ishii A, Kojima T, Wakai S, Kizawa T, Fujimoto Y, Kikkawa K, Yoshimura K, Inoue T, Yasumoto S, Ogawa A, Kaneko S, Hirose S. Kurahashi H, et al. Among authors: hirose s. Neurology. 2009 Oct 13;73(15):1214-7. doi: 10.1212/WNL.0b013e3181bc0158. Neurology. 2009. PMID: 19822871

7

A novel SSCP variant (c.828G>A) within the M2 domain of the human neuronal nicotinic acetylcholine receptor alpha 4 subunit gene, CHRNA4.

Akiyoshi H, Iwata H, Fukuma G, Yonetani M, Wada K, Kaneko S, Mitsudome A, Hirose S. Akiyoshi H, et al. Among authors: hirose s. Hum Mutat. 2000 Nov;16(5):450. doi: 10.1002/1098-1004(200011)16:5<450::AID-HUMU27>3.0.CO;2-4. Hum Mutat. 2000. PMID: 11058920 No abstract available.

8

Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A.

Ito M, Nagafuji H, Okazawa H, Yamakawa K, Sugawara T, Mazaki-Miyazaki E, Hirose S, Fukuma G, Mitsudome A, Wada K, Kaneko S. Ito M, et al. Among authors: hirose s. Epilepsy Res. 2002 Jan;48(1-2):15-23. doi: 10.1016/s0920-1211(01)00313-8. Epilepsy Res. 2002. PMID: 11823106

9

Effect of growth hormone on high plasma levels of glucagon-like peptide-1 (GLP-1) in hypophysectomized rats.

Tateishi K, Kitayama N, Ishikawa H, Mitsudome A, Hirose S. Tateishi K, et al. Among authors: hirose s. Exp Clin Endocrinol Diabetes. 2002 Oct;110(7):361-3. doi: 10.1055/s-2002-34994. Exp Clin Endocrinol Diabetes. 2002. PMID: 12397536

10

A G to A transition at the last nucleotide of exon 6 of the gamma c gene (868G-->A) may result in either a splice or missense mutation in patients with X-linked severe combined immunodeficiency.

Kanai N, Yanai F, Hirose S, Nibu K, Izuhara K, Tani T, Kubota T, Mitsudome A. Kanai N, et al. Among authors: hirose s. Hum Genet. 1999 Jan;104(1):36-42. doi: 10.1007/s004390050907. Hum Genet. 1999. PMID: 10071190

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