Wada K - Search Results

1

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: wada k. Epilepsy Res. 2002 Jan;48(1-2):15-23. doi: 10.1016/s0920-1211(01)00313-8. Epilepsy Res. 2002. PMID: 11823106

2

A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy.

Hirose S, Iwata H, Akiyoshi H, Kobayashi K, Ito M, Wada K, Kaneko S, Mitsudome A. Hirose S, et al. Among authors: wada k. Neurology. 1999 Nov 10;53(8):1749-53. doi: 10.1212/wnl.53.8.1749. Neurology. 1999. PMID: 10563623

3

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction.

Sugawara T, Tsurubuchi Y, Agarwala KL, Ito M, Fukuma G, Mazaki-Miyazaki E, Nagafuji H, Noda M, Imoto K, Wada K, Mitsudome A, Kaneko S, Montal M, Nagata K, Hirose S, Yamakawa K. Sugawara T, et al. Among authors: wada k. Proc Natl Acad Sci U S A. 2001 May 22;98(11):6384-9. doi: 10.1073/pnas.111065098. Proc Natl Acad Sci U S A. 2001. PMID: 11371648 Free PMC article.

4

Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures.

Sugawara T, Mazaki-Miyazaki E, Ito M, Nagafuji H, Fukuma G, Mitsudome A, Wada K, Kaneko S, Hirose S, Yamakawa K. Sugawara T, et al. Among authors: wada k. Neurology. 2001 Aug 28;57(4):703-5. doi: 10.1212/wnl.57.4.703. Neurology. 2001. PMID: 11524484

5

Effect of localization of missense mutations in SCN1A on epilepsy phenotype severity.

Kanai K, Hirose S, Oguni H, Fukuma G, Shirasaka Y, Miyajima T, Wada K, Iwasa H, Yasumoto S, Matsuo M, Ito M, Mitsudome A, Kaneko S. Kanai K, et al. Among authors: wada k. Neurology. 2004 Jul 27;63(2):329-34. doi: 10.1212/01.wnl.0000129829.31179.5b. Neurology. 2004. PMID: 15277629 Review.

6

A novel mutation of KCNQ3 (c.925T-->C) in a Japanese family with benign familial neonatal convulsions.

Hirose S, Zenri F, Akiyoshi H, Fukuma G, Iwata H, Inoue T, Yonetani M, Tsutsumi M, Muranaka H, Kurokawa T, Hanai T, Wada K, Kaneko S, Mitsudome A. Hirose S, et al. Among authors: wada k. Ann Neurol. 2000 Jun;47(6):822-6. Ann Neurol. 2000. PMID: 10852552

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: wada k. 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

Effects of non-toxic and toxic concentrations of phenytoin on monoamines levels in rat brain.

Okada M, Kawata Y, Kiryu K, Mizuno K, Wada K, Inomata H, Tasaki H, Kaneko S. Okada M, et al. Among authors: wada k. Epilepsy Res. 1997 Sep;28(2):155-63. doi: 10.1016/s0920-1211(97)00043-0. Epilepsy Res. 1997. PMID: 9267780

9

[Molecular genetic studies of epilepsies].

Kaneko S, Wada K. Kaneko S, et al. Among authors: wada k. No To Shinkei. 1998 Dec;50(12):1071-7. No To Shinkei. 1998. PMID: 9989351 Review. Japanese. No abstract available.

10

Effects of carbamazepine on hippocampal serotonergic system.

Okada M, Hirano T, Mizuno K, Kawata Y, Wada K, Murakami T, Tasaki H, Kaneko S. Okada M, et al. Among authors: wada k. Epilepsy Res. 1998 Aug;31(3):187-98. doi: 10.1016/s0920-1211(98)00025-4. Epilepsy Res. 1998. PMID: 9722029

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