Fukuyama Y - Search Results

1

PRRT2 mutations are the major cause of benign familial infantile seizures.

Schubert J, Paravidino R, Becker F, Berger A, Bebek N, Bianchi A, Brockmann K, Capovilla G, Dalla Bernardina B, Fukuyama Y, Hoffmann GF, Jurkat-Rott K, Anttonen AK, Kurlemann G, Lehesjoki AE, Lehmann-Horn F, Mastrangelo M, Mause U, Müller S, Neubauer B, Püst B, Rating D, Robbiano A, Ruf S, Schroeder C, Seidel A, Specchio N, Stephani U, Striano P, Teichler J, Turkdogan D, Vigevano F, Viri M, Bauer P, Zara F, Lerche H, Weber YG. Schubert J, et al. Among authors: fukuyama y. Hum Mutat. 2012 Oct;33(10):1439-43. doi: 10.1002/humu.22126. Epub 2012 Jun 11. Hum Mutat. 2012. PMID: 22623405

2

Benign familial infantile convulsions: linkage to chromosome 16p12-q12 in 14 families.

Weber YG, Berger A, Bebek N, Maier S, Karafyllakes S, Meyer N, Fukuyama Y, Halbach A, Hikel C, Kurlemann G, Neubauer B, Osawa M, Püst B, Rating D, Saito K, Stephani U, Tauer U, Lehmann-Horn F, Jurkat-Rott K, Lerche H. Weber YG, et al. Among authors: fukuyama y. Epilepsia. 2004 Jun;45(6):601-9. doi: 10.1111/j.0013-9580.2004.48203.x. Epilepsia. 2004. PMID: 15144424 Free article.

3

Bibliography of congenital muscular dystrophies: Series V (2001).

Fukuyama Y, Saito K. Fukuyama Y, et al. Brain Dev. 2003 Mar;25(2):137-43. doi: 10.1016/s0387-7604(02)00156-0. Brain Dev. 2003. PMID: 12645609 No abstract available.

4

Rasmussen syndrome: multifocal spread of inflammation suggested from MRI and PET findings.

Maeda Y, Oguni H, Saitou Y, Mutoh A, Imai K, Osawa M, Fukuyama Y, Hori T, Yamane F, Kubo O, Ishii K, Ishiwata K. Maeda Y, et al. Among authors: fukuyama y. Epilepsia. 2003 Aug;44(8):1118-21. doi: 10.1046/j.1528-1157.2003.67602.x. Epilepsia. 2003. PMID: 12887447 Free article.

5

Bibliography of congenital muscular dystrophies: Series IV (2000) with Appendix II.

Fukuyama Y, Saito K. Fukuyama Y, et al. Brain Dev. 2002 Mar;24(2):118-28. doi: 10.1016/s0387-7604(02)00009-8. Brain Dev. 2002. PMID: 12148488 No abstract available.

6

[Acute non-herpetic encephalitis with severe refractory status epilepticus --its overwhelming ictogenicity, epileptogenicity, long-term prognosis and review of the literature].

Awaya Y, Fukuyama Y, Hayashi K, Osawa M. Awaya Y, et al. Among authors: fukuyama y. No To Hattatsu. 2007 Mar;39(2):138-44. No To Hattatsu. 2007. PMID: 17370636 Review. Japanese.

7

[A case of idiopathic torsion dystonia showing blepharospasm at the onset].

Ohtsu M, Hayashi K, Tanaka T, Imai K, Osawa M, Fukuyama Y. Ohtsu M, et al. Among authors: fukuyama y. No To Hattatsu. 2002 May;34(3):254-61. No To Hattatsu. 2002. PMID: 12030016 Japanese.

8

Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort.

Oguni H, Hayashi K, Osawa M, Awaya Y, Fukuyama Y, Fukuma G, Hirose S, Mitsudome A, Kaneko S. Oguni H, et al. Among authors: fukuyama y. Adv Neurol. 2005;95:103-17. Adv Neurol. 2005. PMID: 15508916 Review. No abstract available.

9

Paroxysmal kinesigenic choreoathetosis: from first discovery in 1892 to genetic linkage with benign familial infantile convulsions.

Kato N, Sadamatsu M, Kikuchi T, Niikawa N, Fukuyama Y. Kato N, et al. Among authors: fukuyama y. Epilepsy Res. 2006 Aug;70 Suppl 1:S174-84. doi: 10.1016/j.eplepsyres.2006.02.009. Epub 2006 Aug 9. Epilepsy Res. 2006. PMID: 16901678 Review.

10

Severe myoclonic epilepsy in infancy: Dravet syndrome.

Dravet C, Bureau M, Oguni H, Fukuyama Y, Cokar O. Dravet C, et al. Among authors: fukuyama y. Adv Neurol. 2005;95:71-102. Adv Neurol. 2005. PMID: 15508915 Review. No abstract available.

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