Kurahashi H - Search Results

1

A patient with a GNAO1 mutation with decreased spontaneous movements, hypotonia, and dystonic features.

Okumura A, Maruyama K, Shibata M, Kurahashi H, Ishii A, Numoto S, Hirose S, Kawai T, Iso M, Kataoka S, Okuno Y, Muramatsu H, Kojima S. Okumura A, et al. Among authors: kurahashi h. Brain Dev. 2018 Nov;40(10):926-930. doi: 10.1016/j.braindev.2018.06.005. Epub 2018 Jun 21. Brain Dev. 2018. PMID: 29935962

2

Long-term follow-up of patients with benign partial epilepsy in infancy.

Okumura A, Watanabe K, Negoro T, Hayakawa F, Kato T, Maruyama K, Kubota T, Suzuki M, Kurahashi H, Azuma Y. Okumura A, et al. Among authors: kurahashi h. Epilepsia. 2006 Jan;47(1):181-5. doi: 10.1111/j.1528-1167.2006.00385.x. Epilepsia. 2006. PMID: 16417547 Free article.

3

Posterior reversible encephalopathy syndrome in a child with bronchial asthma.

Kurahashi H, Okumura A, Koide T, Ando Y, Hirata H, Magota M, Watabane K. Kurahashi H, et al. Brain Dev. 2006 Sep;28(8):544-6. doi: 10.1016/j.braindev.2006.02.008. Epub 2006 Apr 17. Brain Dev. 2006. PMID: 16617001

4

The mildest form of acute necrotizing encephalopathy associated with influenza A.

Okumura A, Kidokoro H, Mizuguchi M, Kurahashi H, Hirabayashi Y, Morishima T, Watanabe K. Okumura A, et al. Among authors: kurahashi h. Neuropediatrics. 2006 Aug;37(4):261-3. doi: 10.1055/s-2006-924431. Neuropediatrics. 2006. PMID: 17177155

5

Phenytoin desensitization monitored by antigen specific T cell response using carboxyfluorescein succinimidyl ester dilution assay.

Okumura A, Tsuge I, Kubota T, Kurahashi H, Natsume J, Negoro T, Watanabe K. Okumura A, et al. Among authors: kurahashi h. Eur J Paediatr Neurol. 2007 Nov;11(6):385-8. doi: 10.1016/j.ejpn.2007.03.001. Epub 2007 Apr 10. Eur J Paediatr Neurol. 2007. PMID: 17428709

6

Focal epilepsy resulting from a de novo SCN1A mutation.

Okumura A, Kurahashi H, Hirose S, Okawa N, Watanabe K. Okumura A, et al. Among authors: kurahashi h. Neuropediatrics. 2007 Oct;38(5):253-6. doi: 10.1055/s-2008-1062703. Neuropediatrics. 2007. PMID: 18330841

7

Outcome of acute necrotizing encephalopathy in relation to treatment with corticosteroids and gammaglobulin.

Okumura A, Mizuguchi M, Kidokoro H, Tanaka M, Abe S, Hosoya M, Aiba H, Maegaki Y, Yamamoto H, Tanabe T, Noda E, Imataka G, Kurahashi H. Okumura A, et al. Among authors: kurahashi h. Brain Dev. 2009 Mar;31(3):221-7. doi: 10.1016/j.braindev.2008.03.005. Epub 2008 May 5. Brain Dev. 2009. PMID: 18456443

8

Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy.

Wang JW, Kurahashi H, Ishii A, Kojima T, Ohfu M, Inoue T, Ogawa A, Yasumoto S, Oguni H, Kure S, Fujii T, Ito M, Okuno T, Shirasaka Y, Natsume J, Hasegawa A, Konagaya A, Kaneko S, Hirose S. Wang JW, et al. Among authors: kurahashi h. Epilepsia. 2008 Sep;49(9):1528-34. doi: 10.1111/j.1528-1167.2008.01609.x. Epub 2008 Apr 21. Epilepsia. 2008. PMID: 18479393 Free article.

9

Novel de novo splice-site mutation of SCN1A in a patient with partial epilepsy with febrile seizures plus.

Kumakura A, Ito M, Hata D, Oh N, Kurahashi H, Wang JW, Hirose S. Kumakura A, et al. Among authors: kurahashi h. Brain Dev. 2009 Feb;31(2):179-82. doi: 10.1016/j.braindev.2008.06.001. Epub 2008 Jul 15. Brain Dev. 2009. PMID: 18632234

10

Hemiconvulsion-hemiplegia syndrome in a patient with severe myoclonic epilepsy in infancy.

Sakakibara T, Nakagawa E, Saito Y, Sakuma H, Komaki H, Sugai K, Sasaki M, Kurahashi H, Hirose S. Sakakibara T, et al. Among authors: kurahashi h. Epilepsia. 2009 Sep;50(9):2158-62. doi: 10.1111/j.1528-1167.2009.02175.x. Epub 2009 Jun 26. Epilepsia. 2009. PMID: 19563349 Free article.

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