Kurahashi H - Search Results

1

Fournier's gangrene during ACTH therapy.

Numoto S, Kurahashi H, Azuma Y, Numaguchi A, Nakahara K, Tainaka T, Takasu M, Yamakawa K, Nago N, Muto T, Kitagawa Y, Okumura A. Numoto S, et al. Among authors: kurahashi h. Brain Dev. 2017 May;39(5):435-438. doi: 10.1016/j.braindev.2016.11.012. Epub 2016 Dec 20. Brain Dev. 2017. PMID: 28007393

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

Spinocerebellar ataxias type 27 derived from a disruption of the fibroblast growth factor 14 gene with mimicking phenotype of paroxysmal non-kinesigenic dyskinesia.

Shimojima K, Okumura A, Natsume J, Aiba K, Kurahashi H, Kubota T, Yokochi K, Yamamoto T. Shimojima K, et al. Among authors: kurahashi h. Brain Dev. 2012 Mar;34(3):230-3. doi: 10.1016/j.braindev.2011.04.014. Epub 2011 May 19. Brain Dev. 2012. PMID: 21600715

9

On the likelihood of SCN1A microdeletions or duplications in Dravet syndrome with missense mutation.

Shi X, Wang J, Kurahashi H, Ishii A, Higurashi N, Kaneko S, Hirose S. Shi X, et al. Among authors: kurahashi h. Brain Dev. 2012 Sep;34(8):617-9. doi: 10.1016/j.braindev.2011.11.005. Epub 2011 Dec 27. Brain Dev. 2012. PMID: 22206733

10

Thalamic lesions in acute encephalopathy with biphasic seizures and late reduced diffusion.

Kurahashi N, Tsuji T, Kato T, Ogaya S, Umemura A, Yamada K, Kurahashi H, Maruyama K, Takeuchi T, Kubota T, Saitoh S, Natsume J, Okumura A. Kurahashi N, et al. Among authors: kurahashi h. Pediatr Neurol. 2014 Nov;51(5):701-5. doi: 10.1016/j.pediatrneurol.2014.07.013. Epub 2014 Jul 16. Pediatr Neurol. 2014. PMID: 25193414

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