Hamano SI - Search Results

1

First Patient With Salla Disease Confirmed by Genomic Analysis in Japan.

Matsuura R, Hamano SI, Iwamoto T, Shimizu K, Ohashi H. Matsuura R, et al. Among authors: hamano si. Pediatr Neurol. 2018 Apr;81:52-53. doi: 10.1016/j.pediatrneurol.2018.01.002. Epub 2018 Jan 31. Pediatr Neurol. 2018. PMID: 29472023 No abstract available.

2

Interstitial duplication 8q22-q24: report of a case proven by FISH with mapped cosmid probes.

Wakui K, Ohashi H, Yamagishi A, Hamano S, Nara T, Ishikiriyama S, Nakamura Y, Fukushima Y. Wakui K, et al. Am J Med Genet. 1996 Oct 2;65(1):36-9. doi: 10.1002/(SICI)1096-8628(19961002)65:1<36::AID-AJMG5>3.0.CO;2-W. Am J Med Genet. 1996. PMID: 8914738 Review.

3

Human herpesvirus 6 encephalopathy predominantly affecting the frontal lobes.

Yoshinari S, Hamano S, Minamitani M, Tanaka M, Eto Y. Yoshinari S, et al. Pediatr Neurol. 2007 Jan;36(1):13-6. doi: 10.1016/j.pediatrneurol.2006.09.002. Pediatr Neurol. 2007. PMID: 17162191

4

Posterior reversible encephalopathy syndrome associated with IVIG in a patient with Guillain-Barré syndrome.

Koichihara R, Hamano S, Yamashita S, Tanaka M. Koichihara R, et al. Pediatr Neurol. 2008 Aug;39(2):123-5. doi: 10.1016/j.pediatrneurol.2008.04.005. Pediatr Neurol. 2008. PMID: 18639758

5

Gaucher disease patient with myoclonus epilepsy and a novel mutation.

Tajima A, Ohashi T, Hamano S, Higurashi N, Ida H. Tajima A, et al. Pediatr Neurol. 2010 Jan;42(1):65-8. doi: 10.1016/j.pediatrneurol.2009.08.007. Pediatr Neurol. 2010. PMID: 20004867

6

Nonthalamic generalization of ictal spikes in atypical absence seizures.

Higurashi N, Hamano S, Yoshinari S, Tanaka M, Ida H. Higurashi N, et al. Pediatr Neurol. 2010 Aug;43(2):131-4. doi: 10.1016/j.pediatrneurol.2010.04.009. Pediatr Neurol. 2010. PMID: 20610125

7

PIGA mutations cause early-onset epileptic encephalopathies and distinctive features.

Kato M, Saitsu H, Murakami Y, Kikuchi K, Watanabe S, Iai M, Miya K, Matsuura R, Takayama R, Ohba C, Nakashima M, Tsurusaki Y, Miyake N, Hamano S, Osaka H, Hayasaka K, Kinoshita T, Matsumoto N. Kato M, et al. Neurology. 2014 May 6;82(18):1587-96. doi: 10.1212/WNL.0000000000000389. Epub 2014 Apr 4. Neurology. 2014. PMID: 24706016

8

The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations.

Yamada Y, Nomura N, Yamada K, Matsuo M, Suzuki Y, Sameshima K, Kimura R, Yamamoto Y, Fukushi D, Fukuhara Y, Ishihara N, Nishi E, Imataka G, Suzumura H, Hamano S, Shimizu K, Iwakoshi M, Ohama K, Ohta A, Wakamoto H, Kajita M, Miura K, Yokochi K, Kosaki K, Kuroda T, Kosaki R, Hiraki Y, Saito K, Mizuno S, Kurosawa K, Okamoto N, Wakamatsu N. Yamada Y, et al. Am J Med Genet A. 2014 Aug;164A(8):1899-908. doi: 10.1002/ajmg.a.36551. Epub 2014 Apr 8. Am J Med Genet A. 2014. PMID: 24715670

9

Difficulty of Early Diagnosis and Requirement of Long-Term Follow-Up in Benign Infantile Seizures.

Kikuchi K, Hamano S, Higurashi N, Matsuura R, Suzuki K, Tanaka M, Minamitani M. Kikuchi K, et al. Pediatr Neurol. 2015 Aug;53(2):157-62. doi: 10.1016/j.pediatrneurol.2015.03.025. Epub 2015 Apr 10. Pediatr Neurol. 2015. PMID: 26096618

10

Intravenous immunoglobulin therapy is rarely effective as the initial treatment in West syndrome: A retrospective study of 70 patients.

Matsuura R, Hamano S, Hirata Y, Oba A, Suzuki K, Kikuchi K. Matsuura R, et al. J Neurol Sci. 2016 Sep 15;368:140-4. doi: 10.1016/j.jns.2016.07.001. Epub 2016 Jul 4. J Neurol Sci. 2016. PMID: 27538618

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