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WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects.
Yokote K, Chanprasert S, Lee L, Eirich K, Takemoto M, Watanabe A, Koizumi N, Lessel D, Mori T, Hisama FM, Ladd PD, Angle B, Baris H, Cefle K, Palanduz S, Ozturk S, Chateau A, Deguchi K, Easwar TK, Federico A, Fox A, Grebe TA, Hay B, Nampoothiri S, Seiter K, Streeten E, Piña-Aguilar RE, Poke G, Poot M, Posmyk R, Martin GM, Kubisch C, Schindler D, Oshima J. Yokote K, et al. Among authors: deguchi k. Hum Mutat. 2017 Jan;38(1):7-15. doi: 10.1002/humu.23128. Epub 2016 Oct 7. Hum Mutat. 2017. PMID: 27667302 Free PMC article. Review.
Characteristic Clinical Features of Werner Syndrome with a Novel Compound Heterozygous WRN Mutation c.1720+1G>A Plus c.3139-1G>C.
Matsumoto N, Ohta Y, Deguchi K, Kishida M, Sato K, Shang J, Takemoto M, Hishikawa N, Yamashita T, Watanabe A, Yokote K, Takemoto M, Oshima J, Abe K. Matsumoto N, et al. Among authors: deguchi k. Intern Med. 2019 Apr 1;58(7):1033-1036. doi: 10.2169/internalmedicine.1816-18. Epub 2018 Dec 18. Intern Med. 2019. PMID: 30568144 Free PMC article.
A forgotten disease in Japan.
Matsuura H, Deguchi K. Matsuura H, et al. Among authors: deguchi k. Eur J Intern Med. 2021 Mar;85:110-111. doi: 10.1016/j.ejim.2021.01.008. Epub 2021 Jan 31. Eur J Intern Med. 2021. PMID: 33531201 No abstract available.
Tissue plasminogen activator thrombolytic therapy for acute ischemic stroke in 4 hospital groups in Japan.
Kono S, Deguchi K, Morimoto N, Kurata T, Deguchi S, Yamashita T, Ikeda Y, Matsuura T, Narai H, Omori N, Manabe Y, Yunoki T, Takao Y, Kawata S, Kashihara K, Abe K. Kono S, et al. Among authors: deguchi s, deguchi k. J Stroke Cerebrovasc Dis. 2013 Apr;22(3):190-6. doi: 10.1016/j.jstrokecerebrovasdis.2011.07.016. Epub 2011 Oct 2. J Stroke Cerebrovasc Dis. 2013. PMID: 21968092
799 results