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Page 1
Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1.
Yoshimura H, Iwasaki S, Nishio SY, Kumakawa K, Tono T, Kobayashi Y, Sato H, Nagai K, Ishikawa K, Ikezono T, Naito Y, Fukushima K, Oshikawa C, Kimitsuki T, Nakanishi H, Usami S. Yoshimura H, et al. Among authors: ishikawa k. PLoS One. 2014 Mar 11;9(3):e90688. doi: 10.1371/journal.pone.0090688. eCollection 2014. PLoS One. 2014. PMID: 24618850 Free PMC article.
[Problem and assignment for distinguishing the Usher syndrome type].
Iwasaki S, Yoshimura H, Takeichi N, Satou H, Ishikawa K, Kaga K, Kumakawa K, Nagai K, Furuya N, Ikezono T, Nakanishi H, Naitou Y, Fukushima K, Tono T, Kimitsuki T, Nishio S, Takumi Y, Usami S. Iwasaki S, et al. Among authors: ishikawa k. Nihon Jibiinkoka Gakkai Kaiho. 2012 Oct;115(10):894-901. doi: 10.3950/jibiinkoka.115.894. Nihon Jibiinkoka Gakkai Kaiho. 2012. PMID: 23214047 Japanese.
WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis.
Kobayashi M, Miyagawa M, Nishio SY, Moteki H, Fujikawa T, Ohyama K, Sakaguchi H, Miyanohara I, Sugaya A, Naito Y, Morita SY, Kanda Y, Takahashi M, Ishikawa K, Nagano Y, Tono T, Oshikawa C, Kihara C, Takahashi H, Noguchi Y, Usami SI. Kobayashi M, et al. Among authors: ishikawa k. PLoS One. 2018 Mar 12;13(3):e0193359. doi: 10.1371/journal.pone.0193359. eCollection 2018. PLoS One. 2018. PMID: 29529044 Free PMC article.
Comprehensive analysis of syndromic hearing loss patients in Japan.
Ideura M, Nishio SY, Moteki H, Takumi Y, Miyagawa M, Sato T, Kobayashi Y, Ohyama K, Oda K, Matsui T, Ito T, Suzumura H, Nagai K, Izumi S, Nishiyama N, Komori M, Kumakawa K, Takeda H, Kishimoto Y, Iwasaki S, Furutate S, Ishikawa K, Fujioka M, Nakanishi H, Nakayama J, Horie R, Ohta Y, Naito Y, Kakudo M, Sakaguchi H, Kataoka Y, Sugahara K, Hato N, Nakagawa T, Tsuchihashi N, Kanda Y, Kihara C, Tono T, Miyanohara I, Ganaha A, Usami SI. Ideura M, et al. Among authors: ishikawa k. Sci Rep. 2019 Aug 19;9(1):11976. doi: 10.1038/s41598-019-47141-4. Sci Rep. 2019. PMID: 31427586 Free PMC article.
The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss.
Yasukawa R, Moteki H, Nishio SY, Ishikawa K, Abe S, Honkura Y, Hyogo M, Mihashi R, Ikezono T, Shintani T, Ogasawara N, Shirai K, Yoshihashi H, Ishino T, Otsuki K, Ito T, Sugahara K, Usami SI. Yasukawa R, et al. Among authors: ishikawa k. Genes (Basel). 2019 Sep 24;10(10):744. doi: 10.3390/genes10100744. Genes (Basel). 2019. PMID: 31554319 Free PMC article.
The clinical features and prognosis of mumps-associated hearing loss: a retrospective, multi-institutional investigation in Japan.
Morita S, Fujiwara K, Fukuda A, Fukuda S, Nishio SY, Kitoh R, Hato N, Ikezono T, Ishikawa K, Kaga K, Matsubara A, Matsunaga T, Murata T, Naito Y, Nishizaki K, Ogawa K, Sano H, Sato H, Sone M, Suzuki M, Takahashi H, Tono T, Yamashita H, Yamasoba T, Usami SI. Morita S, et al. Among authors: ishikawa k. Acta Otolaryngol. 2017;137(sup565):S44-S47. doi: 10.1080/00016489.2017.1290826. Epub 2017 Mar 24. Acta Otolaryngol. 2017. PMID: 28338374
4,487 results