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Browsing by Author Miyata, Toshiyuki

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Issue DateTitleAuthor(s)
7-May-2015A novel quantitative hemolytic assay coupled with restriction fragment length polymorphisms analysis enabled early diagnosis of atypical hemolytic uremic syndrome and identified unique predisposing mutations in Japan.Yoshida, Yoko; Miyata, Toshiyuki; Matsumoto, Masanori; Shirotani-Ikejima, Hiroko; Uchida, Yumiko; Ohyama, Yoshifumi; Kokubo, Tetsuro; Fujimura, Yoshihiro
Oct-2012ADAMTS13 gene deletion enhances plasma high-mobility group box1 elevation and neuroinflammation in brain ischemia-reperfusion injury.Fujioka, Masayuki; Nakano, Takafumi; Hayakawa, Kazuhide; Irie, Keiichi; Akitake, Yoshiharu; Sakamoto, Yuya; Mishima, Kenichi; Muroi, Carl; Yonekawa, Yasuhiro; Banno, Fumiaki; Kokame, Koichi; Miyata, Toshiyuki; Nishio, Kenji; Okuchi, Kazuo; Iwasaki, Katsunori; Fujiwara, Michihiro; Siesjö, Bo K.
22-Jul-2011Natural history of Upshaw-Schulman syndrome based on ADAMTS13 gene analysis in JapanFujimura, Yoshihiro; Matsumoto, Masanori; Isonishi, Ayami; Yagi, Hideo; Kokame, Koichi; Soejima, Kenji; Murata, Mitsuru; Miyata, Toshiyuki
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