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Yoshihiro Fujimura

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Pediatrics International : Official Journal of the Japan Pediatric Society|February 20, 2014
Diagnostic criteria for atypical hemolytic uremic syndrome proposed by the Joint Committee of the Japanese Society of Nephrology and the Japan Pediatric SocietyToshihiro Sawai, Masaomi Nangaku, Akira Ashida, et al.
Internal Medicine (Tokyo, Japan)|May 17, 2013
Drug-induced thrombotic thrombocytopenic purpura successfully treated with recombinant human soluble thrombomodulinYu Nishijima, Haruhiko Hirata, Aiko Himeno, et al.
Acta Haematologica|May 5, 2005
Von Willebrand factor-cleaving protease activity remains at the intermediate level in thrombotic thrombocytopenic purpuraTakeshi Sugimoto, Katsuyasu Saigo, Tomohiro Shin, et al.
Thrombosis Research|May 6, 2019
Involvement of the ADAMTS13-VWF axis in acute Kawasaki disease and effects of intravenous immunoglobulinNobuyuki Tsujii, Keiji Nogami, Masanori Matsumoto, et al.
Thrombosis Research|March 2, 2018
Alternative pathway activation due to low level of complement factor H in primary antiphospholipid syndromeHiroyuki Nakamura, Kenji Oku, Yusuke Ogata, et al.
Thrombosis and Haemostasis|June 4, 2008
Comprehensive analysis of ADAMTS13 in patients with liver cirrhosisMasahito Uemura, Yoshihiro Fujimura, Masanori Matsumoto, et al.
Nihon Jinzo Gakkai Shi|May 2, 2013
[Diagnostic criteria of atypical hemolytic uremic syndrome]Shoji Kagami, Hirokazu Okada, Shinya Kaname, et al.
Clinical and Experimental Nephrology|December 18, 2013
Diagnostic criteria for atypical hemolytic uremic syndrome proposed by the Joint Committee of the Japanese Society of Nephrology and the Japan Pediatric SocietyToshihiro Sawai, Masaomi Nangaku, Akira Ashida, et al.
The Journal of Biological Chemistry|July 22, 2022
Correction: Antibody recognition of complement factor H reveals a flexible loop involved in atypical hemolytic uremic syndrome pathogenesisTakanori Yokoo, Aki Tanabe, Yoko Yoshida, et al.
European Journal of Haematology|December 15, 2012
A novel Wiskott-Aldrich syndrome protein mutation in an infant with thrombotic thrombocytopenic purpuraYukako Kawasaki, Hidemi Toyoda, Shoichiro Otsuki, et al.
Pageof 18

Showing results (141-150 of 176) with videos related to

Sort By:
Pageof 18
Pediatrics International : Official Journal of the Japan Pediatric Society|February 20, 2014
Diagnostic criteria for atypical hemolytic uremic syndrome proposed by the Joint Committee of the Japanese Society of Nephrology and the Japan Pediatric SocietyToshihiro Sawai, Masaomi Nangaku, Akira Ashida, et al.
Internal Medicine (Tokyo, Japan)|May 17, 2013
Drug-induced thrombotic thrombocytopenic purpura successfully treated with recombinant human soluble thrombomodulinYu Nishijima, Haruhiko Hirata, Aiko Himeno, et al.
Acta Haematologica|May 5, 2005
Von Willebrand factor-cleaving protease activity remains at the intermediate level in thrombotic thrombocytopenic purpuraTakeshi Sugimoto, Katsuyasu Saigo, Tomohiro Shin, et al.
Thrombosis Research|May 6, 2019
Involvement of the ADAMTS13-VWF axis in acute Kawasaki disease and effects of intravenous immunoglobulinNobuyuki Tsujii, Keiji Nogami, Masanori Matsumoto, et al.
Thrombosis Research|March 2, 2018
Alternative pathway activation due to low level of complement factor H in primary antiphospholipid syndromeHiroyuki Nakamura, Kenji Oku, Yusuke Ogata, et al.
Thrombosis and Haemostasis|June 4, 2008
Comprehensive analysis of ADAMTS13 in patients with liver cirrhosisMasahito Uemura, Yoshihiro Fujimura, Masanori Matsumoto, et al.
Nihon Jinzo Gakkai Shi|May 2, 2013
[Diagnostic criteria of atypical hemolytic uremic syndrome]Shoji Kagami, Hirokazu Okada, Shinya Kaname, et al.
Clinical and Experimental Nephrology|December 18, 2013
Diagnostic criteria for atypical hemolytic uremic syndrome proposed by the Joint Committee of the Japanese Society of Nephrology and the Japan Pediatric SocietyToshihiro Sawai, Masaomi Nangaku, Akira Ashida, et al.
The Journal of Biological Chemistry|July 22, 2022
Correction: Antibody recognition of complement factor H reveals a flexible loop involved in atypical hemolytic uremic syndrome pathogenesisTakanori Yokoo, Aki Tanabe, Yoko Yoshida, et al.
European Journal of Haematology|December 15, 2012
A novel Wiskott-Aldrich syndrome protein mutation in an infant with thrombotic thrombocytopenic purpuraYukako Kawasaki, Hidemi Toyoda, Shoichiro Otsuki, et al.
Pageof 18