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Yoshihiro Fujimura

Showing results (161-170 of 176) with videos related to

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Clinical and Experimental Nephrology|July 1, 2018
Safety and effectiveness of eculizumab for adult patients with atypical hemolytic-uremic syndrome in Japan: interim analysis of post-marketing surveillanceHideki Kato, Yoshitaka Miyakawa, Yoshihiko Hidaka, et al.
International Journal of Hematology|February 3, 2016
Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiencyXinping Fan, Johanna A Kremer Hovinga, Hiroko Shirotani-Ikejima, et al.
BMC Nephrology|July 23, 2013
Long term follow up of congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) on hemodialysis for 19 years: a case reportKoki Mise, Yoshifumi Ubara, Masanori Matsumoto, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|July 28, 2016
Clinical guides for atypical hemolytic uremic syndrome in JapanHideki Kato, Masaomi Nangaku, Hiroshi Hataya, et al.
Clinical and Experimental Nephrology|July 17, 2016
Clinical guides for atypical hemolytic uremic syndrome in JapanHideki Kato, Masaomi Nangaku, Hiroshi Hataya, et al.
Internal Medicine (Tokyo, Japan)|September 3, 2013
Therapeutic modality of 11 patients with TTP in a single institution in Miyazaki from 2000 to 2011Noriaki Kawano, Naoko Yokota-Ikeda, Shuro Yoshida, et al.
British Journal of Haematology|July 25, 2020
The Kg-antigen, RhAG with a Lys164Gln mutation, gives rise to haemolytic disease of the newbornMitsunobu Tanaka, Takaaki Abe, Takeharu Minamitani, et al.
Blood|October 18, 2003
Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndromeMasanori Matsumoto, Koichi Kokame, Kenji Soejima, et al.
Scandinavian Journal of Gastroenterology|July 9, 2008
Plasma ADAMTS13 activity parallels the APACHE II score, reflecting an early prognostic indicator for patients with severe acute pancreatitisChie Morioka, Masahito Uemura, Tomomi Matsuyama, et al.
British Journal of Haematology|December 6, 2008
Pregnancy-induced thrombocytopenia and TTP, and the risk of fetal death, in Upshaw-Schulman syndrome: a series of 15 pregnancies in 9 genotyped patientsYoshihiro Fujimura, Masanori Matsumoto, Koichi Kokame, et al.
Pageof 18

Showing results (161-170 of 176) with videos related to

Sort By:
Pageof 18
Clinical and Experimental Nephrology|July 1, 2018
Safety and effectiveness of eculizumab for adult patients with atypical hemolytic-uremic syndrome in Japan: interim analysis of post-marketing surveillanceHideki Kato, Yoshitaka Miyakawa, Yoshihiko Hidaka, et al.
International Journal of Hematology|February 3, 2016
Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiencyXinping Fan, Johanna A Kremer Hovinga, Hiroko Shirotani-Ikejima, et al.
BMC Nephrology|July 23, 2013
Long term follow up of congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) on hemodialysis for 19 years: a case reportKoki Mise, Yoshifumi Ubara, Masanori Matsumoto, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|July 28, 2016
Clinical guides for atypical hemolytic uremic syndrome in JapanHideki Kato, Masaomi Nangaku, Hiroshi Hataya, et al.
Clinical and Experimental Nephrology|July 17, 2016
Clinical guides for atypical hemolytic uremic syndrome in JapanHideki Kato, Masaomi Nangaku, Hiroshi Hataya, et al.
Internal Medicine (Tokyo, Japan)|September 3, 2013
Therapeutic modality of 11 patients with TTP in a single institution in Miyazaki from 2000 to 2011Noriaki Kawano, Naoko Yokota-Ikeda, Shuro Yoshida, et al.
British Journal of Haematology|July 25, 2020
The Kg-antigen, RhAG with a Lys164Gln mutation, gives rise to haemolytic disease of the newbornMitsunobu Tanaka, Takaaki Abe, Takeharu Minamitani, et al.
Blood|October 18, 2003
Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndromeMasanori Matsumoto, Koichi Kokame, Kenji Soejima, et al.
Scandinavian Journal of Gastroenterology|July 9, 2008
Plasma ADAMTS13 activity parallels the APACHE II score, reflecting an early prognostic indicator for patients with severe acute pancreatitisChie Morioka, Masahito Uemura, Tomomi Matsuyama, et al.
British Journal of Haematology|December 6, 2008
Pregnancy-induced thrombocytopenia and TTP, and the risk of fetal death, in Upshaw-Schulman syndrome: a series of 15 pregnancies in 9 genotyped patientsYoshihiro Fujimura, Masanori Matsumoto, Koichi Kokame, et al.
Pageof 18