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Yoko Yoshida

Showing results (141-150 of 174) with videos related to

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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.
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.
Journal of Human Genetics|March 21, 2018
Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genesTomohiko Yamamura, Kandai Nozu, Hiroaki Ueda, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|July 14, 2007
Hepatic differentiation of human bone marrow-derived UE7T-13 cells: Effects of cytokines and CCN family gene expressionTakashi Shimomura, Yoko Yoshida, Tomohiko Sakabe, 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.
BMC Gastroenterology|December 23, 2011
Postprandial fullness correlates with rapid inflow of gastric content into duodenum but not with chronic gastritisNobutake Yamamichi, Takeshi Shimamoto, Chihiro Minatsuki, et al.
The Journal of Biological Chemistry|April 22, 2022
Antibody recognition of complement factor H reveals a flexible loop involved in atypical hemolytic uremic syndrome pathogenesisTakanori Yokoo, Aki Tanabe, Yoko Yoshida, et al.
JACC. Clinical Electrophysiology|March 25, 2022
Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With Brugada SyndromeKeisuke Suzuki, Keiko Sonoda, Hisaaki Aoki, et al.
International Journal of Hematology|August 20, 2014
Analysis of patients with atypical hemolytic uremic syndrome treated at the Mie University Hospital: concentration of C3 p.I1157T mutationTakeshi Matsumoto, Xinping Fan, Eiji Ishikawa, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|June 28, 2023
Calmodulinopathy in Japanese Children　- Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and InfancyMegumi Fukuyama, Minoru Horie, Koichi Kato, et al.
Pageof 18

Showing results (141-150 of 174) with videos related to

Sort By:
Pageof 18
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.
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.
Journal of Human Genetics|March 21, 2018
Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genesTomohiko Yamamura, Kandai Nozu, Hiroaki Ueda, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|July 14, 2007
Hepatic differentiation of human bone marrow-derived UE7T-13 cells: Effects of cytokines and CCN family gene expressionTakashi Shimomura, Yoko Yoshida, Tomohiko Sakabe, 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.
BMC Gastroenterology|December 23, 2011
Postprandial fullness correlates with rapid inflow of gastric content into duodenum but not with chronic gastritisNobutake Yamamichi, Takeshi Shimamoto, Chihiro Minatsuki, et al.
The Journal of Biological Chemistry|April 22, 2022
Antibody recognition of complement factor H reveals a flexible loop involved in atypical hemolytic uremic syndrome pathogenesisTakanori Yokoo, Aki Tanabe, Yoko Yoshida, et al.
JACC. Clinical Electrophysiology|March 25, 2022
Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With Brugada SyndromeKeisuke Suzuki, Keiko Sonoda, Hisaaki Aoki, et al.
International Journal of Hematology|August 20, 2014
Analysis of patients with atypical hemolytic uremic syndrome treated at the Mie University Hospital: concentration of C3 p.I1157T mutationTakeshi Matsumoto, Xinping Fan, Eiji Ishikawa, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|June 28, 2023
Calmodulinopathy in Japanese Children　- Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and InfancyMegumi Fukuyama, Minoru Horie, Koichi Kato, et al.
Pageof 18