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Molecular Genetics & Genomic Medicine|June 18, 2014
Candidate gene analysis using genomic quantitative PCR: identification of ADAMTS13 large deletions in two patients with Upshaw-Schulman syndromeYuka Eura, Koichi Kokame, Toshiro Takafuta, et al.
Scientific Reports|October 19, 2017
Herpud1 negatively regulates pathological cardiac hypertrophy by inducing IP3 receptor degradationNatalia Torrealba, Mario Navarro-Marquez, Valeria Garrido, 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.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 28, 2018
Herpud1 impacts insulin-dependent glucose uptake in skeletal muscle cells by controlling the Ca2+-calcineurin-Akt axisMario Navarro-Marquez, Natalia Torrealba, Rodrigo Troncoso, et al.
Journal of Artificial Organs : the Official Journal of the Japanese Society for Artificial Organs|July 25, 2019
Experience of the use of octreotide for refractory gastrointestinal bleeding in a patient with Jarvik2000® left ventricular assist deviceSeiko Nakajima-Doi, Osamu Seguchi, Yasuhiro Shintani, et al.
Research and Practice in Thrombosis and Haemostasis|June 6, 2024
Mitral regurgitation is associated with similar loss of von Willebrand factor large multimers but lower frequency of anemia compared with aortic stenosisHiroshi Takiguchi, Mizuki Miura, Shin-Ichi Shirai, et al.
Research and Practice in Thrombosis and Haemostasis|January 25, 2024
von Willebrand factor Ristocetin co-factor activity to von Willebrand factor antigen level ratio for diagnosis of acquired von Willebrand syndrome caused by aortic stenosisNoriyuki Okubo, Shingo Sugawara, Tohru Fujiwara, et al.
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