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Journal of Clinical Medicine|January 22, 2021
Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic DiagnosisBarbara Preisler, Behnaz Pezeshkpoor, Atanas Banchev, et al.The Journal of Clinical Investigation|May 8, 2025
Thrombospondin-1 inhibits alternative complement pathway activation in antineutrophil cytoplasmic antibody-associated vasculitisSwagata Konwar, Sophie Schroda, Manuel Rogg, et al.The Journal of Biological Chemistry|October 18, 2024
Suppressed ORAI1-STIM1-dependent Ca2+ entry by protein kinase C isoforms regulating platelet procoagulant activityJinmi Zou, Pengyu Zhang, Fiorella A Solari, et al.Blood Cells, Molecules & Diseases|December 18, 2020
Acquired von Willebrand syndrome in ECMO patients: A 3-year cohort studyBernd Panholzer, Tido Bajorat, Assad Haneya, et al.Thrombosis and Haemostasis|November 7, 2014
Characterisation of patients with Glanzmann thrombasthenia and identification of 17 novel mutationsKirstin Sandrock-Lang, Johannes Oldenburg, Verena Wiegering, et al.Haematologica|December 16, 2017
Variable impairment of platelet functions in patients with severe, genetically linked immune deficienciesMagdolna Nagy, Tom G Mastenbroek, Nadine J A Mattheij, et al.Journal of Thrombosis and Haemostasis : JTH|December 16, 2023
Aggregates of nonmuscular myosin IIA in erythrocytes associate with GATA1- and GFI1B-related thrombocytopeniaCarlo Zaninetti, Jose' Rivera, Leonard Vater, et al.Journal of Thrombosis and Haemostasis : JTH|March 24, 2020
Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalenceStefano Barco, Stefanie Sollfrank, Alice Trinchero, et al.Nature Communications|September 5, 2014
Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott-Aldrich syndrome-like platelet defectMarkus Bender, Simon Stritt, Paquita Nurden, et al.Hemasphere|January 17, 2020
Fundamentals for a Systematic Approach to Mild and Moderate Inherited Bleeding Disorders: An EHA Consensus ReportFrancesco Rodeghiero, Ingrid Pabinger, Margaret Ragni, et al.Pageof 14