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Showing results (381-390 of 442) with videos related to

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BMJ Open|October 18, 2019
Comparative effectiveness of surgery in traumatic acute subdural and intracerebral haematoma: study protocol for a prospective observational study within CENTER-TBI and Net-QuReThomas A Van Essen, Victor Volovici, Maryse C Cnossen, et al.
American Journal of Clinical Oncology|April 26, 2019
Small Cell Carcinoma of the Esophagus: A Nationwide Analysis of Treatment and Outcome at Patient Level in Locoregional DiseasePaul M Jeene, Elisabeth D Geijsen, Christina T Muijs, et al.
Journal of Thrombosis and Haemostasis : JTH|November 6, 2018
Population pharmacokinetics of factor IX in hemophilia B patients undergoing surgeryT Preijers, H C A M Hazendonk, R Liesner, et al.
British Journal of Haematology|September 27, 2022
Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patientsMaurice Swinkels, Ferdows Atiq, Petra E Bürgisser, et al.
Blood Advances|May 9, 2022
The bleeding phenotype in people with nonsevere hemophiliaFabienne R Kloosterman, Anne-Fleur Zwagemaker, Catherine N Bagot, et al.
Research and Practice in Thrombosis and Haemostasis|July 30, 2024
Targeted exome analysis in patients with rare bleeding disorders: data from the Rare Bleeding Disorders in the Netherlands studySterre P E Willems, Annet Simons, Joline L Saes, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 1, 2018
Perioperative replacement therapy in haemophilia B: An appeal to "B" more preciseH C A M Hazendonk, T Preijers, R Liesner, et al.
Blood Advances|November 17, 2023
Oxygen gradient ektacytometry-derived biomarkers are associated with acute complications in sickle cell diseaseMinke A E Rab, Celeste K Kanne, Camille Boisson, et al.
Hemasphere|June 24, 2022
Importance of Genotyping in von Willebrand Disease to Elucidate Pathogenic Mechanisms and Variability in PhenotypeFerdows Atiq, Johan Boender, Waander L van Heerde, et al.
British Journal of Haematology|May 17, 2018
Comorbidities associated with higher von Willebrand factor (VWF) levels may explain the age-related increase of VWF in von Willebrand diseaseFerdows Atiq, Karina Meijer, Jeroen Eikenboom, et al.
Pageof 45

Showing results (381-390 of 442) with videos related to

Sort By:
Pageof 45
BMJ Open|October 18, 2019
Comparative effectiveness of surgery in traumatic acute subdural and intracerebral haematoma: study protocol for a prospective observational study within CENTER-TBI and Net-QuReThomas A Van Essen, Victor Volovici, Maryse C Cnossen, et al.
American Journal of Clinical Oncology|April 26, 2019
Small Cell Carcinoma of the Esophagus: A Nationwide Analysis of Treatment and Outcome at Patient Level in Locoregional DiseasePaul M Jeene, Elisabeth D Geijsen, Christina T Muijs, et al.
Journal of Thrombosis and Haemostasis : JTH|November 6, 2018
Population pharmacokinetics of factor IX in hemophilia B patients undergoing surgeryT Preijers, H C A M Hazendonk, R Liesner, et al.
British Journal of Haematology|September 27, 2022
Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patientsMaurice Swinkels, Ferdows Atiq, Petra E Bürgisser, et al.
Blood Advances|May 9, 2022
The bleeding phenotype in people with nonsevere hemophiliaFabienne R Kloosterman, Anne-Fleur Zwagemaker, Catherine N Bagot, et al.
Research and Practice in Thrombosis and Haemostasis|July 30, 2024
Targeted exome analysis in patients with rare bleeding disorders: data from the Rare Bleeding Disorders in the Netherlands studySterre P E Willems, Annet Simons, Joline L Saes, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 1, 2018
Perioperative replacement therapy in haemophilia B: An appeal to "B" more preciseH C A M Hazendonk, T Preijers, R Liesner, et al.
Blood Advances|November 17, 2023
Oxygen gradient ektacytometry-derived biomarkers are associated with acute complications in sickle cell diseaseMinke A E Rab, Celeste K Kanne, Camille Boisson, et al.
Hemasphere|June 24, 2022
Importance of Genotyping in von Willebrand Disease to Elucidate Pathogenic Mechanisms and Variability in PhenotypeFerdows Atiq, Johan Boender, Waander L van Heerde, et al.
British Journal of Haematology|May 17, 2018
Comorbidities associated with higher von Willebrand factor (VWF) levels may explain the age-related increase of VWF in von Willebrand diseaseFerdows Atiq, Karina Meijer, Jeroen Eikenboom, et al.
Pageof 45