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Showing results (11-20 of 20) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|August 26, 2010
Systematic review on the effect of glucocorticoid use on procoagulant, anti-coagulant and fibrinolytic factorsB van Zaane, E Nur, A Squizzato, et al.
British Journal of Haematology|January 2, 2025
Plasma inflammatory and angiogenic protein profiling of patients with sickle cell diseaseL A de Ligt, A E Gaartman, K Konté, et al.
The Netherlands Journal of Medicine|August 27, 2011
An unusual cause of a usual presentation. Hantavirus infectionM Goeijenbier, E Nur, M Goris, et al.
British Journal of Haematology|December 16, 2024
Exhaled breath analysis during vaso-occlusive events in sickle cell diseaseC Vuong, P Brinkman, H Heijboer, et al.
The American Journal of Tropical Medicine and Hygiene|April 9, 2024
The 2023 Dengue Outbreak in Bangladesh: Exploring the Epidemiology in Hospitalized PatientsUrby Saraf Anika, Muna Islam, Fatema E Nur Mou, et al.
Blood Cells, Molecules & Diseases|November 25, 2025
Oxidantscan: A novel biomarker to assess red blood cell susceptibility to oxidative stress in sickle cell diseaseC A Hernández, M J M Traets, W W van Solinge, et al.
Journal of Thrombosis and Haemostasis : JTH|May 1, 2017
Dynamics of von Willebrand factor reactivity in sickle cell disease during vaso-occlusive crisis and steady stateJ W R Sins, M Schimmel, B M Luken, et al.
Blood Reviews|May 27, 2019
Sickle cell disease: Clinical presentation and management of a global health challengeM E Houwing, P J de Pagter, E J van Beers, et al.
Annals of Hematology|January 22, 2026
Anti-thymocyte globulin-based treatment frequently leads to enduring treatment success in both old and young adult patients with aplastic anaemia: a real-world analysis from the Dutch aplastic anaemia registryC J M Halkes, E A S Koster, E J M Bogers, et al.
American Journal of Hematology|February 21, 2025
Pyruvate Kinase Function Correlates With Red Blood Cell Properties and Clinical Manifestations in Sickle Cell DiseaseM J M Traets, J F Bos, S van der Veen, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

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Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Journal of Thrombosis and Haemostasis : JTH|August 26, 2010
Systematic review on the effect of glucocorticoid use on procoagulant, anti-coagulant and fibrinolytic factorsB van Zaane, E Nur, A Squizzato, et al.
British Journal of Haematology|January 2, 2025
Plasma inflammatory and angiogenic protein profiling of patients with sickle cell diseaseL A de Ligt, A E Gaartman, K Konté, et al.
The Netherlands Journal of Medicine|August 27, 2011
An unusual cause of a usual presentation. Hantavirus infectionM Goeijenbier, E Nur, M Goris, et al.
British Journal of Haematology|December 16, 2024
Exhaled breath analysis during vaso-occlusive events in sickle cell diseaseC Vuong, P Brinkman, H Heijboer, et al.
The American Journal of Tropical Medicine and Hygiene|April 9, 2024
The 2023 Dengue Outbreak in Bangladesh: Exploring the Epidemiology in Hospitalized PatientsUrby Saraf Anika, Muna Islam, Fatema E Nur Mou, et al.
Blood Cells, Molecules & Diseases|November 25, 2025
Oxidantscan: A novel biomarker to assess red blood cell susceptibility to oxidative stress in sickle cell diseaseC A Hernández, M J M Traets, W W van Solinge, et al.
Journal of Thrombosis and Haemostasis : JTH|May 1, 2017
Dynamics of von Willebrand factor reactivity in sickle cell disease during vaso-occlusive crisis and steady stateJ W R Sins, M Schimmel, B M Luken, et al.
Blood Reviews|May 27, 2019
Sickle cell disease: Clinical presentation and management of a global health challengeM E Houwing, P J de Pagter, E J van Beers, et al.
Annals of Hematology|January 22, 2026
Anti-thymocyte globulin-based treatment frequently leads to enduring treatment success in both old and young adult patients with aplastic anaemia: a real-world analysis from the Dutch aplastic anaemia registryC J M Halkes, E A S Koster, E J M Bogers, et al.
American Journal of Hematology|February 21, 2025
Pyruvate Kinase Function Correlates With Red Blood Cell Properties and Clinical Manifestations in Sickle Cell DiseaseM J M Traets, J F Bos, S van der Veen, et al.
Pageof 2