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Showing results (401-410 of 442) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|January 25, 2023
Little discrepancy between one-stage and chromogenic factor VIII (FVIII)/IX assays in a large international cohort of persons with nonsevere hemophilia A and BAnne-Fleur Zwagemaker, Fabienne R Kloosterman, Samantha C Gouw, et al.
Journal of Thrombosis and Haemostasis : JTH|March 8, 2025
Bleeding symptoms in persons with rare bleeding disorders and a heterozygous genotype: data from the Rare Bleeding Disorders in the Netherlands studySterre P E Willems, Marjon H Cnossen, Nick van Es, et al.
Frontiers in Neurology|April 27, 2019
Pre-injury Comorbidities Are Associated With Functional Impairment and Post-concussive Symptoms at 3- and 6-Months After Mild Traumatic Brain Injury: A TRACK-TBI StudyJohn K Yue, Maryse C Cnossen, Ethan A Winkler, et al.
Research and Practice in Thrombosis and Haemostasis|April 14, 2025
Sexuality and bleeding in von Willebrand diseaseCalvin B van Kwawegen, Hester Pastoor, Jeroen Eikenboom, et al.
American Journal of Hematology|April 23, 2016
Early occurrence of red blood cell alloimmunization in patients with sickle cell diseaseJoep W R Sins, Bart J Biemond, Sil M van den Bersselaar, et al.
Thrombosis and Haemostasis|May 12, 2017
Joint assessment in von Willebrand disease. Validation of the Haemophilia Joint Health score and Haemophilia Activities ListKarin P M van Galen, Merel A Timmer, Piet de Kleijn, et al.
Blood Advances|April 21, 2022
Desmopressin response depends on the presence and type of genetic variants in patients with type 1 and type 2 von Willebrand diseaseFerdows Atiq, Jessica Heijdra, Fleur Snijders, et al.
Blood Reviews|September 13, 2025
Metabolomics in sickle cell disease: Current knowledge and gaps - A scoping reviewSigrid van der Veen, Judith J M Jans, Eduard J van Beers, et al.
Thrombosis and Haemostasis|May 6, 2020
A Novel, Enriched Population Pharmacokinetic Model for Recombinant Factor VIII-Fc Fusion Protein Concentrate in Hemophilia A PatientsLaura H Bukkems, Jessica M Heijdra, Mary Mathias, et al.
Research and Practice in Thrombosis and Haemostasis|July 30, 2024
Psychometrics of patient-reported outcomes measurement information system in von Willebrand disease, inherited platelet function disorders, and rare bleeding disordersEvelien S van Hoorn, Sterre P E Willems, Wala Al Arashi, et al.
Pageof 45

Showing results (401-410 of 442) with videos related to

Sort By:
Pageof 45
Journal of Thrombosis and Haemostasis : JTH|January 25, 2023
Little discrepancy between one-stage and chromogenic factor VIII (FVIII)/IX assays in a large international cohort of persons with nonsevere hemophilia A and BAnne-Fleur Zwagemaker, Fabienne R Kloosterman, Samantha C Gouw, et al.
Journal of Thrombosis and Haemostasis : JTH|March 8, 2025
Bleeding symptoms in persons with rare bleeding disorders and a heterozygous genotype: data from the Rare Bleeding Disorders in the Netherlands studySterre P E Willems, Marjon H Cnossen, Nick van Es, et al.
Frontiers in Neurology|April 27, 2019
Pre-injury Comorbidities Are Associated With Functional Impairment and Post-concussive Symptoms at 3- and 6-Months After Mild Traumatic Brain Injury: A TRACK-TBI StudyJohn K Yue, Maryse C Cnossen, Ethan A Winkler, et al.
Research and Practice in Thrombosis and Haemostasis|April 14, 2025
Sexuality and bleeding in von Willebrand diseaseCalvin B van Kwawegen, Hester Pastoor, Jeroen Eikenboom, et al.
American Journal of Hematology|April 23, 2016
Early occurrence of red blood cell alloimmunization in patients with sickle cell diseaseJoep W R Sins, Bart J Biemond, Sil M van den Bersselaar, et al.
Thrombosis and Haemostasis|May 12, 2017
Joint assessment in von Willebrand disease. Validation of the Haemophilia Joint Health score and Haemophilia Activities ListKarin P M van Galen, Merel A Timmer, Piet de Kleijn, et al.
Blood Advances|April 21, 2022
Desmopressin response depends on the presence and type of genetic variants in patients with type 1 and type 2 von Willebrand diseaseFerdows Atiq, Jessica Heijdra, Fleur Snijders, et al.
Blood Reviews|September 13, 2025
Metabolomics in sickle cell disease: Current knowledge and gaps - A scoping reviewSigrid van der Veen, Judith J M Jans, Eduard J van Beers, et al.
Thrombosis and Haemostasis|May 6, 2020
A Novel, Enriched Population Pharmacokinetic Model for Recombinant Factor VIII-Fc Fusion Protein Concentrate in Hemophilia A PatientsLaura H Bukkems, Jessica M Heijdra, Mary Mathias, et al.
Research and Practice in Thrombosis and Haemostasis|July 30, 2024
Psychometrics of patient-reported outcomes measurement information system in von Willebrand disease, inherited platelet function disorders, and rare bleeding disordersEvelien S van Hoorn, Sterre P E Willems, Wala Al Arashi, et al.
Pageof 45