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Samantha C Gouw

Showing results (1-10 of 67) with videos related to

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Blood|February 23, 2013
Unraveling the genetics of inhibitors in hemophiliaSamantha C Gouw, Karin Fijnvandraat
Seminars in Thrombosis and Hemostasis|September 10, 2013
Identifying nongenetic risk factors for inhibitor development in severe hemophilia aSamantha C Gouw, Karin Fijnvandraat
Current Treatment Options in Cardiovascular Medicine|August 31, 2001
Tetralogy of FallotSamantha C. Gouw, Thuy-Nga Le, Narayanswami Sreeram
Seminars in Thrombosis and Hemostasis|February 20, 2010
The multifactorial etiology of inhibitor development in hemophilia: genetics and environmentSamantha C Gouw, H Marÿke van den Berg
European Journal of Pediatrics|June 12, 2025
Improving shared decision‑making between paediatric haematologists, children with sickle cell disease, and their parents: an observational post-intervention studyRicardo O Wijngaarde, Samantha C Gouw, Dirk T Ubbink
Nederlands Tijdschrift Voor Geneeskunde|March 17, 2023
[Personal health records: a promising tool?]Martijn R Brands, Samantha C Gouw, Mariëtte H E Driessens
The Cochrane Database of Systematic Reviews|January 20, 2016
Antibody therapies for lymphoma in childrenVerena de Zwart, Samantha C Gouw, Friederike A G Meyer-Wentrup
Seminars in Thrombosis and Hemostasis|July 26, 2018
Preventing or Eradicating Factor VIII Antibody Formation in Patients with Hemophilia A: What Can We Learn from Other Disorders?Shermarke Hassan, Karin Fijnvandraat, Johanna G van der Bom, et al.
BMJ Open|February 17, 2025
How healthcare providers' IT identity is formed and how it affects the use of telemonitoring: a qualitative interview study in COPD careNienke Renting, Martijn R Brands, Emmie A B Velthausz, et al.
Research and Practice in Thrombosis and Haemostasis|October 19, 2023
Patient-relevant health outcomes for von Willebrand disease, platelet function disorders, and rare bleeding disorders: a Delphi studyEvelien S van Hoorn, Hester F Lingsma, Marjon H Cnossen, et al.
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 7
Blood|February 23, 2013
Unraveling the genetics of inhibitors in hemophiliaSamantha C Gouw, Karin Fijnvandraat
Seminars in Thrombosis and Hemostasis|September 10, 2013
Identifying nongenetic risk factors for inhibitor development in severe hemophilia aSamantha C Gouw, Karin Fijnvandraat
Current Treatment Options in Cardiovascular Medicine|August 31, 2001
Tetralogy of FallotSamantha C. Gouw, Thuy-Nga Le, Narayanswami Sreeram
Seminars in Thrombosis and Hemostasis|February 20, 2010
The multifactorial etiology of inhibitor development in hemophilia: genetics and environmentSamantha C Gouw, H Marÿke van den Berg
European Journal of Pediatrics|June 12, 2025
Improving shared decision‑making between paediatric haematologists, children with sickle cell disease, and their parents: an observational post-intervention studyRicardo O Wijngaarde, Samantha C Gouw, Dirk T Ubbink
Nederlands Tijdschrift Voor Geneeskunde|March 17, 2023
[Personal health records: a promising tool?]Martijn R Brands, Samantha C Gouw, Mariëtte H E Driessens
The Cochrane Database of Systematic Reviews|January 20, 2016
Antibody therapies for lymphoma in childrenVerena de Zwart, Samantha C Gouw, Friederike A G Meyer-Wentrup
Seminars in Thrombosis and Hemostasis|July 26, 2018
Preventing or Eradicating Factor VIII Antibody Formation in Patients with Hemophilia A: What Can We Learn from Other Disorders?Shermarke Hassan, Karin Fijnvandraat, Johanna G van der Bom, et al.
BMJ Open|February 17, 2025
How healthcare providers' IT identity is formed and how it affects the use of telemonitoring: a qualitative interview study in COPD careNienke Renting, Martijn R Brands, Emmie A B Velthausz, et al.
Research and Practice in Thrombosis and Haemostasis|October 19, 2023
Patient-relevant health outcomes for von Willebrand disease, platelet function disorders, and rare bleeding disorders: a Delphi studyEvelien S van Hoorn, Hester F Lingsma, Marjon H Cnossen, et al.
Pageof 7