Lize D. Van Vulpen
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
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Found 56 publications
Mim8 Bispecific Antibody Prophylaxis in Hemophilia A with or without Inhibitors.
Journal: The New England journal of medicine
Published: April 29, 2026
Long-term prosthesis survival of total hip and total knee arthroplasty in people with inherited bleeding disorders.
Journal: Research and practice in thrombosis and haemostasis
Published: February 26, 2026
Predicting Recovery After Joint Bleeding in Persons With Bleeding Disorders.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: December 02, 2025
An 80-year-old man with a rare disease manifestation of disseminated cryptococcosis.
Journal: IDCases
Published: July 10, 2025
Pharmacokinetic-guided dose reduction of emicizumab in congenital hemophilia A: interim analysis of the DosEmi study.
Journal: Journal of thrombosis and haemostasis : JTH
Published: June 05, 2025
Inhibitor Formation in the Era of Novel Haemophilia Treatment-A Humanized Mouse Model to Answer Our Questions?
Journal: Thrombosis and haemostasis
Published: March 06, 2025
No correlation between thrombin generation and emicizumab levels: implications for monitoring emicizumab therapy.
Journal: Research and practice in thrombosis and haemostasis
Published: November 07, 2024
Letter in response to Bounaix et al. "Management of anticoagulation and factor XIII replacement in a patient with severe factor XIII deficiency and recurrent venous thromboembolic disease: case report and review of literature".
Journal: Research and practice in thrombosis and haemostasis
Published: June 28, 2024
A clinical practice guideline for primary care physiotherapy in patients with haemophilia.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: April 04, 2024
Efficacy of a 1:1 ratio VWF/FVIII concentrate in patients with von Willebrand disease.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: March 18, 2024
Limited value of testing for factor XIII and α2-antiplasmin deficiency in patients with a bleeding disorder of unknown cause.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: March 18, 2024
Towards Personalized Treatment in Haemophilia: The Role of Genetic Factors in Iron and Heme Control to Identify Patients at Risk for Haemophilic Arthropathy.
Journal: Journal of personalized medicine
Published: December 29, 2023
Last Updated: 09/26/2026