Paul R. Van Der Valk
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
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Found 10 publications
Health care resources and costs associated with delivering gene therapy for hemophilia in clinical practice.
Journal: Research and practice in thrombosis and haemostasis
Published: July 28, 2025
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
Transition readiness among adolescents and young adults with haemophilia in the Netherlands: Nationwide questionnaire study.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: June 16, 2023
Clotting factor activity levels and bleeding risk in people with haemophilia playing sports.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: October 14, 2022
Liver-related complications before and after successful treatment of chronic hepatitis C virus infection in people with inherited bleeding disorders.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: June 02, 2022
Real-Life Pharmacokinetics of rFVIII-Fc and rFIX-Fc.
Journal: TH open : companion journal to thrombosis and haemostasis
Published: November 12, 2020
Catheter Ablation for Atrial Fibrillation in Patients with Hemophilia or von Willebrand Disease.
Journal: TH open : companion journal to thrombosis and haemostasis
Published: May 23, 2019
Continuous infusion of extended half-life factor VIII (efmoroctocog alpha) for surgery in severe haemophilia A.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: May 26, 2018
The association of haemophilic arthropathy with Health-Related Quality of Life: a post hoc analysis.
The association of haemophilic arthropathy with Health-Related Quality of Life: a post hoc analysis.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: September 25, 2016
APOE1 mutation in a patient with type III hyperlipoproteinaemia: detailed genetic analysis required.
APOE1 mutation in a patient with type III hyperlipoproteinaemia: detailed genetic analysis required.
Journal: The Netherlands journal of medicine
Published: August 04, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026