Schutgens REG

ORCID: 0000-0002-2762-6033 · 5 papers in corpus
other 2026
Haemophilia : the official journal of the World Federation of Hemophilia ·doi:10.1111/hae.70186

BACKGROUND: Glanzmann thrombasthenia (GT) is an inherited platelet disorder resulting in severely reduced platelet aggregation and increased bleeding tendency. Pregnancy and childbirth in women with GT present significant challenges for bot…

review 2025
British journal of haematology ·doi:10.1111/bjh.70056

To illustrate the challenges in the management of women with Glanzmann thrombasthenia (GT) planning a pregnancy, we conducted a literature review and present a case series of eight women giving detailed descriptions of reproductive health p…

observational 2023
Research and practice in thrombosis and haemostasis ·doi:10.1016/j.rpth.2023.102229

BACKGROUND: Heavy menstrual bleeding (HMB), self-reported by 37% of adolescents, can be the first sign of a bleeding disorder (BD) during adolescence. The Dutch general practitioner (GP) guideline demands laboratory diagnostics and referral…

meta-analysis 2022
Haemophilia : the official journal of the World Federation of Hemophilia ·doi:10.1111/hae.14492

AIM: Currently, it is unknown which patient-reported outcomes are important for patients with autosomal inherited bleeding disorders. Therefore, the purpose of this study is to systematically review the available literature assessing patien…

observational 2020
Research and practice in thrombosis and haemostasis ·doi:10.1002/rth2.12281

BACKGROUND: Patients with congenital blood platelet disorders (CPDs) demonstrate a predominantly mucocutaneous bleeding tendency. Repeated bleeds throughout life can have a significant impact on health status-related quality of life (HR-QoL…