about
Efficacy, cycle control, and user acceptability of a novel combined contraceptive vaginal ringEfficacy, tolerability and acceptability of a novel contraceptive vaginal ring releasing etonogestrel and ethinyl oestradiol.Disproportionate Intrauterine Growth Intervention Trial At Term: DIGITATInduction of labour versus expectant monitoring in women with pregnancy induced hypertension or mild preeclampsia at term: the HYPITAT trial.Well being of obstetric patients on minimal blood transfusions (WOMB trial).Early versus late epidural analgesia and risk of instrumental delivery in nulliparous women: a systematic review.Induction versus expectant monitoring for intrauterine growth restriction at term: randomised equivalence trial (DIGITAT)Effect of alpha-linolenic acid supplementation during pregnancy on maternal and neonatal polyunsaturated fatty acid status and pregnancy outcome.Induction of labour with a Foley catheter or oral misoprostol at term: the PROBAAT-II study, a multicentre randomised controlled trialDilemma in timing of delivery in a patient with an acute myocardial infarctionWhich intrauterine growth restricted fetuses at term benefit from early labour induction? A secondary analysis of the DIGITAT randomised trial.Maternal health-related quality of life after induction of labor or expectant monitoring in pregnancy complicated by intrauterine growth retardation beyond 36 weeksAvulsion of puborectalis muscle and other risk factors for cystocele recurrence: a 2-year follow-up study.The contraceptive vaginal ring compared with the combined oral contraceptive pill: a comprehensive review of randomized controlled trials.The contraceptive vaginal ring, NuvaRing(®), a decade after its introduction.Epidural analgesia during labour, routinely or on request: a cost-effectiveness analysis.Involving women in personalised decision-making on mode of delivery after caesarean section: the development and pilot testing of a patient decision aid.Neonatal sepsis is mediated by maternal fever in labour epidural analgesia.Clinical indicators associated with the mode of twin delivery: an analysis of 22,712 twin pairs.Clinical acceptability of an ethylene-vinyl-acetate nonmedicated vaginal ring.Human parvovirus B19 infection and unbalanced translocation in a case of hydrops fetalis.Planning the mode of delivery for twin pregnancies: A web-based questionnaire.Epidural analgesia and operative delivery: a ten-year population-based cohort study in The Netherlands.Comparison of uterine concentrations of ethinyl estradiol and etonogestrel after use of a contraceptive vaginal ring and an oral contraceptive.The clinical acceptability of a non-medicated vaginal ring.[Pregnancy after isotretinoin use].[Successful treatment and pregnancy in a women with the non-classic form of congenital adrenal hyperplasia]The CHOICE study: effect of counselling on the selection of combined hormonal contraceptive methods in 11 countries.Women's prelabour preference for epidural analgesia: a cross-sectional study among women from the Netherlands and Belgium.Suspected versus non-suspected small-for-gestational age fetuses at term: perinatal outcomes.Induction of labour versus expectant monitoring for gestational hypertension or mild pre-eclampsia after 36 weeks' gestation (HYPITAT): a multicentre, open-label randomised controlled trial.Neonatal and maternal outcomes in twin gestations > or =32 weeks according to the planned mode of delivery.[Term breech presentation: an indication for cesarean section]Birth weight and neurodevelopmental outcome of children at 2 years of age after planned vaginal delivery for breech presentation at term.Industry-sponsored research: how to eliminate bias?[Diagnostic image (213). A pregnant woman with premature contractions and vaginal blood loss]Routine labour epidural analgesia versus labour analgesia on request: a randomised non-inferiority trial.Vaginal birth after a caesarean section: the development of a Western European population-based prediction model for deliveries at term.The combined contraceptive vaginal ring (NuvaRing): first experience in daily clinical practice in The Netherlands.Pregnancy and delivery with an abdominal mesh graft.
P50
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P50
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onderzoeker
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researcher ORCID ID = 0000-0003-2319-4808
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name
Frans Roumen
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Frans Roumen
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Frans Roumen
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Frans Roumen
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Frans Roumen
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Frans Roumen
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Frans Roumen
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Frans Roumen
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Frans Roumen
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Frans Roumen
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Frans Roumen
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Frans Roumen
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P106
P21
P31
P496
0000-0003-2319-4808