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Disease burden in primary sclerosing cholangitis in the Netherlands
Disease burden in primary sclerosing cholangitis in the Netherlands
Effectiveness of routine third trimester ultrasonography to reduce adverse perinatal outcomes in low risk pregnancy (the IRIS study): nationwide, pragmatic, multicentre, stepped wedge cluster randomised trial
Cost-effectiveness of laparoscopy as diagnostic tool before primary cytoreductive surgery in ovarian cancer
A dynamic approach to estimating the chances of a live birth in couples with unexplained subfertility with and without treatment: a population-based record-linkage study
Laparoscopy to Predict the Result of Primary Cytoreductive Surgery in Patients With Advanced Ovarian Cancer: A Randomized Controlled Trial
Induction of labor at term with oral misoprostol or Foley catheter, the PROBAAT-II trial (NTR3466)
Temporizing management versus termination of pregnancy in women with severe preeclampsia at 28-34 weeks (TOTEM-Trial)
Nifedipine versus atosiban for tocolysis in preterm labour (Assessment of Perinatal Outcome after Specific Tocolysis in Early Labour: APOSTEL III-trial)
Repeated measurement of short cervical length does not influence the risk of preterm delivery
Screening Low-Risk Women with a Singleton Pregnancy for Short Cervical Length to Identify Increased Risk for Preterm Birth: The Triple P Screening Study
Preventing Preterm Birth with Progesterone (The Triple P Treat Study): A Randomized Controlled Trial
Assessment of obstetric-teams' non-technical skills in the management of postpartum hemorrhage using actual care video recordings
Comparison of the Actim Partus test and fetal fibronectin test in combination with cervical length in the prediction of spontaneous preterm delivery in symptomatic women: a post-hoc analysis
False-positive, false-negative and uninterpretable results in fetal fibronectin testing during the APOSTEL1 study; which factors do contribute?
Effectiveness and safety of different methods for induction of labor in women with a previous cesarean section
Delivery versus expectant monitoring for late preterm hypertensive disorders of pregnancy (HYPITAT-II): a multicenter, open label, randomized controlled trial
The risk of preterm delivery in women with signs of preterm labor before 34 weeks who do not deliver within 7 days: the APOSTEL-1 cohort
Does quantitative fetal fibronectin testing improve the prediction of spontaneous preterm delivery as compared to qualitative fetal fibronectin testing in symptomatic women: a post-hoc analysis
The contribution of vaginal examination to risk stratification of women with signs of preterm labor before 34 weeks gestation: the APOSTEL1-cohort

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