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IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control|February 2, 2008
Rotary encoding for intravascular ultrasonic imaging systemsE Verdonk, P Webb, M Greenstein
Diabetes Research and Clinical Practice|October 28, 1998
Effects of acarbose (Glucobay) in persons with type 1 diabetes: a multicentre studyJ P Sels, H E Verdonk, B H Wolffenbuttel
Molecular Ecology|July 21, 2021
Adaptive and nonadaptive causes of heterogeneity in genetic differentiation across the Mimulus guttatus genomeJack M Colicchio, Lauren N Hamm, Hannah E Verdonk, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 15, 2019
Estradiol reference intervals in women during the menstrual cycle, postmenopausal women and men using an LC-MS/MS methodSara J E Verdonk, Hubert W Vesper, Frans Martens, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|February 1, 1995
Phase II trial of CPT-11 in patients with advanced pancreatic cancer, an EORTC early clinical trials group studyD J Wagener, H E Verdonk, L Y Dirix, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1992
Melatonin and melatonin-progestin combinations alter pituitary-ovarian function in women and can inhibit ovulationB C Voordouw, R Euser, R E Verdonk, et al.
Frontiers in Medicine|January 5, 2024
Bronchial obstruction in osteogenesis imperfecta can be detected by forced oscillation techniqueSilvia Storoni, Sara J E Verdonk, Dimitra Micha, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 27, 2024
Case Series of 6 Fetuses With Osteogenesis Imperfecta Type II: A Retrospective Study of Heart PathologySara J E Verdonk, Silvia Storoni, Lidiia Zhytnik, et al.
Physiological Reports|July 4, 2023
Altered collagen I and premature pulmonary embryonic differentiation in patients with OI type IIS Storoni, L Celli, M Breur, et al.
Calcified Tissue International|June 5, 2023
Medical Care Use Among Patients with Monogenic Osteoporosis Due to Rare Variants in LRP5, PLS3, or WNT1S J E Verdonk, S Storoni, L Zhytnik, et al.
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