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Advances in Medical Education and Practice|January 23, 2015
Leading teams during simulated pediatric emergencies: a pilot studyEster H Coolen, Jos M Draaisma, Sabien den Hamer, et al.
BMC Emergency Medicine|March 10, 2010
Advanced medical life support procedures in vitally compromised children by a helicopter emergency medical serviceBastiaan M Gerritse, Annelies Schalkwijk, Ben J Pelzer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 2, 2022
Head circumference in glucose transporter 1 deficiency syndrome: Normal for individuals, abnormal as a groupLoes A van Gemert, Wilhelmina G Leen, Jos M Draaisma, et al.
American Journal of Medical Genetics. Part A|September 9, 2017
Variable phenotypic expression in a large Noonan syndrome family segregating a novel SOS1 mutationDorothée C van Trier, Tuula Rinne, Kees Noordam, et al.
European Journal of Pediatrics|June 28, 2018
Ocular findings in Noonan syndrome: a retrospective cohort study of 105 patientsDorothée C van Trier, Ineke van der Burgt, Renske W Draaijer, et al.
American Journal of Medical Genetics. Part A|June 20, 2017
Motor performance in children with Noonan syndromeEllen A Croonen, Marlou Essink, Ineke van der Burgt, et al.
Plos One|March 4, 2014
Methods to quantify soft tissue-based cranial growth and treatment outcomes in children: a systematic reviewSander Brons, Machteld E van Beusichem, Ewald M Bronkhorst, et al.
American Journal of Medical Genetics. Part A|June 25, 2016
Perceived motor problems in daily life: Focus group interviews with people with Noonan syndrome and their relativesEllen A Croonen, Mirjam Harmsen, Ineke Van der Burgt, et al.
American Journal of Medical Genetics. Part A|May 3, 2008
Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotypeMariëlle E M Swinkels, Annet Simons, Dominique F Smeets, et al.
Kidney International|April 22, 2019
SON haploinsufficiency causes impaired pre-mRNA splicing of CAKUT genes and heterogeneous renal phenotypesJung-Hyun Kim, Eun Young Park, David Chitayat, et al.
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