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European Journal of Ophthalmology|February 7, 2015
Primary cataract as a key to recognition of myotonic dystrophy type 1Nicol C Voermans, Corrie E Erasmus, Charlotte W Ockeloen, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|May 28, 2008
Pre-transplant quality of life does not predict survival after lung transplantationKarin M Vermeulen, Elisabeth M TenVergert, Erik A M Verschuuren, et al.
Developmental Medicine and Child Neurology|November 16, 2019
Changes in severity and impact of drooling after submandibular gland botulinum neurotoxin A injections in children with neurodevelopmental disabilitiesKaren Van Hulst, Jan Jw Van Der Burg, Peter H Jongerius, et al.
Journal of Pediatric Rehabilitation Medicine|April 2, 2025
Reliability and validity of the Mini-Eating and Drinking Ability Classification System (Mini-EDACS) among Dutch preschoolers with cerebral palsyFloor van der Klift, Lynn B Orriëns, Bea Spek, et al.
Journal of Child Neurology|May 28, 2016
Diagnosis and Management of Drooling in Children With Progressive Dystonia: A Case Series of Patients With MEGDEL SyndromeDorian Blommaert, Karen van Hulst, Frank J A van den Hoogen, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 8, 2023
Recognising symptoms of congenital myasthenic syndromes in children: A guide for paediatriciansLynn B Orriëns, Dilan Eker, Hilde M H Braakman, et al.
Transplantation|February 24, 2010
Lung transplantation from nonheparinized category III non-heart-beating donors. A single-centre reportMichiel E Erasmus, Erik A M Verschuuren, Danielle M Nijkamp, et al.
American Journal of Respiratory and Critical Care Medicine|August 1, 1997
Effects of early surfactant treatment persisting for one week after lung transplantation in ratsM E Erasmus, G J Hofstede, A H Petersen, et al.
European Journal of Pediatrics|September 21, 2011
Clinical practice: swallowing problems in cerebral palsyCorrie E Erasmus, Karen van Hulst, Jan J Rotteveel, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Prenatal analysis in two suspected cases of glutathione synthetase deficiencyE Erasmus, L J Mienie, W N de Vries, et al.
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