Showing results (1-10 of 10) with videos related to
Sort By:
Pageof 1
Tijdschrift Voor Psychiatrie|May 4, 2011
[Rating scales for assessing catatonia; which ones are the best?]J Rooseleer, A Willaert, P SienaertB-ENT|February 20, 2016
Swallowing dysfunction in myotonic dystrophy: a retrospective study of symptomatology and radiographic findingsA Willaert, M Jorissen, A GoelevenInternational Journal of Pediatric Otorhinolaryngology|September 15, 2023
Otological problems in ichthyosis: A literature reviewR Van Oosterwyck, E Loos, A WillaertFrontiers in Pharmacology|March 23, 2022
The Abcc6a Knockout Zebrafish Model as a Novel Tool for Drug Screening for Pseudoxanthoma ElasticumM Van Gils, A Willaert, P J Coucke, et al.Methods in Cell Biology|July 23, 2016
RT-qPCR gene expression analysis in zebrafish: Preanalytical precautions and use of expressed repetitive elements for normalizationS Vanhauwaert, S Lefever, P Coucke, et al.The Journal of Investigative Dermatology|July 22, 2018
Generation and Validation of a Complete Knockout Model of abcc6a in ZebrafishM Van Gils, A Willaert, E Y G De Vilder, et al.Journal of Medical Genetics|December 18, 2008
Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylationA Willaert, F Malfait, S Symoens, et al.Genesis (New York, N.Y. : 2000)|August 12, 2008
Absence of arterial phenotype in mice with homozygous slc2A10 missense substitutionsB L Callewaert, B L Loeys, C Casteleyn, et al.Scientific Reports|February 16, 2016
Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and SkinC Gistelinck, R Gioia, A Gagliardi, et al.Human Mutation|October 16, 2007
Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified familiesB L Callewaert, A Willaert, W S Kerstjens-Frederikse, et al.Pageof 1