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American Journal of Human Genetics|January 1, 1989
Linkage analysis of chromosome 17 markers in British and South African families with neurofibromatosis type IC G Mathew, K Thorpe, D F Easton, et al.Apoptosis : an International Journal on Programmed Cell Death|January 1, 1997
Butyrate-induced reversal of dexamethasone resistance in autonomous rat Nb2 lymphoma cellsA R Buckley, J S Krumenacker, D J Buckley, et al.The Journal of Dermatological Treatment|July 9, 2008
Validation of clinical and image skin scoring systems for a single chronic discoid lupus erythematosus lesionAngelina Erceg, Elke M J G De Jong, Rosanne G Van Lingen, et al.Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|October 28, 2023
Do depressive and anxiety symptoms influence the quality of life of patients with atrial fibrillation after cryoballoon ablation: a comparison studyGabriela Raileanu, Norzad Jawid, Evelien Bohte, et al.International Journal of Dental Hygiene|September 11, 2023
Dutch dental hygiene students' knowledge of HPV-related oropharyngeal squamous cell carcinoma and HPV vaccinationMarcella R Poelman, Henk S Brand, Deborah G de Jong, et al.The British Journal of Dermatology|May 20, 2004
Memory effector (CD45RO+) and cytotoxic (CD8+) T cells appear early in the margin zone of spreading psoriatic lesions in contrast to cells expressing natural killer receptors, which appear lateW H P M Vissers, C H M Arndtz, L Muys, et al.Lung|January 22, 2020
Ranking Self-reported Gastrointestinal Side Effects of Pharmacotherapy in SarcoidosisM Drent, V L J Proesmans, M D P Elfferich, et al.Tissue Engineering. Part B, Reviews|September 29, 2015
Environmental Influences on Endothelial to Mesenchymal Transition in Developing Implanted Cardiovascular Tissue-Engineered GraftsDimitri E P Muylaert, Olivier G de Jong, Gisela G G Slaats, et al.Human Genetics|September 10, 1999
The frequency of lysosomal storage diseases in The NetherlandsB J Poorthuis, R A Wevers, W J Kleijer, et al.Human Genetics|September 1, 1995
Metachromatic leukodystrophy: a 12-bp deletion in exon 2 of the arylsulfatase A gene in a late infantile variantJ A Luyten, P W Wenink, G C Steenbergen-Spanjers, et al.Pageof 37