Taco W Kuijpers

发表

Effectiveness of a Web-Based Application to Monitor Health-Related Quality of Life

Lotte Haverman, T. Kuijpers, K. Dolman, 2013, Pediatrics.

Association of mannose-binding lectin genotype with cardiovascular abnormalities in Kawasaki disease

J. Ottenkamp, C. Hack, T. Kuijpers, 2003, The Lancet.

Disruption of vascular homeostasis in patients with Kawasaki disease: involvement of vascular endothelial growth factor and angiopoietins.

Michael Levin, David Burgner, Martin L Hibberd, 2012, Arthritis and rheumatism.

Genome-wide analysis of differential transcriptional and epigenetic variability across human immune cell types

Alfonso Valencia, Nicole Soranzo, Daniel Rico, 2016, bioRxiv.

Polymorphisms in the mannose-binding lectin gene as determinants of age-defined risk of coronary artery lesions in Kawasaki disease.

Jaap Ottenkamp, Gerrit Jan Weverling, J. Ottenkamp, 2006, Arthritis and rheumatism.

Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease

Tien Yin Wong, Paul Mitchell, Nagib Dahdah, 2011, Nature Genetics.

LAD-1/variant syndrome is caused by mutations in FERMT3.

Dirk Roos, Frank Baas, Arthur J Verhoeven, 2009, Blood.

A novel flow cytometry-based platelet aggregation assay.

Arthur J Verhoeven, Sergio Rutella, Karl Seeger, 2013, Blood.

Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

Fengyuan Hu, Kevin Rue-Albrecht, Patrick Deegan, 2017, Circulation.

Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities

Tatsuhiko Tsunoda, Hariklia Eleftherohorinou, Nagib Dahdah, 2016, Circulation. Cardiovascular genetics.

Dynamic contrast-enhanced magnetic resonance imaging can play a role in predicting flare in juvenile idiopathic arthritis.

Cristina Lavini, Mario Maas, T. Kuijpers, 2017, European journal of radiology.