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American Journal of Respiratory and Critical Care Medicine|May 12, 2000
Virus- and bradykinin-induced airway hyperresponsiveness in guinea pigsG Folkerts, J W Vlieger, A de Vries, et al.
European Journal of Gastroenterology & Hepatology|October 2, 2009
Influence of alpha-1 antitrypsin heterozygosity on treatment efficacy of HCV combination therapyKarin F Kok, Hanneke van Soest, Antonius E van Herwaarden, et al.
British Journal of Cancer|May 10, 2014
Mammary gland-specific ablation of focal adhesion kinase reduces the incidence of p53-mediated mammary tumour formationM H A M van Miltenburg, M J van Nimwegen, I Tijdens, et al.
BMJ Open|July 13, 2026
A multidisciplinary active lifestyle aftercare programme for individuals with acquired brain injury (ABI-MOTION): protocol of a practice-based implementation studyElisabeth A de Vries, Erik Grauwmeijer, Erwin Ista, et al.
European Journal of Human Genetics : EJHG|February 19, 2021
Quantitative facial phenotyping for Koolen-de Vries and 22q11.2 deletion syndromeAlexander J M Dingemans, Diante E Stremmelaar, Roos van der Donk, et al.
Seminars in Arthritis and Rheumatism|August 21, 2019
Quantitative subchondral bone perfusion imaging in knee osteoarthritis using dynamic contrast enhanced MRIBas A de Vries, Rianne A van der Heijden, Joost Verschueren, et al.
Cardiovascular Research|December 27, 2011
Connexin43 silencing in myofibroblasts prevents arrhythmias in myocardial cultures: role of maximal diastolic potentialSaïd F Askar, Brian O Bingen, Jim Swildens, et al.
Neurology|August 28, 2002
Clinical and genetic heterogeneity in benign hereditary choreaG J Breedveld, A K Percy, M E MacDonald, et al.
Clinical Genetics|September 14, 2007
Pure subtelomeric microduplications as a cause of mental retardationE M Ruiter, D A Koolen, T Kleefstra, et al.
Clinical Genetics|January 12, 2016
De novo loss-of-function mutations in X-linked SMC1A cause severe ID and therapy-resistant epilepsy in females: expanding the phenotypic spectrumS Jansen, T Kleefstra, M H Willemsen, et al.
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