Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
NGS panel analysis in 24 ectopia lentis patients; a clinically relevant test with a high diagnostic yield.
European journal of medical genetics·2017
A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability.
European journal of medical genetics·2014
Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy.
Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation·2010
Knowledge, attitudes, and practices regarding premature ventricular contractions among patients: a cross-sectional study.
Frontiers in public health·2026
Diagnostic Accuracy and Optimal Thresholds of Salivary Pepsin (Peptest) in Laryngopharyngeal Reflux: A Systematic Review and Meta-Analysis.
Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery·2026
Anti-inflammatory and antioxidant effects of propolis: A systematic review and meta-analysis of the influences of the geographical origin and phenotype.
Complementary therapies in medicine·2026
Metabolic Stress Testing Reveals Persistent Lipid-Handling Dysfunction in Women With Polycystic Ovary Syndrome Despite Exercise Training.
Diabetes, obesity & metabolism·2026