Multiple sclerosis - How common variants influence disease phenotype and rare variants trigger onset of disease
An update on the use of tolvaptan for autosomal dominant polycystic kidney disease: consensus statement on behalf of the ERA Working Group on Inherited Kidney Disorders, the European Rare Kidney Disease Reference Network and Polycystic Kidney Disease Inte
Leveraging consanguinity in inherited retinal diseases uncovers missing genetic variation : rare novel disease genes and a multitude of novel variants in known disease genes
Developing a rare disease chronic care model: Management of systemic sclerosis (MANOSS) study protocol
Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers
An automated platform for multiparameter data collection on live pathogens of higher or unknown biosafety risk (CAPS-IT)
Seroprevalence of IgG antibodies against SARS coronavirus 2 in Belgium – a serial prospective cross-sectional nationwide study of residual samples