- Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome2006 | First Faculty of Medicine
- Familial juvenile hyperuricaemic nephropathy (FJHN): linkage analysis in 15 families, physical and transcriptional characterisation of the FJHN critical region on chromosome 16p11.2 and the analysis of seven candidate genes2003 | First Faculty of Medicine
- Hereditary Interstitial Kidney Disease2010 | First Faculty of Medicine
- Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management-A KDIGO consensus report2015 | First Faculty of Medicine
