Publications
- Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene2013 | Second Faculty of Medicine
- Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis2001 | Publication without faculty affiliation
- Diversity of kidney care referral pathways in national child health systems of 48 European countries2024 | Second Faculty of Medicine
- Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease2023 | First Faculty of Medicine, Second Faculty of Medicine
- Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 22023 | Second Faculty of Medicine
- Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension2023 | Second Faculty of Medicine
- Tolvaptan for Children and Adolescents with Autosomal Dominant Polycystic Kidney Disease: Randomized Controlled Trial2023 | Second Faculty of Medicine
- Design of two ongoing clinical trials of tolvaptan in the treatment of pediatric patients with autosomal recessive polycystic kidney disease2023 | Second Faculty of Medicine
- Unattended automated office blood pressure measurement in children2023 | Second Faculty of Medicine
- Hypertension in pediatric kidney transplantation2023 | Second Faculty of Medicine
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