- Parapelvic renal cysts2023 | First Faculty of Medicine
- Renal cysts and diabetes syndrome2015 | Second Faculty of Medicine
- Magnetic resonance imaging as an adjunct diagnostic tool in computed tomography defined Bosniak IIF-III renal cysts: a multicenter study2018 | Faculty of Medicine in Pilsen
- Blood pressure in children with renal cysts and diabetes syndrome2021 | Second Faculty of Medicine
- Miniinvasive treatment of the renal cysts in childrenPublication without faculty affiliation
- Renal cyst mimicking metastasis on a bone scan - advantage of a hybrid imaging2020 | Publication without faculty affiliation
- Ambulatory blood pressure correlates with renal volume and number of renal cysts in children with autosomal dominant polycystic kidney disease2003 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Ambulatory blood pressure correlates with renal volume and number of renal cysts in children with autosomal recessive polycystic kidney disease.2003 | Central Library of Charles University
- Hepatic phenotypes of HNF1B gene mutations: A case of neonatal cholestasis requiring portoenterostomy and literature review2015 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- A practical guide and decision-making protocol for the management of complex renal cystic masses2017 | Faculty of Medicine in Pilsen
- Ambulatory Blood Pressure Monitoring in Children with Cystic Kidney Diseases2001 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Hypomagnesaemia is absent in children with autosomal dominant polycystic kidney disease2019 | Second Faculty of Medicine
- Hypertension in children with cystic kidney diseases2006 | Second Faculty of Medicine
- Gastrointestinal tract involvement in hereditary kidney diseases2018 | First Faculty of Medicine
- Genotype-phenotype correlation in children with autosomal dominant polycystic kidney disease2009 | Second Faculty of Medicine
- Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: Results of the ESCAPE study2006 | Second Faculty of Medicine
- Cerebral hemangioblastomas in Von Hippel-Lindau disease2009 | Second Faculty of Medicine
- Types and characteristics of renal lesions - diagnosis, treatment and prognosis2023 | Faculty of Medicine in Hradec Králové
- MODY diabetes: what should we know for proper diagnostics and treatment?2012 | Second Faculty of Medicine
- Genotype/phenotype correlation in Czech tuberous sclerosis patients2016 | Second Faculty of Medicine
- A unique coincidence of a 17q12 deletion and duplication in a Czech family led to a refined genotype–phenotype correlation2023 | Second Faculty of Medicine
- Laparoendoscopic single-site surgery (LESS) in urology - a new frontier in minimally invasive surgery?2012 | Second Faculty of Medicine
- DCDC2 Mutations Cause a Renal-Hepatic Ciliopathy by Disrupting Wnt Signaling2015 | First Faculty of Medicine
- Renal concentrating capacity is linked to blood pressure in children with autosomal dominant polycystic kidney disease2004 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Liver, kidneys and diabetes: three faces of HNF1B gene deficit2014 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome2006 | First Faculty of Medicine
- Both 17q12 duplication and deletion detected in the patient with normal phenotype and their segregation in family with variably affected members2020 | Second Faculty of Medicine
- Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease2018 | Second Faculty of Medicine
- TSC2 pathogenic variants are predictive of severe clinical manifestations in TSC infants: results of the EPISTOP study2020 | Second Faculty of Medicine
- HNF1B nephropathy has a slow-progressive phenotype in childhood-with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry2019 | Second Faculty of Medicine
