- Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome2012 | First Faculty of Medicine
- Plasmapheresis-induced clinical improvement in a patient with steroid-resistant nephrotic syndrome due to Podocin (NPHS2) gene mutation2010 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Faculty of Physical Education and Sport
- Genetically Determined Forms of Nephrotic Syndrome in Children2009 | Second Faculty of Medicine
- Mutational Analysis of the NPHS2 Gene in Czech Patients with Idiopathic Nephrotic Syndrome2012 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Partial remission with cyclosporine A in a patient with nephrotic syndrome due to NPHS2 mutation2009 | Second Faculty of Medicine
- The most common founder pathogenic variant c.868G > A (p.Val290Met) in the NPHS2 gene in a representative adult Czech cohort with focal segmental glomerulosclerosis is associated with a milder disease and its underdiagnosis in childhood2023 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Second Faculty of Medicine, Faculty of Medicine in Pilsen, Third Faculty of Medicine
- Screening for NPHS2 Mutations May Help Predict FSGS Recurrence after Transplantation2011 | Second Faculty of Medicine
- The verification of the applicability of NPHS2/SYNPO ratio for diagnosis of FSGS and MCD2016 | First Faculty of Medicine
- Plasmapheresis-induced Clinical Improvement in a Patient with Steroid-Resitant Nephrotic Syndrome Due to Podocin (NPHS2) Gene Mutation2010 | Second Faculty of Medicine
- Genetic screening in adolescents with steroid-resistant nephrotic syndrome2013 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Steroid-resistant nephrotic syndrome (SRNS) due to mutation in the NPHS2 gene encoding podocin - case reportPublication without faculty affiliation
- Monogenic forms of steroid-resistant nephrotic syndrome2018 | Second Faculty of Medicine, Faculty of Medicine in Pilsen
- Genetic diagnosis of steroid-resistant nephrotic syndrome in a longitudinal collection of Czech and Slovak patients: a high proportion of causative variants in NUP932018 | Second Faculty of Medicine
- Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 92006 | Second Faculty of Medicine
- Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome2012 | Second Faculty of Medicine
- A single-gene cause in 29,5 % of cases of steroid-resistant nephrotic syndrom2015 | Faculty of Medicine in Hradec Králové
- Management of children with congenital nephrotic syndrome: challenging treatment paradigms2019 | Second Faculty of Medicine
