- The possible role of the skin biopsy in the diagnosis of Alport syndrome in clinical practice.2003 | Central Library of Charles University
- Pregnancy in Alportś syndrome2001 | First Faculty of Medicine
- New Diagnostic Possibilities of Alport Syndrome1999 | Second Faculty of Medicine
- Current and Future Therapeutical Options in Alport Syndrome2023 | First Faculty of Medicine
- Alports's Syndrome and Benign Familial Haematuria1999 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Is a chance for slowing down progression CKD in Alport syndrom?Commentary on:KI 81,2012,494-5012012 | First Faculty of Medicine
- Alport syndrome2006 | First Faculty of Medicine
- Alport's syndrom to look ophthalmologist2007 | First Faculty of Medicine
- Novinky v léčbě Alportova syndromu2023 | First Faculty of Medicine
- A founder COL4A4 pathogenic variant resulting in autosomal recessive Alport syndrome accounts for most genetic kidney failure in Romani people2023 | Central Library of Charles University, Second Faculty of Medicine, Faculty of Medicine in Pilsen, Third Faculty of Medicine
- Alport syndrome and benign recurrent hematuria are casued ba the mutations of collagen IV genes2003 | First Faculty of Medicine
- Mutation Analysis of COL4A5 and COL4A3 Genes in Alport´s Syndrome1999 | Central Library of Charles University, Second Faculty of Medicine
- Aberrant splicing of the COL4A5 gene in patients with Alport syndrome1994 | Central Library of Charles University
- Introduction of molecular genetic diagnosis in syndromes with a hearing defect1998 | Second Faculty of Medicine
- The possible role of the skin biopsy in the diagnostics OF ALPORT syndrome in clinical practice2003 | Central Library of Charles University
- Familial hematuria: A review2017 | Second Faculty of Medicine
- The Possible Role of the Skin Biopsy in the Diagnostic of Alport Syndrome in Clinical PracticePublication without faculty affiliation
- Benign familial hematuria2001 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Partial remission with cyclosporine A in a patient with nephrotic syndrome due to NPHS2 mutation2009 | Second Faculty of Medicine
- Dlouhodobé sledování žen s Alportovým syndromem - zkušenost z pediatrického centra2021 | First Faculty of Medicine
- Genetic etiology of kidney disease - overview and case studies in accordance with massive parallel sequencing2021 | Second Faculty of Medicine
- Sparsentan. Dual angiotensin II AT1 receptor blocker and endothelin ETA receptor antagonist, Treatment of focal segmental glomerulosclerosis, Treatment of IgA nephropathy2020 | First Faculty of Medicine
- Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the Phenotype2021 | Second Faculty of Medicine