- Molecular Genetic Testing of Diabetes Insipidus Renalis2019 | Faculty of Medicine in Pilsen
- Molecuclar Genetic Examination in Cystic Fibrosis1999 | Central Library of Charles University, Second Faculty of Medicine
- congenital and genetic causes and molecular genetic examination nephropathy and uropathy2013 | Second Faculty of Medicine
- Léri-Weill Syndrome on the Principle of Structural Aberration of Chromosome Y (Case Report)2018 | Faculty of Medicine in Pilsen
- Molecular genetic testing in patients with autosomal recessive non syndromic hearing loss and deafness2003 | Second Faculty of Medicine
- Molekulárně genetická vyšetření u pacientů a rodin s vrozenou autosomálně recesivní nesyndromovou ztrátou sluchu a hluchotou.2002 | Second Faculty of Medicine
- Complex approach towards patients with hypertrophic cardiomyopathy and indications to genetic testing2020 | Central Library of Charles University, Second Faculty of Medicine
- Familial hypercholesterolemia is still unknown?2014 | First Faculty of Medicine
- Heart rhythm disorders in children, current topics in paediatric arrhythmology2019 | Publication without faculty affiliation
- Monogenic diabetes MODY in childhood: a retrospective study of patients diagnosed at the Department of Pediatrics, University Hospital in Pilsen in 2000-20172019 | Second Faculty of Medicine, Faculty of Medicine in Pilsen
- Best Practices-Molecular genetic testing for thrombophilia associated with venous thromboembolism and its complications-the consensus of the Czech Society of Thrombosis and Haemostasis CLS JEP, the Society for Medical Genetics CLS JEP, Czech Society of Hematology CSL JEP, Czech Society of Internal Medicine CSL JEP and the Czech Society of Clinical Biochemistry CSL JEP2011 | First Faculty of Medicine
- Introduction of molecular genetic diagnosis in syndromes with a hearing defect1998 | Second Faculty of Medicine
- New WHO classification of lung tumours2016 | Faculty of Medicine in Pilsen
- Midline defect of facial skeleton, pigment naevi and growth failure - interactive case-report2011 | Faculty of Medicine in Hradec Králové
- Monitoring of the expensive pneumooncological first-line treatment of the advanced non-small cell lung cancer in the TULUNG register in the Czech Republic2017 | Faculty of Medicine in Hradec Králové, Second Faculty of Medicine, Faculty of Medicine in Pilsen
- Genetically Determined Forms of Nephrotic Syndrome in Children2009 | Second Faculty of Medicine
- Congenital muscular dystrophies +12012 | Second Faculty of Medicine
- Systemic mastocytosis2009 | Third Faculty of Medicine
- Neonatal Screening for Cystic Fibrosis (Review)2005 | Second Faculty of Medicine, Third Faculty of Medicine
- Nález patogenní varianty genu PALB2 v rodině sledované pro nefrogenní diabetes insipidus2018 | Faculty of Medicine in Pilsen
- Tuberculosis from surgical point of viewPublication without faculty affiliation
- CANVAS - a newly identified genetic cause of late-onset ataxia. Description of the first cases in the Czech Republic2021 | First Faculty of Medicine, Second Faculty of Medicine
- Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation2010 | First Faculty of Medicine
- Current Diagnostic Strategies and Overview of Preimplantation, Prenatal and Postnatal DNA Diagnostics of Cystic Fibrosis in the Czech Republic2008 | Second Faculty of Medicine, Third Faculty of Medicine
- Congenital developmental defects of the skin2017 | Publication without faculty affiliation
- Modern diagnosis of lung cancer - a task for close multidisciplinary cooperation2011 | Faculty of Medicine in Hradec Králové
- Interdisciplinary consensus for predictive testing of activation mutations of the epidermal growth factor receptor (EGFR) in non-small cell lung cancer2011 | Faculty of Medicine in Hradec Králové, Central Library of Charles University, First Faculty of Medicine
- Substitution in the promoter region ofthe CYP21 affects a phenotype ofthe disease in patients with 21-hydroxylase deficiency2009 | Third Faculty of Medicine
- Diagnostics algorithm of muscular dystrophies2019 | Second Faculty of Medicine