- congenital and genetic causes and molecular genetic examination nephropathy and uropathy2013 | Second Faculty of Medicine
- Complex morphological and molecular genetic examination of amelogenesis imperfecta: A case presentation of two Czech siblings with a non-syndrome form of the disease2014 | Second Faculty of Medicine
- Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A2007 | Faculty of Medicine in Hradec Králové
- Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A2007 | Faculty of Medicine in Hradec Králové, Central Library of Charles University
- Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A2007 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Central Library of Charles University, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A2007 | First Faculty of Medicine
- Implication of molecular genetic examination in a Ihree generational family with multiple endoerine neoplasia type 2A2007 | First Faculty of Medicine, Second Faculty of Medicine
- Molecular Genetic Testing of Diabetes Insipidus Renalis2019 | Faculty of Medicine in Pilsen
- Introduction of molecular genetic diagnosis in syndromes with a hearing defect1998 | Second Faculty of Medicine
- Monogenic forms of diabetes: they are more common than we have thought so far2014 | Second Faculty of Medicine
- Biochemical nad molecular characteristics in 11 czech children with tyrosinemia type I2010 | First Faculty of Medicine
- 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 Pilsen, Faculty of Medicine in Hradec Králové, Second Faculty of Medicine
- Diagnostics algorithm of muscular dystrophies2019 | Second Faculty of Medicine
- Léri-Weill Syndrome on the Principle of Structural Aberration of Chromosome Y (Case Report)2018 | Faculty of Medicine in Pilsen
- 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
- Next generation sequencing and the molecular tumor board from the point of view of oncologists2021 | First Faculty of Medicine
- Current perspectives on the aetiology of tall stature in children and adolescents (1): Syndromes associated with tall stature2022 | Second Faculty of Medicine
- We have a daughter or not? Androgen insensivity syndrome2014 | First Faculty of Medicine
- Acute lymphoblastic leukemia in a child with Leri-Weill syndrome and complete SHOX gene deletion: A Case Report2018 | Second Faculty of Medicine
- Total Knee Arthroplasty in Severe Valgus Deformity in a Patient with Achondroplasia2011 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Stomatological Problems in Child with the II Type Mucopolysaccharidosis2013 | Faculty of Medicine in Pilsen
- Fabry's disease from the point of view of nephrology2015 | First Faculty of Medicine
- Molecular classification of endometrial cancers translated into practice2021 | Faculty of Medicine in Pilsen
- Increased frequency of deltaF508 mutation carriers in men with non-obstructive azoospermia1999 | Second Faculty of Medicine
- The first Obesity Unit in Czechoslovakia was established twenty years ago2009 | Third Faculty of Medicine
- Acute myeloid leukemia in children2015 | Second Faculty of Medicine
- Neonatal hyperbilirubinemia in a Vietnamese child - case report2020 | First Faculty of Medicine
- Wiskott-Aldrich Syndrome - Disease Requiring Early Transplantation of Hemopoietic Stem Cells2009 | Central Library of Charles University, Second Faculty of Medicine
- Novel FBN1 gene mutation and maternal germinal mosaicism as the cause of neonatal form of Marfan syndrome2014 | First Faculty of Medicine
- Unique presentation of LHON/MELAS overlap syndrome caused by m.13046T > C in MTND52016 | First Faculty of Medicine, Second Faculty of Medicine