- Non-sarcomeric hypertrophic cardiomyopathies in adults2011 | First Faculty of Medicine
- Which conformation of the MM-CK molecule is responsible for a strong bond in the M-line of sarcomere?Publication without faculty affiliation
- Simulation of some dynamic properties of sarcomere inside the cardiomyocyte2000 | First Faculty of Medicine
- Model of intracelellar calcium dynamics of cardiomyocyte including sarcomere contractility2001 | First Faculty of Medicine
- Genetic screening of patients for mutations in sarcomeric genes resposible for hypertrophic cardiomyopathy, prelminary resultsPublication without faculty affiliation
- Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in ACTN22023 | Faculty of Science
- Hypertrophic cardiomyopathy - Molecular genetic analysis of exons 9 and 11 of the TNNT2 gene in Czech patients2006 | Faculty of Science
- Low Prevalence and Variable Clinical Presentation of Troponin I and Troponin T Gene Mutations in Hypertrophic Cardiomyopathy2009 | Third Faculty of Medicine
- Low Prevalence and Variable Clinical Presentation of Troponin I and Troponin T Gene Mutations in Hypertrophic Cardiomyopathy2009 | Publication without faculty affiliation
- The effects of candesartan on left ventricular hypertrophy and function in nonobstructive hypertrophic cardiomyopathy2009 | Third Faculty of Medicine
- Genetic testing in patients with hypertrophic cardiomyopathy +12021 | Publication without faculty affiliation
- Usefulness of Alcohol Septal Ablation in the Left Ventricular Outflow Tract Obstruction in Fabry Disease Cardiomyopathy2021 | First Faculty of Medicine
- Is Hypertrophic Cardiomyopathy Always a Familial and Inherited Disease?2023 | Publication without faculty affiliation
- Sequence analysis of myozenin 2 in 438 European patients with familial hypertrophic cardiomyopathy2008 | Publication without faculty affiliation
- Variants in miRNA Regulating Cardiac Growth Are Not a Common Cause of Hypertrophic Cardiomyopathy2015 | Faculty of Science, Third Faculty of Medicine
- Cellular mechanisms of myocardial depression in porcine septic shock2018 | Faculty of Medicine in Pilsen
- PRKAG2 syndrome as a highly arrhythmogenic eventuality in the differential diagnosis of hypertrophic cardiomyopathy - an example of two families with a confirmed causative DNA variant2023 | Second Faculty of Medicine, Central Library of Charles University
- Genetics of hypertrophic cardiomyopathy2008 | Publication without faculty affiliation
- Common presentation of rare diseases: Left ventricular hypertrophy and diastolic dysfunction2018 | First Faculty of Medicine
- Molecular genetic in hypertrophic cardiomyopathy2007 | Third Faculty of Medicine
- Clinical and morphological variables influencing the results of genetic testing of patients with hypertrophic cardiomyopathy2014 | Publication without faculty affiliation
- Congenital-infantile fibrosarcoma: A clinicopathological study of five patients entered on the Prague Children s Tumor Registry1996 | Second Faculty of Medicine
- Fibrosis and expression of extracellular matrix proteins in human interventricular septum in aortic valve stenosis and regurgitation2024 | First Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University, Faculty of Physical Education and Sport
- Molecular Remodeling of Left and Right Ventricular Myocardium in Chronic Anthracycline Cardiotoxicity and Post-Treatment Follow Up2014 | Faculty of Pharmacy in Hradec Králové, Faculty of Medicine in Hradec Králové
- New Developments in Hypertrophic Cardiomyopathy2017 | Publication without faculty affiliation
- HNK-1 in Morphological Study of Development of the Cardiac Conduction System in Selected Groups of Sauropsida2019 | First Faculty of Medicine
- Spectrum and clinical manifestations of mutations in genes responsible for hypertrophic cardiomyopathy2012 | Third Faculty of Medicine
- Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry2023 | First Faculty of Medicine
- The prevalence of genetic variations in patients with hypertrophic and dilated cardiomyopathyPublication without faculty affiliation