Publications
- Gene variants at FTO, 9p21, and 2q36.3 are age-independently associated with myocardial infarction in Czech men2016 | First Faculty of Medicine
- Characterization of Early Disease Status in Treatment-Naive Male Paediatric Patients with Fabry Disease Enrolled in a Randomized Clinical Trial2015 | First Faculty of Medicine
- Anderson-Fabry disease2013 | First Faculty of Medicine
- Fabry disease - more common than you think2011 | First Faculty of Medicine
- CCAAT/Enhancer-Binding Protein alpha (CEBPA) Polymorphisms and Mutations in Healthy Individuals and in Patients with Peripheral Artery Disease, Ischaemic Heart Disease and Hyperlipidaemia2010 | First Faculty of Medicine
- Association of bilirubin in the blood serum and promoters UGT1A1 gene variants with atherosclerosis.Publication without faculty affiliation
- Genetic screening of patients for mutations in sarcomeric genes resposible for hypertrophic cardiomyopathy, prelminary resultsPublication without faculty affiliation
- Variations of the Saphenopopliteal Junction: An Ultrasonography Study in a Young Population, A Systematic Review and A Meta-Analysis2024 | First Faculty of Medicine, Second Faculty of Medicine
- Missed diagnosis of Fabry disease: should we screen patients with multiple sclerosis?2024 | First Faculty of Medicine
- Screening of Fabry disease in patients with an implanted permanent pacemaker2023 | First Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Hradec Králové, Central Library of Charles University
Loading network view...