- Anderson-Fabry disease and gastrointestinal tract involvement2020 | First Faculty of Medicine
- Anderson-Fabry disease2013 | First Faculty of Medicine
- Study of urinary proteomes in Anderson-Fabry disease2010 | First Faculty of Medicine
- Onset and progression of the Anderson-Fabry disease related cardiomyopathy2008 | First Faculty of Medicine, Third Faculty of Medicine
- Early cardiac changes in children with Anderson-Fabry disease2013 | First Faculty of Medicine
- The Role of Cardiac Imaging in the Diagnosis and Management of Anderson-Fabry Disease2019 | First Faculty of Medicine
- The heart in Anderson-Fabry disease and other lysosomal storage disorders2007 | First Faculty of Medicine
- Natural history of the respiratory involvement in Anderson-Fabry disease2007 | First Faculty of Medicine
- Cardiac manifestations of Anderson-Fabry disease: results from the international Fabry outcome survey2007 | First Faculty of Medicine
- Study of urinary proteomes in Anderson-Fabry disease2010 | Faculty of Science, Faculty of Physical Education and Sport, First Faculty of Medicine
- Serial ECG, Echocardiography and Holter monitoring in children with Anderson-Fabry disease.Publication without faculty affiliation
- A unique case of extensive myocardial late iodine enhancement on CT in Anderson-Fabry disease2023 | First Faculty of Medicine
- Standard ECG for differential diagnosis between Anderson-Fabry disease and hypertrophic cardiomyopathy2022 | First Faculty of Medicine
- Anderson-Fabry disease: No histological signs of pathological accumulation in arterial and venous endothelium during pegunigalsidase alfa therapy2021 | First Faculty of Medicine
- Misdiagnosis of Anderson Fabry disease: data from FOS - the Fabry Outcome SurveyPublication without faculty affiliation
- Anderson - Fabry Disease Homozygosity: Rare Case of Late-Onset VariantPublication without faculty affiliation
- Preliminary results of screening in Anderson-Fabry Disease (AF) in patients on chronic hemodialysis (HD) in the Czech republicSecondary causes of membranous glomerulonephritis +1Publication without faculty affiliation
- Rheumatological misdiagnosis of Anderson-Fabry disease, a treatable lysosomal storage disorder - Data from the European Fabry Outcome Survey (2)Publication without faculty affiliation
- Rheumatological misdiagnosis of Anderson-Fabry disease, a treatable lysosomal storage disorder - Data from the European Fabry Outcome Survey (1)Publication without faculty affiliation
- Effect of enzyme replacement therapy with agalsidase alfa on left ventricular mass in patients with Anderson Fabry disease: two-year results from FOS- the Fabry Outcome SurveyPublication without faculty affiliation
- Effect of enzyme replacement therapy with agalsidase alfa on left ventricular mass in patients with Anderson Fabry disease: two-year results from FOS - the Fabry Outcome SurveyPublication without faculty affiliation
- Common presentation of rare diseases: Left ventricular hypertrophy and diastolic dysfunction2018 | First Faculty of Medicine
- peliminary results of the screening Anderson-Fabry deisease in patients in regular dialysed treatment in Czech RepublicPublication without faculty affiliation
- Conundrum of implantable electric devices in Anderson-Fabry cardiomyopathy2019 | First Faculty of Medicine
- Screening of Fabry disease in patients with an implanted permanent pacemaker2023 | First Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University, Faculty of Medicine in Hradec Králové