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Polymorfní komorová tachykardie
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publication
Clinical characteristics of three Czech families with catecholaminergic polymorphic ventricular tachycardia and pilot results of RyR2 gene mutation analysis
2010 |
First Faculty of Medicine, Faculty of Physical Education and Sport
publication
The role of genetic examination in the diagnosis of causes of circulatory arrest in a young patient without structural heart disease
2019 |
Second Faculty of Medicine
publication
Inherited arrhythmias
+1
2008 |
Faculty of Medicine in Hradec Králové
publication
Case Study of Asymptomatic Long QT Syndrome Detected with Preparticipation Screening
2011 |
Second Faculty of Medicine
publication
Genetic causes of sudden infant death syndrome in the era of next generation sequencing. Review
2020 |
First Faculty of Medicine, Third Faculty of Medicine
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Inherited arrhythmic syndromes in children
2020 |
Central Library of Charles University
publication
ECG ruler for graphic screening of corrected QT interval prolongation
2013 |
Second Faculty of Medicine