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Search for publications relevant for "Catecholaminergic Polymorphic Ventricular Tachycardia"
Catecholaminergic Polymorphic Ventricular Tachycardia
Publication
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A Classic Electrocardiographic Manifestation of Catecholaminergic Polymorphic Ventricular Tachycardia
2012 |
Central Library of Charles University
publication
Flecainide Is Associated With a Lower Incidence of Arrhythmic Events in a Large Cohort of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
2023 |
Publication without faculty affiliation
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The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registry
2018 |
Publication without faculty affiliation
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An International Multi-Center Cohort Study on β-blockers for the Treatment of Symptomatic Children with Catecholaminergic Polymorphic Ventricular Tachycardia
2022 |
Publication without faculty affiliation
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An Evaluation of Age at Symptom-Onset, Proband Status and Sex as Predictors of Disease Severity in Pediatric Catecholaminergic Polymorphic Ventricular Tachycardia
2021 |
Publication without faculty affiliation
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Catecholaminergic Polymorphic Ventricular Tachycardia in Children Analysis of Therapeutic Strategies and Outcomes From an International Multicenter Registry
2015 |
Publication without faculty affiliation
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Clinical Characteristics and Mutational Analysis of the RyR2 Gene in Seven Czech Families with Catecholaminergic Polymorphic Ventricular Tachycardia
2012 |
Publication without faculty affiliation
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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
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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
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Inherited arrhythmic syndromes in children
2020 |
Central Library of Charles University
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Genetic causes of sudden infant death syndrome in the era of next generation sequencing. Review
2020 |
First Faculty of Medicine, Third Faculty of Medicine