Total number of publications: 23
2022
-
Inherited arrhythmias: from gene variants to ionic channel dysfunctions
Year: 2022, type:
-
Translational research in the field of inherited arrhythmias
Year: 2022, type: Conference abstract
-
Změny v elektrické aktivitě varianty Y4734C-RYR2 asociované s idiopatickou fibrilací komor.
Year: 2022, type: Conference abstract
2021
-
Clinical, genetic and functional analysis of R562S-Kv7.1 mutation associated with long QT syndrome type 1
Year: 2021, type: Conference abstract
-
Dysfunkce na podkladě mutace R562S asociované se syndromem dlouhého QT typu 1
Year: 2021, type: Conference abstract
-
Long-QT founder variant T309I-Kv7.1 with dominant negative pattern may predispose delayed afterdepolarizations under β-adrenergic stimulation
Nature Scientific Reports, year: 2021, volume: 11, edition: 1, DOI
2020
-
Out-of-Hospital Cardiac Arrest Due to Ventricular Fibrillation in a 5-Year-Old Pediatric Patient
PEDIATRIC EMERGENCY CARE, year: 2020, volume: 36, edition: 7, DOI
2019
-
Molecular analysis confirmed common ancestor of 10 Czech families with long QT syndrome carrying C926T-KCNQ1 variant
Year: 2019, type: Conference abstract
-
Mutace T309I asociovaná se syndromem dlouhého QT typu 1: akumulace IKs jako mechanismus ochrany srdce proti arytmii
Year: 2019, type: Conference abstract
-
Mutation R591C associated with long QT syndrome type 1: clinical, genetic, and functional analysis
Year: 2019, type: Conference abstract