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Nature Communications|February 4, 2026
Two-step voltage-sensor activation of the human KV7.4 channel and effect of a deafness-associated mutationMario Nappi, Damon J A Frampton, Ali S Kusay, et al.Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|February 13, 2013
Arrhythmogenic right ventricular cardiomyopathy mimics: role of cardiovascular magnetic resonanceGiovanni Quarta, Syed I Husain, Andrew S Flett, et al.The Journal of General Physiology|October 26, 2021
Suppression of ventricular arrhythmias by targeting late L-type Ca2+ currentMarina Angelini, Arash Pezhouman, Nicoletta Savalli, et al.The Journal of Physiology|October 26, 2023
Two epilepsy-associated variants in KCNA2 (KV 1.2) at position H310 oppositely affect channel functional expressionTeresa Mínguez-Viñas, Varsha Prakash, Kaiqian Wang, et al.Circulation|January 18, 2006
Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathyPetros Syrris, Deirdre Ward, Angeliki Asimaki, et al.European Heart Journal|November 20, 2012
Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and CanadaAnnika F M Haywood, Nancy D Merner, Kathy A Hodgkinson, et al.Nature Communications|May 16, 2026
The four voltage-sensing domains of T-type calcium channels activate near the resting membrane potentialMarina Angelini, Moira McVicar, Savana Maxfield, et al.Journal of Cardiovascular Medicine (Hagerstown, Md.)|May 1, 2026
Pregnancy in the broad phenotype and genotype spectrum of disease-causing desmosomal variant-positive womenSilvia Castelletti, Annina S Vischer, Rachel Bastiaenen, et al.International Journal of Cardiology|May 21, 2019
Risk score for the exclusion of arrhythmic events in arrhythmogenic right ventricular cardiomyopathy at first presentationAnnina S Vischer, Silvia Castelletti, Petros Syrris, et al.Pageof 5