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Heart Rhythm|February 4, 2009
A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndromeLia Crotti, Marzena A Lewandowska, Peter J Schwartz, et al.
European Heart Journal|May 16, 2024
Long QT syndrome: importance of reassessing arrhythmic risk after treatment initiationVeronica Dusi, Federica Dagradi, Carla Spazzolini, et al.
International Journal of Cardiology|November 29, 2017
Cardiac arrest and Brugada syndrome: Is drug-induced type 1 ECG pattern always a marker of low risk?Pietro Delise, Giuseppe Allocca, Nadir Sitta, et al.
European Heart Journal|June 4, 2018
For neonatal ECG screening there is no reason to relinquish old Bazett's correctionMarco Stramba-Badiale, Dilip R Karnad, Karine M Goulene, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|July 15, 2025
TP-fusion at peak exercise: a novel marker for the recognition of unsuspected long QT syndrome patientsCarlo Boeri, Patrizio Sarto, Paolo Cerea, et al.
Stem Cell Research|April 21, 2018
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 geneManuela Mura, Yee-Ki Lee, Monia Ginevrino, et al.
JACC. Clinical Electrophysiology|March 25, 2022
Left Cardiac Sympathetic Denervation for Long QT Syndrome: 50 Years' Experience Provides Guidance for ManagementVeronica Dusi, Luigi Pugliese, Gaetano M De Ferrari, et al.
Heart Rhythm|October 4, 2024
Frequency of and outcomes associated with nonadherence to guideline-based recommendations for an implantable cardioverter-defibrillator in patients with congenital long QT syndromeRaquel Neves, Lia Crotti, Sahej Bains, et al.
Journal of the American College of Cardiology|July 31, 2012
Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testingLia Crotti, Cherisse A Marcou, David J Tester, et al.
Heart Rhythm|February 18, 2012
Torsades de pointes following acute myocardial infarction: evidence for a deadly link with a common genetic variantLia Crotti, Dan Hu, Hector Barajas-Martinez, et al.
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