Lia Crotti

发表

Filtering approach based on empirical mode decomposition improves the assessment of short scale complexity in long QT syndrome type 1 population

Sergio Cerutti, A. Porta, Vlasta Bari, 2014, 2014 36th Annual International Conference of the IEEE Engineering in Medicine and Biology Society.

Refined multiscale entropy analysis of heart period and QT interval variabilities in long QT syndrome type-1 patients

Pere Caminal, Sergio Cerutti, A. Porta, 2013, 2013 35th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC).

Ion channels and beating heart: the players and the music

Giuseppe Limongelli, Charles Antzelevitch, Lia Crotti, 2011 .

Multiscale Complexity Analysis of Short QT Interval Variability Series Stratifies the Arrhythmic Risk of Long QT Syndrome Type 1 Patients

A. Porta, Vlasta Bari, Beatrice De Maria, 2018, 2018 Computing in Cardiology Conference (CinC).

A Refined Multiscale Self-Entropy Approach for the Assessment of Cardiac Control Complexity: Application to Long QT Syndrome Type 1 Patients

A. Porta, Vlasta Bari, Beatrice De Maria, 2015, Entropy.

Time, frequency and information domain analysis of heart period and QT variability in asymptomatic long QT syndrome type 2 patients

A. Porta, Vlasta Bari, Beatrice De Maria, 2015, 2015 37th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC).

Low-Pass Filtering Approach via Empirical Mode Decomposition Improves Short-Scale Entropy-Based Complexity Estimation of QT Interval Variability in Long QT Syndrome Type 1 Patients

Sergio Cerutti, A. Porta, Vlasta Bari, 2014, Entropy.

Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility

Takeshi Tsuchiya, Thomas Meitinger, Tatsuhiko Tsunoda, 2014, Circulation. Cardiovascular genetics.

A Novel Disease Gene for Brugada SyndromeClinical Perspective

Peter J. Schwartz, Michael John Ackerman, Kiyoshi Nakazawa, 2012 .

Autonomic control of heart rate and QT interval variability influences arrhythmic risk in long QT syndrome type 1.

Alberto Porta, Vlasta Bari, Peter J. Schwartz, 2015, Journal of the American College of Cardiology.

Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

Thomas Meitinger, Peter J. Schwartz, Walter J. Chazin, 2013, Circulation.

Elucidating arrhythmogenic mechanisms of long-QT syndrome CALM1-F142L mutation in patient-specific induced pluripotent stem cell-derived cardiomyocytes

Stefano Severi, Antonio Zaza, Alberto Porta, 2017, Cardiovascular research.

Nature Genetics Advance Online Publication Genetic Association Study of Qt Interval Highlights Role for Calcium Signaling Pathways in Myocardial Repolarization

Michael J Ackerman, Christian Gieger, Thomas Meitinger, 2022 .

Arrhythmogenic Calmodulin Mutations Disrupt Intracellular Cardiomyocyte Ca2+ Regulation by Distinct Mechanisms

Peter J. Schwartz, Alfred L. George, Lia Crotti, 2014, Journal of the American Heart Association.

Prevalence of Long-QT Syndrome Gene Variants in Sudden Infant Death Syndrome

Peter J. Schwartz, Alfred L. George, Lia Crotti, 2007, Circulation.

Multiscale Complexity Analysis of the Cardiac Control Identifies Asymptomatic and Symptomatic Patients in Long QT Syndrome Type 1

Pere Caminal, Sergio Cerutti, Alberto Porta, 2014, PloS one.

The Jervell and Lange-Nielsen Syndrome: Natural History, Molecular Basis, and Clinical Outcome

Lauri Toivonen, Peter J. Schwartz, Minoru Horie, 2006, Archives des maladies du coeur et des vaisseaux.

Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes.

Lia Crotti, Christopher N. Johnson, Nicole Sekarski, 2016, Heart rhythm.

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Dan M Roden, Beverley Balkau, Pierre Lindenbaum, 2013, Nature Genetics.

A Novel Disease Gene for Brugada Syndrome: Sarcolemmal Membrane–Associated Protein Gene Mutations Impair Intracellular Trafficking of hNav1.5

Michael J. Ackerman, Peter J. Schwartz, Kiyoshi Nakazawa, 2012, Circulation. Arrhythmia and electrophysiology.

Long-QT syndrome: from genetics to management.

Lia Crotti, P. Schwartz, L. Crotti, 2012, Circulation. Arrhythmia and electrophysiology.

KCNH2-K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome

Dan M Roden, Alessandro Vicentini, Lia Crotti, 2005, Circulation.

Symbolic analysis of heart period and QT interval variabilities in LQT1 patients

Sergio Cerutti, Alberto Porta, Tito Bassani, 2014 .

Long QT syndrome-associated mutations in intrauterine fetal death.

Michael J Ackerman, Brian Brost, Alice Ghidoni, 2013, JAMA.

Prevalence of the Congenital Long-QT Syndrome

Fabio Mosca, Peter J. Schwartz, Marco Stramba-Badiale, 2009, Circulation.

Cardiac potassium channel dysfunction in sudden infant death syndrome.

Dan M Roden, Carlos G Vanoye, Lia Crotti, 2007, Journal of molecular and cellular cardiology.