Rezultati pretrage autora

1

QTc Behavior During Exercise and Genetic Testing for the Long-QT Syndrome od Peter J. Schwartz, Lia Crotti

Izdano 2011

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Long-QT Syndrome od Peter J. Schwartz, Lia Crotti, Roberto Insolia

Izdano 2012

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Modifier genes for sudden cardiac death od Peter J. Schwartz, Lia Crotti, Alfred L. George

Izdano 2018

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Long QT Syndrome: From Genetics to Management od Schwartz, Peter J., MD, Lia Crotti, Insolia, Roberto

Izdano 2012

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Congenital long QT syndrome od Lia Crotti, Giuseppe G. A. Celano, Federica Dagradi, Peter J. Schwartz

Izdano 2008

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6

The Elusive Link Between LQT3 and Brugada Syndrome od Silvia G. Priori, Carlo Napolitano, Peter J. Schwartz, Raffaella Bloise, Lia Crotti, E Ronchetti

Izdano 2000

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7

Adenosine and the Cardiovascular System: The Good and the Bad od Régis Guieu, Jean‐Claude Deharo, Baptiste Maille, Lia Crotti, Ermino Torresani, Michele Brignole, Gianfranco Parati

Izdano 2020

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Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome od Federica Dagradi, Carla Spazzolini, Silvia Castelletti, Matteo Pedrazzini, Maria‐Christina Kotta, Lia Crotti, Peter J. Schwartz

Izdano 2020

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From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2 od Peter J. Schwartz, Massimiliano Gnecchi, Federica Dagradi, Silvia Castelletti, Gianfranco Parati, Carla Spazzolini, Luca Sala, Lia Crotti

Izdano 2019

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10

Mexiletine Shortens the QT Interval in Patients With Potassium Channel–Mediated Type 2 Long QT Syndrome od J. Martijn Bos, Lia Crotti, Ram K. Rohatgi, Silvia Castelletti, Federica Dagradi, Peter J. Schwartz, Michael J. Ackerman

Izdano 2019

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11

Autonomic Control of Heart Rate and QT Interval Variability Influences Arrhythmic Risk in Long QT Syndrome Type 1 od Alberto Porta, Giulia Girardengo, Vlasta Bari, Alfred L. George, Paul A. Brink, Althea Goosen, Lia Crotti, Peter J. Schwartz

Izdano 2015

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Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation od Neeti Hindocha, Lina Nashef, Frances Elmslie, Rachael Birch, Sameer M. Zuberi, Ammar Al‐Chalabi, Lia Crotti, Peter J. Schwartz, Andrew Makoff

Izdano 2008

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13

Arrhythmogenic Calmodulin Mutations Disrupt Intracellular Cardiomyocyte Ca 2+ Regulation by Distinct Mechanisms od Yin Guo, Faisal Hassan, Ayman R. Haroun, Lisa L. Salazar Murphy, Lia Crotti, Peter J. Schwartz, Alfred L. George, Jonathan Satin

Izdano 2014

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14

Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathies od Maryam Fish, Gasnat Shaboodien, Sarah Kraus, Karen Sliwa, Christine E. Seidman, Michael A. Burke, Lia Crotti, Peter J. Schwartz, Bongani M. Mayosi

Izdano 2016

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15

From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies od Lia Crotti, Pedro Brugada, Hugh Calkins, Philippe Chevalier, Giulio Conte, Gherardo Finocchiaro, Pieter G. Postema, Vincent Probst, Peter J. Schwartz, Elijah R. Behr

Izdano 2023

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16

Long QT syndrome: importance of reassessing arrhythmic risk after treatment initiation od Veronica Dusi, Federica Dagradi, Carla Spazzolini, Lia Crotti, Paolo Cerea, Fulvio L F Giovenzana, Giulia Musu, Matteo Pedrazzini, Margherita Torchio, Peter J. Schwartz

Izdano 2024

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17

NOS1AP Is a Genetic Modifier of the Long-QT Syndrome od Lia Crotti, Maria Cristina Monti, Roberto Insolia, Anna L. Peljto, Althea Goosen, Paul A. Brink, David A. Greenberg, Peter J. Schwartz, Alfred L. George

Izdano 2009

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18

Transient outward current (Ito) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndrome od John R. Giudicessi, Dan Ye, David J. Tester, Lia Crotti, Alessandra Mugione, Vladislav V. Nesterenko, Richard M. Albertson, Charles Antzelevitch, Peter J. Schwartz, Michael J. Ackerman

Izdano 2011

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19

Identification of a targeted and testable antiarrhythmic therapy for long-QT syndrome type 2 using a patient-specific cellular model od Ashish Mehta, Chrishan J. A. Ramachandra, Pritpal Singh, Anuja Chitre, Chong Hui Lua, Manuela Mura, Lia Crotti, Philip Wong, Peter J. Schwartz, Massimiliano Gnecchi, Winston Shim

Izdano 2017

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20

Contemporary genetic testing in inherited cardiac disease od Francesca Girolami, Giulia Frisso, Matteo Benelli, Lia Crotti, Maria Iascone, Ruggiero Mango, Cristina Mazzaccara, Kalliopi Pilichou, Eloisa Arbustini, Benedetta Tomberli, Giuseppe Limongelli, Cristina Basso, Iacopo Olivotto

Izdano 2017

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QTc Behavior During Exercise and Genetic Testing for the Long-QT Syndrome od Peter J. Schwartz, Lia Crotti

Long-QT Syndrome od Peter J. Schwartz, Lia Crotti, Roberto Insolia

Modifier genes for sudden cardiac death od Peter J. Schwartz, Lia Crotti, Alfred L. George

Long QT Syndrome: From Genetics to Management od Schwartz, Peter J., MD, Lia Crotti, Insolia, Roberto

Congenital long QT syndrome od Lia Crotti, Giuseppe G. A. Celano, Federica Dagradi, Peter J. Schwartz

The Elusive Link Between LQT3 and Brugada Syndrome od Silvia G. Priori, Carlo Napolitano, Peter J. Schwartz, Raffaella Bloise, Lia Crotti, E Ronchetti

Adenosine and the Cardiovascular System: The Good and the Bad od Régis Guieu, Jean‐Claude Deharo, Baptiste Maille, Lia Crotti, Ermino Torresani, Michele Brignole, Gianfranco Parati

Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome od Federica Dagradi, Carla Spazzolini, Silvia Castelletti, Matteo Pedrazzini, Maria‐Christina Kotta, Lia Crotti, Peter J. Schwartz

From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2 od Peter J. Schwartz, Massimiliano Gnecchi, Federica Dagradi, Silvia Castelletti, Gianfranco Parati, Carla Spazzolini, Luca Sala, Lia Crotti

Mexiletine Shortens the QT Interval in Patients With Potassium Channel–Mediated Type 2 Long QT Syndrome od J. Martijn Bos, Lia Crotti, Ram K. Rohatgi, Silvia Castelletti, Federica Dagradi, Peter J. Schwartz, Michael J. Ackerman

Autonomic Control of Heart Rate and QT Interval Variability Influences Arrhythmic Risk in Long QT Syndrome Type 1 od Alberto Porta, Giulia Girardengo, Vlasta Bari, Alfred L. George, Paul A. Brink, Althea Goosen, Lia Crotti, Peter J. Schwartz

Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an <i>SCN1A</i> mutation od Neeti Hindocha, Lina Nashef, Frances Elmslie, Rachael Birch, Sameer M. Zuberi, Ammar Al‐Chalabi, Lia Crotti, Peter J. Schwartz, Andrew Makoff

Arrhythmogenic Calmodulin Mutations Disrupt Intracellular Cardiomyocyte Ca <sup>2+</sup> Regulation by Distinct Mechanisms od Yin Guo, Faisal Hassan, Ayman R. Haroun, Lisa L. Salazar Murphy, Lia Crotti, Peter J. Schwartz, Alfred L. George, Jonathan Satin

From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies od Lia Crotti, Pedro Brugada, Hugh Calkins, Philippe Chevalier, Giulio Conte, Gherardo Finocchiaro, Pieter G. Postema, Vincent Probst, Peter J. Schwartz, Elijah R. Behr

Long QT syndrome: importance of reassessing arrhythmic risk after treatment initiation od Veronica Dusi, Federica Dagradi, Carla Spazzolini, Lia Crotti, Paolo Cerea, Fulvio L F Giovenzana, Giulia Musu, Matteo Pedrazzini, Margherita Torchio, Peter J. Schwartz

<i>NOS1AP</i> Is a Genetic Modifier of the Long-QT Syndrome od Lia Crotti, Maria Cristina Monti, Roberto Insolia, Anna L. Peljto, Althea Goosen, Paul A. Brink, David A. Greenberg, Peter J. Schwartz, Alfred L. George

Contemporary genetic testing in inherited cardiac disease od Francesca Girolami, Giulia Frisso, Matteo Benelli, Lia Crotti, Maria Iascone, Ruggiero Mango, Cristina Mazzaccara, Kalliopi Pilichou, Eloisa Arbustini, Benedetta Tomberli, Giuseppe Limongelli, Cristina Basso, Iacopo Olivotto

Rezultati pretrage - Lia Crotti

QTc Behavior During Exercise and Genetic Testing for the Long-QT Syndrome od Peter J. Schwartz, Lia Crotti

Long-QT Syndrome od Peter J. Schwartz, Lia Crotti, Roberto Insolia

Modifier genes for sudden cardiac death od Peter J. Schwartz, Lia Crotti, Alfred L. George

Long QT Syndrome: From Genetics to Management od Schwartz, Peter J., MD, Lia Crotti, Insolia, Roberto

Congenital long QT syndrome od Lia Crotti, Giuseppe G. A. Celano, Federica Dagradi, Peter J. Schwartz

The Elusive Link Between LQT3 and Brugada Syndrome od Silvia G. Priori, Carlo Napolitano, Peter J. Schwartz, Raffaella Bloise, Lia Crotti, E Ronchetti

Adenosine and the Cardiovascular System: The Good and the Bad od Régis Guieu, Jean‐Claude Deharo, Baptiste Maille, Lia Crotti, Ermino Torresani, Michele Brignole, Gianfranco Parati

Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome od Federica Dagradi, Carla Spazzolini, Silvia Castelletti, Matteo Pedrazzini, Maria‐Christina Kotta, Lia Crotti, Peter J. Schwartz

From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2 od Peter J. Schwartz, Massimiliano Gnecchi, Federica Dagradi, Silvia Castelletti, Gianfranco Parati, Carla Spazzolini, Luca Sala, Lia Crotti

Mexiletine Shortens the QT Interval in Patients With Potassium Channel–Mediated Type 2 Long QT Syndrome od J. Martijn Bos, Lia Crotti, Ram K. Rohatgi, Silvia Castelletti, Federica Dagradi, Peter J. Schwartz, Michael J. Ackerman

Autonomic Control of Heart Rate and QT Interval Variability Influences Arrhythmic Risk in Long QT Syndrome Type 1 od Alberto Porta, Giulia Girardengo, Vlasta Bari, Alfred L. George, Paul A. Brink, Althea Goosen, Lia Crotti, Peter J. Schwartz

Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an <i>SCN1A</i> mutation od Neeti Hindocha, Lina Nashef, Frances Elmslie, Rachael Birch, Sameer M. Zuberi, Ammar Al‐Chalabi, Lia Crotti, Peter J. Schwartz, Andrew Makoff

Arrhythmogenic Calmodulin Mutations Disrupt Intracellular Cardiomyocyte Ca <sup>2+</sup> Regulation by Distinct Mechanisms od Yin Guo, Faisal Hassan, Ayman R. Haroun, Lisa L. Salazar Murphy, Lia Crotti, Peter J. Schwartz, Alfred L. George, Jonathan Satin

From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies od Lia Crotti, Pedro Brugada, Hugh Calkins, Philippe Chevalier, Giulio Conte, Gherardo Finocchiaro, Pieter G. Postema, Vincent Probst, Peter J. Schwartz, Elijah R. Behr

Long QT syndrome: importance of reassessing arrhythmic risk after treatment initiation od Veronica Dusi, Federica Dagradi, Carla Spazzolini, Lia Crotti, Paolo Cerea, Fulvio L F Giovenzana, Giulia Musu, Matteo Pedrazzini, Margherita Torchio, Peter J. Schwartz

<i>NOS1AP</i> Is a Genetic Modifier of the Long-QT Syndrome od Lia Crotti, Maria Cristina Monti, Roberto Insolia, Anna L. Peljto, Althea Goosen, Paul A. Brink, David A. Greenberg, Peter J. Schwartz, Alfred L. George

Contemporary genetic testing in inherited cardiac disease od Francesca Girolami, Giulia Frisso, Matteo Benelli, Lia Crotti, Maria Iascone, Ruggiero Mango, Cristina Mazzaccara, Kalliopi Pilichou, Eloisa Arbustini, Benedetta Tomberli, Giuseppe Limongelli, Cristina Basso, Iacopo Olivotto

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