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Lia Crotti

Showing results (61-70 of 245) with videos related to

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Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 7, 2016
Time, frequency and information domain analysis of heart period and QT variability in asymptomatic long QT syndrome type 2 patientsVlasta Bari, Giulia Girardengo, Andrea Marchi, et al.
Human Genetics|October 21, 2010
Gene symbol: KCNH2. Disease: Long QT syndromeLia Crotti, M Pedrazzini, R Insolia, et al.
Oxidative Medicine and Cellular Longevity|February 17, 2016
Novel Perspectives in Redox Biology and Pathophysiology of Failing Myocytes: Modulation of the Intramyocardial Redox Milieu for Therapeutic Interventions-A Review Article from the Working Group of Cardiac Cell Biology, Italian Society of CardiologyAlessia Arcaro, Flora Pirozzi, Annalisa Angelini, et al.
Human Genetics|October 21, 2010
Gene symbol: KCNQ1. Disease: Long QT syndromeLia Crotti, C Ferrandi, M Pedrazzini, et al.
Epilepsia|February 7, 2008
Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutationNeeti Hindocha, Lina Nashef, Frances Elmslie, et al.
Circulation. Genomic and Precision Medicine|April 2, 2021
Importance of Dedicated Units for the Management of Patients With Inherited Arrhythmia SyndromesGiulio Conte, Arthur Wilde, Elijah R Behr, et al.
Journal of the American Heart Association|June 25, 2014
Arrhythmogenic calmodulin mutations disrupt intracellular cardiomyocyte Ca2+ regulation by distinct mechanismsGuo Yin, Faisal Hassan, Ayman R Haroun, et al.
Human Genetics|October 21, 2010
Gene symbol: KCNH2. Disease: Long QT syndromeLia Crotti, L Crotti, M Pedrazzini, et al.
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.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 9, 2015
Filtering approach based on empirical mode decomposition improves the assessment of short scale complexity in long QT syndrome type 1 populationVlasta Bari, Andrea Marchi, Giulia Girardengo, et al.
Pageof 25

Showing results (61-70 of 245) with videos related to

Sort By:
Pageof 25
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 7, 2016
Time, frequency and information domain analysis of heart period and QT variability in asymptomatic long QT syndrome type 2 patientsVlasta Bari, Giulia Girardengo, Andrea Marchi, et al.
Human Genetics|October 21, 2010
Gene symbol: KCNH2. Disease: Long QT syndromeLia Crotti, M Pedrazzini, R Insolia, et al.
Oxidative Medicine and Cellular Longevity|February 17, 2016
Novel Perspectives in Redox Biology and Pathophysiology of Failing Myocytes: Modulation of the Intramyocardial Redox Milieu for Therapeutic Interventions-A Review Article from the Working Group of Cardiac Cell Biology, Italian Society of CardiologyAlessia Arcaro, Flora Pirozzi, Annalisa Angelini, et al.
Human Genetics|October 21, 2010
Gene symbol: KCNQ1. Disease: Long QT syndromeLia Crotti, C Ferrandi, M Pedrazzini, et al.
Epilepsia|February 7, 2008
Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutationNeeti Hindocha, Lina Nashef, Frances Elmslie, et al.
Circulation. Genomic and Precision Medicine|April 2, 2021
Importance of Dedicated Units for the Management of Patients With Inherited Arrhythmia SyndromesGiulio Conte, Arthur Wilde, Elijah R Behr, et al.
Journal of the American Heart Association|June 25, 2014
Arrhythmogenic calmodulin mutations disrupt intracellular cardiomyocyte Ca2+ regulation by distinct mechanismsGuo Yin, Faisal Hassan, Ayman R Haroun, et al.
Human Genetics|October 21, 2010
Gene symbol: KCNH2. Disease: Long QT syndromeLia Crotti, L Crotti, M Pedrazzini, et al.
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.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 9, 2015
Filtering approach based on empirical mode decomposition improves the assessment of short scale complexity in long QT syndrome type 1 populationVlasta Bari, Andrea Marchi, Giulia Girardengo, et al.
Pageof 25