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Lia Crotti

Showing results (71-80 of 246) with videos related to

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Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: SCN5A. Disease: Brugada SyndromeLia Crotti, M Pedrazzini, R Insolia, et al.
Human Genetics|October 21, 2010
Gene symbol: SCN5A. Disease: Brugada syndromeLia Crotti, M Pedrazzini, R Insolia, et al.
Human Genetics|October 21, 2010
Gene symbol: SCN5A. Disease: Brugada syndromeLia Crotti, C Ferrandi, M Pedrazzini, et al.
Stem Cell Research|December 1, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi006-A from a patient affected by an autosomal recessive form of long QT syndrome type 1Manuela Mura, Francesca Bastaroli, Marzia Corli, et al.
Human Genetics|October 21, 2010
Gene symbol: KCNH2. Disease: Long QT syndromeLia Crotti, M Pedrazzini, C Ferrandi, et al.
Stem Cell Research|April 24, 2018
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1Manuela Mura, Monia Ginevrino, Rita Zappatore, et al.
Scientific Reports|February 27, 2016
Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathiesMaryam Fish, Gasnat Shaboodien, Sarah Kraus, et al.
Scientific Reports|May 19, 2016
Corrigendum: Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathiesMaryam Fish, Gasnat Shaboodien, Sarah Kraus, et al.
Journal of Proteome Research|February 3, 2026
Metabolic Adaptation during Cardiac Exercise Rehabilitation in Patients after a First Myocardial InfarctionEleonora Bossi, Marta Nobile, Federico Paoletti, et al.
Cardiovascular Research|February 16, 2020
NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesisCarlotta Ronchi, Joyce Bernardi, Manuela Mura, et al.
Pageof 25

Showing results (71-80 of 246) with videos related to

Sort By:
Pageof 25
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: SCN5A. Disease: Brugada SyndromeLia Crotti, M Pedrazzini, R Insolia, et al.
Human Genetics|October 21, 2010
Gene symbol: SCN5A. Disease: Brugada syndromeLia Crotti, M Pedrazzini, R Insolia, et al.
Human Genetics|October 21, 2010
Gene symbol: SCN5A. Disease: Brugada syndromeLia Crotti, C Ferrandi, M Pedrazzini, et al.
Stem Cell Research|December 1, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi006-A from a patient affected by an autosomal recessive form of long QT syndrome type 1Manuela Mura, Francesca Bastaroli, Marzia Corli, et al.
Human Genetics|October 21, 2010
Gene symbol: KCNH2. Disease: Long QT syndromeLia Crotti, M Pedrazzini, C Ferrandi, et al.
Stem Cell Research|April 24, 2018
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1Manuela Mura, Monia Ginevrino, Rita Zappatore, et al.
Scientific Reports|February 27, 2016
Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathiesMaryam Fish, Gasnat Shaboodien, Sarah Kraus, et al.
Scientific Reports|May 19, 2016
Corrigendum: Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathiesMaryam Fish, Gasnat Shaboodien, Sarah Kraus, et al.
Journal of Proteome Research|February 3, 2026
Metabolic Adaptation during Cardiac Exercise Rehabilitation in Patients after a First Myocardial InfarctionEleonora Bossi, Marta Nobile, Federico Paoletti, et al.
Cardiovascular Research|February 16, 2020
NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesisCarlotta Ronchi, Joyce Bernardi, Manuela Mura, et al.
Pageof 25