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Human Genetics
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August 21, 2009
Novel human pathological mutations. Gene symbol: SCN5A. Disease: Brugada Syndrome
Lia Crotti, M Pedrazzini, R Insolia, et al.
Human Genetics
|
October 21, 2010
Gene symbol: SCN5A. Disease: Brugada syndrome
Lia Crotti, M Pedrazzini, R Insolia, et al.
Human Genetics
|
October 21, 2010
Gene symbol: SCN5A. Disease: Brugada syndrome
Lia 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 1
Manuela Mura, Francesca Bastaroli, Marzia Corli, et al.
Human Genetics
|
October 21, 2010
Gene symbol: KCNH2. Disease: Long QT syndrome
Lia 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 1
Manuela 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 cardiomyopathies
Maryam 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 cardiomyopathies
Maryam 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 Infarction
Eleonora Bossi, Marta Nobile, Federico Paoletti, et al.
Cardiovascular Research
|
February 16, 2020
NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis
Carlotta Ronchi, Joyce Bernardi, Manuela Mura, et al.
Page
of 25
Search research articles
Search
Showing results (71-80 of 246) with videos related to
Sort By:
Page
of 25
Human Genetics
|
August 21, 2009
Novel human pathological mutations. Gene symbol: SCN5A. Disease: Brugada Syndrome
Lia Crotti, M Pedrazzini, R Insolia, et al.
Human Genetics
|
October 21, 2010
Gene symbol: SCN5A. Disease: Brugada syndrome
Lia Crotti, M Pedrazzini, R Insolia, et al.
Human Genetics
|
October 21, 2010
Gene symbol: SCN5A. Disease: Brugada syndrome
Lia 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 1
Manuela Mura, Francesca Bastaroli, Marzia Corli, et al.
Human Genetics
|
October 21, 2010
Gene symbol: KCNH2. Disease: Long QT syndrome
Lia 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 1
Manuela 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 cardiomyopathies
Maryam 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 cardiomyopathies
Maryam 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 Infarction
Eleonora Bossi, Marta Nobile, Federico Paoletti, et al.
Cardiovascular Research
|
February 16, 2020
NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis
Carlotta Ronchi, Joyce Bernardi, Manuela Mura, et al.
Page
of 25