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Circulation. Arrhythmia and Electrophysiology
|
May 25, 2016
Inverted U-Shaped Relation Between the Risk of Sudden Cardiac Death and Maximal Left Ventricular Wall Thickness in Hypertrophic Cardiomyopathy
Constantinos O'Mahony, Fatima Jichi, Lorenzo Monserrat, et al.
European Heart Journal
|
July 6, 2007
Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects
Lorenzo Monserrat, Manuel Hermida-Prieto, Xusto Fernandez, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
June 21, 2013
Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy
Lucía Núñez, Juan Ramón Gimeno-Blanes, María Isabel Rodríguez-García, et al.
JAMA Cardiology
|
November 28, 2019
Mortality Among Referral Patients With Hypertrophic Cardiomyopathy vs the General European Population
Massimiliano Lorenzini, Zacharias Anastasiou, Constantinos O'Mahony, et al.
Scientific Reports
|
May 4, 2022
Identification of an elusive spliceogenic MYBPC3 variant in an otherwise genotype-negative hypertrophic cardiomyopathy pedigree
Mario Torrado, Emilia Maneiro, Arsonval Lamounier Junior, et al.
Circulation
|
November 4, 2005
Gene mutations in apical hypertrophic cardiomyopathy
Michael Arad, Manual Penas-Lado, Lorenzo Monserrat, et al.
Revista Espanola De Cardiologia
|
June 23, 2006
[The implantable cardioverter-defibrillator and hypertrophic cardiomyopathy. Experience at three centers]
Francisco Marín, Juan R Gimeno, Eduardo Payá, et al.
Journal of the American College of Cardiology
|
December 25, 2007
Prevalence of fabry disease in a cohort of 508 unrelated patients with hypertrophic cardiomyopathy
Lorenzo Monserrat, Juan Ramón Gimeno-Blanes, Francisco Marín, et al.
Heart Rhythm
|
October 23, 2012
p.D1690N Nav1.5 rescues p.G1748D mutation gating defects in a compound heterozygous Brugada syndrome patient
Lucía Núñez, Adriana Barana, Irene Amorós, et al.
Heart (British Cardiac Society)
|
November 1, 2016
Predictors of atrial fibrillation in hypertrophic cardiomyopathy
Oliver P Guttmann, Menelaos Pavlou, Constantinos O'Mahony, et al.
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Search research articles
Search
Showing results (91-100 of 160) with videos related to
Sort By:
Page
of 16
Circulation. Arrhythmia and Electrophysiology
|
May 25, 2016
Inverted U-Shaped Relation Between the Risk of Sudden Cardiac Death and Maximal Left Ventricular Wall Thickness in Hypertrophic Cardiomyopathy
Constantinos O'Mahony, Fatima Jichi, Lorenzo Monserrat, et al.
European Heart Journal
|
July 6, 2007
Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects
Lorenzo Monserrat, Manuel Hermida-Prieto, Xusto Fernandez, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
June 21, 2013
Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy
Lucía Núñez, Juan Ramón Gimeno-Blanes, María Isabel Rodríguez-García, et al.
JAMA Cardiology
|
November 28, 2019
Mortality Among Referral Patients With Hypertrophic Cardiomyopathy vs the General European Population
Massimiliano Lorenzini, Zacharias Anastasiou, Constantinos O'Mahony, et al.
Scientific Reports
|
May 4, 2022
Identification of an elusive spliceogenic MYBPC3 variant in an otherwise genotype-negative hypertrophic cardiomyopathy pedigree
Mario Torrado, Emilia Maneiro, Arsonval Lamounier Junior, et al.
Circulation
|
November 4, 2005
Gene mutations in apical hypertrophic cardiomyopathy
Michael Arad, Manual Penas-Lado, Lorenzo Monserrat, et al.
Revista Espanola De Cardiologia
|
June 23, 2006
[The implantable cardioverter-defibrillator and hypertrophic cardiomyopathy. Experience at three centers]
Francisco Marín, Juan R Gimeno, Eduardo Payá, et al.
Journal of the American College of Cardiology
|
December 25, 2007
Prevalence of fabry disease in a cohort of 508 unrelated patients with hypertrophic cardiomyopathy
Lorenzo Monserrat, Juan Ramón Gimeno-Blanes, Francisco Marín, et al.
Heart Rhythm
|
October 23, 2012
p.D1690N Nav1.5 rescues p.G1748D mutation gating defects in a compound heterozygous Brugada syndrome patient
Lucía Núñez, Adriana Barana, Irene Amorós, et al.
Heart (British Cardiac Society)
|
November 1, 2016
Predictors of atrial fibrillation in hypertrophic cardiomyopathy
Oliver P Guttmann, Menelaos Pavlou, Constantinos O'Mahony, et al.
Page
of 16