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JAMA Cardiology
|
August 10, 2017
Role of Genetic Testing in Inherited Cardiovascular Disease: A Review
Allison L Cirino, Stephanie Harris, Neal K Lakdawala, et al.
Journal of the American College of Cardiology
|
October 16, 2012
Quantitative expression of the mutated lamin A/C gene in patients with cardiolaminopathy
Nupoor Narula, Valentina Favalli, Paolo Tarantino, et al.
Archives of Medical Science : AMS
|
May 18, 2016
Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies
Andreas Perrot, Pavol Tomasov, Eric Villard, et al.
Clinical Genetics
|
January 23, 2025
Exploring the Familial Phenotypic Variability Associated With TTN Truncating Variants in Cardiomyopathies: Variant Spectrum, Genotype-Phenotype Correlation and Consequences in Genetic Counseling
Marie Massier, Pascal de Groote, Erwan Donal, et al.
European Heart Journal
|
September 9, 2010
Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases
Philippe Charron, Michael Arad, Eloisa Arbustini, et al.
European Journal of Heart Failure
|
February 22, 2019
High risk of heart failure associated with desmoglein-2 mutations compared to plakophilin-2 mutations in arrhythmogenic right ventricular cardiomyopathy/dysplasia
Alexis Hermida, Véronique Fressart, Francoise Hidden-Lucet, et al.
Circulation. Genomic and Precision Medicine
|
January 23, 2024
Prevalence and Significance of Rare Genetic Variants in <i>AKAP9</i> in Inherited Cardiac Diseases
Alexis Hermida, Flavie Ader, Guillaume Jedraszak, et al.
European Journal of Heart Failure
|
November 16, 2012
A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activity
Felix W Friedrich, Gilles Dilanian, Patricia Khattar, et al.
Annals of Medicine
|
June 30, 2025
Diagnostic pathway for cardiac amyloidosis from the healthcare professional's perspective: results from the French DIAM-ATTR survey
Silvia Oghina, Damien Legallois, Fabien Hyafil, et al.
Revista Espanola De Cardiologia (English Ed.)
|
December 18, 2015
2015 ESC Guidelines for the Diagnosis and Management of Pericardial Diseases
Yehuda Adler, Philippe Charron, Massimo Imazio, et al.
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of 21
Search research articles
Search
Showing results (101-110 of 203) with videos related to
Sort By:
Page
of 21
JAMA Cardiology
|
August 10, 2017
Role of Genetic Testing in Inherited Cardiovascular Disease: A Review
Allison L Cirino, Stephanie Harris, Neal K Lakdawala, et al.
Journal of the American College of Cardiology
|
October 16, 2012
Quantitative expression of the mutated lamin A/C gene in patients with cardiolaminopathy
Nupoor Narula, Valentina Favalli, Paolo Tarantino, et al.
Archives of Medical Science : AMS
|
May 18, 2016
Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies
Andreas Perrot, Pavol Tomasov, Eric Villard, et al.
Clinical Genetics
|
January 23, 2025
Exploring the Familial Phenotypic Variability Associated With TTN Truncating Variants in Cardiomyopathies: Variant Spectrum, Genotype-Phenotype Correlation and Consequences in Genetic Counseling
Marie Massier, Pascal de Groote, Erwan Donal, et al.
European Heart Journal
|
September 9, 2010
Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases
Philippe Charron, Michael Arad, Eloisa Arbustini, et al.
European Journal of Heart Failure
|
February 22, 2019
High risk of heart failure associated with desmoglein-2 mutations compared to plakophilin-2 mutations in arrhythmogenic right ventricular cardiomyopathy/dysplasia
Alexis Hermida, Véronique Fressart, Francoise Hidden-Lucet, et al.
Circulation. Genomic and Precision Medicine
|
January 23, 2024
Prevalence and Significance of Rare Genetic Variants in <i>AKAP9</i> in Inherited Cardiac Diseases
Alexis Hermida, Flavie Ader, Guillaume Jedraszak, et al.
European Journal of Heart Failure
|
November 16, 2012
A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activity
Felix W Friedrich, Gilles Dilanian, Patricia Khattar, et al.
Annals of Medicine
|
June 30, 2025
Diagnostic pathway for cardiac amyloidosis from the healthcare professional's perspective: results from the French DIAM-ATTR survey
Silvia Oghina, Damien Legallois, Fabien Hyafil, et al.
Revista Espanola De Cardiologia (English Ed.)
|
December 18, 2015
2015 ESC Guidelines for the Diagnosis and Management of Pericardial Diseases
Yehuda Adler, Philippe Charron, Massimo Imazio, et al.
Page
of 21