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Circulation. Genomic and Precision Medicine
|
August 28, 2019
Genetic Mosaicism in Calmodulinopathy
Lisa M Wren, Juan Jiménez-Jáimez, Saleh Al-Ghamdi, et al.
Revista Espanola De Cardiologia (English Ed.)
|
January 24, 2012
Comments on the ESC guidelines on the management of cardiovascular diseases during pregnancy. A critical vision of Spanish cardiology
Angel M Alonso Gómez, Josep Comín, Xavier Borrás, et al.
European Heart Journal
|
March 20, 2026
Genetic counselling implementation in dilated cardiomyopathy
Job A J Verdonschot, Karin Y van Spaendonck-Zwarts, Debby M E I Hellebrekers, et al.
Circulation
|
November 3, 2022
A Human Hereditary Cardiomyopathy Shares a Genetic Substrate With Bicuspid Aortic Valve
Marcos Siguero-Álvarez, Alejandro Salguero-Jiménez, Joaquim Grego-Bessa, et al.
Heart (British Cardiac Society)
|
May 27, 2020
Mutations in <i>TRIM63</i> cause an autosomal-recessive form of hypertrophic cardiomyopathy
Joel Salazar-Mendiguchía, Juan Pablo Ochoa, Julian Palomino-Doza, et al.
Circulation. Genomic and Precision Medicine
|
August 18, 2023
Risks of Ventricular Arrhythmia and Heart Failure in Carriers of <i>RBM20</i> Variants
Douglas E Cannie, Alexandros Protonotarios, Athanasios Bakalakos, et al.
Circulation. Heart Failure
|
September 23, 2020
Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the <i>TTN</i> Gene
Mohammed Majid Akhtar, Massimiliano Lorenzini, Marcos Cicerchia, et al.
Journal of the American College of Cardiology
|
April 18, 2020
Natural History and Risk Stratification in Andersen-Tawil Syndrome Type 1
Andrea Mazzanti, Dmitri Guz, Alessandro Trancuccio, et al.
Journal of Clinical Medicine
|
April 3, 2021
Prognostic Value of Reduced Heart Rate Reserve during Exercise in Hypertrophic Cardiomyopathy
Quirino Ciampi, Iacopo Olivotto, Jesus Peteiro, et al.
Journal of the American College of Cardiology
|
December 3, 2016
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies
Martín F Ortiz-Genga, Sofía Cuenca, Matteo Dal Ferro, et al.
Page
of 16
Search research articles
Search
Showing results (141-150 of 160) with videos related to
Sort By:
Page
of 16
Circulation. Genomic and Precision Medicine
|
August 28, 2019
Genetic Mosaicism in Calmodulinopathy
Lisa M Wren, Juan Jiménez-Jáimez, Saleh Al-Ghamdi, et al.
Revista Espanola De Cardiologia (English Ed.)
|
January 24, 2012
Comments on the ESC guidelines on the management of cardiovascular diseases during pregnancy. A critical vision of Spanish cardiology
Angel M Alonso Gómez, Josep Comín, Xavier Borrás, et al.
European Heart Journal
|
March 20, 2026
Genetic counselling implementation in dilated cardiomyopathy
Job A J Verdonschot, Karin Y van Spaendonck-Zwarts, Debby M E I Hellebrekers, et al.
Circulation
|
November 3, 2022
A Human Hereditary Cardiomyopathy Shares a Genetic Substrate With Bicuspid Aortic Valve
Marcos Siguero-Álvarez, Alejandro Salguero-Jiménez, Joaquim Grego-Bessa, et al.
Heart (British Cardiac Society)
|
May 27, 2020
Mutations in <i>TRIM63</i> cause an autosomal-recessive form of hypertrophic cardiomyopathy
Joel Salazar-Mendiguchía, Juan Pablo Ochoa, Julian Palomino-Doza, et al.
Circulation. Genomic and Precision Medicine
|
August 18, 2023
Risks of Ventricular Arrhythmia and Heart Failure in Carriers of <i>RBM20</i> Variants
Douglas E Cannie, Alexandros Protonotarios, Athanasios Bakalakos, et al.
Circulation. Heart Failure
|
September 23, 2020
Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the <i>TTN</i> Gene
Mohammed Majid Akhtar, Massimiliano Lorenzini, Marcos Cicerchia, et al.
Journal of the American College of Cardiology
|
April 18, 2020
Natural History and Risk Stratification in Andersen-Tawil Syndrome Type 1
Andrea Mazzanti, Dmitri Guz, Alessandro Trancuccio, et al.
Journal of Clinical Medicine
|
April 3, 2021
Prognostic Value of Reduced Heart Rate Reserve during Exercise in Hypertrophic Cardiomyopathy
Quirino Ciampi, Iacopo Olivotto, Jesus Peteiro, et al.
Journal of the American College of Cardiology
|
December 3, 2016
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies
Martín F Ortiz-Genga, Sofía Cuenca, Matteo Dal Ferro, et al.
Page
of 16