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Lorenzo Monserrat

Showing results (101-110 of 160) with videos related to

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European Journal of Heart Failure|July 18, 2015
Prediction of thrombo-embolic risk in patients with hypertrophic cardiomyopathy (HCM Risk-CVA)Oliver P Guttmann, Menelaos Pavlou, Constantinos O'Mahony, et al.
Heart (British Cardiac Society)|November 20, 2010
Insights into genotype-phenotype correlation in hypertrophic cardiomyopathy. Findings from 18 Spanish families with a single mutation in MYBPC3M José Oliva-Sandoval, Francisco Ruiz-Espejo, Lorenzo Monserrat, et al.
European Heart Journal|October 6, 2007
Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial DiseasesPerry Elliott, Bert Andersson, Eloisa Arbustini, et al.
Kardiologia Polska|July 18, 2008
[Classification of the cardiomyopathies]Perry Elliott, Bert Andersson, Eloisa Arbustini, et al.
Stem Cell Reports|November 6, 2018
Isogenic Pairs of hiPSC-CMs with Hypertrophic Cardiomyopathy/LVNC-Associated ACTC1 E99K Mutation Unveil Differential Functional DeficitsJames G W Smith, Thomas Owen, Jamie R Bhagwan, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|June 19, 2014
Desmoplakin truncations and arrhythmogenic left ventricular cardiomyopathy: characterizing a phenotypeJose María López-Ayala, Ivan Gómez-Milanés, Juan José Sánchez Muñoz, et al.
Plos One|April 22, 2016
Calmodulin 2 Mutation N98S Is Associated with Unexplained Cardiac Arrest in Infants Due to Low Clinical Penetrance Electrical DisordersJuan Jiménez-Jáimez, Julián Palomino Doza, Ángeles Ortega, et al.
Circulation|December 8, 2017
Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/DysplasiaFrancisco José Bermúdez-Jiménez, Víctor Carriel, Andreas Brodehl, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 30, 2023
A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish familyAnabel Cámara-Checa, Francesca Perin, Marcos Rubio-Alarcón, et al.
International Journal of Cardiology|June 14, 2020
Reduction in Filamin C transcript is associated with arrhythmogenic cardiomyopathy in Ashkenazi JewsShimrit Oz, Hagith Yonath, Leonid Visochyk, et al.
Pageof 16

Showing results (101-110 of 160) with videos related to

Sort By:
Pageof 16
European Journal of Heart Failure|July 18, 2015
Prediction of thrombo-embolic risk in patients with hypertrophic cardiomyopathy (HCM Risk-CVA)Oliver P Guttmann, Menelaos Pavlou, Constantinos O'Mahony, et al.
Heart (British Cardiac Society)|November 20, 2010
Insights into genotype-phenotype correlation in hypertrophic cardiomyopathy. Findings from 18 Spanish families with a single mutation in MYBPC3M José Oliva-Sandoval, Francisco Ruiz-Espejo, Lorenzo Monserrat, et al.
European Heart Journal|October 6, 2007
Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial DiseasesPerry Elliott, Bert Andersson, Eloisa Arbustini, et al.
Kardiologia Polska|July 18, 2008
[Classification of the cardiomyopathies]Perry Elliott, Bert Andersson, Eloisa Arbustini, et al.
Stem Cell Reports|November 6, 2018
Isogenic Pairs of hiPSC-CMs with Hypertrophic Cardiomyopathy/LVNC-Associated ACTC1 E99K Mutation Unveil Differential Functional DeficitsJames G W Smith, Thomas Owen, Jamie R Bhagwan, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|June 19, 2014
Desmoplakin truncations and arrhythmogenic left ventricular cardiomyopathy: characterizing a phenotypeJose María López-Ayala, Ivan Gómez-Milanés, Juan José Sánchez Muñoz, et al.
Plos One|April 22, 2016
Calmodulin 2 Mutation N98S Is Associated with Unexplained Cardiac Arrest in Infants Due to Low Clinical Penetrance Electrical DisordersJuan Jiménez-Jáimez, Julián Palomino Doza, Ángeles Ortega, et al.
Circulation|December 8, 2017
Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/DysplasiaFrancisco José Bermúdez-Jiménez, Víctor Carriel, Andreas Brodehl, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 30, 2023
A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish familyAnabel Cámara-Checa, Francesca Perin, Marcos Rubio-Alarcón, et al.
International Journal of Cardiology|June 14, 2020
Reduction in Filamin C transcript is associated with arrhythmogenic cardiomyopathy in Ashkenazi JewsShimrit Oz, Hagith Yonath, Leonid Visochyk, et al.
Pageof 16