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Microbiology Spectrum
|
March 26, 2026
Two novel real-time PCR assays for <i>Brucella</i> detection: a species-specific multiplex and a genus-level singleplex developed via large-scale whole genome sequencing data analysis
Emily Hoover, John Chmara, Marc-Olivier Duceppe, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society
|
May 27, 2021
Hypertrophic cardiomyopathies requiring more monitoring for less atrial fibrillation-related complications: a clustering analysis based on the French registry on hypertrophic cardiomyopathy (REMY)
Marion Hourqueig, Guillaume Bouzille, Mariana Mirabel, et al.
Plos One
|
August 3, 2017
Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasia
Joel Fedida, Veronique Fressart, Philippe Charron, et al.
European Heart Journal
|
June 16, 2009
Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy
Laëtitia Duboscq-Bidot, Philippe Charron, Volker Ruppert, et al.
Neuromuscular Disorders : NMD
|
December 14, 2011
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study
Karim Wahbi, Anthony Béhin, Philippe Charron, et al.
JACC. Clinical Electrophysiology
|
March 15, 2025
Pulsed-Field vs Thermal Catheter Ablation of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy
Samy Gribissa, Thomas Kueffer, Sven Knecht, et al.
Stem Cell Research
|
February 20, 2021
Generation of iPSC line from MYH7 R403L mutation carrier with severe hypertrophic cardiomyopathy and isogenic CRISPR/Cas9 corrected control
Vincent Fontaine, Laetitia Duboscq-Bidot, Charlène Jouve, et al.
Frontiers in Physiology
|
January 8, 2013
Brugada ECG pattern: a physiopathological prospective study based on clinical, electrophysiological, angiographic, and genetic findings
Guillaume Duthoit, Véronique Fressart, Françoise Hidden-Lucet, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
February 28, 2025
Imaging features of desmoplakin arrhythmogenic cardiomyopathy: A comparative cardiovascular magnetic resonance study
Mikael Laredo, Etienne Charpentier, Shannon Soulez, et al.
Clinical Genetics
|
October 31, 2023
DNA-pools targeted-sequencing as a robust cost-effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosis
Claire Perret, Carole Proust, Ulrike Esslinger, et al.
Page
of 21
Search research articles
Search
Showing results (71-80 of 203) with videos related to
Sort By:
Page
of 21
Microbiology Spectrum
|
March 26, 2026
Two novel real-time PCR assays for <i>Brucella</i> detection: a species-specific multiplex and a genus-level singleplex developed via large-scale whole genome sequencing data analysis
Emily Hoover, John Chmara, Marc-Olivier Duceppe, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society
|
May 27, 2021
Hypertrophic cardiomyopathies requiring more monitoring for less atrial fibrillation-related complications: a clustering analysis based on the French registry on hypertrophic cardiomyopathy (REMY)
Marion Hourqueig, Guillaume Bouzille, Mariana Mirabel, et al.
Plos One
|
August 3, 2017
Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasia
Joel Fedida, Veronique Fressart, Philippe Charron, et al.
European Heart Journal
|
June 16, 2009
Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy
Laëtitia Duboscq-Bidot, Philippe Charron, Volker Ruppert, et al.
Neuromuscular Disorders : NMD
|
December 14, 2011
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study
Karim Wahbi, Anthony Béhin, Philippe Charron, et al.
JACC. Clinical Electrophysiology
|
March 15, 2025
Pulsed-Field vs Thermal Catheter Ablation of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy
Samy Gribissa, Thomas Kueffer, Sven Knecht, et al.
Stem Cell Research
|
February 20, 2021
Generation of iPSC line from MYH7 R403L mutation carrier with severe hypertrophic cardiomyopathy and isogenic CRISPR/Cas9 corrected control
Vincent Fontaine, Laetitia Duboscq-Bidot, Charlène Jouve, et al.
Frontiers in Physiology
|
January 8, 2013
Brugada ECG pattern: a physiopathological prospective study based on clinical, electrophysiological, angiographic, and genetic findings
Guillaume Duthoit, Véronique Fressart, Françoise Hidden-Lucet, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
February 28, 2025
Imaging features of desmoplakin arrhythmogenic cardiomyopathy: A comparative cardiovascular magnetic resonance study
Mikael Laredo, Etienne Charpentier, Shannon Soulez, et al.
Clinical Genetics
|
October 31, 2023
DNA-pools targeted-sequencing as a robust cost-effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosis
Claire Perret, Carole Proust, Ulrike Esslinger, et al.
Page
of 21