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Circulation
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March 17, 2025
Correction to: Low Penetrance Sarcomere Variants Contribute to Additive Risk in Hypertrophic Cardiomyopathy
Joshua K Meisner, Aaron Renberg, Eric D Smith, et al.
Circulation
|
April 17, 2026
The Natural History of Massive Left Ventricular Hypertrophy in Pediatric Hypertrophic Cardiomyopathy: A Multiregistry Analysis
Robert Przybylski, Gabrielle Norrish, Brian Claggett, et al.
Circulation
|
September 30, 2021
Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants
Marta Gigli, Davide Stolfo, Sharon L Graw, et al.
Science (New York, N.Y.)
|
October 30, 2025
The functional landscape of coding variation in the familial hypercholesterolemia gene <i>LDLR</i>
Daniel R Tabet, Atina G Coté, Megan C Lancaster, et al.
The American Journal of Sports Medicine
|
October 30, 2023
Relationship Between Age and Pathology With Treatment of Pediatric and Adolescent Discoid Lateral Meniscus: A Report From the SCORE Multicenter Database
Rachel S Silverstein, Scott D McKay, Pablo Coello, et al.
Circulation
|
June 22, 2026
Correction to: The Natural History of Massive Left Ventricular Hypertrophy in Pediatric Hypertrophic Cardiomyopathy: A Multiregistry Analysis
Robert Przybylski, Gabrielle Norrish, Brian Claggett, et al.
Orthopaedic Journal of Sports Medicine
|
February 23, 2026
Risk Factors for Complication and Reoperation in the Treatment of Discoid Lateral Meniscus in Children and Adolescents: A Multicenter Study
Suzanna Ohlsen, Michelle Son, Waylon Howard, et al.
JACC. Heart Failure
|
July 18, 2025
Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric Study
Maria Perotto, Alessia Paldino, Francesco Mazzarotto, et al.
Journal of the American College of Cardiology
|
May 20, 2026
Sex and Age Specific Genetic Risk Across the Dilated and Arrhythmogenic Cardiomyopathy Spectrum: Insights From the SHaRe Registry
Sophie L V M Stroeks, Nicole K Bart, Joseph Rossano, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 8, 2025
The contribution of <i>RBM20</i> truncating variants to human cardiomyopathy
Brendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
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of 48
Search research articles
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Showing results (451-460 of 474) with videos related to
Sort By:
Page
of 48
Circulation
|
March 17, 2025
Correction to: Low Penetrance Sarcomere Variants Contribute to Additive Risk in Hypertrophic Cardiomyopathy
Joshua K Meisner, Aaron Renberg, Eric D Smith, et al.
Circulation
|
April 17, 2026
The Natural History of Massive Left Ventricular Hypertrophy in Pediatric Hypertrophic Cardiomyopathy: A Multiregistry Analysis
Robert Przybylski, Gabrielle Norrish, Brian Claggett, et al.
Circulation
|
September 30, 2021
Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants
Marta Gigli, Davide Stolfo, Sharon L Graw, et al.
Science (New York, N.Y.)
|
October 30, 2025
The functional landscape of coding variation in the familial hypercholesterolemia gene <i>LDLR</i>
Daniel R Tabet, Atina G Coté, Megan C Lancaster, et al.
The American Journal of Sports Medicine
|
October 30, 2023
Relationship Between Age and Pathology With Treatment of Pediatric and Adolescent Discoid Lateral Meniscus: A Report From the SCORE Multicenter Database
Rachel S Silverstein, Scott D McKay, Pablo Coello, et al.
Circulation
|
June 22, 2026
Correction to: The Natural History of Massive Left Ventricular Hypertrophy in Pediatric Hypertrophic Cardiomyopathy: A Multiregistry Analysis
Robert Przybylski, Gabrielle Norrish, Brian Claggett, et al.
Orthopaedic Journal of Sports Medicine
|
February 23, 2026
Risk Factors for Complication and Reoperation in the Treatment of Discoid Lateral Meniscus in Children and Adolescents: A Multicenter Study
Suzanna Ohlsen, Michelle Son, Waylon Howard, et al.
JACC. Heart Failure
|
July 18, 2025
Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric Study
Maria Perotto, Alessia Paldino, Francesco Mazzarotto, et al.
Journal of the American College of Cardiology
|
May 20, 2026
Sex and Age Specific Genetic Risk Across the Dilated and Arrhythmogenic Cardiomyopathy Spectrum: Insights From the SHaRe Registry
Sophie L V M Stroeks, Nicole K Bart, Joseph Rossano, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 8, 2025
The contribution of <i>RBM20</i> truncating variants to human cardiomyopathy
Brendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
Page
of 48