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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 27, 2021
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
Francesco Mazzarotto, Megan H Hawley, Matteo Beltrami, et al.
European Journal of Human Genetics : EJHG
|
May 31, 2025
MYBPC3 c.2309-2A>G: exploring a founder variant in Italian hypertrophic cardiomyopathy patients
Marco Fabiani, Caterina Micolonghi, Silvia Caroselli, 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.
European Heart Journal Supplements : Journal of the European Society of Cardiology
|
May 19, 2025
ANMCO position paper 'Hypertrophic cardiomyopathy: from diagnosis to treatment'
Cristina Chimenti, Attilio Iacovoni, Andrea Montalto, et al.
Giornale Italiano Di Cardiologia (2006)
|
April 28, 2025
[ANMCO Position paper: Hypertrophic cardiomyopathy: from diagnosis to treatment]
Cristina Chimenti, Attilio Iacovoni, Andrea Montalto, 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.
European Journal of Heart Failure
|
May 29, 2021
Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy
Maria A Restrepo-Cordoba, Karim Wahbi, Anca R Florian, et al.
Journal of the American College of Cardiology
|
August 25, 2022
Natural History of MYH7-Related Dilated Cardiomyopathy
Fernando de Frutos, Juan Pablo Ochoa, Marina Navarro-Peñalver, et al.
European Heart Journal
|
August 2, 2023
Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry
Lia Crotti, Carla Spazzolini, Mette Nyegaard, et al.
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Search research articles
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Showing results (71-80 of 79) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 79 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 27, 2021
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
Francesco Mazzarotto, Megan H Hawley, Matteo Beltrami, et al.
European Journal of Human Genetics : EJHG
|
May 31, 2025
MYBPC3 c.2309-2A>G: exploring a founder variant in Italian hypertrophic cardiomyopathy patients
Marco Fabiani, Caterina Micolonghi, Silvia Caroselli, 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.
European Heart Journal Supplements : Journal of the European Society of Cardiology
|
May 19, 2025
ANMCO position paper 'Hypertrophic cardiomyopathy: from diagnosis to treatment'
Cristina Chimenti, Attilio Iacovoni, Andrea Montalto, et al.
Giornale Italiano Di Cardiologia (2006)
|
April 28, 2025
[ANMCO Position paper: Hypertrophic cardiomyopathy: from diagnosis to treatment]
Cristina Chimenti, Attilio Iacovoni, Andrea Montalto, 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.
European Journal of Heart Failure
|
May 29, 2021
Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy
Maria A Restrepo-Cordoba, Karim Wahbi, Anca R Florian, et al.
Journal of the American College of Cardiology
|
August 25, 2022
Natural History of MYH7-Related Dilated Cardiomyopathy
Fernando de Frutos, Juan Pablo Ochoa, Marina Navarro-Peñalver, et al.
European Heart Journal
|
August 2, 2023
Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry
Lia Crotti, Carla Spazzolini, Mette Nyegaard, et al.
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of 8