Related references
Note: Only part of the references are listed.Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry
Roberto Barriales-Villa et al.
REVISTA ESPANOLA DE CARDIOLOGIA (2021)
Association of Genetic Variants With Outcomes in Patients With Nonischemic Dilated Cardiomyopathy
Luis Escobar-Lopez et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2021)
Improved Risk Stratification for Ventricular Arrhythmias and Sudden Death in Patients With Nonischemic Dilated Cardiomyopathy
Andrea Di Marco et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2021)
Clinical Risk Prediction in Patients With Left Ventricular Myocardial Noncompaction
Guillem Casas et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2021)
Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy
Francesco Mazzarotto et al.
CIRCULATION (2020)
Desmoplakin Cardiomyopathy, a Fibrotic and Inflammatory Form of Cardiomyopathy Distinct From Typical Dilated or Arrhythmogenic Right Ventricular Cardiomyopathy
Eric D. Smith et al.
CIRCULATION (2020)
Effects of danicamtiv, a novel cardiac myosin activator, in heart failure with reduced ejection fraction: experimental data and clinical results from a phase 2a trial
Adriaan A. Voors et al.
EUROPEAN JOURNAL OF HEART FAILURE (2020)
Implications of Genetic Testing in Dilated Cardiomyopathy
Job A. J. Verdonschot et al.
CIRCULATION-GENOMIC AND PRECISION MEDICINE (2020)
Pathogenic RBM20-Variants Are Associated With a Severe Disease Expression in Male Patients With Dilated Cardiomyopathy
Thomas Morris Hey et al.
CIRCULATION-HEART FAILURE (2019)
Clinical diversity of MYH7-related cardiomyopathies: Insights into genotype-phenotype correlations
Tova Hershkovitz et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2019)
Precision Medicine in the Management of Dilated Cardiomyopathy JACC State-of-the-Art Review
Diane Fatkin et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2019)
Role of titin in cardiomyopathy: from DNA variants to patient stratification
James S. Ware et al.
NATURE REVIEWS CARDIOLOGY (2018)
Titin cardiomyopathy leads to altered mitochondrial energetics, increased fibrosis and long-termlife-threatening arrhythmias
Job A. J. Verdonschot et al.
EUROPEAN HEART JOURNAL (2018)
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel
Melissa A. Kelly et al.
GENETICS IN MEDICINE (2018)
Dilated cardiomyopathy myosin mutants have reduced force-generating capacity
Zoltan Ujfalusi et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2018)
Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights From the Sarcomeric Human Cardiomyopathy Registry (SHaRe)
Carolyn Y. Ho et al.
CIRCULATION (2018)
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
Roddy Walsh et al.
GENETICS IN MEDICINE (2017)
Clinical genetics and outcome of left ventricular non-compaction cardiomyopathy
Farbod Sedaghat-Hamedani et al.
EUROPEAN HEART JOURNAL (2017)
Dilated Cardiomyopathy Genetic Determinants and Mechanisms
Elizabeth M. McNally et al.
CIRCULATION RESEARCH (2017)
Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases
Yigal M. Pinto et al.
EUROPEAN HEART JOURNAL (2016)
The Diagnosis and Evaluation of Dilated Cardiomyopathy
Alan G. Japp et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2016)
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies
Martin F. Ortiz-Genga et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2016)
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients
C. Fiorillo et al.
ORPHANET JOURNAL OF RARE DISEASES (2016)
A Novel MYH7 Gene Mutation in a Fetus With Left Ventricular Noncompaction
Yasuhisa Nomura et al.
CANADIAN JOURNAL OF CARDIOLOGY (2015)
Structural Implications of β-Cardiac Myosin Heavy Chain Mutations in Human Disease
Melanie Colegrave et al.
ANATOMICAL RECORD-ADVANCES IN INTEGRATIVE ANATOMY AND EVOLUTIONARY BIOLOGY (2014)
The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy
Daniel Vega Moller et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2009)
Left ventricular non-compaction - Insights from cardiovascular magnetic resonance imaging
SE Petersen et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2005)
Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene
E Villard et al.
EUROPEAN HEART JOURNAL (2005)
Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy
R Jenni et al.
HEART (2001)
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy
M Kamisago et al.
NEW ENGLAND JOURNAL OF MEDICINE (2000)