Related references
Note: Only part of the references are listed.Titin-truncating mutations associated with dilated cardiomyopathy alter length-dependent activation and its modulation via phosphorylation
Petr G. Vikhorev et al.
CARDIOVASCULAR RESEARCH (2022)
Burden of heart failure and underlying causes in 195 countries and territories from 1990 to 2017
Nicola Luigi Bragazzi et al.
EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY (2021)
2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure
Theresa A. McDonagh et al.
EUROPEAN HEART JOURNAL (2021)
Desmocollin-2 promotes intestinal mucosal repair by controlling integrin-dependent cell adhesion and migration
Sven Flemming et al.
MOLECULAR BIOLOGY OF THE CELL (2020)
Genotype-phenotype correlations in recessive titinopathies
Marco Savarese et al.
GENETICS IN MEDICINE (2020)
Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene
Mohammed Majid Akhtar et al.
CIRCULATION-HEART FAILURE (2020)
Arrhythmogenic right ventricular cardiomyopathy in patients with biallelic JUP-associated skin fragility
Hassan Vahidnezhad et al.
SCIENTIFIC REPORTS (2020)
Heart Failure in the Middle East Arab Countries: Current and Future Perspectives
Abdelfatah A. Elasfar et al.
JOURNAL OF THE SAUDI HEART ASSOCIATION (2020)
Untying the knot: protein quality control in inherited cardiomyopathies
Larissa M. Dorsch et al.
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY (2019)
Genomic Reorganization of Lamin-Associated Domains in Cardiac Myocytes Is Associated With Differential Gene Expression and DNA Methylation in Human Dilated Cardiomyopathy
Sirisha M. Cheedipudi et al.
CIRCULATION RESEARCH (2019)
DNA Damage Response/TP53 Pathway Is Activated and Contributes to the Pathogenesis of Dilated Cardiomyopathy Associated With LMNA (Lamin A/C) Mutations
Suet Nee Chen et al.
CIRCULATION RESEARCH (2019)
High risk of heart failure associated with desmoglein-2 mutations compared to plakophilin-2 mutations in arrhythmogenic right ventricular cardiomyopathy/dysplasia
Alexis Hermida et al.
EUROPEAN JOURNAL OF HEART FAILURE (2019)
Association of single nucleotide polymorphisms in the 3′UTR region of TPM1 gene with dilated cardiomyopathy A case-control study
Qiang Yao et al.
MEDICINE (2019)
Screening of MYH7 gene mutation sites in hypertrophic cardiomyopathy and its significance
Hui-Ting Liu et al.
CHINESE MEDICAL JOURNAL (2019)
Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Ray E. Hershberger et al.
GENETICS IN MEDICINE (2018)
Spectrum of Restrictive and Infiltrative Cardiomyopathies Part 2 of a 2-Part Series
Naveen L. Pereira et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2018)
Role of Lamin A/C Gene Mutations in the Signaling Defects Leading to Cardiomyopathies
Andrea Gerbino et al.
FRONTIERS IN PHYSIOLOGY (2018)
Homozygous missense MYBPC3 Pro873His mutation associated with increased risk for heart failure development in hypertrophic cardiomyopathy
Antheia Kissopoulou et al.
ESC HEART FAILURE (2018)
The LifeLines Cohort Study: Prevalence and treatment of cardiovascular disease and risk factors
M. Yldau van der Ende et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY (2017)
Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects
Jennifer England et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2017)
Arrhythmogenic Right Ventricular Cardiomyopathy
Domenico Corrado et al.
NEW ENGLAND JOURNAL OF MEDICINE (2017)
The role of desmosomes in carcinogenesis
Guangxin Zhou et al.
ONCOTARGETS AND THERAPY (2017)
Plakophilin-2 is required for transcription of genes that control calcium cycling and cardiac rhythm
Marina Cerrone et al.
NATURE COMMUNICATIONS (2017)
Prevalence and Clinical Implication of Double Mutations in Hypertrophic Cardiomyopathy Revisiting the Gene-Dose Effect
Dana Fourey et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2017)
Arrhythmogenic cardiomyopathy related DSG2 mutations affect desmosomal cadherin binding kinetics
Mareike Dieding et al.
SCIENTIFIC REPORTS (2017)
Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis
Anneline S. J. M. te Riele et al.
CARDIOVASCULAR RESEARCH (2017)
Restrictive Cardiomyopathy Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy
Eli Muchtar et al.
CIRCULATION RESEARCH (2017)
Whole-Exome Sequencing Identifies a Novel Mutation of Desmocollin 2 in a Chinese Family With Arrhythmogenic Right Ventricular Cardiomyopathy
Ji-Shi Liu et al.
AMERICAN JOURNAL OF CARDIOLOGY (2017)
Prevalence and risk factors of heart failure in the USA: NHANES 2013 - 2014 epidemiological follow-up study
Saketram Komanduri et al.
JOURNAL OF COMMUNITY HOSPITAL INTERNAL MEDICINE PERSPECTIVES (2017)
Arrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy
Alexandros Protonotarios et al.
EUROPACE (2016)
Biochemical Comparison of Tpm1.1 (α) and Tpm2.2 (β) Tropomyosins from Rabbit Skeletal Muscle
Elke M. Lohmeier-Vogel et al.
BIOCHEMISTRY (2016)
Prevalence of heart failure in Australia: a systematic review
Berhe W. Sahle et al.
BMC CARDIOVASCULAR DISORDERS (2016)
Characterizing the Molecular Pathology of Arrhythmogenic Cardiomyopathy in Patient Buccal Mucosa Cells
Angeliki Asimaki et al.
CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY (2016)
2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure
Piotr Ponikowski et al.
EUROPEAN HEART JOURNAL (2016)
Inhibition of late sodium current attenuates ionic arrhythmia mechanism in ventricular myocytes expressing LaminA-N195K mutation
Yogananda S. Markandeya et al.
HEART RHYTHM (2016)
Sibling risk of hospitalization for heart failure - A nationwide study
Magnus P. Lindgren et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY (2016)
Arrhythmogenic right-ventricular cardiomyopathy: molecular genetics into clinical practice in the era of next generation sequencing
Giulia Poloni et al.
JOURNAL OF CARDIOVASCULAR MEDICINE (2016)
Idiopathic Restrictive Cardiomyopathy Is Primarily a Genetic Disease
Maria Gallego-Delgado et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2016)
Epidemiology and aetiology of heart failure
Boback Ziaeian et al.
NATURE REVIEWS CARDIOLOGY (2016)
A small-molecule inhibitor of sarcomere contractility suppresses hypertrophic cardiomyopathy in mice
Eric M. Green et al.
SCIENCE (2016)
Laminopathies disrupt epigenomic developmental programs and cell fate
Jelena Perovanovic et al.
SCIENCE TRANSLATIONAL MEDICINE (2016)
Prevalence of Heart Failure and Adherence to Process Indicators: Which Socio-Demographic Determinants are Involved?
Alessandra Buja et al.
INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH (2016)
Burden of Heart Failure in Latin America: A Systematic Review and Meta-analysis
Agustin Ciapponi et al.
REVISTA ESPANOLA DE CARDIOLOGIA (2016)
Homozygous Desmocollin-2 Mutations and Arrhythmogenic Cardiomyopathy
Alessandra Lorenzon et al.
AMERICAN JOURNAL OF CARDIOLOGY (2015)
A Systematic Review of Phenotypic Features Associated With Cardiac Troponin I Mutations in Hereditary Cardiomyopathies
Jens Mogensen et al.
CANADIAN JOURNAL OF CARDIOLOGY (2015)
Genetic Landscape of Cardiomyopathy and Its Role in Heart Failure
Elizabeth M. McNally et al.
CELL METABOLISM (2015)
Recent Developments in Heart Failure
Sujith Dassanayaka et al.
CIRCULATION RESEARCH (2015)
Incidence, prevalence and 1-year all-cause mortality of heart failure in Germany: a study based on electronic healthcare data of more than six million persons
Christoph Ohlmeier et al.
CLINICAL RESEARCH IN CARDIOLOGY (2015)
Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers
Aditya Bhonsale et al.
EUROPEAN HEART JOURNAL (2015)
Cardiac myosin-binding protein C (MYBPC3) in cardiac pathophysiology
Lucie Carrier et al.
GENE (2015)
Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity
Ahmed A. Alfares et al.
GENETICS IN MEDICINE (2015)
Cardiovascular risk assessment: a global perspective
Dong Zhao et al.
NATURE REVIEWS CARDIOLOGY (2015)
Arrhythmogenic Cardiomyopathy in a Patient With a Rare Loss-of-Function KCNQ1 Mutation
Qinmei Xiong et al.
JOURNAL OF THE AMERICAN HEART ASSOCIATION (2015)
Genetics and Heart Failure: A Concise Guide for the Clinician
Cecile Skrzynia et al.
CURRENT CARDIOLOGY REVIEWS (2015)
Inherited Cardiomyopathies
Jeffrey A. Towbin
CIRCULATION JOURNAL (2014)
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing
Trevor J. Pugh et al.
GENETICS IN MEDICINE (2014)
Contemporary aetiology, clinical characteristics and prognosis of adults with heart failure observed in a tertiary hospital in Tanzania: the prospective Tanzania Heart Failure (TaHeF) study
Abel Makubi et al.
HEART (2014)
The Hypertrophic Cardiomyopathy Myosin Mutation R453C Alters ATP Binding and Hydrolysis of Human Cardiac β- Myosin*
Marieke Bloemink et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2014)
The MOGE(S) Classification of Cardiomyopathy for Clinicians
Eloisa Arbustini et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2014)
Cardiovascular Risk and Events in 17 Low-, Middle-, and High-Income Countries
S. Yusuf et al.
NEW ENGLAND JOURNAL OF MEDICINE (2014)
Single point mutation in Rabenosyn-5 in a female with intractable seizures and evidence of defective endocytotic trafficking
Sylvia Stockler et al.
ORPHANET JOURNAL OF RARE DISEASES (2014)
Heart failure: preventing disease and death worldwide
Piotr Ponikowski et al.
ESC HEART FAILURE (2014)
Cardiomyopathies: Evolution of pathogenesis concepts and potential for new therapies
Hamayak Sisakian
WORLD JOURNAL OF CARDIOLOGY (2014)
Arrhythmogenic right ventricular cardiomyopathy: From genetics to diagnostic and therapeutic challenges
Bruno Pinamonti et al.
WORLD JOURNAL OF CARDIOLOGY (2014)
Age-Dependent Clinical and Genetic Characteristics in Japanese Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia
Seiko Ohno et al.
CIRCULATION JOURNAL (2013)
Epidemiology of Heart Failure in Asia
Yasuhiko Sakata et al.
CIRCULATION JOURNAL (2013)
Incidence and epidemiology of new onset heart failure with preserved vs. reduced ejection fraction in a community-based cohort: 11-year follow-up of PREVEND
Frank P. Brouwers et al.
EUROPEAN HEART JOURNAL (2013)
The epidemiology of heart failure, based on data for 2.1 million inhabitants in Sweden
Ramin Zarrinkoub et al.
EUROPEAN JOURNAL OF HEART FAILURE (2013)
Clinical utility gene card for: dilated cardiomyopathy (CMD)
Anna Posafalvi et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2013)
Recent advances in the epidemiology, diagnosis and treatment of endomyocardial fibrosis in Africa
Ana Olga H. Mocumbi et al.
HEART (2013)
Natriuretic Peptide-Based Screening and Collaborative Care for Heart Failure The STOP-HF Randomized Trial
Mark Ledwidge et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2013)
Alpha-tropomyosin mutations in inherited cardiomyopathies
Charles Redwood et al.
JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY (2013)
PONTIAC (NT-proBNP Selected PreventiOn of cardiac eveNts in a populaTion of dIabetic patients without A history of Cardiac disease)
Martin Huelsmann et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2013)
Clinical and Genetic Characterization of Patients with Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Caused by a Plakophilin-2 Splice Mutation
Jasper J. van der Smagt et al.
CARDIOLOGY (2012)
Cardiomyopathies and myocardial disorders in Africa: present status and the way forward
Ayodele O. Falase et al.
CARDIOVASCULAR JOURNAL OF AFRICA (2012)
Genetics of inherited cardiomyopathy
Daniel Jacoby et al.
EUROPEAN HEART JOURNAL (2012)
Diastolic stiffness as assessed by diastolic wall strain is associated with adverse remodelling and poor outcomes in heart failure with preserved ejection fraction
Tomohito Ohtani et al.
EUROPEAN HEART JOURNAL (2012)
Double or compound sarcomere mutations in hypertrophic cardiomyopathy: A potential link to sudden death in the absence of conventional risk factors
Barry J. Maron et al.
HEART RHYTHM (2012)
Dual Specificity Phosphatase 4 Mediates Cardiomyopathy Caused by Lamin A/C (LMNA) Gene Mutation
Jason C. Choi et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers A European Cohort Study
Ingrid A. W. van Rijsingen et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2012)
Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010
Theo Vos et al.
LANCET (2012)
Rapamycin Reverses Elevated mTORC1 Signaling in Lamin A/C-Deficient Mice, Rescues Cardiac and Skeletal Muscle Function, and Extends Survival
Fresnida J. Ramos et al.
SCIENCE TRANSLATIONAL MEDICINE (2012)
Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations
Katja Gehmlich et al.
CARDIOVASCULAR RESEARCH (2011)
Mitogen-Activated Protein Kinase Inhibitors Improve Heart Function and Prevent Fibrosis in Cardiomyopathy Caused by Mutation in Lamin A/C Gene
Wei Wu et al.
CIRCULATION (2011)
Contribution of Genetic Factors to the Pathogenesis of Dilated Cardiomyopathy - The Cause of Dilated Cardiomyopathy: Genetic or Acquired? (Genetic-Side)
Akinori Kimura
CIRCULATION JOURNAL (2011)
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy
Eric Villard et al.
EUROPEAN HEART JOURNAL (2011)
Clinical utility gene card for: hypertrophic cardiomyopathy (type 1-14)
Yigal M. Pinto et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2011)
Desmosomal protein gene mutations in patients with idiopathic dilated cardiomyopathy undergoing cardiac transplantation: a clinicopathological study
Pablo Garcia-Pavia et al.
HEART (2011)
Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity
Manuela Pigors et al.
HUMAN MOLECULAR GENETICS (2011)
Incidence and mortality of heart failure: A community-based study
Francisco M. Gomez-Soto et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY (2011)
Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia-Associated Mutations From Background Genetic Noise
Jamie D. Kapplinger et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2011)
Is there nascent structure in the intrinsically disordered region of troponin I?
Olivier Julien et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2011)
Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy
A. van den Wijngaard et al.
NETHERLANDS HEART JOURNAL (2011)
Cardiomyopathy: A Systematic Review of Disease-Causing Mutations in Myosin Heavy Chain 7 and Their Phenotypic Manifestations
R. Walsh et al.
CARDIOLOGY (2010)
The C Terminus of Cardiac Troponin I Stabilizes the Ca2+-Activated State of Tropomyosin on Actin Filaments
Agnieszka Galinska et al.
CIRCULATION RESEARCH (2010)
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathy
Marzia De Bortoli et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2010)
Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all
Thomas E. Callis et al.
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS (2010)
Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia
Barbara Bauce et al.
HEART RHYTHM (2010)
Homozygous Mutations in the 5′ Region of the JUP Gene Result in Cutaneous Disease but Normal Heart Development in Children
Rita M. Cabral et al.
JOURNAL OF INVESTIGATIVE DERMATOLOGY (2010)
Wide spectrum of desmosomal mutations in Danish patients with arrhythmogenic right ventricular cardiomyopathy
A. H. Christensen et al.
JOURNAL OF MEDICAL GENETICS (2010)
Malignant and benign mutations in familial cardiomyopathies: Insights into mutations linked to complex cardiovascular phenotypes
Qian Xu et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2010)
Correcting diastolic dysfunction by Ca2+ desensitizing troponin in a transgenic mouse model of restrictive cardiomyopathy
Yuejin Li et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2010)
Striated muscle tropomyosin isoforms differentially regulate cardiac performance and myofilament calcium sensitivity
Ganapathy Jagatheesan et al.
JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY (2010)
Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients With Dilated Cardiomyopathy
Ray E. Hershberger et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2009)
Progress With Genetic Cardiomyopathies Screening, Counseling, and Testing in Dilated, Hypertrophic, and Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
Ray E. Hershberger et al.
CIRCULATION-HEART FAILURE (2009)
Genetic and biochemical heterogeneity of cardiac troponins: clinical and laboratory implications
Giuseppe Lippi et al.
CLINICAL CHEMISTRY AND LABORATORY MEDICINE (2009)
The Nuclear Envelope as a Signaling Node in Development and Disease
William T. Dauer et al.
DEVELOPMENTAL CELL (2009)
Heart failure and chronic obstructive pulmonary disease: diagnostic pitfalls and epidemiology
Nathaniel Mark Hawkins et al.
EUROPEAN JOURNAL OF HEART FAILURE (2009)
Clinical features, survival experience, and profile of plakophylin-2 gene mutations in participants of the Arrhythmogenic Right Ventricular Cardiomyopathy Registry of South Africa
David A. Watkins et al.
HEART RHYTHM (2009)
Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy
Sharie B. Parks et al.
AMERICAN HEART JOURNAL (2008)
Troponin and cardiomyopathy
Audrey N. Chang et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2008)
Impending epidemic - Future projection of heart failure in Japan to the year 2055
Yuji Okura et al.
CIRCULATION JOURNAL (2008)
Is the 2006 American Heart Association classification of cardiomyopathies the gold standard?
Barry J. Maron
CIRCULATION-HEART FAILURE (2008)
Plakophilin 2:: a critical scaffold for PKCα that regulates intercellular junction assembly
Amanda E. Bass-Zubek et al.
JOURNAL OF CELL BIOLOGY (2008)
Left-Dominant Arrhythmogenic Cardiomyopathy
Srijita Sen-Chowdhry et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2008)
A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy
Maximilian G. Posch et al.
MOLECULAR GENETICS AND METABOLISM (2008)
A novel dominant mutation in plakoglobin causes Arrhythmogenic right ventricular cardiomyopathy
Angeliki Asimaki et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro
Giorgia Beffagna et al.
BMC MEDICAL GENETICS (2007)
Ectopic expression and dynamics of TPM1α and TPM1κ in myofibrils of avian myotubes
Jushuo Wang et al.
CELL MOTILITY AND THE CYTOSKELETON (2007)
Clinical epidemiology of heart failure
Arend Mosterd et al.
HEART (2007)
Hereditary myosin myopathies
Anders Oldfors
NEUROMUSCULAR DISORDERS (2007)
Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy
Antoine Muchir et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression
Srijita Sen-Chowdhry et al.
CIRCULATION (2007)
Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy
Arnd Heuser et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Cardiac myosin binding protein C phosphorylation is cardioprotective
Sakthivel Sadayappan et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2
Petros Syrris et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Advances in the diagnostic management of arrhythmogenic right ventricular dysplasia-cardiomyopathy
Stefan Peters
INTERNATIONAL JOURNAL OF CARDIOLOGY (2006)
Incidence, causes, and outcomes of dilated cardiomyopathy in children
Jeffrey A. Towbin et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2006)
Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function
Joachim P. Schmitt et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Association of parental heart failure with risk of heart failure in offspring
Douglas S. Lee et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
Contemporary definitions and classification of the cardiomyopathies - An American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; And Council on Epidemiology and Prevention
BJ Maron et al.
CIRCULATION (2006)
Epidemiology and etiology of cardiomyopathy in Africa
K Sliwa et al.
CIRCULATION (2005)
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype
M Mirza et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy
A Perrot et al.
JOURNAL OF MOLECULAR MEDICINE-JMM (2005)
Role of troponin T in disease
AV Gomes et al.
MOLECULAR AND CELLULAR BIOCHEMISTRY (2004)
Prevalence of right ventricular dysplasia-cardiomyopathy in a non-referral hospital
S Peters et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY (2004)
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy
B Gerull et al.
NATURE GENETICS (2004)
Hypertrophic cardiomyopathy:: Low frequency of mutations in the β-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients
M García-Castro et al.
CLINICAL CHEMISTRY (2003)
A recessive mutation in desmoplakin causes arrhythmogenic right ventricular dysplasia, skin disorder, and woolly hair
R Alcalai et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2003)
Natural history of dilated cardiomyopathy due to lamin A/C gene mutations
MRG Taylor et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2003)
Utility of genetic screening in hypertrophic cardiomyopathy:: Prevalence and significance of novel and double (homozygous and heterozygous) β-myosin mutations
SA Mohiddin et al.
GENETIC TESTING (2003)
Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations
J Mogensen et al.
JOURNAL OF CLINICAL INVESTIGATION (2003)
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy
A Rampazzo et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
Prevalence of chronic heart failure in Southwestern Europe: the EPICA study
F Ceia et al.
EUROPEAN JOURNAL OF HEART FAILURE (2002)
Familial dilated cardiomyopathy in patients transplanted for idiopathic dilated cardiomyopathy
L Monserrat et al.
REVISTA ESPANOLA DE CARDIOLOGIA (2002)
Cardiac troponin T is essential in sarcomere assembly and cardiac contractility
AJ Sehnert et al.
NATURE GENETICS (2002)
Hypertrophic cardiomyopathy - A systematic review
BJ Maron
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2002)
Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly
H Niimura et al.
CIRCULATION (2002)
Left bundle-branch block is associated with increased 1-year sudden and total mortality rate in 5517 outpatients with congestive heart failure: A report from the Italian Network on Congestive Heart Failure
S Baldasseroni et al.
AMERICAN HEART JOURNAL (2002)
The complete gene sequence of titin, expression of an unusual ≈700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system
ML Bang et al.
CIRCULATION RESEARCH (2001)
Disease-causing mutations in cardiac troponin T: Identification of a critical tropomyosin-binding region
T Palm et al.
BIOPHYSICAL JOURNAL (2001)
Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy
TM Olson et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2001)
ABC of heart failure - Aetiology
GYH Lip et al.
BRITISH MEDICAL JOURNAL (2000)