4.3 Review

Accurate Classification of Non-ischemic Cardiomyopathy

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Review Pediatrics

Pediatric Restrictive Cardiomyopathies

Raffaello Ditaranto et al.

Summary: Restrictive cardiomyopathy (RCM) is a rare type of pediatric heart muscle disease with poor prognosis and high incidence of complications. Heart transplantation is the only effective treatment option. Although RCM has shared hemodynamic characteristics, the causes and natural course vary.

FRONTIERS IN PEDIATRICS (2022)

Review Cardiac & Cardiovascular Systems

Hypereosinophilic syndrome: considerations for the cardiologist

Antoine Bondue et al.

Summary: Eosinophil-mediated endomyocardial damage is a well-known complication in patients with hypereosinophilic syndromes. Management and survival have improved, but some patients still develop severe cardiomyopathy. Treatment of HES should be managed by clinicians with expertise, while cardiologists play a key role in managing associated cardiopathy.
Article Cardiac & Cardiovascular Systems

Dilated cardiomyopathy in the era of precision medicine: latest concepts and developments

Nicoletta Orphanou et al.

Summary: Dilated cardiomyopathy (DCM) is a complex disease with various genetic and non-genetic causes, leading to a range of clinical presentations. Recent advancements in understanding the genetic basis of DCM have provided insights into genotype-directed therapies, paving the way for more efficient diagnosis and prevention strategies.

HEART FAILURE REVIEWS (2022)

Article Cardiac & Cardiovascular Systems

Proteomics profiling reveals a distinct high-risk molecular subtype of hypertrophic cardiomyopathy

Lusha W. Liang et al.

Summary: This study used proteomics profiling to identify molecular subtypes of hypertrophic cardiomyopathy (HCM) and examined their associations with major adverse cardiovascular events (MACE) in a multicenter prospective cohort. Four molecular subtypes of HCM were identified, and a high-risk subtype (subtype D) was found to be associated with upregulation of pathways related to inflammation, fibrosis, and Ras/mitogen-activated protein kinase. This prospective plasma proteomics study not only identified HCM molecular subtypes but also revealed pathobiological mechanisms associated with a high-risk subtype of HCM.
Review Cardiac & Cardiovascular Systems

Restrictive cardiomyopathy: from genetics and clinical overview to animal modeling

Michelle Chintanaphol et al.

Summary: Restrictive cardiomyopathy is a rare but potentially devastating heart muscle disorder characterized by abnormal muscle relaxation, restricted ventricular filling, and often accompanied by diastolic dysfunction and atrial enlargement. Approximately 30% of cases are familial and the pathogenesis involves various genetic mutations and other diseases.

REVIEWS IN CARDIOVASCULAR MEDICINE (2022)

Article

A Review of Left Ventricular Noncompaction cardiomyopathy (LVNC)

Hasan Mirza et al.

Journal of Community Hospital Internal Medicine Perspectives (2022)

Review Cardiac & Cardiovascular Systems

Atrial cardiomyopathy: from cell to bedside

Mengmeng Li et al.

Summary: Atrial cardiomyopathy involves structural and electrical remodeling of the atria, potentially leading to impaired mechanical function. It may be an important yet underestimated contributor to cardioembolic stroke. Further prospective studies are needed to define the relationship between atrial cardiomyopathy, atrial fibrillation, and embolic stroke.

ESC HEART FAILURE (2022)

Review Cardiac & Cardiovascular Systems

Viral Myocarditis: Classification, Diagnosis, and Clinical Implications

Fabiola B. Sozzi et al.

Summary: Myocarditis is an inflammatory disease of the myocardium, with viral infections being the most common cause. The diagnosis of myocarditis is challenging due to its wide range of clinical manifestations, which can lead to heart failure and arrhythmias. Cardiac magnetic resonance imaging (CMR) plays a crucial role in diagnosing myocarditis. Arrhythmias, including atrial fibrillation and ventricular tachycardia, are common complications, but the mechanisms are not fully understood. Myocarditis carries a significant risk, especially in patients with extensive myocardial fibrosis. CMR can serve as a predictor of sudden cardiac death (SCD) and cardiovascular mortality.

FRONTIERS IN CARDIOVASCULAR MEDICINE (2022)

Article Cardiac & Cardiovascular Systems

Left ventricular non-compaction cardiomyopathy: restrictive subtype with MYH7 gene mutation

Kazim Oztarhan et al.

Summary: Left ventricular non-compaction is a rare and unclassified congenital cardiomyopathy. There are nine distinct subtypes identified, and ongoing studies focus on the prognosis and mortality of these subtypes. This study presents the first case of the restrictive subtype of left ventricular non-compaction with a family history and MYH7 gene mutation, contributing new information to the understanding of this disease.

CARDIOLOGY IN THE YOUNG (2022)

Article Genetics & Heredity

Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood

A. Muravyev et al.

Summary: This study provides a detailed analysis of the clinical, genetic, and structural predictions of distinct FLNC-associated phenotypes in pediatric cases. It reveals a unique clinical form of filaminopathies characterized by early-onset restrictive cardiomyopathy and congenital myopathy. The amino acid substitution A1186V is identified as a hotspot mutation for the combination of myopathy and cardiomyopathy.

ORPHANET JOURNAL OF RARE DISEASES (2022)

Article Biology

Subtypes and Mechanisms of Hypertrophic Cardiomyopathy Proposed by Machine Learning Algorithms

Mila Glavaski et al.

Summary: This study uses machine learning algorithms to identify subtypes of hypertrophic cardiomyopathy (HCM) and explore its mechanisms. By analyzing clinical and laboratory findings, four HCM subtypes are determined, and models to predict the presence of different HCM features are generated. These findings provide deeper insights into the mechanisms of HCM.

LIFE-BASEL (2022)

Review Cardiac & Cardiovascular Systems

Arrhythmogenic Right Ventricular Cardiomyopathy

Andrew D. Krahn et al.

Summary: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a condition characterized by right ventricular fibrofatty infiltration and arrhythmias. The diagnosis relies on the fulfillment of task force criteria incorporating electrophysiological parameters, cardiac imaging findings, genetic factors, and histopathologic features. Risk stratification of ARVC aims to identify individuals at higher risk of sudden cardiac death or sustained ventricular tachycardia. Current management options for ARVC include exercise restriction, medication therapy, consideration for implantable cardioverter-defibrillator insertion, and catheter ablation.

JACC-CLINICAL ELECTROPHYSIOLOGY (2022)

Article Medicine, General & Internal

A special case of hypertrophic cardiomyopathy with a differential diagnosis of isolated cardiac amyloidosis or junctophilin type 2 associated cardiomyopathy

Severine De Bruijn et al.

Summary: Differential diagnosis between hypertrophic cardiomyopathy and cardiac amyloidosis is crucial, yet challenging due to similarities in their presentation. Advancements in non-invasive diagnostic methods may eliminate the need for invasive studies. A new variant of the junctophilin 2 gene related to hypertrophic cardiomyopathy was found in a patient diagnosed with the disease.

ACTA CLINICA BELGICA (2021)

Article Cardiac & Cardiovascular Systems

Emerging concepts in arrhythmogenic dilated cardiomyopathy

Thomas Zegkos et al.

Summary: This article discusses the importance of phenotypic and genotypic analysis in dilated cardiomyopathy with arrhythmic burden, and emphasizes early preventive measures for sudden cardiac death, with special attention given to the overlap with left dominant arrhythmogenic cardiomyopathy.

HEART FAILURE REVIEWS (2021)

Article Medicine, General & Internal

Prevalence and Clinical Characteristics of Fabry Disease in Chinese Patients with Hypertrophic Cardiomyopathy

Yan Xiao et al.

AMERICAN JOURNAL OF THE MEDICAL SCIENCES (2021)

Review Biochemistry & Molecular Biology

Recent Findings Related to Cardiomyopathy and Genetics

Takanobu Yamada et al.

Summary: Advancements in NGS have made genetic analysis more accessible, leading to discoveries about the role of rare variants in cardiomyopathy and the variability of clinical courses based on causative genes. These findings extend beyond traditional types of cardiomyopathy to include conditions like PPCM, CTRCD, and ACM, sparking progress in understanding mechanisms and developing new therapies. Recent studies also suggest a contribution of common variants in cardiomyopathy development, marking a new era in the field of cardiomyopathy and genetics.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2021)

Article Cardiac & Cardiovascular Systems

Cadherin 2-Related Arrhythmogenic Cardiomyopathy Prevalence and Clinical Features

Alice Ghidoni et al.

Summary: In a cohort of previously genotype-negative ACM patients, the prevalence of probands with CDH2 pathogenic variants was found to be low at 1.2%. However, those with CDH2 mutations showed a high incidence of ventricular arrhythmic events and rare occurrences of heart failure.

CIRCULATION-GENOMIC AND PRECISION MEDICINE (2021)

Article Cardiac & Cardiovascular Systems

Diagnosis and treatment of cardiac amyloidosis. A position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

Pablo Garcia-Pavia et al.

Summary: Cardiac amyloidosis is a serious and progressive infiltrative disease caused by the deposition of amyloid fibrils in the heart. With advances in imaging techniques and non-invasive diagnosis, it is now recognized as more common than traditionally believed. The Working Group on Myocardial and Pericardial Disease has proposed definitions, diagnostic algorithms, and treatment strategies to help bridge the gap between the latest research and clinical practice in managing cardiac amyloidosis.

EUROPEAN JOURNAL OF HEART FAILURE (2021)

Article Cardiac & Cardiovascular Systems

Myocardial Histopathology in Patients With Obstructive Hypertrophic Cardiomyopathy

Hao Cui et al.

Summary: This study analyzed the myocardial histopathology of 1,836 patients with obstructive HCM undergoing septal myectomy, finding associations between myocyte hypertrophy, myocyte disarray, and interstitial fibrosis with severity of heart disease. Older age, lower degree of myocyte hypertrophy, and lower degree of endocardial thickening were independently associated with worse post-myectomy survival.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2021)

Article Cardiac & Cardiovascular Systems

Left Ventricular Longitudinal Dyssynchrony by CMR Feature Tracking Is Related to Adverse Prognosis in Advanced Arrhythmogenic Cardiomyopathy

Yanyan Song et al.

Summary: LV involvement assessed by CMR-FT is an independent risk factor for cardiovascular and arrhythmic events in ACM patients, providing prognostic value for this subtype.

FRONTIERS IN CARDIOVASCULAR MEDICINE (2021)

Review Medicine, General & Internal

Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and Phenocopies

Riccardo Vio et al.

Summary: HCM and primary RCM have a similar genetic background, primarily caused by variants in sarcomeric genes. These sarcomeric cardiomyopathies share diastolic dysfunction as the prevalent pathophysiological mechanism, and familial forms of primary RCM may be part of the phenotypic spectrum of HCM. Infiltrative and storage diseases may show either a hypertrophic or restrictive phenotype based on left ventricular wall thickness and filling pattern.

JOURNAL OF CLINICAL MEDICINE (2021)

Review Biology

Update on Biomarkers Associated to Cardioembolic Stroke: A Narrative Review

Ana Catarina Fonseca et al.

Summary: NT-proBNP and BNP are the most widely studied biomarkers for cardioembolic stroke, with NT-proBNP currently being used for patient selection in clinical trials and risk prediction tools. Other biomarkers have limited use in clinical practice due to methodological quality issues. Validation studies for most biomarkers are lacking.

LIFE-BASEL (2021)

Article Cardiac & Cardiovascular Systems

Phenotypic clustering of dilated cardiomyopathy patients highlights important pathophysiological differences

Job A. J. Verdonschot et al.

Summary: This study identified four different DCM phenogroups with significant differences in clinical presentation, underlying molecular profiles, and outcome. The use of phenogrouping could lead to a more personalized treatment approach for DCM patients.

EUROPEAN HEART JOURNAL (2021)

Article Cardiac & Cardiovascular Systems

Phenotypic clustering of dilated cardiomyopathy patients highlights important pathophysiological differences

Job A. J. Verdonschot et al.

Summary: This study identified four different DCM phenogroups with distinct molecular profiles and outcomes, paving the way for a more personalized treatment approach. Decision tree modeling helped classify DCM patients into different phenogroups, offering a new avenue for individualized therapy.

EUROPEAN HEART JOURNAL (2021)

Review Medicine, Research & Experimental

Cardiac Amyloidosis: Overlooked, Underappreciated, and Treatable

Jonah Rubin et al.

ANNUAL REVIEW OF MEDICINE, VOL 71, 2020 (2020)

Article Genetics & Heredity

FLNC truncations cause arrhythmogenic right ventricular cardiomyopathy

Francesca Brun et al.

JOURNAL OF MEDICAL GENETICS (2020)

Article Computer Science, Interdisciplinary Applications

Classification model based on strain measurements to identify patients with arrhythmogenic cardiomyopathy with left ventricular involvement

Yolanda Vives-Gilabert et al.

COMPUTER METHODS AND PROGRAMS IN BIOMEDICINE (2020)

Article Cardiac & Cardiovascular Systems

Penetrance of Hypertrophic Cardiomyopathy in Sarcomere Protein Mutation Carriers

Massimiliano Lorenzini et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2020)

Article Genetics & Heredity

The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals

Joel Salazar-Mendiguchia et al.

EUROPEAN JOURNAL OF MEDICAL GENETICS (2020)

Article Cardiac & Cardiovascular Systems

A founder homozygous DSG2 variant in East Asia results in ARVC with full penetrance and heart failure phenotype

Liang Chen et al.

INTERNATIONAL JOURNAL OF CARDIOLOGY (2019)

Review Cardiac & Cardiovascular Systems

Clinical and genetic insights into non-compaction: a meta-analysis and systematic review on 7598 individuals

Elham Kayvanpour et al.

CLINICAL RESEARCH IN CARDIOLOGY (2019)

Review Medicine, General & Internal

Dilated cardiomyopathy: from epidemiologic to genetic phenotypes A translational review of current literature

D. Reichart et al.

JOURNAL OF INTERNAL MEDICINE (2019)

Editorial Material Cardiac & Cardiovascular Systems

Risk Stratification and Hypertrophic Cardiomyopathy Subtypes

Mark V. Sherrid et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2019)

Article Cardiac & Cardiovascular Systems

Distinct Subgroups in Hypertrophic Cardiomyopathy in the NHLBI HCM Registry

Stefan Neubauer et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2019)

Editorial Material Medicine, General & Internal

Cardiology: hypertrophic cardiomyopathy

John Firth

CLINICAL MEDICINE (2019)

Review Cardiac & Cardiovascular Systems

Arrhythmic Genotypes in Familial Dilated Cardiomyopathy: Implications for Genetic Testing and Clinical Management

Stacey Peters et al.

HEART LUNG AND CIRCULATION (2019)

Review Cardiac & Cardiovascular Systems

Cancer Therapy-Related Cardiac Dysfunction: An Overview for the Clinician

Irving E. Perez et al.

CLINICAL MEDICINE INSIGHTS-CARDIOLOGY (2019)

Article Cardiac & Cardiovascular Systems

Prognosis of adult obstructive hypertrophic cardiomyopathy patients with different morphological types after surgical myectomy

Bing Tang et al.

EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY (2018)

Article Cardiac & Cardiovascular Systems

Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy

Jaap I. van Waning et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2018)

Article Cardiac & Cardiovascular Systems

Epidemiology and Clinical Aspects of Genetic Cardiomyopathies

Daniele Masarone et al.

HEART FAILURE CLINICS (2018)

Article Genetics & Heredity

Clinical and genetic backgrounds of hypertrophic cardiomyopathy with mid-ventricular obstruction

Natsuko Inagaki et al.

JOURNAL OF HUMAN GENETICS (2018)

Review Genetics & Heredity

Genetics of hypertrophic cardiomyopathy: A review of current state

M. Sabater-Molina et al.

CLINICAL GENETICS (2018)

Article Cardiac & Cardiovascular Systems

Clinical outcomes associated with sarcomere mutations in hypertrophic cardiomyopathy: a meta-analysis on 7675 individuals

Farbod Sedaghat-Hamedani et al.

CLINICAL RESEARCH IN CARDIOLOGY (2018)

Article Cardiac & Cardiovascular Systems

Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals

Elham Kayvanpour et al.

CLINICAL RESEARCH IN CARDIOLOGY (2017)

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A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation

Daniel F. Gudbjartsson et al.

EUROPEAN HEART JOURNAL (2017)

Article Cardiac & Cardiovascular Systems

Women with hypertrophic cardiomyopathy have worse survival

Jeffrey B. Geske et al.

EUROPEAN HEART JOURNAL (2017)

Review Medicine, General & Internal

Dilated cardiomyopathy

Robert G. Weintraub et al.

LANCET (2017)

Review Cardiac & Cardiovascular Systems

Neonatal dilated cardiomyopathy

Paulo Soares et al.

REVISTA PORTUGUESA DE CARDIOLOGIA (2017)

Article Cardiac & Cardiovascular Systems

Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy

Hugh Calkins et al.

CIRCULATION (2017)

Article Cardiac & Cardiovascular Systems

Dilated Cardiomyopathy Genetic Determinants and Mechanisms

Elizabeth M. McNally et al.

CIRCULATION RESEARCH (2017)

Review Cardiac & Cardiovascular Systems

Severe cardiac involvement in Gaucher type IIIC: a case report and review of the literature

Yilmaz Kor et al.

CARDIOLOGY IN THE YOUNG (2017)

Article Cardiac & Cardiovascular Systems

Safety of American Heart Association-recommended minimum exercise for desmosomal mutation carriers

Abhishek C. Sawant et al.

HEART RHYTHM (2016)

Review Cardiac & Cardiovascular Systems

Stress cardiomyopathy: Is it limited to Takotsubo syndrome? Problems of definition

Petr A. Sarapultsev et al.

INTERNATIONAL JOURNAL OF CARDIOLOGY (2016)

Review Cardiac & Cardiovascular Systems

The Diagnosis and Evaluation of Dilated Cardiomyopathy

Alan G. Japp et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2016)

Review Cardiac & Cardiovascular Systems

Left Ventricular Noncompaction A Distinct Genetic Cardiomyopathy?

Eloisa Arbustini et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2016)

Article Genetics & Heredity

The prevalence and distribution of the amyloidogenic transthyretin (TTR) V122I allele in Africa

Daniel R. Jacobson et al.

MOLECULAR GENETICS & GENOMIC MEDICINE (2016)

Review Cardiac & Cardiovascular Systems

New Perspectives on the Prevalence of Hypertrophic Cardiomyopathy

Christopher Semsarian et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2015)

Article Medicine, General & Internal

Left ventricular non-compaction cardiomyopathy

Jeffrey A. Towbin et al.

LANCET (2015)

Article Cardiac & Cardiovascular Systems

Genotype-Phenotype Correlations in Apical Variant Hypertrophic Cardiomyopathy

Eric C. Towe et al.

CONGENITAL HEART DISEASE (2015)

Review Cardiac & Cardiovascular Systems

CNS disease triggering Takotsubo stress cardiomyopathy

Josef Finsterer et al.

INTERNATIONAL JOURNAL OF CARDIOLOGY (2014)

Article Immunology

Cardiac fibroblasts mediate IL-17A-driven inflammatory dilated cardiomyopathy

Lei Wu et al.

JOURNAL OF EXPERIMENTAL MEDICINE (2014)

Article Cardiac & Cardiovascular Systems

Clinical Phenotype and Outcome of Hypertrophic Cardiomyopathy Associated With Thin-Filament Gene Mutations

Raffaele Coppini et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2014)

Article Cardiac & Cardiovascular Systems

The Relationship of Left Ventricular Trabeculation to Ventricular Function and Structure Over a 9.5-Year Follow-Up The MESA Study

Filip Zemrak et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2014)

Article Multidisciplinary Sciences

Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

Rafael Valdes-Mas et al.

NATURE COMMUNICATIONS (2014)

Article Cardiac & Cardiovascular Systems

Mortality and Sudden Death in Pediatric Left Ventricular Noncompaction in a Tertiary Referral Center

Samuel T. Brescia et al.

CIRCULATION (2013)

Article Cardiac & Cardiovascular Systems

Homozygous Founder Mutation in Desmocollin-2 (DSC2) Causes Arrhythmogenic Cardiomyopathy in the Hutterite Population

Brenda Gerull et al.

CIRCULATION-CARDIOVASCULAR GENETICS (2013)

Article Cardiac & Cardiovascular Systems

Autosomal Recessive Atrial Dilated Cardiomyopathy With Standstill Evolution Associated With Mutation of Natriuretic Peptide Precursor A

Marcello Disertori et al.

CIRCULATION-CARDIOVASCULAR GENETICS (2013)

Article Genetics & Heredity

Syndromic non-compaction of the left ventricle: associated chromosomal anomalies

M. C. Digilio et al.

CLINICAL GENETICS (2013)

Article Cardiac & Cardiovascular Systems

Left ventricular hypertrophy in Fabry disease: a practical approach to diagnosis

Zaheer Yousef et al.

EUROPEAN HEART JOURNAL (2013)

Review Cardiac & Cardiovascular Systems

Dilated cardiomyopathy: the complexity of a diverse genetic architecture

Ray E. Hershberger et al.

NATURE REVIEWS CARDIOLOGY (2013)

Article Cardiac & Cardiovascular Systems

Senile Systemic Amyloidosis: Clinical Features at Presentation and Outcome

Jennifer H. Pinney et al.

JOURNAL OF THE AMERICAN HEART ASSOCIATION (2013)

Review Cardiac & Cardiovascular Systems

Surgical treatment of hypertrophic cardiomyopathy

Sameh M. Said et al.

EXPERT REVIEW OF CARDIOVASCULAR THERAPY (2013)

Article Cardiac & Cardiovascular Systems

Testosterone and interleukin-1β increase cardiac remodeling during coxsackievirus B3 myocarditis via serpin A 3n

Michael J. Coronado et al.

AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY (2012)

Article Medicine, Research & Experimental

Beyond the Cardiac Myofilament: Hypertrophic Cardiomyopathy- Associated Mutations in Genes that Encode Calcium-Handling Proteins

A. P. Landstrom et al.

CURRENT MOLECULAR MEDICINE (2012)

Article Clinical Neurology

Cardiomyopathy in Friedreich Ataxia: Clinical Findings and Research

R. Mark Payne et al.

JOURNAL OF CHILD NEUROLOGY (2012)

Article Medicine, General & Internal

Truncations of Titin Causing Dilated Cardiomyopathy

Daniel S. Herman et al.

NEW ENGLAND JOURNAL OF MEDICINE (2012)

Article Genetics & Heredity

Coffin-Lowry syndrome and left ventricular noncompaction cardiomyopathy with a restrictive pattern

Hugo R. Martinez et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2011)

Article Cardiac & Cardiovascular Systems

Sarcomere Gene Mutations in Isolated Left Ventricular Noncompaction Cardiomyopathy Do Not Predict Clinical Phenotype

Susanne Probst et al.

CIRCULATION-CARDIOVASCULAR GENETICS (2011)

Article Urology & Nephrology

Isolated ventricular noncompaction in patients with chronic renal failure

N.S. Markovic et al.

CLINICAL NEPHROLOGY (2011)

Article Genetics & Heredity

Natural history of Danon disease

Dana Boucek et al.

GENETICS IN MEDICINE (2011)

Article Cardiac & Cardiovascular Systems

Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

Francesca Girolami et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2010)

Article Cardiac & Cardiovascular Systems

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)

Editorial Material Cardiac & Cardiovascular Systems

Hypertrophic Cardiomyopathy: Identification of Morphological Subtypes by Echocardiography and Cardiac Magnetic Resonance Imaging

Imran S. Syed et al.

JACC-CARDIOVASCULAR IMAGING (2008)

Review Cardiac & Cardiovascular Systems

Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy

Mark M. Awad et al.

NATURE CLINICAL PRACTICE CARDIOVASCULAR MEDICINE (2008)

Review Cardiac & Cardiovascular Systems

Diagnostic approaches to pediatric cardiomyopathy of metabolic genetic etiologies and their relation to therapy

Gerald F. Cox

PROGRESS IN PEDIATRIC CARDIOLOGY (2007)

Article Cardiac & Cardiovascular Systems

Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype

Toru Kubo et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2007)

Article Medicine, General & Internal

Incidence, causes, and outcomes of dilated cardiomyopathy in children

Jeffrey A. Towbin et al.

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2006)

Article Cardiac & Cardiovascular Systems

Myocardial biopsy based classification and treatment in patients with dilated cardiomyopathy

O Zimmermann et al.

INTERNATIONAL JOURNAL OF CARDIOLOGY (2005)

Article Cardiac & Cardiovascular Systems

Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations

M Hermida-Prieto et al.

AMERICAN JOURNAL OF CARDIOLOGY (2004)

Article Cardiac & Cardiovascular Systems

Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction

M Vatta et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2003)

Article Cardiac & Cardiovascular Systems

Left ventricular hypertrabeculation/noncompaction and association with additional cardiac abnormalities and neuromuscular disorders

C Stöllberger et al.

AMERICAN JOURNAL OF CARDIOLOGY (2002)