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1164-131 Clinical significance of lamin A/C mutations in dilated cardiomyopathy

article published in 2004

2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Developed in collaboration with the Ameri

artículo científico publicado en 2011

2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines

artículo científico publicado en 2011

2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines

artículo científico publicado en 2011

2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines

artículo científico publicado en 2011

A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy.

artículo científico publicado en 2005

A common SCN5A variant alters the responsiveness of human sodium channels to class I antiarrhythmic agents

artículo científico publicado en 2007

A family-based association study of congenital left-sided heart malformations and 5,10 methylenetetrahydrofolate reductase

artículo científico publicado en 2004

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.

artículo científico publicado en 2016

A noninvasive means of detecting preclinical cardiomyopathy in Duchenne muscular dystrophy?

artículo científico publicado en 2003

A nonsense SCN5A mutation associated with Brugada-type electrocardiogram and intraventricular conduction defects

artículo científico publicado en 2009

A novel Alu-mediated Xq28 microdeletion ablates TAZ and partially deletes DNL1L in a patient with Barth syndrome

artículo científico publicado en 2009

A novel SCN5A mutation V1340I in Brugada syndrome augmenting arrhythmias during febrile illness

artículo científico publicado en 2009

A role for Toll-like receptor 3 variants in host susceptibility to enteroviral myocarditis and dilated cardiomyopathy.

artículo científico publicado en 2010

A woman with incidental findings of ventricular aneurysms and a desmosomal cardiomyopathy

artículo científico publicado en 2008

ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy gene

artículo científico publicado en 2009

Accelerated cardiac remodeling in desmoplakin transgenic mice in response to endurance exercise is associated with perturbed Wnt/β-catenin signaling

artículo científico publicado en 2015

Administration of a large nesiritide bolus dose in a pediatric patient: case report and review of nesiritide use in pediatrics

artículo científico publicado en 2006

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

artículo científico publicado en 2009

Arginine vasopressin levels are elevated and correlate with functional status in infants and children with congestive heart failure

artículo científico publicado en 2004

Arrhythmias and dilated cardiomyopathy common pathogenetic pathways?

artículo científico publicado en 2011

Arrhythmogenic Phenotype in Dilated Cardiomyopathy: Natural History and Predictors of Life-Threatening Arrhythmias.

artículo científico publicado en 2015

Arrhythmogenic right ventricular cardiomyopathy causing sudden cardiac death in boxer dogs: a new animal model of human disease

artículo científico publicado en 2004

Arrhythmogenic right ventricular cardiomyopathy type 1 (ARVD1): confirmation of locus assignment and mutation screening of four candidate genes

artículo científico publicado en 2003

Arrhythmogenic right ventricular cardiomyopathy/dysplasia clinical presentation and diagnostic evaluation: results from the North American Multidisciplinary Study

artículo científico publicado en 2009

Arrhythmogenic right ventricular cardiomyopathy: a 'final common pathway' that defines clinical phenotype

scientific article published on 15 February 2007

Arrhythmogenic right ventricular cardiomyopathy: a paradigm of overlapping disorders

artículo científico publicado en 2008

Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C): a multidisciplinary study: design and protocol

artículo científico publicado en 2003

Assessing the global and regional impact of primary cardiomyopathies: The Global Burden of Diseases, Injuries and Risk Factors (GBD 2010) Study

Assessment and management of the failing heart in children

artículo científico publicado en 2008

Assessment of large copy number variants in patients with apparently isolated congenital left-sided cardiac lesions reveals clinically relevant genomic events.

artículo científico publicado en 2017

Assessment of the CTNNA3 gene encoding human alpha T-catenin regarding its involvement in dilated cardiomyopathy

artículo científico publicado en 2002

Assessment of the Cylex ImmuKnow cell function assay in pediatric heart transplant patients

artículo científico publicado en 2008

Association between diffuse myocardial fibrosis and diastolic dysfunction in sickle cell anemia

artículo científico publicado en 2017

Association of common variants in ERBB4 with congenital left ventricular outflow tract obstruction defects

artículo científico publicado en 2011

Association of competitive and recreational sport participation with cardiac events in patients with arrhythmogenic right ventricular cardiomyopathy: results from the North American multidisciplinary study of arrhythmogenic right ventricular cardiom

artículo científico publicado en 2015

Association of left ventricular dilation at listing for heart transplant with postlisting and early posttransplant mortality in children with dilated cardiomyopathy

artículo científico publicado en 2009

B-type natriuretic peptide is a sensitive screening test for acute rejection in pediatric heart transplant patients

scientific article published on 24 April 2008

B-type natriuretic peptide predicts adverse cardiovascular events in pediatric outpatients with chronic left ventricular systolic dysfunction

artículo científico publicado en 2006

Beta2-adrenergic receptor genetic variants and risk of sudden cardiac death

scientific article published on 01 April 2006

Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy

scientific journal article

Biomarkers of cardiovascular stress and fibrosis in preclinical hypertrophic cardiomyopathy

artículo científico publicado en 2017

Brugada syndrome: 1992-2002: a historical perspective

artículo científico publicado en 2003

CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs

artículo científico publicado en 2011

Cardiac Biomarkers in Pediatric Cardiomyopathy: Study Design and Recruitment Results from the Pediatric Cardiomyopathy Registry

artículo científico publicado en 2019

Cardiac ankyrin repeat protein gene (ANKRD1) mutations in hypertrophic cardiomyopathy

artículo científico publicado en 2009

Cardiac metabolic pathways affected in the mouse model of barth syndrome

artículo científico publicado en 2015

Cardiac transplantation in children with Down syndrome, Turner syndrome, and other chromosomal anomalies: A multi-institutional outcomes analysis

artículo científico publicado en 2018

Cardiac-specific VLCAD deficiency induces dilated cardiomyopathy and cold intolerance

artículo científico publicado en 2013

Cardiomyopathies Due to Left Ventricular Noncompaction, Mitochondrial and Storage Diseases, and Inborn Errors of Metabolism

artículo científico publicado en 2017

Cardiomyopathy Phenotypes and Outcomes for Children With Left Ventricular Myocardial Noncompaction: Results From the Pediatric Cardiomyopathy Registry

artículo científico publicado en 2015

Cardiomyopathy and heart transplantation in children

artículo científico publicado en 2002

Cardiomyopathy in muscular dystrophy workshop. 28-30 September 2003, Tucson, Arizona

artículo científico publicado en 2004

Cardiotropic viruses in the myocardium of children with end-stage heart disease

artículo científico publicado en 2004

Cardiovascular Family History Increases Risk for Late-Onset Adverse Cardiovascular Outcomes in Childhood Cancer Survivors: A St. Jude Lifetime Cohort Report

artículo científico publicado en 2020

Cardiovascular Health Promotion in Children: Challenges and Opportunities for 2020 and Beyond: A Scientific Statement From the American Heart Association

artículo científico publicado en 2016

Characteristics and outcomes of cardiomyopathy in children with Duchenne or Becker muscular dystrophy: a comparative study from the Pediatric Cardiomyopathy Registry

scientific article published on 19 March 2008

Characteristics and outcomes of heart failure-related intensive care unit admissions in children with cardiomyopathy

artículo científico publicado en 2013

Characterization of left ventricular diastolic function by tissue Doppler imaging and clinical status in children with hypertrophic cardiomyopathy

artículo científico publicado en 2004

Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study

artículo científico publicado en 2016

Clinical Presentation and Outcomes by Sex in Arrhythmogenic Right Ventricular Cardiomyopathy: Findings from the North American ARVC Registry

artículo científico publicado en 2016

Clinical approaches to tachyarrhythmias, volume 10: The brugada syndrome

Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene

artículo científico publicado en 2007

Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy

artículo científico publicado en 2003

Clinical course and risk stratification of patients affected with the Jervell and Lange-Nielsen syndrome

artículo científico publicado en 2006

Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2

artículo científico publicado en 2006

Clinical implications for patients with long QT syndrome who experience a cardiac event during infancy

artículo científico publicado en 2009

Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease.

artículo científico publicado en 2004

Combined assessment of sex- and mutation-specific information for risk stratification in type 1 long QT syndrome

artículo científico publicado en 2012

Competing risks for death and cardiac transplantation in children with dilated cardiomyopathy: results from the pediatric cardiomyopathy registry

artículo científico publicado en 2011

Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2010

Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome

artículo científico publicado en 2002

Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathy

artículo científico publicado en 2002

Concentrations of brain natriuretic peptide in the plasma predicts outcomes of treatment of children with decompensated heart failure admitted to the Intensive Care unit

artículo científico publicado en 2007

Conditional ablation of nonmuscle myosin II-B delineates heart defects in adult mice

artículo científico publicado en 2009

Conduction abnormalities in pediatric patients with restrictive cardiomyopathy

artículo científico publicado en 2012

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly

artículo científico publicado en 2009

Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart Association.

artículo científico publicado en 2016

D-transposition of the great arteries: the current era of the arterial switch operation

artículo científico publicado en 2014

Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children

scientific article published on 06 September 2005

Danon disease presenting with dilated cardiomyopathy and a complex phenotype

artículo científico publicado en 2007

Defective human Ether-à-go-go-related gene trafficking linked to an endoplasmic reticulum retention signal in the C terminus

scientific article published on 20 May 2002

Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome

artículo científico publicado en 2002

Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy

artículo científico publicado en 2006

Desmosomal gene variants in patients with “possible ARVC” ⬇️

artículo científico publicado el 17 de marzo de 2011

Detection of viral deoxyribonucleic acid in amniotic fluid: association with fetal malformation and pregnancy abnormalities

artículo científico publicado en 2005

Detection of viruses in myocardial tissues by polymerase chain reaction. evidence of adenovirus as a common cause of myocarditis in children and adults

artículo científico publicado en 2003

Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria

artículo científico publicado en 2010

Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria.

artículo científico publicado en 2010

Diagnostic value of epinephrine test for genotyping LQT1, LQT2, and LQT3 forms of congenital long QT syndrome

artículo científico publicado en 2004

Diagnostic, prognostic, and therapeutic implications of genetic testing for hypertrophic cardiomyopathy

artículo científico publicado en 2009

Differences in Presentation and Outcomes Between Children With Familial Dilated Cardiomyopathy and Children With Idiopathic Dilated Cardiomyopathy: A Report From the Pediatric Cardiomyopathy Registry Study Group

artículo científico

Differential effects of beta-blockade on dispersion of repolarization in the absence and presence of sympathetic stimulation between the LQT1 and LQT2 forms of congenital long QT syndrome

artículo científico publicado en 2002

Dilated cardiomyopathy

artículo científico publicado en 2010

Dilated cardiomyopathy: a tale of cytoskeletal proteins and beyond

artículo científico publicado en 2006

Dilation of the aortic root in mitochondrial disease patients

article

Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010

artículo científico publicado en 2012

Dissection of Z-disc myopalladin gene network involved in the development of restrictive cardiomyopathy using system genetics approach

artículo científico publicado en 2017

Disturbance in Z-disk mechanosensitive proteins induced by a persistent mutant myopalladin causes familial restrictive cardiomyopathy

artículo científico publicado en 2014

Dystrophin genotype-cardiac phenotype correlations in Duchenne and Becker muscular dystrophies using cardiac magnetic resonance imaging

artículo científico publicado en 2015

Early predictors of survival to and after heart transplantation in children with dilated cardiomyopathy.

artículo científico publicado en 2012

Echocardiographic evaluation of asymptomatic parental and sibling cardiovascular anomalies associated with congenital left ventricular outflow tract lesions

artículo científico publicado en 2004

Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy

artículo científico publicado en 2006

Effect of body mass index on outcome in pediatric heart transplant patients

scientific article published on 01 July 2007

Effect of solute temperature in the measurement of cardiac output in children using the thermodilution technique

artículo científico publicado en 2016

Effectiveness of mechanical circulatory support in children with acute fulminant and persistent myocarditis.

artículo científico publicado en 2011

Epidemiology and cause-specific outcome of hypertrophic cardiomyopathy in children: findings from the Pediatric Cardiomyopathy Registry

artículo científico publicado en 2007

Epinephrine unmasks latent mutation carriers with LQT1 form of congenital long-QT syndrome.

artículo científico publicado en 2003

Factors associated with establishing a causal diagnosis for children with cardiomyopathy.

artículo científico publicado en 2006

FasL expression in cardiomyocytes activates the ERK1/2 pathway, leading to dilated cardiomyopathy and advanced heart failure.

artículo científico publicado en 2015

Fibrillin-1 Gene Mutations in Left Ventricular Non-compaction Cardiomyopathy

artículo científico publicado en 2016

Fkbp1a controls ventricular myocardium trabeculation and compaction by regulating endocardial Notch1 activity.

artículo científico publicado en 2013

Frequency of cardiac death in children with idiopathic dilated cardiomyopathy.

artículo científico publicado en 2009

Further Associations of Congenital Heart Disease and Genetic Syndromes: Report of a Case of Tetralogy of Fallot and Fabry’s Disease

Future research directions in pediatric cardiomyopathy

GSK3- and PRMT-1-dependent modifications of desmoplakin control desmoplakin-cytoskeleton dynamics

artículo científico publicado en 2015

Genetic Modulation of Brugada Syndrome by a Common Polymorphism

artículo científico publicado en 2009

Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity

artículo científico publicado en 2006

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome

artículo científico publicado en 2002

Genetic architecture of laterality defects revealed by whole exome sequencing

artículo científico publicado en 2019

Genetic aspects of dilated cardiomyopathy

Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline

artículo científico publicado en 2009

Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy

artículo científico publicado en 2005

Genetics and cardiac arrhythmias

artículo científico publicado en 2002

Genetics and cardiovascular disease: a policy statement from the American Heart Association.

artículo científico publicado en 2012

Genetics of arrhythmogenic right ventricular cardiomyopathy: a practical guide for physicians

artículo científico publicado en 2013

Genetics of dilated cardiomyopathy: more genes that kill

scientific article published on 01 November 2004

Genotype-phenotype aspects of type 2 long QT syndrome

artículo científico publicado en 2009

Genotype-phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin

artículo científico publicado en 2006

Genotype-specific QT correction for heart rate and the risk of life-threatening cardiac events in adolescents with congenital long-QT syndrome

artículo científico publicado en 2011

Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010

artículo científico publicado en 2012

Global, regional, and national comparative risk assessment of 79 behavioural, environmental and occupational, and metabolic risks or clusters of risks in 188 countries, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013

artículo científico publicado en 2015

Global, regional, and national incidence and mortality for HIV, tuberculosis, and malaria during 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013.

artículo científico publicado en 2014

Global, regional, and national levels and causes of maternal mortality during 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013.

artículo científico publicado en 2014

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

artículo científico

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

artículo científico publicado en 2011

Health-Related Quality of Life and Functional Status Are Associated with Cardiac Status and Clinical Outcome in Children with Cardiomyopathy

artículo científico publicado en 2015

Heart Transplants in Pediatric Patients: Viral Infection As a Loss Predictor ⬇️

artículo científico publicado el 1 de noviembre de 2010

Hot topics in tetralogy of Fallot.

artículo científico publicado en 2013

How accurately, reproducibly, and efficiently can we measure left ventricular indices using M-mode, 2-dimensional, and 3-dimensional echocardiography in children?

artículo científico publicado en 2008

How should hypertrophic cardiomyopathy be classified?: What's in a name? Dilemmas in nomenclature characterizing hypertrophic cardiomyopathy and left ventricular hypertrophy

artículo científico publicado en 2009

Hypertrophic cardiomyopathy

artículo científico publicado en 2009

Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects

artículo científico publicado en 2003

Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations

artículo científico publicado en 2008

Idiopathic and Primary Cardiomyopathies in Children

Impaired binding of ZASP/Cypher with phosphoglucomutase 1 is associated with dilated cardiomyopathy

scientific journal article

Improved outcomes of pediatric dilated cardiomyopathy with utilization of heart transplantation

artículo científico publicado en 2004

Incidence of and risk factors for sudden cardiac death in children with dilated cardiomyopathy: a report from the Pediatric Cardiomyopathy Registry

artículo científico publicado en 2012

Incidence, causes, and outcomes of dilated cardiomyopathy in children

artículo científico publicado en 2006

Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel

artículo científico publicado en 2002

Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability.

artículo científico publicado en 2005

Inherited Cardiomyopathies

article

Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutation

artículo científico publicado en 2007

Initial Observations of the Effects of Calcium Chloride Infusions in Pediatric Patients with Low Cardiac Output

artículo científico publicado en 2015

International Society for Heart and Lung Transplantation: Practice guidelines for management of heart failure in children.

artículo científico publicado en 2004

Intrafamilial variability of noncompaction of the ventricular myocardium

scientific article published on 01 May 2006

Ion channel dysfunction associated with arrhythmia, ventricular noncompaction, and mitral valve prolapse: a new overlapping phenotype

artículo científico publicado en 2014

Is adenovirus a fetal pathogen? ⬇️

artículo científico publicado el 1 de septiembre de 2003

Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12.

artículo científico publicado en 2004

KCNE2 modulation of Kv4.3 current and its potential role in fatal rhythm disorders

artículo científico publicado en 2009

LAMP2 microdeletions in patients with Danon disease

artículo científico publicado en 2010

Late pacemaker requirement after pediatric orthotopic heart transplantation may predict the presence of transplant coronary artery disease

artículo científico publicado en 2004

Left Atrial structure and function in hypertrophic cardiomyopathy sarcomere mutation carriers with and without left ventricular hypertrophy

artículo científico publicado en 2017

Left Ventricular Noncompaction: A New Form of Heart Failure ⬇️

artículo científico publicado el 1 de octubre de 2010

Left ventricular non-compaction cardiomyopathy

artículo científico publicado en 2015

Left ventricular non-compaction cardiomyopathy in children: characterisation of clinical status using tissue Doppler-derived indices of left ventricular diastolic relaxation

artículo científico publicado en 2006

Left ventricular noncompaction cardiomyopathy and aortopathy in a patient with recessive dystrophic epidermolysis bullosa

artículo científico publicado en 2012

Left ventricular noncompaction cardiomyopathy in Barth syndrome: an example of an undulating cardiac phenotype necessitating mechanical circulatory support as a bridge to transplantation

artículo científico publicado en 2012

Left ventricular noncompaction cardiomyopathy: cardiac, neuromuscular, and genetic factors

artículo científico publicado en 2017

Left ventricular noncompaction in a family with lamin A/C gene mutation

artículo científico publicado en 2015

Leukocyte suppression is associated with improved clinical outcomes in children's status after orthotopic heart transplantation

artículo científico publicado en 2005

Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome).

artículo científico publicado en 2009

Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome

artículo científico publicado en 2003

Long QT syndrome and pregnancy

artículo científico publicado en 2007

Long QT syndrome in adults.

artículo científico publicado en 2007

Long-QT syndrome after age 40.

artículo científico publicado en 2008

Long-term follow-up of individuals with the electrocardiographic pattern of right bundle-branch block and ST-segment elevation in precordial leads V1 to V3.

artículo científico publicado en 2002

Malonyl coenzyme A decarboxylase deficiency: early dietary restriction and time course of cardiomyopathy

artículo científico publicado en 2012

Mechanical circulatory support as a bridge to combined dual organ transplantation in children

artículo científico publicado en 2006

Mediators in HIV-associated cardiovascular disease: a focus on cytokines and genes

artículo científico publicado en 2003

Medical Therapy Leads to Favorable Remodeling in Left Ventricular Non-compaction Cardiomyopathy: Dilated Phenotype

artículo científico

Milder clinical course of Type IV 3-methylglutaconic aciduria due to a novel mutation in TMEM70 ⬇️

artículo científico publicado el 24 de julio de 2010

Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro

artículo científico publicado en 2007

Modification of a volume-overload heart failure model to track myocardial remodeling and device-related reverse remodeling

artículo científico publicado en 2011

Modulating effects of age and gender on the clinical course of long QT syndrome by genotype

artículo científico publicado en 2003

Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations

artículo científico publicado en 2012

Molecular diagnosis of myocardial disease

artículo científico publicado en 2002

Molecular genetic basis of sudden cardiac death

scientific article published on 01 October 2004

Molecular genetics of heterotaxy syndromes

artículo científico publicado en 2004

Molecular normalization of dystrophin in the failing left and right ventricle of patients treated with either pulsatile or continuous flow-type ventricular assist devices

artículo científico publicado en 2004

Molecular remodelling of dystrophin in patients with end-stage cardiomyopathies and reversal in patients on assistance-device therapy.

artículo científico publicado en 2002

Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosis

artículo científico publicado en 2005

Mortality and sudden death in pediatric left ventricular noncompaction in a tertiary referral center

artículo científico publicado en 2013

Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome

artículo científico publicado en 2006

Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction

artículo científico publicado en 2002

Mutation and gender-specific risk in type 2 long QT syndrome: implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome

artículo científico publicado en 2011

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2002

Mutation screening for the genes causing cardiac arrhythmias

artículo científico publicado en 2006

Mutation site-specific differences in arrhythmic risk and sensitivity to sympathetic stimulation in the LQT1 form of congenital long QT syndrome: multicenter study in Japan

artículo científico publicado en 2004

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

artículo científico publicado en 2003

Mutations in KCNE1 in long QT syndrome (LQTS): insights into mechanism of LQTS and drug sensitivity?

artículo científico publicado en 2006

Mutations in PDLIM3 and MYOZ1 encoding myocyte Z line proteins are infrequently found in idiopathic dilated cardiomyopathy

artículo científico publicado en 2007

Mutations in conserved amino acids in the KCNQ1 channel and risk of cardiac events in type-1 long-QT syndrome

artículo científico publicado en 2009

Mutations in cytoplasmic loops of the KCNQ1 channel and the risk of life-threatening events: implications for mutation-specific response to β-blocker therapy in type 1 long-QT syndrome

artículo científico publicado en 2012

Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2006

Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy

artículo científico publicado en 2002

Mutations in the muscle LIM protein and α-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis ⬇️

artículo científico publicado el 1 de septiembre de 2003

Myocardial Fas ligand expression increases susceptibility to AZT-induced cardiomyopathy

artículo científico publicado en 2007

Myocardial deformation abnormalities in pediatric hypertrophic cardiomyopathy: are all etiologies identical?

artículo científico publicado en 2008

Myocardial fibrosis burden predicts left ventricular ejection fraction and is associated with age and steroid treatment duration in duchenne muscular dystrophy

artículo científico publicado en 2015

Myocardial infarction, viral infection, and the cytoskeleton final common pathways of a common disease?

artículo científico publicado en 2007

Myocardial pro-inflammatory cytokine expression and cellular rejection in pediatric heart transplant recipients

artículo científico publicado en 2008

NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling

artículo científico publicado en 2008

Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis ⬇️

artículo científico publicado el 26 de octubre de 2010

Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism

artículo científico publicado en 2002

Nesiritide therapy in a term neonate with renal disease

artículo científico publicado en 2006

No Obesity Paradox in Pediatric Patients With Dilated Cardiomyopathy

artículo científico publicado en 2018

Novel mutations in domain I of SCN5A cause Brugada syndrome

artículo científico publicado en 2002

Outcomes in children with Noonan syndrome and hypertrophic cardiomyopathy: a study from the Pediatric Cardiomyopathy Registry

artículo científico publicado en 2012

Outcomes of congenital heart surgery patients after extracorporeal life support at Texas Children's Hospital

artículo científico publicado en 2004

Outcomes of restrictive cardiomyopathy in childhood and the influence of phenotype: a report from the Pediatric Cardiomyopathy Registry.

artículo científico

Outpatient continuous parenteral inotropic therapy as bridge to transplantation in children with advanced heart failure

artículo científico publicado en 2006

Over two decades of pediatric heart transplantation: How has survival changed?

article

PTPN11 mutation associated with aortic dilation and hypertrophic cardiomyopathy in a pediatric patient with Noonan syndrome

artículo científico publicado en 2009

Parvovirus B19 myocarditis causes significant morbidity and mortality in children

artículo científico publicado en 2012

Paucity of skeletal manifestations in Hispanic families with FBN1 mutations

artículo científico publicado en 2009

Pediatric Cardiomyopathies

artículo científico publicado en 2017

Pediatric and adult dilated cardiomyopathy represent distinct pathological entities

artículo científico publicado en 2017

Pediatric cardiomyopathy: importance of genetic and metabolic evaluation

artículo científico publicado en 2012

Phenotypic characterization of a large European family with Brugada syndrome displaying a sudden unexpected death syndrome mutation in SCN5A:.

artículo científico publicado en 2004

Phospholipid abnormalities in children with Barth syndrome

artículo científico publicado en 2003

Postmortem cardiomegaly and echocardiographic measurements of left ventricular size and function in children infected with the human immunodeficiency virus. The Prospective P2C2 HIV Multicenter Study

artículo científico publicado en 2003

Preface: Heart failure in children

scientific article published on 01 October 2010

Prevalence, morbidity, and mortality of heart failure-related hospitalizations in children in the United States: a population-based study

artículo científico publicado en 2012

Prevalence, predictors, and outcomes of cardiorenal syndrome in children with dilated cardiomyopathy: a report from the Pediatric Cardiomyopathy Registry

artículo científico publicado en 2015

Preventing pediatric cardiomyopathy: a 2015 outlook

artículo científico publicado en 2015

Prognostic implications of mutation-specific QTc standard deviation in congenital long QT syndrome

artículo científico publicado en 2013

Progress in Pediatric Cardiology

Prolonged QT in a 13-year-old patient with Down syndrome and complete atrioventricular canal defect

scientific article published on 01 October 2011

Proposed diagnostic criteria for the Brugada syndrome: consensus report

artículo científico publicado en 2002

Provocation testing in inherited arrhythmia disorders: can we be more specific?

artículo científico publicado en 2005

Radio-frequency catheter ablation of accessory pathway mediated tachycardia in a child after orthotopic heart transplantation

artículo científico publicado en 2005

Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

artículo científico publicado en 2011

Recommendations for physical activity and recreational sports participation for young patients with genetic cardiovascular diseases.

artículo científico publicado en 2004

Recovery of echocardiographic function in children with idiopathic dilated cardiomyopathy: results from the pediatric cardiomyopathy registry

artículo científico publicado en 2014

Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly

artículo científico publicado en 2008

Regional myocardial deformation in children with hypertrophic cardiomyopathy: morphological and clinical correlations

scientific article published on 30 October 2007

Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1

article

Reply: Pregnancy in arrhythmogenic right ventricular dysplasia/cardiomyopathy

artículo científico publicado en 2013

Response by Towbin and Jefferies to Letter Regarding Article, "Cardiomyopathies Due to Left Ventricular Noncompaction, Mitochondrial and Storage Diseases, and Inborn Errors of Metabolism".

artículo científico publicado en 2017

Response to letter regarding article, "mortality and sudden death in pediatric left ventricular noncompaction in a tertiary referral center".

artículo científico publicado en 2014

Risk factors and mode of death in isolated hypertrophic cardiomyopathy in children

artículo científico publicado en 2009

Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT syndrome

artículo científico publicado en 2008

Risk factors for recurrent syncope and subsequent fatal or near-fatal events in children and adolescents with long QT syndrome

artículo científico publicado en 2011

Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals

artículo científico publicado en 2011

Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndrome

artículo científico publicado en 2006

Risk of death in the long QT syndrome when a sibling has died

artículo científico publicado en 2008

Risk of life-threatening cardiac events among patients with long QT syndrome and multiple mutations

artículo científico publicado en 2012

Risk of recurrent cardiac events after onset of menopause in women with congenital long-QT syndrome types 1 and 2

artículo científico publicado en 2011

Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutation

artículo científico publicado en 2011

Risk stratification at diagnosis for children with hypertrophic cardiomyopathy: an analysis of data from the Pediatric Cardiomyopathy Registry

artículo científico publicado en 2013

SCN5A variants in Japanese patients with left ventricular noncompaction and arrhythmia

artículo científico publicado en 2008

SNP genotyping to screen for a common deletion in CHARGE syndrome

artículo científico publicado en 2005

Safety and efficacy of nesiritide in pediatric heart failure.

artículo científico publicado en 2007

Scarring in the heart--a reversible phenomenon?

artículo científico publicado en 2007

Shared genetic causes of cardiac hypertrophy in children and adults

artículo científico publicado en 2008

Short-term mechanical unloading and reverse remodeling of failing hearts in children

artículo científico publicado en 2009

Sickle cell anemia mice develop a unique cardiomyopathy with restrictive physiology

scientific article published on 08 August 2016

Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation

artículo científico publicado en 2005

Strategies to Prevent Cast Formation in Patients with Plastic Bronchitis Undergoing Heart Transplantation

artículo científico publicado en 2017

Survival Without Cardiac Transplantation Among Children With Dilated Cardiomyopathy

artículo científico publicado en 2017

Symptom complex is associated with transplant coronary artery disease and sudden death/resuscitated sudden death in pediatric heart transplant recipients

artículo científico publicado en 2005

Task Force 2: congenital heart disease

artículo científico publicado en 2005

Task Force 4: HCM and other cardiomyopathies, mitral valve prolapse, myocarditis, and Marfan syndrome

artículo científico publicado en 2005

The A, B, Cs of sudden infant death syndrome: an electrical disorder?

scientific article published on 20 February 2010

The Brugada Syndrome

The Burden of Early Phenotypes and the Influence of Wall Thickness in Hypertrophic Cardiomyopathy Mutation Carriers: Findings From the HCMNet Study.

artículo científico publicado en 2017

The Impact of Concomitant Left Ventricular Non-compaction with Congenital Heart Disease on Perioperative Outcomes

artículo científico publicado en 2016

The Incidence of Pediatric Cardiomyopathy in Two Regions of the United States ⬇️

artículo científico publicado el 24 de abril de 2003

The International Society of Heart and Lung Transplantation Guidelines for the care of heart transplant recipients

artículo científico publicado en 2010

The detection of cardiotropic viruses in the myocardium of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy

artículo científico publicado en 2002

The detection of viral genomes by polymerase chain reaction in the myocardium of pediatric patients with advanced HIV disease

article

The efficacy of mitral valve surgery in children with dilated cardiomyopathy and severe mitral regurgitation

artículo científico publicado en 2007

The impact of heart failure severity at time of listing for cardiac transplantation on survival in pediatric cardiomyopathy

artículo científico publicado en 2011

The mystery of arrhythmogenic right ventricular dysplasia/cardiomyopathy: from observation to mechanistic explanation

artículo científico publicado en 2006

The pediatric cardiomyopathy registry and heart failure: key results from the first 15 years

artículo científico publicado en 2010

The role of endomyocardial biopsy in the management of cardiovascular disease: a scientific statement from the American Heart Association, the American College of Cardiology, and the European Society of Cardiology

scientific article published on 24 October 2007

The role of endomyocardial biopsy in the management of cardiovascular disease: a scientific statement from the American Heart Association, the American College of Cardiology, and the European Society of Cardiology Endorsed by the Heart Failure Socie

artículo científico publicado en 2007

The role of endomyocardial biopsy in the management of cardiovascular disease: a scientific statement from the American Heart Association, the American College of Cardiology, and the European Society of Cardiology. Endorsed by the Heart Failure Soci

scientific article published on 01 November 2007

Tinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regulate heart function across species

scientific journal article

Toward a genetic etiology of CHARGE syndrome: I. A systematic scan for submicroscopic deletions

article

Transcription factor neuromancer/TBX20 is required for cardiac function in Drosophila with implications for human heart disease

artículo científico publicado en 2008

Treating children with idiopathic dilated cardiomyopathy (from the Pediatric Cardiomyopathy Registry).

artículo científico publicado en 2009

Trigger-specific ion-channel mechanisms, risk factors, and response to therapy in type 1 long QT syndrome

artículo científico publicado en 2011

Trigger-specific risk factors and response to therapy in long QT syndrome type 2.

artículo científico publicado en 2010

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

article

Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations

artículo científico publicado en 2004

Variable expression of long QT syndrome among gene carriers from families with five different HERG mutations

artículo científico publicado en 2002

Ventricular remodeling and survival are more favorable for myocarditis than for idiopathic dilated cardiomyopathy in childhood: an outcomes study from the Pediatric Cardiomyopathy Registry.

artículo científico

Viral endomyocardial infection in the 1st year post transplant is associated with persistent inflammation in children who have undergone cardiac transplant

artículo científico

Viral endomyocardial infection is an independent predictor and potentially treatable risk factor for graft loss and coronary vasculopathy in pediatric cardiac transplant recipients

artículo científico publicado en 2010

Viral epidemiologic shift in inflammatory heart disease: the increasing involvement of parvovirus B19 in the myocardium of pediatric cardiac transplant patients

artículo científico publicado en 2010

Viral genomic detection and outcome in myocarditis

artículo científico publicado en 2005

Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns

artículo científico publicado en 2017

Worsening renal function in children hospitalized with decompensated heart failure: evidence for a pediatric cardiorenal syndrome?

artículo científico publicado en 2008

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

scholarly article

alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption

artículo científico publicado en 2008

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