Lista de obras - William McKenna - Dominio Público Uruguay

2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC).

artículo científico publicado en 2014

A new diagnostic test for arrhythmogenic right ventricular cardiomyopathy.

artículo científico publicado en 2009

A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD).

artículo científico publicado en 2013

A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions

artículo científico publicado en 2011

A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2007

A validation study of the 2003 American College of Cardiology/European Society of Cardiology and 2011 American College of Cardiology Foundation/American Heart Association risk stratification and treatment algorithms for sudden cardiac death in [...]

artículo científico publicado en 2013

Abnormal cardiac formation in hypertrophic cardiomyopathy: fractal analysis of trabeculae and preclinical gene expression.

artículo científico

Abnormal septal convexity into the left ventricle occurs in subclinical hypertrophic cardiomyopathy ⬇️

artículo científico publicado en 2015

Alcohol Septal Ablation in Hypertrophic Cardiomyopathy: An Opportunity to Be Taken

artículo científico publicado en 2012

Altered desmosomal proteins in granulomatous myocarditis and potential pathogenic links to arrhythmogenic right ventricular cardiomyopathy.

artículo científico publicado en 2011

Anomalous left coronary artery in hypertrophic cardiomyopathy.

artículo científico publicado en 2014

Appropriate interpretation of the athlete's electrocardiogram saves lives as well as moneyThe opinions expressed in this article are not necessarily those of the Editors of the European Heart Journal or of the European Society of Cardiology

artículo científico publicado en 2007

Are We Nearly There Yet Progress in the Prevention of Sudden Cardiac Death in the Young

article

Arrhythmogenic cardiomyopathy: etiology, diagnosis, and treatment

artículo científico publicado en 2010

Arrhythmogenic left ventricular cardiomyopathy

artículo científico

Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis

artículo científico publicado en 2006

Arrhythmogenic right ventricular cardiomyopathy mimics: role of cardiovascular magnetic resonance

artículo científico publicado en 2013

Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2

artículo científico publicado en 2006

Cardiac Magnetic Resonance Imaging and Sudden Death Risk in Patients With Hypertrophic Cardiomyopathy

article

Cardiac myosin binding protein-C mutations in families with hypertrophic cardiomyopathy: disease expression in relation to age, gender, and long term outcome.

artículo científico publicado en 2012

Cardiomyopathy mutations reveal variable region of myosin converter as major element of cross-bridge compliance.

artículo científico publicado en 2009

Cardiovascular Magnetic Resonance in Arrhythmogenic Right Ventricular Cardiomyopathy Revisited

article

Cardiovascular magnetic resonance measurement of myocardial extracellular volume in health and disease

artículo científico

Cellular mechanisms underlying the increased disease severity seen for patients with long QT syndrome caused by compound mutations in KCNQ1.

artículo científico publicado en 2014

Clinical Significance of Epsilon Waves in Arrhythmogenic Cardiomyopathy

article

Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression

artículo científico publicado en 2007

Comparison of Prognostic Value of Tissue Doppler Imaging in Carcinoid Heart Disease Versus the Value in Patients With the Carcinoid Syndrome but Without Carcinoid Heart Disease

article

Comparison of electrocardiographic criteria for the detection of cardiac abnormalities in elite black and white athletes.

artículo científico publicado en 2014

Current electrocardiographic criteria for diagnosis of Brugada pattern: a consensus report

article

Current state of knowledge on aetiology, diagnosis, management, and therapy of myocarditis: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases.

artículo científico publicado en 2013

Detection of hypertrophic cardiomyopathy is improved when using advanced rather than strictly conventional 12-lead electrocardiogram

article

Diagnosis of apical hypertrophic cardiomyopathy: T-wave inversion and relative but not absolute apical left ventricular hypertrophy

artículo científico publicado en 2015

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

Disease pathways and novel therapeutic targets in hypertrophic cardiomyopathy

artículo científico publicado en 2011

Dynamic conduction and repolarisation changes in early arrhythmogenic right ventricular cardiomyopathy versus benign outflow tract ectopy demonstrated by high density mapping & paced surface ECG analysis

artículo científico publicado en 2014

Dynamic electrocardiographic changes in patients with arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2010

Electrophysiological abnormalities precede overt structural changes in arrhythmogenic right ventricular cardiomyopathy due to mutations in desmoplakin-A combined murine and human study.

artículo científico publicado en 2012

Epidemiology of the inherited cardiomyopathies

artículo científico publicado en 2020

Evaluation of suspected right ventricular pathology in the athlete

artículo científico publicado en 2012

Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency

artículo científico publicado en 2009

Exercise-induced ventricular arrhythmias and risk of sudden cardiac death in patients with hypertrophic cardiomyopathy

artículo científico publicado en 2009

Exercise: friend or foe?

artículo científico publicado en 2013

Familial Evaluation in Arrhythmogenic Right Ventricular Cardiomyopathy

article

Family History of Premature Death and Risk of Early Onset Cardiovascular Disease

article

Functional effects of the DCM mutant Gly159Asp Troponin C in skinned muscle fibres

article

Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing

artículo científico publicado en 2013

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

artículo científico publicado en 2010

Genetic variation in SCN10A influences cardiac conduction

artículo científico publicado en 2010

Genetics of inherited cardiomyopathy.

artículo científico publicado en 2011

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

High-density substrate mapping in Brugada syndrome: combined role of conduction and repolarization heterogeneities in arrhythmogenesis.

artículo científico publicado en 2009

Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair.

artículo científico publicado en 2008

How should hypertrophic cardiomyopathy be classified?

article

Imaging phenotype versus genotype in hypertrophic cardiomyopathy

artículo científico publicado en 2011

Left ventricular outflow tract obstruction and sudden death risk in patients with hypertrophic cardiomyopathy.

artículo científico publicado en 2006

Left ventricular strain and untwist in hypertrophic cardiomyopathy: relation to exercise capacity.

artículo científico publicado en 2010

Left-dominant arrhythmogenic cardiomyopathy in a large family: associated desmosomal or nondesmosomal genotype?

artículo científico publicado en 2013

Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T gene.

artículo científico publicado en 2011

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations

artículo científico publicado en 2011

Metabolic modulator perhexiline corrects energy deficiency and improves exercise capacity in symptomatic hypertrophic cardiomyopathy.

artículo científico publicado en 2010

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

artículo científico publicado en 2012

Molecular changes in the heart of a severe case of arrhythmogenic right ventricular cardiomyopathy caused by a desmoglein-2 null allele

article

Mutation screening of the PTPN11 gene in hypertrophic cardiomyopathy

artículo científico publicado en 2006

Mutational Heterogeneity, Modifier Genes, and Environmental Influences Contribute to Phenotypic Diversity of Arrhythmogenic Cardiomyopathy

article

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

artículo científico publicado en 2007

Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy.

artículo científico publicado en 2011

Myocardial Crypts

article

Myocarditis and the military patient.

artículo científico

Myofibrillar Ca(2+) sensitivity is uncoupled from troponin I phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin T.

artículo científico publicado en 2012

Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis ⬇️

artículo científico publicado el 26 de octubre de 2010

Normal passive viscoelasticity but abnormal myofibrillar force generation in human hypertrophic cardiomyopathy

artículo científico publicado en 2010

Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy

artículo científico publicado en 2014

Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy?

artículo científico publicado en 2010

Outcomes after implantable cardioverter-defibrillator treatment in children with hypertrophic cardiomyopathy.

artículo científico publicado en 2006

Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chain

artículo científico publicado en 2015

Prediction of sarcomere mutations in subclinical hypertrophic cardiomyopathy

artículo científico publicado en 2014

Prediction of thrombo-embolic risk in patients with hypertrophic cardiomyopathy (HCM Risk-CVA).

artículo científico publicado en 2015

Prevalence and clinical significance of cardiovascular abnormalities in patients with the LEOPARD syndrome.

artículo científico publicado en 2007

Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy

article

Prevalence of J-point elevation in sudden arrhythmic death syndrome families

artículo científico publicado en 2011

Prevalence of sequence variants in the RAS-mitogen activated protein kinase signaling pathway in pre-adolescent children with hypertrophic cardiomyopathy

artículo científico publicado en 2012

Prevalence, Clinical Significance, and Genetic Basis of Hypertrophic Cardiomyopathy With Restrictive Phenotype

article

Prognostic significance of myocardial fibrosis in hypertrophic cardiomyopathy.

artículo científico

Prophylactic implantable defibrillator in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia and no prior ventricular fibrillation or sustained ventricular tachycardia

artículo científico publicado en 2010

Quantification of left ventricular trabeculae using fractal analysis.

artículo científico publicado en 2013

Rare nonconservative LRP6 mutations are associated with metabolic syndrome.

artículo científico publicado en 2013

Recommendations for interpretation of 12-lead electrocardiogram in the athlete

artículo científico publicado en 2009

Reconciling the Protean Manifestations of Arrhythmogenic Cardiomyopathy

article

Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada.

artículo científico publicado en 2012

Relation between serum N-terminal pro-brain natriuretic peptide and prognosis in patients with hypertrophic cardiomyopathy

artículo científico publicado en 2013

Reply

Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy

artículo científico publicado en 2007

Role of late gadolinium enhancement cardiovascular magnetic resonance in the risk stratification of hypertrophic cardiomyopathy

artículo científico

Significance of maximal and regional left ventricular wall thickness in association with arrhythmic events in patients with hypertrophic cardiomyopathy.

artículo científico publicado en 2010

Skeletal muscle involvement in cardiomyopathies

artículo científico publicado en 2013

Sudden Cardiac Death in Hypertrophic Cardiomyopathy

article

Sudden cardiac death in the young: a strategy for prevention by targeted evaluation.

artículo científico publicado en 2006

Sudden death from genetic and acquired cardiomyopathies

artículo científico publicado en 2012

T-Wave Alternans and Left Ventricular Wall Thickness in Predicting Arrhythmic Risk in Patients With Hypertrophic Cardiomyopathy

article

The cardiac desmosome and arrhythmogenic cardiomyopathies: from gene to disease.

artículo científico publicado en 2010

The implications of inheritance for clinical management

artículo científico publicado en 2012

The long-term survival and the risks and benefits of implantable cardioverter defibrillators in patients with hypertrophic cardiomyopathy

article

The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43

artículo científico publicado en 2012

The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygote

artículo científico publicado en 2013

The variation of the sarcolipin gene (SLN) in atrial fibrillation, long QT syndrome and sudden arrhythmic death syndrome

article

Treatment of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: An International Task Force Consensus Statement

artículo científico publicado en 2015

Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathy.

artículo científico publicado en 2011

Usefulness of N-terminal pro-B-type natriuretic peptide levels to predict exercise capacity in hypertrophic cardiomyopathy

artículo científico publicado en 2006

Value of the signal-averaged electrocardiogram in arrhythmogenic right ventricular cardiomyopathy/dysplasia

artículo científico publicado en 2010

Variable Interatrial Conduction Illustrated in a Hypertrophic Cardiomyopathy Population

article

When rare illuminates common: how cardiocutaneous syndromes transformed our perspective on arrhythmogenic cardiomyopathy

artículo científico

Lista de obras de William McKenna

2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC).

A new diagnostic test for arrhythmogenic right ventricular cardiomyopathy.

A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD).

A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions

A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy

A validation study of the 2003 American College of Cardiology/European Society of Cardiology and 2011 American College of Cardiology Foundation/American Heart Association risk stratification and treatment algorithms for sudden cardiac death in [...]

Abnormal cardiac formation in hypertrophic cardiomyopathy: fractal analysis of trabeculae and preclinical gene expression.

Abnormal septal convexity into the left ventricle occurs in subclinical hypertrophic cardiomyopathy ⬇️

Alcohol Septal Ablation in Hypertrophic Cardiomyopathy: An Opportunity to Be Taken

Altered desmosomal proteins in granulomatous myocarditis and potential pathogenic links to arrhythmogenic right ventricular cardiomyopathy.

Anomalous left coronary artery in hypertrophic cardiomyopathy.

Appropriate interpretation of the athlete's electrocardiogram saves lives as well as moneyThe opinions expressed in this article are not necessarily those of the Editors of the European Heart Journal or of the European Society of Cardiology

Are We Nearly There Yet Progress in the Prevention of Sudden Cardiac Death in the Young

Arrhythmogenic cardiomyopathy: etiology, diagnosis, and treatment

Arrhythmogenic left ventricular cardiomyopathy

Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis

Arrhythmogenic right ventricular cardiomyopathy mimics: role of cardiovascular magnetic resonance

Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2

Cardiac Magnetic Resonance Imaging and Sudden Death Risk in Patients With Hypertrophic Cardiomyopathy

Cardiac myosin binding protein-C mutations in families with hypertrophic cardiomyopathy: disease expression in relation to age, gender, and long term outcome.

Cardiomyopathy mutations reveal variable region of myosin converter as major element of cross-bridge compliance.

Cardiovascular Magnetic Resonance in Arrhythmogenic Right Ventricular Cardiomyopathy Revisited

Cardiovascular magnetic resonance measurement of myocardial extracellular volume in health and disease

Cellular mechanisms underlying the increased disease severity seen for patients with long QT syndrome caused by compound mutations in KCNQ1.

Clinical Significance of Epsilon Waves in Arrhythmogenic Cardiomyopathy

Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression

Comparison of Prognostic Value of Tissue Doppler Imaging in Carcinoid Heart Disease Versus the Value in Patients With the Carcinoid Syndrome but Without Carcinoid Heart Disease

Comparison of electrocardiographic criteria for the detection of cardiac abnormalities in elite black and white athletes.

Current electrocardiographic criteria for diagnosis of Brugada pattern: a consensus report

Current state of knowledge on aetiology, diagnosis, management, and therapy of myocarditis: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases.

Detection of hypertrophic cardiomyopathy is improved when using advanced rather than strictly conventional 12-lead electrocardiogram

Diagnosis of apical hypertrophic cardiomyopathy: T-wave inversion and relative but not absolute apical left ventricular hypertrophy

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

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

Disease pathways and novel therapeutic targets in hypertrophic cardiomyopathy

Dynamic conduction and repolarisation changes in early arrhythmogenic right ventricular cardiomyopathy versus benign outflow tract ectopy demonstrated by high density mapping & paced surface ECG analysis

Dynamic electrocardiographic changes in patients with arrhythmogenic right ventricular cardiomyopathy

Electrophysiological abnormalities precede overt structural changes in arrhythmogenic right ventricular cardiomyopathy due to mutations in desmoplakin-A combined murine and human study.

Epidemiology of the inherited cardiomyopathies

Evaluation of suspected right ventricular pathology in the athlete

Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency

Exercise-induced ventricular arrhythmias and risk of sudden cardiac death in patients with hypertrophic cardiomyopathy

Exercise: friend or foe?

Familial Evaluation in Arrhythmogenic Right Ventricular Cardiomyopathy

Family History of Premature Death and Risk of Early Onset Cardiovascular Disease

Functional effects of the DCM mutant Gly159Asp Troponin C in skinned muscle fibres

Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

Genetic variation in SCN10A influences cardiac conduction

Genetics of inherited cardiomyopathy.

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).

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).

High-density substrate mapping in Brugada syndrome: combined role of conduction and repolarization heterogeneities in arrhythmogenesis.

Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair.

How should hypertrophic cardiomyopathy be classified?

Imaging phenotype versus genotype in hypertrophic cardiomyopathy

Left ventricular outflow tract obstruction and sudden death risk in patients with hypertrophic cardiomyopathy.

Left ventricular strain and untwist in hypertrophic cardiomyopathy: relation to exercise capacity.

Left-dominant arrhythmogenic cardiomyopathy in a large family: associated desmosomal or nondesmosomal genotype?

Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T gene.

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations

Metabolic modulator perhexiline corrects energy deficiency and improves exercise capacity in symptomatic hypertrophic cardiomyopathy.

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

Molecular changes in the heart of a severe case of arrhythmogenic right ventricular cardiomyopathy caused by a desmoglein-2 null allele

Mutation screening of the PTPN11 gene in hypertrophic cardiomyopathy

Mutational Heterogeneity, Modifier Genes, and Environmental Influences Contribute to Phenotypic Diversity of Arrhythmogenic Cardiomyopathy

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

Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy.

Myocardial Crypts

Myocarditis and the military patient.

Myofibrillar Ca(2+) sensitivity is uncoupled from troponin I phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin T.

Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis ⬇️

Normal passive viscoelasticity but abnormal myofibrillar force generation in human hypertrophic cardiomyopathy

Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy

Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy?

Outcomes after implantable cardioverter-defibrillator treatment in children with hypertrophic cardiomyopathy.

Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chain

Prediction of sarcomere mutations in subclinical hypertrophic cardiomyopathy

Prediction of thrombo-embolic risk in patients with hypertrophic cardiomyopathy (HCM Risk-CVA).