Lista de obras - Michael H Gollob - Dominio Público Uruguay

A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation

artículo científico publicado en 2013

A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation

artículo científico publicado en 2014

A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation.

artículo científico publicado en 2016

A novel mutation in the RYR2 gene leading to catecholaminergic polymorphic ventricular tachycardia and paroxysmal atrial fibrillation: dose-dependent arrhythmia-event suppression by β-blocker therapy

artículo científico publicado en 2011

A practical guide to early repolarization.

artículo científico publicado en 2015

A prospective randomized evaluation of a pharmacogenomic approach to antiplatelet therapy among patients with ST-elevation myocardial infarction: the RAPID STEMI study.

artículo científico publicado en 2015

AMP-activated protein kinase and familial Wolff-Parkinson-White syndrome: new perspectives on heart development and arrhythmogenesis

artículo científico publicado en 2002

Accelerating risk of Fidelis lead fracture.

artículo científico publicado en 2008

An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition

scientific article published on 16 January 2020

An unusual accessory pathway: anteroseptal to ventricular outflow region connection

scientific article published on 01 May 2005

Appropriate result from an inappropriate ICD shock.

artículo científico publicado en 2006

Arrhythmia characterization and long-term outcomes in catecholaminergic polymorphic ventricular tachycardia ⬇️

artículo científico publicado el 9 de febrero de 2011

Atrial arrhythmias in the young: early onset atrial arrhythmias preceding a diagnosis of a primary muscular dystrophy

artículo científico publicado en 2014

Atrial fibrillation as an autoimmune disease?

artículo científico publicado en 2013

Atrioventricular block as the initial manifestation of cardiac sarcoidosis in middle-aged adults.

artículo científico publicado en 2014

Begetting atrial fibrillation: Connexins and arrhythmogenesis.

artículo científico publicado en 2007

Bundle Branch Re-Entrant Ventricular Tachycardia: Novel Genetic Mechanisms in a Life-Threatening Arrhythmia

artículo científico publicado en 2016

Cardiac connexins as candidate genes for idiopathic atrial fibrillation.

artículo científico publicado en 2006

Characterization of a novel mutation in the cardiac ryanodine receptor that results in catecholaminergic polymorphic ventricular tachycardia ⬇️

artículo científico publicado el 14 de julio de 2010

Chronic AMPK activity dysregulation produces myocardial insulin resistance in the human Arg302Gln-PRKAG2 glycogen storage disease mouse model.

artículo científico publicado en 2013

Clinical trials, the renin angiotensin system and atrial fibrillation.

artículo científico publicado en 2006

Comment on "Familial pseudo-Wolff-Parkinson-White syndrome".

artículo científico publicado en 2006

Corrigendum to: 'HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies' [Europace 2011;13:1077-109, doi: 10.1093/europace/eur245]

artículo científico publicado en 2012

Degenerating regenerating torsades de pointes.

artículo científico publicado en 2012

Derivation and validation of a simple exercise-based algorithm for prediction of genetic testing in relatives of LQTS probands

artículo científico publicado en 2011

Discrepant DNA analysis in three patients with inherited arrhythmia: molecular genetic test results deserve a second glance

scientific article published on 01 June 2008

Distinct early signaling events resulting from the expression of the PRKAG2 R302Q mutant of AMPK contribute to increased myocardial glycogen.

artículo científico publicado en 2009

Distinguishing pathogenic mutations from innocuous rare variants in gene discovery for Brugada syndrome

artículo científico publicado en 2012

Early repolarization: a rare primary arrhythmic syndrome and common modifier of arrhythmic risk

artículo científico publicado en 2013

Editorial commentary: Genetic testing in the absence of phenotype: When genetic testing may cause harm.

artículo científico publicado en 2016

Epinephrine infusion in the evaluation of unexplained cardiac arrest and familial sudden death: from the cardiac arrest survivors with preserved Ejection Fraction Registry

artículo científico

Epsilon wave uncovered by exercise test in a patient with desmoplakin-positive arrhythmogenic right ventricular cardiomyopathy

scientific article published on 29 January 2015

Evaluation of Prolonged QT Interval: Structural Heart Disease Mimicking Long QT Syndrome

artículo científico publicado en 2017

Evaluation of genes encoding for the transient outward current (Ito) identifies the KCND2 gene as a cause of J-wave syndrome associated with sudden cardiac death

artículo científico publicado en 2014

Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation

artículo científico publicado en 2010

Evolution of a genetic diagnosis

scientific article published on 20 December 2013

Evolution of clinical diagnosis in patients presenting with unexplained cardiac arrest or syncope due to polymorphic ventricular tachycardia

artículo científico publicado en 2013

Exercise testing in asymptomatic gene carriers exposes a latent electrical substrate of arrhythmogenic right ventricular cardiomyopathy.

artículo científico publicado en 2013

Feasibility study of endocardial mapping of ganglionated plexuses during catheter ablation of atrial fibrillation.

artículo científico publicado en 2006

First report of a large duplication of the KCNQ1 gene in a patient with long QT syndrome.

artículo científico publicado en 2014

Frequency of peripartum cardiomyopathy.

artículo científico publicado en 2006

Gain-of-function mutation of Nav1.5 in atrial fibrillation enhances cellular excitability and lowers the threshold for action potential firing

artículo científico publicado en 2009

Genetic determinants of atrial fibrillation: SNPs are riding the wave(lets)

artículo científico publicado en 2006

Genetics of cardiac electrical disease

artículo científico

Genetics of inherited primary arrhythmia disorders

artículo científico publicado en 2015

Go protein subunit Goα and the secretory process of the natriuretic peptide hormones ANF and BNP.

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

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

In vivo assessment of myocardial glucose uptake by positron emission tomography in adults with the PRKAG2 cardiac syndrome.

artículo científico publicado en 2009

In-hospital mortality in 13,263 survivors of out-of-hospital cardiac arrest in Canada

artículo científico publicado en 2010

Influence of gender on ICD implantation for primary and secondary prevention of sudden cardiac death.

artículo científico publicado en 2006

Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy.

artículo científico publicado en 2009

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

artículo científico publicado en 2014

Isorhythmic interaction between a dual-chamber pacemaker and an intrinsic rhythm: pacemaker malfunctioning or not?

artículo científico publicado en 2004

Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?

artículo científico

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

artículo científico publicado en 2012

Modulating phenotypic expression of the PRKAG2 cardiac syndrome.

artículo científico publicado en 2008

Myocardial infarction in a teenager

artículo científico publicado en 2014

No long-term psychological morbidity living with an implantable cardioverter defibrillator under advisory: the Medtronic Marquis experience.

artículo científico publicado en 2008

Normal atrial activation and voltage during sinus rhythm in the human heart: an endocardial and epicardial mapping study in patients with a history of atrial fibrillation.

artículo científico publicado en 2007

Outcome of Apparently Unexplained Cardiac Arrest: Results From Investigation and Follow-Up of the Prospective Cardiac Arrest Survivors With Preserved Ejection Fraction Registry

artículo científico

PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy

artículo científico publicado en 2002

Patient Outcomes From a Specialized Inherited Arrhythmia Clinic.

artículo científico publicado en 2016

Predictors of fracture risk of a small caliber implantable cardioverter defibrillator lead.

artículo científico publicado en 2009

Prevalence and Characteristics of Early Repolarization in the CASPER Registry

scientific article published on 01 August 2011

Prevalence and Clinical Implication of Double Mutations in Hypertrophic Cardiomyopathy: Revisiting the Gene-Dose Effect.

artículo científico publicado en 2017

Primary prevention of idiopathic ventricular fibrillation: Not for the faint of heart

artículo científico publicado en 2015

Procainamide infusion in the evaluation of unexplained cardiac arrest: from the Cardiac Arrest Survivors with Preserved Ejection Fraction Registry (CASPER).

artículo científico publicado en 2014

Psychological adjustment in ICD patients living with advisory fidelis leads.

artículo científico publicado en 2010

Rapid Device-Detected Nonsustained Ventricular Tachycardia in the Risk Stratification of Hypertrophic Cardiomyopathy.

artículo científico publicado en 2016

Reasons for escalating pacemaker implants

artículo científico publicado en 2006

Recommendations for the use of genetic testing in the clinical evaluation of inherited cardiac arrhythmias associated with sudden cardiac death: Canadian Cardiovascular Society/Canadian Heart Rhythm Society joint position paper

artículo científico publicado en 2011

Reduced septal glucose metabolism predicts response to cardiac resynchronization therapy

scientific article published on 10 December 2011

Repeatable noninvasive measurement of mouse myocardial glucose uptake with 18F-FDG: evaluation of tracer kinetics in a type 1 diabetes model.

artículo científico publicado en 2013

Reply: Noninvasive measurement of mouse myocardial glucose uptake with 18F-FDG

artículo científico publicado en 2014

Response to Letter Regarding Article, "Outcome of Apparently Unexplained Cardiac Arrest: Results From Investigation and Follow-Up of the Prospective Cardiac Arrest Survivors With Preserved Ejection Fraction Registry".

artículo científico publicado en 2016

Safety of Outpatient Initiation of Disopyramide for Obstructive Hypertrophic Cardiomyopathy Patients.

artículo científico publicado en 2017

Sentinel symptoms in patients with unexplained cardiac arrest: from the cardiac arrest survivors with preserved ejection fraction registry (CASPER).

artículo científico publicado en 2011

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation

artículo científico publicado en 2006

Successful ablation of a concealed parahisian accessory pathway using a remote magnetic navigation system following failure by conventional methods.

artículo científico publicado en 2006

Systematic Assessment of Patients With Unexplained Cardiac Arrest

artículo científico publicado en 2009

Targeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation.

artículo científico publicado en 2014

Ten-year follow-up of cardiac sympathectomy in a young woman with catecholaminergic polymorphic ventricular tachycardia and an implantable cardioverter defibrillator

artículo científico publicado en 2009

The Phenotypic Spectrum of a Mutation Hotspot Responsible for the Short QT Syndrome

scientific article published on 01 February 2017

The evolution of gene discovery and the revelation of truth ⬇️

artículo científico publicado el 11 de enero de 2011

The genetic and clinical features of cardiac channelopathies.

scientific article published on July 2010

The genetics of cardiac disease associated with sudden cardiac death: a paper from the 2011 William Beaumont Hospital Symposium on molecular pathology.

artículo científico

The role of atrial natriuretic peptide in modulating cardiac electrophysiology.

artículo científico publicado en 2011

The short QT syndrome: proposed diagnostic criteria.

artículo científico publicado en 2011

Toward Translation of Genomic Discovery to Clinical Efficacy in Atrial Fibrillation

artículo científico publicado en 2016

Transgenic mouse model of ventricular preexcitation and atrioventricular reentrant tachycardia induced by an AMP-activated protein kinase loss-of-function mutation responsible for Wolff-Parkinson-White syndrome.

artículo científico publicado en 2004

Use of implantable cardioverter defibrillators in Canadian and US survivors of out-of-hospital cardiac arrest

artículo científico publicado en 2007

Usefulness of 14-Day Holter for Detection of Nonsustained Ventricular Tachycardia in Patients With Hypertrophic Cardiomyopathy.

artículo científico publicado en 2016

Voltage-gated sodium channels: biophysics, pharmacology, and related channelopathies.

artículo científico

Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia.

artículo científico publicado en 2015

Lista de obras de Michael H Gollob

A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation

A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation

A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation.

A novel mutation in the RYR2 gene leading to catecholaminergic polymorphic ventricular tachycardia and paroxysmal atrial fibrillation: dose-dependent arrhythmia-event suppression by β-blocker therapy

A practical guide to early repolarization.

A prospective randomized evaluation of a pharmacogenomic approach to antiplatelet therapy among patients with ST-elevation myocardial infarction: the RAPID STEMI study.

AMP-activated protein kinase and familial Wolff-Parkinson-White syndrome: new perspectives on heart development and arrhythmogenesis

Accelerating risk of Fidelis lead fracture.

An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition

An unusual accessory pathway: anteroseptal to ventricular outflow region connection

Appropriate result from an inappropriate ICD shock.

Arrhythmia characterization and long-term outcomes in catecholaminergic polymorphic ventricular tachycardia ⬇️

Atrial arrhythmias in the young: early onset atrial arrhythmias preceding a diagnosis of a primary muscular dystrophy

Atrial fibrillation as an autoimmune disease?

Atrioventricular block as the initial manifestation of cardiac sarcoidosis in middle-aged adults.

Begetting atrial fibrillation: Connexins and arrhythmogenesis.

Bundle Branch Re-Entrant Ventricular Tachycardia: Novel Genetic Mechanisms in a Life-Threatening Arrhythmia

Cardiac connexins as candidate genes for idiopathic atrial fibrillation.

Characterization of a novel mutation in the cardiac ryanodine receptor that results in catecholaminergic polymorphic ventricular tachycardia ⬇️

Chronic AMPK activity dysregulation produces myocardial insulin resistance in the human Arg302Gln-PRKAG2 glycogen storage disease mouse model.

Clinical trials, the renin angiotensin system and atrial fibrillation.

Comment on "Familial pseudo-Wolff-Parkinson-White syndrome".

Corrigendum to: 'HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies' [Europace 2011;13:1077-109, doi: 10.1093/europace/eur245]

Degenerating regenerating torsades de pointes.

Derivation and validation of a simple exercise-based algorithm for prediction of genetic testing in relatives of LQTS probands

Discrepant DNA analysis in three patients with inherited arrhythmia: molecular genetic test results deserve a second glance

Distinct early signaling events resulting from the expression of the PRKAG2 R302Q mutant of AMPK contribute to increased myocardial glycogen.

Distinguishing pathogenic mutations from innocuous rare variants in gene discovery for Brugada syndrome

Early repolarization: a rare primary arrhythmic syndrome and common modifier of arrhythmic risk

Editorial commentary: Genetic testing in the absence of phenotype: When genetic testing may cause harm.

Epinephrine infusion in the evaluation of unexplained cardiac arrest and familial sudden death: from the cardiac arrest survivors with preserved Ejection Fraction Registry

Epsilon wave uncovered by exercise test in a patient with desmoplakin-positive arrhythmogenic right ventricular cardiomyopathy

Evaluation of Prolonged QT Interval: Structural Heart Disease Mimicking Long QT Syndrome

Evaluation of genes encoding for the transient outward current (Ito) identifies the KCND2 gene as a cause of J-wave syndrome associated with sudden cardiac death

Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation

Evolution of a genetic diagnosis

Evolution of clinical diagnosis in patients presenting with unexplained cardiac arrest or syncope due to polymorphic ventricular tachycardia

Exercise testing in asymptomatic gene carriers exposes a latent electrical substrate of arrhythmogenic right ventricular cardiomyopathy.

Feasibility study of endocardial mapping of ganglionated plexuses during catheter ablation of atrial fibrillation.

First report of a large duplication of the KCNQ1 gene in a patient with long QT syndrome.

Frequency of peripartum cardiomyopathy.

Gain-of-function mutation of Nav1.5 in atrial fibrillation enhances cellular excitability and lowers the threshold for action potential firing

Genetic determinants of atrial fibrillation: SNPs are riding the wave(lets)

Genetics of cardiac electrical disease

Genetics of inherited primary arrhythmia disorders

Go protein subunit Goα and the secretory process of the natriuretic peptide hormones ANF and BNP.

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).

In vivo assessment of myocardial glucose uptake by positron emission tomography in adults with the PRKAG2 cardiac syndrome.

In-hospital mortality in 13,263 survivors of out-of-hospital cardiac arrest in Canada

Influence of gender on ICD implantation for primary and secondary prevention of sudden cardiac death.

Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy.

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

Isorhythmic interaction between a dual-chamber pacemaker and an intrinsic rhythm: pacemaker malfunctioning or not?

Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

Modulating phenotypic expression of the PRKAG2 cardiac syndrome.

Myocardial infarction in a teenager

No long-term psychological morbidity living with an implantable cardioverter defibrillator under advisory: the Medtronic Marquis experience.

Normal atrial activation and voltage during sinus rhythm in the human heart: an endocardial and epicardial mapping study in patients with a history of atrial fibrillation.

Outcome of Apparently Unexplained Cardiac Arrest: Results From Investigation and Follow-Up of the Prospective Cardiac Arrest Survivors With Preserved Ejection Fraction Registry

PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy

Patient Outcomes From a Specialized Inherited Arrhythmia Clinic.

Predictors of fracture risk of a small caliber implantable cardioverter defibrillator lead.

Prevalence and Characteristics of Early Repolarization in the CASPER Registry

Prevalence and Clinical Implication of Double Mutations in Hypertrophic Cardiomyopathy: Revisiting the Gene-Dose Effect.

Primary prevention of idiopathic ventricular fibrillation: Not for the faint of heart

Procainamide infusion in the evaluation of unexplained cardiac arrest: from the Cardiac Arrest Survivors with Preserved Ejection Fraction Registry (CASPER).

Psychological adjustment in ICD patients living with advisory fidelis leads.

Rapid Device-Detected Nonsustained Ventricular Tachycardia in the Risk Stratification of Hypertrophic Cardiomyopathy.

Reasons for escalating pacemaker implants

Recommendations for the use of genetic testing in the clinical evaluation of inherited cardiac arrhythmias associated with sudden cardiac death: Canadian Cardiovascular Society/Canadian Heart Rhythm Society joint position paper

Reduced septal glucose metabolism predicts response to cardiac resynchronization therapy

Repeatable noninvasive measurement of mouse myocardial glucose uptake with 18F-FDG: evaluation of tracer kinetics in a type 1 diabetes model.

Reply: Noninvasive measurement of mouse myocardial glucose uptake with 18F-FDG

Response to Letter Regarding Article, "Outcome of Apparently Unexplained Cardiac Arrest: Results From Investigation and Follow-Up of the Prospective Cardiac Arrest Survivors With Preserved Ejection Fraction Registry".

Safety of Outpatient Initiation of Disopyramide for Obstructive Hypertrophic Cardiomyopathy Patients.

Sentinel symptoms in patients with unexplained cardiac arrest: from the cardiac arrest survivors with preserved ejection fraction registry (CASPER).

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation