Inherited arrhythmia syndromes: applying the molecular biology and genetic to the clinical management. (Q35566050)

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20 December 2019

review article

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title

Inherited arrhythmia syndromes: applying the molecular biology and genetic to the clinical management (English)

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20 December 2019

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2

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20 December 2019

author name string

Silvia G Priori

series ordinal

1

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20 December 2019

Alessandro Vicentini

series ordinal

3

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20 December 2019

publication date

1 October 2003

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Journal of Interventional Cardiac Electrophysiology

20 December 2019

published in

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20 December 2019

volume

9

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20 December 2019

issue

2

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20 December 2019

page(s)

93-101

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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

20 December 2019

cites work

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Differential response to Na+ channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long-QT syndrome

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Natural history of Brugada syndrome: insights for risk stratification and management

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Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

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Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum

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Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation

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Foretelling the future in Brugada syndrome: do we have the crystal ball?

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Familial polymorphic ventricular arrhythmias: a quarter century of successful medical treatment based on serial exercise-pharmacologic testing

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Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes

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Mechanisms underlying early and delayed afterdepolarizations induced by catecholamines

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Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

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

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Swimming, a gene-specific arrhythmogenic trigger for inherited long QT syndrome

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Successful prevention of recurrent ventricular fibrillation by intravenous isoproterenol in a patient with Brugada syndrome

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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.

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Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

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A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

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Prognostic value of electrophysiologic investigations in Brugada syndrome

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Brugada syndrome and sudden cardiac death in children

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Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients

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Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

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Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families

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MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

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

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Mapping of a gene for long QT syndrome to chromosome 4q25-27

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Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

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Concealed arrhythmogenic syndromes: the hidden substrate of idiopathic ventricular fibrillation?

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Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

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Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3.

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The Elusive Link Between LQT3 and Brugada Syndrome

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Right bundle-branch block and ST-segment elevation in leads V1 through V3: a marker for sudden death in patients without demonstrable structural heart disease

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12 December 2020

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

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Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

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Risk stratification in the long-QT syndrome.

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12 December 2020

Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients

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Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

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12 December 2020

FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death

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12 December 2020

Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts

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12 December 2020

Chromosome mapping of five human cardiac and skeletal muscle sarcoplasmic reticulum protein genes

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12 December 2020

Cardiac autonomic dysfunction in Brugada syndrome

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12 December 2020

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

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12 December 2020

Mutations in the hminK gene cause long QT syndrome and suppress IKs function

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12 December 2020

KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome

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12 December 2020

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

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12 December 2020

A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN

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12 December 2020

Autonomic and antiarrhythmic drug modulation of ST segment elevation in patients with Brugada syndrome

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12 December 2020

A molecular link between the sudden infant death syndrome and the long-QT syndrome

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12 December 2020

Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts

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12 December 2020

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12 December 2020

Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21.

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12 December 2020

Programmed electrical stimulation in Brugada syndrome: how reproducible are the results?

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12 December 2020

Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1).

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12 December 2020