Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients.
about
Anger, emotion, and arrhythmias: from brain to heartRYR2 sequencing reveals novel missense mutations in a Kazakh idiopathic ventricular tachycardia study cohortCalsequestrin 2 and arrhythmiasFlecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humansCatecholaminergic polymorphic ventricular tachycardia: electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden deathRole of Cytosolic Calcium Diffusion in Murine Cardiac Purkinje CellsNext-Generation Sequencing in Post-mortem Genetic Testing of Young Sudden Cardiac Death CasesCatecholaminergic polymorphic ventricular tachycardia: An exciting new eraMolecular and genetic basis of sudden cardiac deathMechanisms of sudden cardiac deathRole of sodium and calcium dysregulation in tachyarrhythmias in sudden cardiac death.Patient Specific Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Drug Development and Screening In Catecholaminergic Polymorphic Ventricular TachycardiaInherited ion channel diseases: a brief reviewCurrent topics in catecholaminergic polymorphic ventricular tachycardiaCatheter ablation for ventricular tachyarrhythmia in patients with channelopathies2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of theA missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from IsraelInvolvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardiaCalsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardiaInherited conduction system abnormalities--one group of diseases, many genesCalsequestrin mutations and catecholaminergic polymorphic ventricular tachycardiaThe RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading framRyR2 mutations linked to ventricular tachycardia and sudden death reduce the threshold for store-overload-induced Ca2+ release (SOICR)Inherited dysfunction of sarcoplasmic reticulum Ca2+ handling and arrhythmogenesisAntiarrhythmic Effects of Dantrolene in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Replication of the Responses Using iPSC ModelsCasq2 deletion causes sarcoplasmic reticulum volume increase, premature Ca2+ release, and catecholaminergic polymorphic ventricular tachycardiaArrhythmogenic mechanisms in a mouse model of catecholaminergic polymorphic ventricular tachycardia.Epidemiology of ventricular tachyarrhythmia : Any changes in the past decades?Leaky Ca2+ release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice.Prevention of ventricular arrhythmia and calcium dysregulation in a catecholaminergic polymorphic ventricular tachycardia mouse model carrying calsequestrin-2 mutation.Heterogeneity of ryanodine receptor dysfunction in a mouse model of catecholaminergic polymorphic ventricular tachycardiaLeaky RyR2 channels unleash a brainstem spreading depolarization mechanism of sudden cardiac death.Cardiac causes for syncope or sudden death in childhood.Successful catheter ablation in a patient with polymorphic ventricular tachycardia.Exercise-induced bidirectional ventricular tachycardia with alternating right and left bundle branch block-type patterns--a case report.A missense mutation in CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel.Identification of novel missense mutations of cardiac ryanodine receptor gene in exercise-induced sudden death at autopsy.Ventricular tachycardia in the absence of structural heart diseaseCardiac syncope in pediatric patients.Catecholaminergic polymorphic ventricular tachycardia in a child: a case report.
P2860
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P2860
Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients.
description
1995 nî lūn-bûn
@nan
1995 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի մարտին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Catecholaminergic polymorphic ...... year follow-up of 21 patients.
@ast
Catecholaminergic polymorphic ...... year follow-up of 21 patients.
@en
type
label
Catecholaminergic polymorphic ...... year follow-up of 21 patients.
@ast
Catecholaminergic polymorphic ...... year follow-up of 21 patients.
@en
prefLabel
Catecholaminergic polymorphic ...... year follow-up of 21 patients.
@ast
Catecholaminergic polymorphic ...... year follow-up of 21 patients.
@en
P2093
P356
P1433
P1476
Catecholaminergic polymorphic ...... year follow-up of 21 patients.
@en
P2093
P304
P356
10.1161/01.CIR.91.5.1512
P407
P577
1995-03-01T00:00:00Z