Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
about
The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex InheritanceGenetics of inherited primary arrhythmia disordersJ-wave syndromes: Brugada and early repolarization syndromesInherited bradyarrhythmia: A diverse genetic backgroundElectrophysiological Mechanisms of Brugada Syndrome: Insights from Pre-clinical and Clinical StudiesGenetics of Brugada syndromeAtrial arrhythmias in inherited arrhythmogenic disordersThe new kids on the block of arrhythmogenic disorders: Short QT Syndrome and early repolarization.A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore.Novel SCN10A variants associated with Brugada syndrome.The Diagnosis, Risk Stratification, and Treatment of Brugada SyndromeNumerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality.A variant of Brugada syndrome.Deleterious protein-altering mutations in the SCN10A voltage-gated sodium channel gene are associated with prolonged QT.J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledgeGenetics of Brugada syndrome.Isolation and characterization of embryonic stem cell-derived cardiac Purkinje cellsRole of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.SCN10A Mutation in a Patient with Erythromelalgia Enhances C-Fiber Activity Dependent Slowing.Early Repolarisation Syndrome - New Concepts.Brugada Syndrome: Clinical, Genetic, Molecular, Cellular, and Ionic Aspects.Cellular and ionic mechanisms underlying the effects of cilostazol, milrinone, and isoproterenol to suppress arrhythmogenesis in an experimental model of early repolarization syndrome.Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome.Novel Therapeutic Strategies for the Management of Ventricular Arrhythmias Associated with the Brugada SyndromeTwenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram.Engineering prokaryotic channels for control of mammalian tissue excitabilityNeuronal Nav1.8 Channels as a Novel Therapeutic Target of Acute Atrial Fibrillation Prevention.Biallelic SCN10A mutations in neuromuscular disease and epileptic encephalopathy.Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic AdvancesBrugada syndrome in children.Voltage-gated sodium channels in the mammalian heart.Brugada syndrome: clinical and genetic findings.Brugada syndrome and its relevance in the perioperative period.Distinguishing pathogenic mutations from background genetic noise in cardiology: the use of large genome databases for genetic interpretation.Pathogenesis and management of Brugada syndrome.Murine Electrophysiological Models of Cardiac Arrhythmogenesis.Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.Clinical Genetic Testing for the Cardiomyopathies and Arrhythmias: A Systematic Framework for Establishing Clinical Validity and Addressing Genotypic and Phenotypic Heterogeneity.Cardiac Arrhythmias Related to Sodium Channel Dysfunction.Postmortem genetic analysis of sudden unexpected death in infancy: neonatal genetic screening may enable the prevention of sudden infant death.
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P2860
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
description
2014 nî lūn-bûn
@nan
2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
@ast
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
@en
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
@en-gb
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
@nl
type
label
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
@ast
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
@en
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
@en-gb
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
@nl
prefLabel
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
@ast
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
@en
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
@en-gb
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
@nl
P2093
P2860
P50
P921
P3181
P1476
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
@en
P2093
Atul Bhatia
Can Hasdemir
Christian Veltmann
Fabio Dezi
Gi-Byoung Nam
Harry J DeAntonio
Hector Barajas-Martínez
Hiroyuki Ito
Jenna Pfeiffer
Kristopher M Kahlig
P2860
P3181
P356
10.1016/J.JACC.2014.04.032
P407
P577
2014-07-08T00:00:00Z