Mutation and gender-specific risk in type 2 long QT syndrome: implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome.
about
Genetics of inherited primary arrhythmia disordersSex differences in the mechanisms underlying long QT syndromeInherited ion channel diseases: a brief reviewRecent advances in genetic testing and counseling for inherited arrhythmiasChannelopathies - emerging trends in the management of inherited arrhythmiasA presumably benign human ether-a-go-go-related gene mutation (R176W) with a malignant primary manifestation of long QT syndrome.Inherited long QT syndrome: clinical manifestation, genetic diagnostics, and therapy.Genotype-specific risk stratification and management of patients with long QT syndrome.Inherited arrhythmia syndromes leading to sudden cardiac death in the young: a global update and an Indian perspective.How do sex hormones modify arrhythmogenesis in long QT syndrome? Sex hormone effects on arrhythmogenic substrate and triggered activity."QT clock" to improve detection of QT prolongation in long QT syndrome patients.Gene mutations in cardiac arrhythmias: a review of recent evidence in ion channelopathies.Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndromeCongenital long and short QT syndromes.Genetics of congenital and drug-induced long QT syndromes: current evidence and future research perspectives.Must every child with long QT syndrome take a beta blocker?Congenital long QT syndromes: prevalence, pathophysiology and management.Is There a Role for Genetics in the Prevention of Sudden Cardiac Death?Molecular Pathophysiology of Congenital Long QT Syndrome.Genetic biomarkers for the risk of seizures in long QT syndrome.Identification of Low-Risk Adult Congenital LQTS Patients.Risk of cardiac events in Long QT syndrome patients when taking antiseizure medications.Marked, transient, emotion-triggered QT accentuation in an adolescent female with type 1 long QT syndrome.Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients : Koponen et al. Follow-up of adult LQTS patients.HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes
P2860
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P2860
Mutation and gender-specific risk in type 2 long QT syndrome: implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome.
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Mutation and gender-specific r ...... atients with long QT syndrome.
@ast
Mutation and gender-specific r ...... atients with long QT syndrome.
@en
type
label
Mutation and gender-specific r ...... atients with long QT syndrome.
@ast
Mutation and gender-specific r ...... atients with long QT syndrome.
@en
prefLabel
Mutation and gender-specific r ...... atients with long QT syndrome.
@ast
Mutation and gender-specific r ...... atients with long QT syndrome.
@en
P2093
P2860
P50
P1433
P1476
Mutation and gender-specific r ...... atients with long QT syndrome.
@en
P2093
Alon Barsheshet
Arthur J Moss
Coeli M Lopes
Dimitry Migdalovich
Elizabeth S Kaufman
G Michael Vincent
Ilan Goldenberg
Jason Costa
Jennifer L Robinson
Jesaia Benhorin
P2860
P304
P356
10.1016/J.HRTHM.2011.03.049
P577
2011-03-25T00:00:00Z