The Prevalence of Mutations inKCNQ1, KCNH2,andSCN5Ain an Unselected National Cohort of Young Sudden Unexplained Death Cases
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Next-Generation Sequencing in Post-mortem Genetic Testing of Young Sudden Cardiac Death CasesSudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditionsMolecular autopsy in victims of inherited arrhythmiasSudden death associated with QT interval prolongation and KCNQ1 gene mutation in a family of English Springer Spaniels.Sudden cardiac death in children (1-18 years): symptoms and causes of death in a nationwide setting.Symptoms Before Sudden Arrhythmic Death Syndrome: A Nationwide Study Among the Young in Denmark.Cardiac magnetic resonance imaging after ventricular tachyarrhythmias increases diagnostic precision and reduces the need for family screening for inherited cardiac disease.Enhanced risk profiling of implanted defibrillator shocks with circulating SCN5A mRNA splicing variants: a pilot trial.Sudden Unexplained Death - Treating the Family.Genetic screening in sudden cardiac death in the young can save future livesCardiac ion channelopathies and the sudden infant death syndromeVisual automated fluorescence electrophoresis provides simultaneous quality, quantity, and molecular weight spectra for genomic DNA from archived neonatal blood spotsThe investigation of sudden arrhythmic death syndrome (SADS)-the current approach to family screening and the future role of genomics and stem cell technology.Negative autopsy and sudden cardiac death.The usual suspects in sudden cardiac death of the young: a focus on inherited arrhythmogenic diseases.A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classification.Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives.DNA and RNA analysis of blood and muscle from bodies with variable postmortem intervals.Telltale hearts.Genetic investigation of 100 heart genes in sudden unexplained death victims in a forensic setting.Dual LQT1 and HCM phenotypes associated with tetrad heterozygous mutations in KCNQ1, MYH7, MYLK2, and TMEM70 genes in a three-generation Chinese family.
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P2860
The Prevalence of Mutations inKCNQ1, KCNH2,andSCN5Ain an Unselected National Cohort of Young Sudden Unexplained Death Cases
description
im August 2012 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в серпні 2012
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name
The Prevalence of Mutations in ...... Sudden Unexplained Death Cases
@en
The Prevalence of Mutations in ...... Sudden Unexplained Death Cases
@nl
type
label
The Prevalence of Mutations in ...... Sudden Unexplained Death Cases
@en
The Prevalence of Mutations in ...... Sudden Unexplained Death Cases
@nl
prefLabel
The Prevalence of Mutations in ...... Sudden Unexplained Death Cases
@en
The Prevalence of Mutations in ...... Sudden Unexplained Death Cases
@nl
P2093
P2860
P50
P1476
The Prevalence of Mutations in ...... Sudden Unexplained Death Cases
@en
P2093
BO GREGERS WINKEL
INGRID BAYER KRISTENSEN
KNUT ERIK BERGE
MAIKEN KUDAHL LARSEN
NIKOLAJ NIELSEN
PETER HENRIK NISSEN
STIG HAUNSØ
TROND PAUL LEREN
YINMAN WANG
P2860
P304
P356
10.1111/J.1540-8167.2012.02371.X
P50
P577
2012-08-06T00:00:00Z