Postmortem molecular screening in unexplained sudden death.
about
Mechanisms of pharmacological rescue of trafficking-defective hERG mutant channels in human long QT syndromeMolecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndromeNext-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 conditionsThe molecular autopsy: should the evaluation continue after the funeral?Clinical and genetic determinants of torsade de pointes riskMolecular autopsy in victims of inherited arrhythmiasPart 10: Pediatric basic and advanced life support: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations.Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.The value of a family history of sudden death in patients with diagnostic type I Brugada ECG pattern.Distinctive profile of sudden cardiac arrest in middle-aged vs. older adults: a community-based study.Population-based analysis of sudden death in children: The Oregon Sudden Unexpected Death StudyEtiology of sudden death in the community: results of anatomical, metabolic, and genetic evaluationLocalization of a disease-associated mutation site in the three-dimensional structure of the cardiac muscle ryanodine receptorDrug evaluation in cardiomyocytes derived from human induced pluripotent stem cells carrying a long QT syndrome type 2 mutationPostmortem genetic testing for conventional autopsy-negative sudden unexplained death: an evaluation of different DNA extraction protocols and the feasibility of mutational analysis from archival paraffin-embedded heart tissueState of postmortem genetic testing known as the cardiac channel molecular autopsy in the forensic evaluation of unexplained sudden cardiac death in the young.Sudden arrhythmic death syndrome: a national survey of sudden unexplained cardiac death.Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.The investigation of sudden arrhythmic death syndrome (SADS)-the current approach to family screening and the future role of genomics and stem cell technology.Sudden cardiac arrest in patients with preserved left ventricular systolic function: a clinical dilemma.Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.Pediatric basic and advanced life support: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science with Treatment Recommendations.Sudden cardiac death: epidemiology and risk factors.Ryanodine receptor-mediated arrhythmias and sudden cardiac death.A community-based evaluation of sudden death associated with therapeutic levels of methadone.The molecular autopsy: an indispensable step following sudden cardiac death in the young?Allele-specific RNA interference rescues the long-QT syndrome phenotype in human-induced pluripotency stem cell cardiomyocytes.Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic AdvancesGenetics and cardiac channelopathies.Sudden cardiac death and implantable cardioverter defibrillators: two modern epidemics?Restricting sports for athletes with heart disease: are we saving lives, avoiding lawsuits, or just promoting obesity and sedentary living?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.Cardiac channel molecular autopsy for sudden unexpected death in epilepsy.An update on risk factors for drug-induced arrhythmias.Exome sequencing-based molecular autopsy of formalin-fixed paraffin-embedded tissue after sudden death.Pattern of coroner's autopsies at Health Sciences Authority, Singapore: a retrospective study (2009-2010).Molecular and Functional Characterization of Rare CACNA1C Variants in Sudden Unexplained Death in the Young.Sudden death: Neurogenic causes, prediction and prevention.
P2860
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P2860
Postmortem molecular screening in unexplained sudden death.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Postmortem molecular screening in unexplained sudden death.
@en
type
label
Postmortem molecular screening in unexplained sudden death.
@en
prefLabel
Postmortem molecular screening in unexplained sudden death.
@en
P2093
P1476
Postmortem molecular screening in unexplained sudden death
@en
P2093
Allison Watts
Jack L Titus
Olga Senashova
Qiuming Gong
Sumeet S Chugh
Susan J Hayflick
Zhengfeng Zhou
P304
P356
10.1016/J.JACC.2003.11.052
P407
P577
2004-05-01T00:00:00Z