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ECG screening of newborns to avoid sudden infant death syndrome?

作者信息

van Langen I M, Wilde A A M

出版信息

Neth Heart J. 2006 Feb;14(2):43-45.

PMID:25696591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2557158/
Abstract
摘要

相似文献

1
ECG screening of newborns to avoid sudden infant death syndrome?对新生儿进行心电图筛查以避免婴儿猝死综合征?
Neth Heart J. 2006 Feb;14(2):43-45.
2
Erratum: ECG screening of newborns to avoid sudden infant death syndrome?勘误:新生儿心电图筛查可预防婴儿猝死综合征?
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Electrocardiogram screening of infants for long QT syndrome: survey of pediatric cardiologists in North America.对婴儿进行长QT综合征的心电图筛查:北美儿科心脏病专家调查
J Electrocardiol. 2010 Jan-Feb;43(1):4-7. doi: 10.1016/j.jelectrocard.2009.07.004.
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Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.婴幼儿Brugada综合征和长QT综合征的分子生物学及细胞机制
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QT interval in newborns of different ethnic origin: usefulness of neonatal ECG screening.不同种族新生儿的QT间期:新生儿心电图筛查的作用
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Postmortem genetic analysis of sudden unexpected death in infancy: neonatal genetic screening may enable the prevention of sudden infant death.婴儿猝死症的死后遗传学分析:新生儿基因筛查可能有助于预防婴儿猝死。
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A Neonate with Susceptibility to Long QT Syndrome Type 6 who Presented with Ventricular Fibrillation and Sudden Unexpected Infant Death.一名对6型长QT综合征易感的新生儿,出现心室颤动和婴儿不明原因猝死。
Am J Case Rep. 2016 Jul 28;17:544-8. doi: 10.12659/ajcr.898327.
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[Usefulness of electrocardiographic screening in a neonatal population].[心电图筛查在新生儿群体中的效用]
An Pediatr (Barc). 2011 May;74(5):303-8. doi: 10.1016/j.anpedi.2010.12.009. Epub 2011 Feb 20.
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Familial cardiological and targeted genetic evaluation: low yield in sudden unexplained death and high yield in unexplained cardiac arrest syndromes.家族性心脏学和靶向基因评估:不明原因猝死的低检出率和不明原因心律失常综合征的高检出率。
Heart Rhythm. 2013 Nov;10(11):1653-60. doi: 10.1016/j.hrthm.2013.08.022. Epub 2013 Aug 22.
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[Sudden infant death--the QT interval in ECG and bradyarrhythmias].[婴儿猝死——心电图中的QT间期与缓慢性心律失常]
Tidsskr Nor Laegeforen. 1989 Jan 20;109(2):186-92.

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Shwachman Diamond Syndrome with Arrhythmia as the First Manifestation a Case Report and Literature Review.以心律失常为首发表现的施瓦赫曼-戴蒙德综合征:病例报告及文献综述
Pharmgenomics Pers Med. 2022 Oct 11;15:867-872. doi: 10.2147/PGPM.S381695. eCollection 2022.

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1
Attenuated pediatric electrode pads for automated external defibrillator use in children.用于儿童自动体外除颤器的减毒儿科电极片。
Resuscitation. 2005 Jul;66(1):31-7. doi: 10.1016/j.resuscitation.2004.12.025.
2
Sudden infant death syndrome: how significant are the cardiac channelopathies?婴儿猝死综合征:心脏离子通道病的影响有多大?
Cardiovasc Res. 2005 Aug 15;67(3):388-96. doi: 10.1016/j.cardiores.2005.02.013.
3
Implantable cardioverter defibrillator implantation in children in The Netherlands.荷兰儿童植入式心脏复律除颤器植入情况
Eur J Pediatr. 2005 Jul;164(7):436-41. doi: 10.1007/s00431-005-1668-1. Epub 2005 Apr 21.
4
Association of long QT syndrome loci and cardiac events among patients treated with beta-blockers.β受体阻滞剂治疗患者中长QT综合征基因座与心脏事件的关联。
JAMA. 2004 Sep 15;292(11):1341-4. doi: 10.1001/jama.292.11.1341.
5
Family and population strategies for screening and counselling of inherited cardiac arrhythmias.遗传性心律失常筛查与咨询的家庭及人群策略
Ann Med. 2004;36 Suppl 1:116-24. doi: 10.1080/17431380410032526.
6
The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome.基因型-表型相关性在长QT综合征突变分析中的应用。
J Med Genet. 2003 Feb;40(2):141-5. doi: 10.1136/jmg.40.2.141.
7
Appraising organised screening programmes for testing for genetic susceptibility to cancer.评估针对癌症遗传易感性检测的有组织筛查项目。
BMJ. 2001 May 12;322(7295):1174-8. doi: 10.1136/bmj.322.7295.1174.
8
Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.长QT综合征基因的突变谱。KVLQT1、HERG、SCN5A、KCNE1和KCNE2。
Circulation. 2000 Sep 5;102(10):1178-85. doi: 10.1161/01.cir.102.10.1178.
9
Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.荷兰长QT综合征家系中的新型KCNQ1和HERG错义突变
Hum Mutat. 1999;13(4):301-10. doi: 10.1002/(SICI)1098-1004(1999)13:4<301::AID-HUMU7>3.0.CO;2-V.
10
Prolongation of the QT interval and the sudden infant death syndrome.QT间期延长与婴儿猝死综合征
N Engl J Med. 1998 Jun 11;338(24):1709-14. doi: 10.1056/NEJM199806113382401.