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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 16, 2025. (Total: 235382Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Sudden Infant Death and KCNH2[original query]
A mitochondrial DNA polymorphism associated with cardiac arrhythmia investigated in sudden infant death syndrome.
Acta paediatrica (Oslo, Norway : 1992) 2007 Feb 96 (2): 206-10.
Arnestad Marianne, Opdal Siri Hauge, Vege Ashild, Rognum Torleiv O
Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.
Circulation 2007 Jan 115 (3): 361-7.
Arnestad Marianne, Crotti Lia, Rognum Torleiv O, Insolia Roberto, Pedrazzini Matteo, Ferrandi Chiara, Vege Ashild, Wang Dao W, Rhodes Troy E, George Alfred L, Schwartz Peter
Cardiac ion channel gene mutations in sudden infant death syndrome.
Pediatric research 2008 Nov 64 (5): 482-7.
Otagiri Tesshu, Kijima Kazuki, Osawa Motoki, Ishii Kuniaki, Makita Naomasa, Matoba Ryoji, Umetsu Kazuo, Hayasaka Kiyos
Contribution of long-QT syndrome genetic variants in sudden infant death syndrome.
Pediatric cardiology 2009 Mar .
Millat G, Kugener B, Chevalier P, Chahine M, Huang H, Malicier D, Rodriguez-Lafrasse C, Rousson R
Mutations in genes encoding cardiac ion channels previously associated with sudden infant death syndrome (SIDS) are present with high frequency in new exome data.
The Canadian journal of cardiology 2013 Sep 29 (9): 1104-9.
Andreasen Charlotte, Refsgaard Lena, Nielsen Jonas B, Sajadieh Ahmad, Winkel Bo G, Tfelt-Hansen Jacob, Haunsø Stig, Holst Anders G, Svendsen Jesper H, Olesen Morten
Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases.
European journal of human genetics : EJHG 2015 Sep .
Hertz Christin Loeth, Christiansen Sofie Lindgren, Larsen Maiken Kudahl, Dahl Morten, Ferrero-Miliani Laura, Weeke Peter Ejvind, Pedersen Oluf, Hansen Torben, Grarup Niels, Ottesen Gyda Lolk, Frank-Hansen Rune, Banner Jytte, Morling Nie
[High incidence of sudden cardiac death in one family with type-3 long QT syndrome: molecular genetics and electrophysiology mechanism analysis].
Zhonghua xin xue guan bing za zhi 2015 Dec 43 (12): 1046-50.
Zhou Hui, Li Zhang, Ali Raza Ghani, Zhu Wengen, Zhou Qiongqiong, Shen Yang, Xie Jinyan, Cao Qing, Wan Rong, Hu Jinzhu, Hong K
Cardiac Genetic Predisposition in Sudden Infant Death Syndrome.
Journal of the American College of Cardiology 2018 Mar 71 (11): 1217-1227.
Tester David J, Wong Leonie C H, Chanana Pritha, Jaye Amie, Evans Jared M, FitzPatrick David R, Evans Margaret J, Fleming Peter, Jeffrey Iona, Cohen Marta C, Tfelt-Hansen Jacob, Simpson Michael A, Behr Elijah R, Ackerman Michael
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