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Items: 1 to 20 of 132

1.

Genetics of the sudden infant death syndrome.

Courts C, Madea B.

Forensic Sci Int. 2010 Dec 15;203(1-3):25-33. doi: 10.1016/j.forsciint.2010.07.008.

PMID:
20674198
2.

The sudden infant death syndrome gene: does it exist?

Opdal SH, Rognum TO.

Pediatrics. 2004 Oct;114(4):e506-12.

PMID:
15466077
3.

Cardiac ion channel mutations in the sudden infant death syndrome.

Klaver EC, Versluijs GM, Wilders R.

Int J Cardiol. 2011 Oct 20;152(2):162-70. doi: 10.1016/j.ijcard.2010.12.051. Review.

4.

Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.

Arnestad M, Crotti L, Rognum TO, Insolia R, Pedrazzini M, Ferrandi C, Vege A, Wang DW, Rhodes TE, George AL Jr, Schwartz PJ.

Circulation. 2007 Jan 23;115(3):361-7.

5.

Sudden infant death syndrome: how significant are the cardiac channelopathies?

Tester DJ, Ackerman MJ.

Cardiovasc Res. 2005 Aug 15;67(3):388-96. Review.

6.

Sudden Infant Death Syndrome: review of implicated genetic factors.

Weese-Mayer DE, Ackerman MJ, Marazita ML, Berry-Kravis EM.

Am J Med Genet A. 2007 Apr 15;143A(8):771-88. Review.

PMID:
17340630
7.

The triple risk hypotheses in sudden infant death syndrome.

Guntheroth WG, Spiers PS.

Pediatrics. 2002 Nov;110(5):e64. Review.

PMID:
12415070
8.

Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study.

Wedekind H, Bajanowski T, Friederich P, Breithardt G, Wülfing T, Siebrands C, Engeland B, Mönnig G, Haverkamp W, Brinkmann B, Schulze-Bahr E.

Int J Legal Med. 2006 May;120(3):129-37.

PMID:
16012827
9.

Biophysical characterization of a new SCN5A mutation S1333Y in a SIDS infant linked to long QT syndrome.

Huang H, Millat G, Rodriguez-Lafrasse C, Rousson R, Kugener B, Chevalier P, Chahine M.

FEBS Lett. 2009 Mar 4;583(5):890-6. doi: 10.1016/j.febslet.2009.02.007.

10.

Contribution of long-QT syndrome genetic variants in sudden infant death syndrome.

Millat G, Kugener B, Chevalier P, Chahine M, Huang H, Malicier D, Rodriguez-Lafrasse C, Rousson R.

Pediatr Cardiol. 2009 May;30(4):502-9. doi: 10.1007/s00246-009-9417-2.

PMID:
19322600
11.

Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis.

Filonzi L, Magnani C, Lavezzi AM, Rindi G, Parmigiani S, Bevilacqua G, Matturri L, Marzano FN.

Neurogenetics. 2009 Feb;10(1):65-72. doi: 10.1007/s10048-008-0149-x.

PMID:
18810510
13.

Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome.

Nonnis Marzano F, Maldini M, Filonzi L, Lavezzi AM, Parmigiani S, Magnani C, Bevilacqua G, Matturri L.

Genomics. 2008 Jun;91(6):485-91. doi: 10.1016/j.ygeno.2008.01.010.

14.

Serotonin transporter role in identifying similarities between SIDS and idiopathic ALTE.

Filonzi L, Magnani C, Nosetti L, Nespoli L, Borghi C, Vaghi M, Nonnis Marzano F.

Pediatrics. 2012 Jul;130(1):e138-44. doi: 10.1542/peds.2011-3331.

15.

De novo mutation in the SCN5A gene associated with early onset of sudden infant death.

Wedekind H, Smits JP, Schulze-Bahr E, Arnold R, Veldkamp MW, Bajanowski T, Borggrefe M, Brinkmann B, Warnecke I, Funke H, Bhuiyan ZA, Wilde AA, Breithardt G, Haverkamp W.

Circulation. 2001 Sep 4;104(10):1158-64.

16.

Cardiac sodium channel dysfunction in sudden infant death syndrome.

Wang DW, Desai RR, Crotti L, Arnestad M, Insolia R, Pedrazzini M, Ferrandi C, Vege A, Rognum T, Schwartz PJ, George AL Jr.

Circulation. 2007 Jan 23;115(3):368-76.

18.

Cardiac channelopathies and sudden infant death syndrome.

Tfelt-Hansen J, Winkel BG, Grunnet M, Jespersen T.

Cardiology. 2011;119(1):21-33. doi: 10.1159/000329047. Review.

PMID:
21778721
19.

A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y.

Plant LD, Bowers PN, Liu Q, Morgan T, Zhang T, State MW, Chen W, Kittles RA, Goldstein SA.

J Clin Invest. 2006 Feb;116(2):430-5.

20.
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