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Items: 1 to 20 of 33


Wisconsin stillbirth services program: a multifocal approach to stillbirth analysis.

VanderWielen B, Zaleski C, Cold C, McPherson E.

Am J Med Genet A. 2011 May;155A(5):1073-80. doi: 10.1002/ajmg.a.34016. Epub 2011 Apr 7.


A common SCN5A polymorphism modulates the biophysical defects of SCN5A mutations.

Shinlapawittayatorn K, Du XX, Liu H, Ficker E, Kaufman ES, Deschênes I.

Heart Rhythm. 2011 Mar;8(3):455-62. doi: 10.1016/j.hrthm.2010.11.034. Epub 2010 Nov 23.


Structure and function of splice variants of the cardiac voltage-gated sodium channel Na(v)1.5.

Schroeter A, Walzik S, Blechschmidt S, Haufe V, Benndorf K, Zimmer T.

J Mol Cell Cardiol. 2010 Jul;49(1):16-24. doi: 10.1016/j.yjmcc.2010.04.004. Epub 2010 Apr 14. Review.


Clinical characteristics and genetic background of congenital long-QT syndrome diagnosed in fetal, neonatal, and infantile life: a nationwide questionnaire survey in Japan.

Horigome H, Nagashima M, Sumitomo N, Yoshinaga M, Ushinohama H, Iwamoto M, Shiono J, Ichihashi K, Hasegawa S, Yoshikawa T, Matsunaga T, Goto H, Waki K, Arima M, Takasugi H, Tanaka Y, Tauchi N, Ikoma M, Inamura N, Takahashi H, Shimizu W, Horie M.

Circ Arrhythm Electrophysiol. 2010 Feb;3(1):10-7. doi: 10.1161/CIRCEP.109.882159. Epub 2009 Dec 8. Erratum in: Circ Arrhythm Electrophysiol. 2012 Dec;5(6):e120-2.


Malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional cardiac sodium channel.

Wang DW, Crotti L, Shimizu W, Pedrazzini M, Cantu F, De Filippo P, Kishiki K, Miyazaki A, Ikeda T, Schwartz PJ, George AL Jr.

Circ Arrhythm Electrophysiol. 2008 Dec;1(5):370-8. doi: 10.1161/CIRCEP.108.788349. Epub 2008 Dec 2.


Fetal ventricular tachycardia secondary to long QT syndrome treated with maternal intravenous magnesium: case report and review of the literature.

Simpson JM, Maxwell D, Rosenthal E, Gill H.

Ultrasound Obstet Gynecol. 2009 Oct;34(4):475-80. doi: 10.1002/uog.6433. Review.


Prenatal diagnosis and management of fetal Long QT syndrome.

Tomek V, Skovranek J, Gebauer RA.

Pediatr Cardiol. 2009 Feb;30(2):194-6. doi: 10.1007/s00246-008-9294-0. Epub 2008 Aug 15. Erratum in: Pediatr Cardiol. 2009 Nov;30(8):1197.


A novel and lethal de novo LQT-3 mutation in a newborn with distinct molecular pharmacology and therapeutic response.

Bankston JR, Yue M, Chung W, Spyres M, Pass RH, Silver E, Sampson KJ, Kass RS.

PLoS One. 2007 Dec 5;2(12):e1258.


Divergent biophysical defects caused by mutant sodium channels in dilated cardiomyopathy with arrhythmia.

Nguyen TP, Wang DW, Rhodes TH, George AL Jr.

Circ Res. 2008 Feb 15;102(3):364-71. Epub 2007 Nov 29.


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. Epub 2007 Jan 8.


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. Epub 2007 Jan 8.


SCN5A polymorphism restores trafficking of a Brugada syndrome mutation on a separate gene.

Poelzing S, Forleo C, Samodell M, Dudash L, Sorrentino S, Anaclerio M, Troccoli R, Iacoviello M, Romito R, Guida P, Chahine M, Pitzalis M, Deschênes I.

Circulation. 2006 Aug 1;114(5):368-76. Epub 2006 Jul 24.


Tetrodotoxin-resistant Na+ channels in human neuroblastoma cells are encoded by new variants of Nav1.5/SCN5A.

Ou SW, Kameyama A, Hao LY, Horiuchi M, Minobe E, Wang WY, Makita N, Kameyama M.

Eur J Neurosci. 2005 Aug;22(4):793-801.


A novel polyclonal antibody specific for the Na(v)1.5 voltage-gated Na(+) channel 'neonatal' splice form.

Chioni AM, Fraser SP, Pani F, Foran P, Wilkin GP, Diss JK, Djamgoz MB.

J Neurosci Methods. 2005 Sep 30;147(2):88-98.


Efficacy of an implantable cardioverter-defibrillator in a neonate with LQT3 associated arrhythmias.

Ten Harkel AD, Witsenburg M, de Jong PL, Jordaens L, Wijman M, Wilde AA.

Europace. 2005 Jan;7(1):77-84.


A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tachycardia/bradycardia.

Chang CC, Acharfi S, Wu MH, Chiang FT, Wang JK, Sung TC, Chahine M.

Cardiovasc Res. 2004 Nov 1;64(2):268-78.


Recurrent third-trimester fetal loss and maternal mosaicism for long-QT syndrome.

Miller TE, Estrella E, Myerburg RJ, Garcia de Viera J, Moreno N, Rusconi P, Ahearn ME, Baumbach L, Kurlansky P, Wolff G, Bishopric NH.

Circulation. 2004 Jun 22;109(24):3029-34. Epub 2004 Jun 7. Review.


Images in cardiovascular medicine. Life-threatening neonatal arrhythmia: successful treatment and confirmation of clinically suspected extreme long QT-syndrome-3.

Kehl HG, Haverkamp W, Rellensmann G, Yelbuz TM, Krasemann T, Vogt J, Schulze-Bahr E.

Circulation. 2004 May 11;109(18):e205-6. No abstract available.


Postnatal outcome of fetal bradycardia without significant cardiac abnormalities.

Lin MT, Hsieh FJ, Shyu MK, Lee CN, Wang JK, Wu MH.

Am Heart J. 2004 Mar;147(3):540-4.


Long QT syndrome and life threatening arrhythmia in a newborn: molecular diagnosis and treatment response.

Schulze-Bahr E, Fenge H, Etzrodt D, Haverkamp W, Mönnig G, Wedekind H, Breithardt G, Kehl HG.

Heart. 2004 Jan;90(1):13-6.

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