Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 9

1.

Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death.

Goldman AM, Glasscock E, Yoo J, Chen TT, Klassen TL, Noebels JL.

Sci Transl Med. 2009 Oct 14;1(2):2ra6. doi: 10.1126/scitranslmed.3000289.

PMID:
20368164
2.

Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.

Sanguinetti MC.

Ann N Y Acad Sci. 1999 Apr 30;868:406-13. Review.

PMID:
10414310
3.

Cardiac arrhythmia and thyroid dysfunction: a novel genetic link.

Purtell K, Roepke TK, Abbott GW.

Int J Biochem Cell Biol. 2010 Nov;42(11):1767-70. doi: 10.1016/j.biocel.2010.07.013. Epub 2010 Aug 3. Review.

PMID:
20688187
4.

The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.

Vincent GM.

Annu Rev Med. 1998;49:263-74. Review.

PMID:
9509262
5.

Recent molecular insights from mutated IKS channels in cardiac arrhythmia.

Dvir M, Peretz A, Haitin Y, Attali B.

Curr Opin Pharmacol. 2014 Apr;15:74-82. doi: 10.1016/j.coph.2013.12.004. Epub 2013 Dec 30. Review.

PMID:
24721657
6.

KCNQ1 gene mutations and the respective genotype-phenotype correlations in the long QT syndrome.

Herbert E, Trusz-Gluza M, Moric E, SmiƂowska-Dzielicka E, Mazurek U, Wilczok T.

Med Sci Monit. 2002 Oct;8(10):RA240-8. Review.

PMID:
12388934
7.

Molecular genetic basis of sudden cardiac death.

Towbin JA.

Pediatr Clin North Am. 2004 Oct;51(5):1229-55. Review.

PMID:
15331282
8.

The long QT syndromes: genetic basis and clinical implications.

Chiang CE, Roden DM.

J Am Coll Cardiol. 2000 Jul;36(1):1-12. Review.

PMID:
10898405
9.

A clinical approach to inherited arrhythmias.

Cerrone M, Cummings S, Alansari T, Priori SG.

Circ Cardiovasc Genet. 2012 Oct 1;5(5):581-90. doi: 10.1161/CIRCGENETICS.110.959429. Review. No abstract available.

PMID:
23074337

Supplemental Content

Support Center