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Results: 12

1.

Inhibition of late sodium current by mexiletine: a novel pharmotherapeutical approach in timothy syndrome.

Gao Y, Xue X, Hu D, Liu W, Yuan Y, Sun H, Li L, Timothy KW, Zhang L, Li C, Yan GX.

Circ Arrhythm Electrophysiol. 2013 Jun;6(3):614-22. doi: 10.1161/CIRCEP.113.000092. Epub 2013 Apr 11. Review.

PMID:
23580742
[PubMed - indexed for MEDLINE]
Free Article
2.

Case scenario: anesthesia-related cardiac arrest in a child with Timothy syndrome.

Nathan AT, Antzelevitch C, Montenegro LM, Vetter VL.

Anesthesiology. 2012 Nov;117(5):1117-26. doi: 10.1097/ALN.0b013e31826e73b1. Review. No abstract available.

PMID:
23011317
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

L-type Ca2+ channel function during Timothy syndrome.

Dixon RE, Cheng EP, Mercado JL, Santana LF.

Trends Cardiovasc Med. 2012 Apr;22(3):72-6. doi: 10.1016/j.tcm.2012.06.015. Review.

PMID:
22999068
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Arrhythmia-associated cardiac Ca²(+) cycling proteins and gene mutations.

Kochhäuser S, Schulze-Bahr E, Kirchhefer U.

Wien Med Wochenschr. 2012 Jul;162(13-14):292-6. Epub 2012 Jun 25. Review. Erratum in: Wien Med Wochenschr. 2012 Dec;162(23-24):544.

PMID:
22733365
[PubMed - indexed for MEDLINE]
5.

Inherited calcium channelopathies in the pathophysiology of arrhythmias.

Venetucci L, Denegri M, Napolitano C, Priori SG.

Nat Rev Cardiol. 2012 Oct;9(10):561-75. doi: 10.1038/nrcardio.2012.93. Epub 2012 Jun 26. Review.

PMID:
22733215
[PubMed - indexed for MEDLINE]
6.

Hallmarks of the channelopathies associated with L-type calcium channels: a focus on the Timothy mutations in Ca(v)1.2 channels.

Bidaud I, Lory P.

Biochimie. 2011 Dec;93(12):2080-6. doi: 10.1016/j.biochi.2011.05.015. Epub 2011 May 31. Review.

PMID:
21664226
[PubMed - indexed for MEDLINE]
7.

Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels.

Striessnig J, Bolz HJ, Koschak A.

Pflugers Arch. 2010 Jul;460(2):361-74. doi: 10.1007/s00424-010-0800-x. Epub 2010 Mar 7. Review.

PMID:
20213496
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

CaV1.2 channelopathies: from arrhythmias to autism, bipolar disorder, and immunodeficiency.

Liao P, Soong TW.

Pflugers Arch. 2010 Jul;460(2):353-9. doi: 10.1007/s00424-009-0753-0. Epub 2009 Nov 15. Review.

PMID:
19916019
[PubMed - indexed for MEDLINE]
9.

The genetic basis of long QT and short QT syndromes: a mutation update.

Hedley PL, Jørgensen P, Schlamowitz S, Wangari R, Moolman-Smook J, Brink PA, Kanters JK, Corfield VA, Christiansen M.

Hum Mutat. 2009 Nov;30(11):1486-511. doi: 10.1002/humu.21106. Review.

PMID:
19862833
[PubMed - indexed for MEDLINE]
10.

Genetic calcium signaling abnormalities in the central nervous system: seizures, migraine, and autism.

Gargus JJ.

Ann N Y Acad Sci. 2009 Jan;1151:133-56. doi: 10.1111/j.1749-6632.2008.03572.x. Review.

PMID:
19154521
[PubMed - indexed for MEDLINE]
11.

Congenital long QT syndrome.

Crotti L, Celano G, Dagradi F, Schwartz PJ.

Orphanet J Rare Dis. 2008 Jul 7;3:18. doi: 10.1186/1750-1172-3-18. Review.

PMID:
18606002
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Ion channel functional candidate genes in multigenic neuropsychiatric disease.

Gargus JJ.

Biol Psychiatry. 2006 Jul 15;60(2):177-85. Epub 2006 Feb 21. Review.

PMID:
16497276
[PubMed - indexed for MEDLINE]

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