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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2006 | 1 |
2007 | 2 |
2008 | 3 |
2009 | 1 |
2024 | 0 |
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7 results
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Lone atrial fibrillation: influence of familial disease on gender predilection.
J Cardiovasc Electrophysiol. 2008 Aug;19(8):802-6. doi: 10.1111/j.1540-8167.2008.01126.x. Epub 2008 Mar 21.
J Cardiovasc Electrophysiol. 2008.
PMID: 18363686
Free PMC article.
A common polymorphism in SCN5A is associated with lone atrial fibrillation.
Chen LY, Ballew JD, Herron KJ, Rodeheffer RJ, Olson TM.
Chen LY, et al.
Clin Pharmacol Ther. 2007 Jan;81(1):35-41. doi: 10.1038/sj.clpt.6100016.
Clin Pharmacol Ther. 2007.
PMID: 17185997
Free PMC article.
Item in Clipboard
X-linked nonsyndromic sinus node dysfunction and atrial fibrillation caused by emerin mutation.
Karst ML, Herron KJ, Olson TM.
Karst ML, et al.
J Cardiovasc Electrophysiol. 2008 May;19(5):510-5. doi: 10.1111/j.1540-8167.2007.01081.x. Epub 2008 Feb 4.
J Cardiovasc Electrophysiol. 2008.
PMID: 18266676
Free PMC article.
Item in Clipboard
Comprehensive mutation scanning of LMNA in 268 patients with lone atrial fibrillation.
Brauch KM, Chen LY, Olson TM.
Brauch KM, et al.
Am J Cardiol. 2009 May 15;103(10):1426-8. doi: 10.1016/j.amjcard.2009.01.354. Epub 2009 Apr 1.
Am J Cardiol. 2009.
PMID: 19427440
Free PMC article.
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Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation.
Olson TM, Alekseev AE, Liu XK, Park S, Zingman LV, Bienengraeber M, Sattiraju S, Ballew JD, Jahangir A, Terzic A.
Olson TM, et al.
Hum Mol Genet. 2006 Jul 15;15(14):2185-91. doi: 10.1093/hmg/ddl143. Epub 2006 Jun 13.
Hum Mol Genet. 2006.
PMID: 16772329
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Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation.
Hodgson-Zingman DM, Karst ML, Zingman LV, Heublein DM, Darbar D, Herron KJ, Ballew JD, de Andrade M, Burnett JC Jr, Olson TM.
Hodgson-Zingman DM, et al.
N Engl J Med. 2008 Jul 10;359(2):158-65. doi: 10.1056/NEJMoa0706300.
N Engl J Med. 2008.
PMID: 18614783
Free PMC article.
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KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation.
Olson TM, Alekseev AE, Moreau C, Liu XK, Zingman LV, Miki T, Seino S, Asirvatham SJ, Jahangir A, Terzic A.
Olson TM, et al.
Nat Clin Pract Cardiovasc Med. 2007 Feb;4(2):110-6. doi: 10.1038/ncpcardio0792.
Nat Clin Pract Cardiovasc Med. 2007.
PMID: 17245405
Free PMC article.
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