Swan H - Search Results

1

A founder mutation of the potassium channel KCNQ1 in long QT syndrome: implications for estimation of disease prevalence and molecular diagnostics.

Piippo K, Swan H, Pasternack M, Chapman H, Paavonen K, Viitasalo M, Toivonen L, Kontula K. Piippo K, et al. Among authors: swan h. J Am Coll Cardiol. 2001 Feb;37(2):562-8. doi: 10.1016/s0735-1097(00)01124-4. J Am Coll Cardiol. 2001. PMID: 11216980 Free article.

2

Functional characterization of the common amino acid 897 polymorphism of the cardiac potassium channel KCNH2 (HERG).

Paavonen KJ, Chapman H, Laitinen PJ, Fodstad H, Piippo K, Swan H, Toivonen L, Viitasalo M, Kontula K, Pasternack M. Paavonen KJ, et al. Among authors: swan h. Cardiovasc Res. 2003 Sep 1;59(3):603-11. doi: 10.1016/s0008-6363(03)00458-9. Cardiovasc Res. 2003. PMID: 14499861

3

Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland.

Fodstad H, Swan H, Laitinen P, Piippo K, Paavonen K, Viitasalo M, Toivonen L, Kontula K. Fodstad H, et al. Among authors: swan h. Ann Med. 2004;36 Suppl 1:53-63. doi: 10.1080/17431380410032689. Ann Med. 2004. PMID: 15176425

4

Loss-of-function mutations of the K(+) channel gene KCNJ2 constitute a rare cause of long QT syndrome.

Fodstad H, Swan H, Auberson M, Gautschi I, Loffing J, Schild L, Kontula K. Fodstad H, et al. Among authors: swan h. J Mol Cell Cardiol. 2004 Aug;37(2):593-602. doi: 10.1016/j.yjmcc.2004.05.011. J Mol Cell Cardiol. 2004. PMID: 15276028

5

Temporal repolarization lability differences among genotyped patients with the long QT syndrome.

Bilchick K, Viitasalo M, Oikarinen L, Fetics B, Tomaselli G, Swan H, Laitinen PJ, Väänänen H, Kontula K, Berger RD. Bilchick K, et al. Among authors: swan h. Am J Cardiol. 2004 Nov 15;94(10):1312-6. doi: 10.1016/j.amjcard.2004.07.123. Am J Cardiol. 2004. PMID: 15541256

6

Ratio of late to early T-wave peak amplitude in 24-h electrocardiographic recordings as indicator of symptom history in patients with long-QT Syndrome types 1 and 2.

Viitasalo M, Oikarinen L, Swan H, Glatter KA, Väänänen H, Fodstad H, Chiamvimonvat N, Kontula K, Toivonen L, Scheinman MM. Viitasalo M, et al. Among authors: swan h. J Am Coll Cardiol. 2006 Jan 3;47(1):112-20. doi: 10.1016/j.jacc.2005.07.068. Epub 2005 Dec 9. J Am Coll Cardiol. 2006. PMID: 16386673 Free article.

7

Effects of beta-blocker therapy on ventricular repolarization documented by 24-h electrocardiography in patients with type 1 long-QT syndrome.

Viitasalo M, Oikarinen L, Swan H, Väänänen H, Järvenpää J, Hietanen H, Karjalainen J, Toivonen L. Viitasalo M, et al. Among authors: swan h. J Am Coll Cardiol. 2006 Aug 15;48(4):747-53. doi: 10.1016/j.jacc.2006.04.084. Epub 2006 Jul 25. J Am Coll Cardiol. 2006. PMID: 16904544 Free article.

8

Beta1-adrenergic receptor polymorphisms, QTc interval and occurrence of symptoms in type 1 of long QT syndrome.

Paavonen KJ, Swan H, Piippo K, Laitinen P, Fodstad H, Sarna S, Toivonen L, Kontula K, Viitasalo M. Paavonen KJ, et al. Among authors: swan h. Int J Cardiol. 2007 May 31;118(2):197-202. doi: 10.1016/j.ijcard.2006.06.050. Epub 2006 Oct 4. Int J Cardiol. 2007. PMID: 17023080

9

Further evidence of inherited long QT syndrome gene mutations in antiarrhythmic drug-associated torsades de pointes.

Lehtonen A, Fodstad H, Laitinen-Forsblom P, Toivonen L, Kontula K, Swan H. Lehtonen A, et al. Among authors: swan h. Heart Rhythm. 2007 May;4(5):603-7. doi: 10.1016/j.hrthm.2007.01.019. Epub 2007 Jan 18. Heart Rhythm. 2007. PMID: 17467628

10

High prevalence of four long QT syndrome founder mutations in the Finnish population.

Marjamaa A, Salomaa V, Newton-Cheh C, Porthan K, Reunanen A, Karanko H, Jula A, Lahermo P, Väänänen H, Toivonen L, Swan H, Viitasalo M, Nieminen MS, Peltonen L, Oikarinen L, Palotie A, Kontula K. Marjamaa A, et al. Among authors: swan h. Ann Med. 2009;41(3):234-40. doi: 10.1080/07853890802668530. Ann Med. 2009. PMID: 19160088 Free PMC article.

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