Fodstad H - Search Results

1

Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects.

Laitinen P, Fodstad H, Piippo K, Swan H, Toivonen L, Viitasalo M, Kaprio J, Kontula K. Laitinen P, et al. Among authors: fodstad h. Hum Mutat. 2000 Jun;15(6):580-1. doi: 10.1002/1098-1004(200006)15:6<580::AID-HUMU16>3.0.CO;2-0. Hum Mutat. 2000. PMID: 10862094

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: fodstad 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. Ann Med. 2004;36 Suppl 1:53-63. doi: 10.1080/17431380410032689. Ann Med. 2004. PMID: 15176425 Free article.

4

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: fodstad 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

5

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: fodstad 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

6

Association between HERG K897T polymorphism and QT interval in middle-aged Finnish women.

Pietilä E, Fodstad H, Niskasaari E, Laitinen P PJ, Swan H, Savolainen M, Kesäniemi YA, Kontula K, Huikuri HV. Pietilä E, et al. Among authors: fodstad h. J Am Coll Cardiol. 2002 Aug 7;40(3):511-4. doi: 10.1016/s0735-1097(02)01979-4. J Am Coll Cardiol. 2002. PMID: 12142119 Free article. Clinical Trial.

7

Molecular screening of selected long QT syndrome (LQTS) mutations in 165 consecutive bodies found in water.

Lunetta P, Levo A, Laitinen PJ, Fodstad H, Kontula K, Sajantila A. Lunetta P, et al. Among authors: fodstad h. Int J Legal Med. 2003 Apr;117(2):115-7. doi: 10.1007/s00414-002-0331-x. Epub 2003 Feb 28. Int J Legal Med. 2003. PMID: 12690509

8

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. 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

9

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: fodstad 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.

10

Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients.

Fodstad H, Bendahhou S, Rougier JS, Laitinen-Forsblom PJ, Barhanin J, Abriel H, Schild L, Kontula K, Swan H. Fodstad H, et al. Ann Med. 2006;38(4):294-304. doi: 10.1080/07853890600756065. Ann Med. 2006. PMID: 16754261 Free article.

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