Stattin EL - Search Results

1

Two automatic QT algorithms compared with manual measurement in identification of long QT syndrome.

Diamant UB, Winbo A, Stattin EL, Rydberg A, Kesek M, Jensen SM. Diamant UB, et al. Among authors: stattin el. J Electrocardiol. 2010 Jan-Feb;43(1):25-30. doi: 10.1016/j.jelectrocard.2009.09.008. J Electrocardiol. 2010. PMID: 20005993

2

[Genetic testing for long QT syndrome is used in clinical practice].

Stattin EL, Rydberg A, Jensen SM. Stattin EL, et al. Lakartidningen. 2006 Nov 8-14;103(45):3542. Lakartidningen. 2006. PMID: 17140181 Swedish. No abstract available.

3

[Long QT syndrome can be effectively treated. Important to identify mutation carriers].

Jensen SM, Stattin EL, Rydberg A. Jensen SM, et al. Among authors: stattin el. Lakartidningen. 2007 Oct 3-9;104(40):2866-70. Lakartidningen. 2007. PMID: 17966800 Review. Swedish. No abstract available.

4

Low incidence of sudden cardiac death in a Swedish Y111C type 1 long-QT syndrome population.

Winbo A, Diamant UB, Stattin EL, Jensen SM, Rydberg A. Winbo A, et al. Among authors: stattin el. Circ Cardiovasc Genet. 2009 Dec;2(6):558-64. doi: 10.1161/CIRCGENETICS.108.825547. Epub 2009 Sep 14. Circ Cardiovasc Genet. 2009. PMID: 20031635

5

Origin of the Swedish long QT syndrome Y111C/KCNQ1 founder mutation.

Winbo A, Diamant UB, Rydberg A, Persson J, Jensen SM, Stattin EL. Winbo A, et al. Among authors: stattin el. Heart Rhythm. 2011 Apr;8(4):541-7. doi: 10.1016/j.hrthm.2010.11.043. Epub 2010 Nov 30. Heart Rhythm. 2011. PMID: 21129503

6

Prevalence, mutation spectrum, and cardiac phenotype of the Jervell and Lange-Nielsen syndrome in Sweden.

Winbo A, Stattin EL, Diamant UB, Persson J, Jensen SM, Rydberg A. Winbo A, et al. Among authors: stattin el. Europace. 2012 Dec;14(12):1799-806. doi: 10.1093/europace/eus111. Epub 2012 Apr 26. Europace. 2012. PMID: 22539601

7

Vectorcardiographic recordings of the Q-T interval in a pediatric long Q-T syndrome population.

Diamant UB, Jensen SM, Winbo A, Stattin EL, Rydberg A. Diamant UB, et al. Among authors: stattin el. Pediatr Cardiol. 2013 Feb;34(2):245-9. doi: 10.1007/s00246-012-0425-2. Epub 2012 Jul 18. Pediatr Cardiol. 2013. PMID: 22806714

8

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing.

Stattin EL, Boström IM, Winbo A, Cederquist K, Jonasson J, Jonsson BA, Diamant UB, Jensen SM, Rydberg A, Norberg A. Stattin EL, et al. BMC Cardiovasc Disord. 2012 Oct 25;12:95. doi: 10.1186/1471-2261-12-95. BMC Cardiovasc Disord. 2012. PMID: 23098067 Free PMC article.

9

Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene.

Diamant UB, Vahedi F, Winbo A, Rydberg A, Stattin EL, Jensen SM, Bergfeldt L. Diamant UB, et al. Among authors: stattin el. J Appl Physiol (1985). 2013 Nov;115(10):1423-32. doi: 10.1152/japplphysiol.00665.2013. Epub 2013 Sep 19. J Appl Physiol (1985). 2013. PMID: 24052033 Free article.

10

Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families.

Winbo A, Stattin EL, Nordin C, Diamant UB, Persson J, Jensen SM, Rydberg A. Winbo A, et al. Among authors: stattin el. BMC Cardiovasc Disord. 2014 Feb 19;14:22. doi: 10.1186/1471-2261-14-22. BMC Cardiovasc Disord. 2014. PMID: 24552659 Free PMC article.

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