Diamant UB - Search Results

1

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: diamant ub. BMC Cardiovasc Disord. 2014 Feb 19;14:22. doi: 10.1186/1471-2261-14-22. BMC Cardiovasc Disord. 2014. PMID: 24552659 Free PMC article.

2

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: diamant ub. 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

3

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: diamant ub. 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

4

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: diamant ub. Europace. 2012 Dec;14(12):1799-806. doi: 10.1093/europace/eus111. Epub 2012 Apr 26. Europace. 2012. PMID: 22539601

5

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. Pediatr Cardiol. 2013 Feb;34(2):245-9. doi: 10.1007/s00246-012-0425-2. Epub 2012 Jul 18. Pediatr Cardiol. 2013. PMID: 22806714

6

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. Among authors: diamant ub. BMC Cardiovasc Disord. 2012 Oct 25;12:95. doi: 10.1186/1471-2261-12-95. BMC Cardiovasc Disord. 2012. PMID: 23098067 Free PMC article.

7

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. 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.

8

Third trimester fetal heart rate predicts phenotype and mutation burden in the type 1 long QT syndrome.

Winbo A, Fosdal I, Lindh M, Diamant UB, Persson J, Wettrell G, Rydberg A. Winbo A, et al. Among authors: diamant ub. Circ Arrhythm Electrophysiol. 2015 Aug;8(4):806-14. doi: 10.1161/CIRCEP.114.002552. Epub 2015 May 27. Circ Arrhythm Electrophysiol. 2015. PMID: 26019114

9

Implantable cardioverter defibrillator treatment in long QT syndrome patients: a national study on adherence to international guidelines.

Sundström E, Jensen SM, Diamant UB, Rydberg A. Sundström E, et al. Among authors: diamant ub. Scand Cardiovasc J. 2017 Apr;51(2):88-94. doi: 10.1080/14017431.2016.1270463. Epub 2016 Dec 30. Scand Cardiovasc J. 2017. PMID: 27936942 Free article.

10

ICD harm and benefit: risk scores applied to the Swedish ICD-treated LQTS population.

Sundström E, Jensen SM, Diamant UB, Wiklund U, Rydberg A. Sundström E, et al. Among authors: diamant ub. Scand Cardiovasc J. 2022 Dec;56(1):48-55. doi: 10.1080/14017431.2022.2060524. Scand Cardiovasc J. 2022. PMID: 35481393 Free article.

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