Kort QT-syndrom som arvelig sygdom

Publikation: Bidrag til tidsskriftTidsskriftartikel

Standard

Kort QT-syndrom som arvelig sygdom. / Møller, Daniel Vega; Hedley, Paula L; Olesen, Morten; Kanters, Jørgen; Svendsen, Jesper Hastrup; Christiansen, Michael.

I: Ugeskrift for Laeger, Bind 173, Nr. 6, 2011, s. 420-424.

Publikation: Bidrag til tidsskriftTidsskriftartikel

Harvard

Møller, DV, Hedley, PL, Olesen, M, Kanters, J, Svendsen, JH & Christiansen, M 2011, 'Kort QT-syndrom som arvelig sygdom', Ugeskrift for Laeger, bind 173, nr. 6, s. 420-424.

APA

Møller, D. V., Hedley, P. L., Olesen, M., Kanters, J., Svendsen, J. H., & Christiansen, M. (2011). Kort QT-syndrom som arvelig sygdom. Ugeskrift for Laeger, 173(6), 420-424.

Vancouver

Møller DV, Hedley PL, Olesen M, Kanters J, Svendsen JH, Christiansen M. Kort QT-syndrom som arvelig sygdom. Ugeskrift for Laeger. 2011;173(6):420-424.

Author

Møller, Daniel Vega ; Hedley, Paula L ; Olesen, Morten ; Kanters, Jørgen ; Svendsen, Jesper Hastrup ; Christiansen, Michael. / Kort QT-syndrom som arvelig sygdom. I: Ugeskrift for Laeger. 2011 ; Bind 173, Nr. 6. s. 420-424.

Bibtex

@article{f52e57ea22fc4751860a70feb48c46e4,
title = "Kort QT-syndrom som arvelig sygdom",
abstract = "Inherited ion-channel disorders can lead to life-threatening cardiac arrhythmias. A recent, rare entity has been discovered and termed short QT syndrome due to its electrocardiac features in conjunction with atrial and ventricular tachyarrhythmias as well as syncope and sudden cardiac death. The basis of the new syndrome is genetic and this review covers the genes responsible for the condition as well as the pathophysiology and diagnostic challenges involved in the syndrome. Furthermore, treatment for this new arrhythmic syndrome is reviewed.",
author = "M{\o}ller, {Daniel Vega} and Hedley, {Paula L} and Morten Olesen and J{\o}rgen Kanters and Svendsen, {Jesper Hastrup} and Michael Christiansen",
year = "2011",
language = "Dansk",
volume = "173",
pages = "420--424",
journal = "Ugeskrift for Laeger",
issn = "0041-5782",
publisher = "Almindelige Danske Laegeforening",
number = "6",

}

RIS

TY - JOUR

T1 - Kort QT-syndrom som arvelig sygdom

AU - Møller, Daniel Vega

AU - Hedley, Paula L

AU - Olesen, Morten

AU - Kanters, Jørgen

AU - Svendsen, Jesper Hastrup

AU - Christiansen, Michael

PY - 2011

Y1 - 2011

N2 - Inherited ion-channel disorders can lead to life-threatening cardiac arrhythmias. A recent, rare entity has been discovered and termed short QT syndrome due to its electrocardiac features in conjunction with atrial and ventricular tachyarrhythmias as well as syncope and sudden cardiac death. The basis of the new syndrome is genetic and this review covers the genes responsible for the condition as well as the pathophysiology and diagnostic challenges involved in the syndrome. Furthermore, treatment for this new arrhythmic syndrome is reviewed.

AB - Inherited ion-channel disorders can lead to life-threatening cardiac arrhythmias. A recent, rare entity has been discovered and termed short QT syndrome due to its electrocardiac features in conjunction with atrial and ventricular tachyarrhythmias as well as syncope and sudden cardiac death. The basis of the new syndrome is genetic and this review covers the genes responsible for the condition as well as the pathophysiology and diagnostic challenges involved in the syndrome. Furthermore, treatment for this new arrhythmic syndrome is reviewed.

M3 - Tidsskriftartikel

C2 - 21299935

VL - 173

SP - 420

EP - 424

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

SN - 0041-5782

IS - 6

ER -

ID: 32476068