[Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease.]

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Standard

[Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease.]. / Holst, Anders Gaarsdal; Tfelt-Hansen, 1jacob; Olesen, Morten S; Theilade, Juliane; Winkel, Bo G; Christensen, Alex H; Bundgaard, Henning; Haunsø, Stig; Svendsen, Jesper Hastrup.

I: Ugeskrift for læger, Bind 172, Nr. 31, 2010, s. 2140-2144.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Holst, AG, Tfelt-Hansen, Olesen, MS, Theilade, J, Winkel, BG, Christensen, AH, Bundgaard, H, Haunsø, S & Svendsen, JH 2010, '[Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease.]', Ugeskrift for læger, bind 172, nr. 31, s. 2140-2144.

APA

Holst, A. G., Tfelt-Hansen, ., Olesen, M. S., Theilade, J., Winkel, B. G., Christensen, A. H., Bundgaard, H., Haunsø, S., & Svendsen, J. H. (2010). [Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease.]. Ugeskrift for læger, 172(31), 2140-2144.

Vancouver

Holst AG, Tfelt-Hansen, Olesen MS, Theilade J, Winkel BG, Christensen AH o.a. [Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease.]. Ugeskrift for læger. 2010;172(31):2140-2144.

Author

Holst, Anders Gaarsdal ; Tfelt-Hansen, 1jacob ; Olesen, Morten S ; Theilade, Juliane ; Winkel, Bo G ; Christensen, Alex H ; Bundgaard, Henning ; Haunsø, Stig ; Svendsen, Jesper Hastrup. / [Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease.]. I: Ugeskrift for læger. 2010 ; Bind 172, Nr. 31. s. 2140-2144.

Bibtex

@article{5da8e6a0a2fd11df928f000ea68e967b,
title = "[Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease.]",
abstract = "Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease, which can lead to life-threatening ventricular arrhythmias in patients with a structurally normal heart. The age of onset is usually between two and 12 years and the initial symptom is frequently syncope or cardiac arrest. The arrhythmias are usually triggered by exercise or emotional affection. The diagnosis is often made using exercise electrocardiogram, which typically triggers arrhythmias. The treatment consists of beta blockers, frequently in combination with implantation of a cardioverter-defibrillator. Udgivelsesdato: 2010-Aug",
author = "Holst, {Anders Gaarsdal} and 1jacob Tfelt-Hansen and Olesen, {Morten S} and Juliane Theilade and Winkel, {Bo G} and Christensen, {Alex H} and Henning Bundgaard and Stig Hauns{\o} and Svendsen, {Jesper Hastrup}",
year = "2010",
language = "Dansk",
volume = "172",
pages = "2140--2144",
journal = "Ugeskrift for Laeger",
issn = "0041-5782",
publisher = "Almindelige Danske Laegeforening",
number = "31",

}

RIS

TY - JOUR

T1 - [Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease.]

AU - Holst, Anders Gaarsdal

AU - Tfelt-Hansen, 1jacob

AU - Olesen, Morten S

AU - Theilade, Juliane

AU - Winkel, Bo G

AU - Christensen, Alex H

AU - Bundgaard, Henning

AU - Haunsø, Stig

AU - Svendsen, Jesper Hastrup

PY - 2010

Y1 - 2010

N2 - Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease, which can lead to life-threatening ventricular arrhythmias in patients with a structurally normal heart. The age of onset is usually between two and 12 years and the initial symptom is frequently syncope or cardiac arrest. The arrhythmias are usually triggered by exercise or emotional affection. The diagnosis is often made using exercise electrocardiogram, which typically triggers arrhythmias. The treatment consists of beta blockers, frequently in combination with implantation of a cardioverter-defibrillator. Udgivelsesdato: 2010-Aug

AB - Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease, which can lead to life-threatening ventricular arrhythmias in patients with a structurally normal heart. The age of onset is usually between two and 12 years and the initial symptom is frequently syncope or cardiac arrest. The arrhythmias are usually triggered by exercise or emotional affection. The diagnosis is often made using exercise electrocardiogram, which typically triggers arrhythmias. The treatment consists of beta blockers, frequently in combination with implantation of a cardioverter-defibrillator. Udgivelsesdato: 2010-Aug

M3 - Tidsskriftartikel

C2 - 20670590

VL - 172

SP - 2140

EP - 2144

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

SN - 0041-5782

IS - 31

ER -

ID: 21258694