Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom

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Standard

Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom. / Holst, Anders Gaarsdal; Tfelt-Hansen, Jacob; Olesen, Morten S; Theilade, Juliane; Winkel, Bo G; Christensen, Alex H; Bundgaard, Henning; Haunsø, Stig; Svendsen, Jesper Hastrup.

I: Ugeskrift for Laeger, Bind 172, Nr. 31, 02.08.2010, s. 2140-4.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Holst, AG, Tfelt-Hansen, J, Olesen, MS, Theilade, J, Winkel, BG, Christensen, AH, Bundgaard, H, Haunsø, S & Svendsen, JH 2010, 'Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom', Ugeskrift for Laeger, bind 172, nr. 31, s. 2140-4.

APA

Holst, A. G., Tfelt-Hansen, J., Olesen, M. S., Theilade, J., Winkel, B. G., Christensen, A. H., Bundgaard, H., Haunsø, S., & Svendsen, J. H. (2010). Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom. Ugeskrift for Laeger, 172(31), 2140-4.

Vancouver

Holst AG, Tfelt-Hansen J, Olesen MS, Theilade J, Winkel BG, Christensen AH o.a. Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom. Ugeskrift for Laeger. 2010 aug. 2;172(31):2140-4.

Author

Holst, Anders Gaarsdal ; Tfelt-Hansen, Jacob ; Olesen, Morten S ; Theilade, Juliane ; Winkel, Bo G ; Christensen, Alex H ; Bundgaard, Henning ; Haunsø, Stig ; Svendsen, Jesper Hastrup. / Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom. I: Ugeskrift for Laeger. 2010 ; Bind 172, Nr. 31. s. 2140-4.

Bibtex

@article{1dbdd3a3313e49a29de976fb9410615a,
title = "Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom",
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.",
author = "Holst, {Anders Gaarsdal} and Jacob 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",
month = aug,
day = "2",
language = "Dansk",
volume = "172",
pages = "2140--4",
journal = "Ugeskrift for Laeger",
issn = "0041-5782",
publisher = "Almindelige Danske Laegeforening",
number = "31",

}

RIS

TY - JOUR

T1 - Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom

AU - Holst, Anders Gaarsdal

AU - Tfelt-Hansen, Jacob

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 - 2010/8/2

Y1 - 2010/8/2

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.

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.

M3 - Tidsskriftartikel

VL - 172

SP - 2140

EP - 2144

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

SN - 0041-5782

IS - 31

ER -

ID: 34042280