Detalhe da pesquisa
1.
Myocardial scarring and recurrence of ventricular arrhythmia in patients surviving an out-of-hospital cardiac arrest.
J Cardiovasc Electrophysiol
; 34(11): 2286-2295, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37681321
2.
Sudden unexplained death versus nonautopsied possible sudden cardiac death: Findings in relatives.
J Cardiovasc Electrophysiol
; 33(2): 254-261, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34918422
3.
Comparing Seizure-Related Death and Suicide in Younger Adults with Epilepsy.
Ann Neurol
; 90(6): 983-987, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34564866
4.
Wireless Single-Lead ECG Monitoring to Detect New-Onset Postoperative Atrial Fibrillation in Patients After Major Noncardiac Surgery: A Prospective Observational Study.
Anesth Analg
; 135(1): 100-109, 2022 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35213523
5.
Sudden unexpected death in epilepsy in persons younger than 50 years: A retrospective nationwide cohort study in Denmark.
Epilepsia
; 62(10): 2405-2415, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34418071
6.
Clinical characteristics and risk factors of arrhythmia during follow-up of patients with idiopathic ventricular fibrillation.
J Cardiovasc Electrophysiol
; 31(10): 2677-2686, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33462911
7.
Toxicology Screening in Sports-Related Sudden Cardiac Death: A Multinational Observational Study.
JACC Clin Electrophysiol
; 10(3): 515-523, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38127009
8.
Use of Nonrecommended Drugs in Patients With Brugada Syndrome: A Danish Nationwide Cohort Study.
J Am Heart Assoc
; 12(7): e028424, 2023 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36942759
9.
ß-blocker adherence among patients with congenital long QT syndrome: a nationwide study.
Eur Heart J Qual Care Clin Outcomes
; 9(1): 76-84, 2022 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35438152
10.
Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis.
BMC Med Genet
; 12: 22, 2011 Feb 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-21306642
11.
Cause-specific mortality in children and young adults with diabetes mellitus: A Danish nationwide cohort study.
Eur J Prev Cardiol
; 28(2): 159-165, 2021 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30862235
12.
Familial Evaluation in Idiopathic Ventricular Fibrillation: Diagnostic Yield and Significance of J Wave Syndromes.
Circ Arrhythm Electrophysiol
; 14(3): e009089, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33550818
13.
The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy.
Eur J Hum Genet
; 28(1): 17-22, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31534214
14.
Presence of Atrioventricular Nodal Reentrant Tachycardia Is Associated With Cardiomyopathy, Heart Failure, and Death.
J Am Heart Assoc
; 13(9): e034439, 2024 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38686897
15.
Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome.
J Am Coll Cardiol
; 69(17): 2134-2145, 2017 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28449774
16.
Factors Associated With and Outcomes After Ventricular Fibrillation Before and During Primary Angioplasty in Patients With ST-Segment Elevation Myocardial Infarction.
Am J Cardiol
; 116(5): 678-85, 2015 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26150175
17.
Nationwide (Denmark) study of symptoms preceding sudden death due to arrhythmogenic right ventricular cardiomyopathy.
Am J Cardiol
; 113(7): 1250-4, 2014 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24513468
18.
Mutations in genes encoding cardiac ion channels previously associated with sudden infant death syndrome (SIDS) are present with high frequency in new exome data.
Can J Cardiol
; 29(9): 1104-9, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23465283
19.
[Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease]. / Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom.
Ugeskr Laeger
; 172(31): 2140-4, 2010 Aug 02.
Artigo
em Da
| MEDLINE | ID: mdl-20670590
20.
A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease.
Case Rep Med
; 2009: 963645, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19829766