Detalhe da pesquisa
1.
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study.
Eur Heart J
; 44(21): 1927-1939, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37038246
2.
Loss of Nuclear Envelope Integrity and Increased Oxidant Production Cause DNA Damage in Adult Hearts Deficient in PKP2: A Molecular Substrate of ARVC.
Circulation
; 146(11): 851-867, 2022 09 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35959657
3.
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
4.
Carriers of COL3A1 pathogenic variants in Denmark: Interfamilial variability in severity and outcome of elective surgical procedures.
Clin Genet
; 102(3): 191-200, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35699227
5.
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease.
Eur Heart J
; 41(28): 2618-2628, 2020 07 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32702746
6.
Pregnancies, ventricular arrhythmias, and substrate progression in women with arrhythmogenic right ventricular cardiomyopathy in the Nordic ARVC Registry.
Europace
; 22(12): 1873-1879, 2020 12 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-32681178
7.
A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression.
N Engl J Med
; 379(18): 1780-1781, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30380381
8.
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.
Nat Genet
; 55(3): 399-409, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36658437
9.
A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients.
J Cardiovasc Transl Res
; 16(6): 1276-1286, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37418234
10.
Incidence rates of dilated cardiomyopathy in adult first-degree relatives versus matched controls.
Int J Cardiol Heart Vasc
; 41: 101065, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35663623
11.
Family Screening in Dilated Cardiomyopathy: Prevalence, Incidence, and Potential for Limiting Follow-Up.
JACC Heart Fail
; 10(11): 792-803, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36328645
12.
Prevalence of Left Ventricular Noncompaction in Newborns.
Circ Cardiovasc Imaging
; 15(6): e014159, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35727876
13.
Abnormal atrial activation is common in patients with arrhythmogenic right ventricular cardiomyopathy.
J Electrocardiol
; 44(2): 237-41, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21093870
14.
Multifocal atrial and ventricular premature contractions with an increased risk of dilated cardiomyopathy caused by a Nav1.5 gain-of-function mutation (G213D).
Int J Cardiol
; 257: 160-167, 2018 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29506689
15.
New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants.
Eur J Hum Genet
; 21(9): 918-28, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23299917
16.
Usefulness of immunostaining for plakoglobin as a diagnostic marker of arrhythmogenic right ventricular cardiomyopathy.
Am J Cardiol
; 109(2): 272-5, 2012 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22036107
17.
[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 Dinamarquês
| MEDLINE | ID: mdl-20670590