Detalhe da pesquisa
1.
Andersen-Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity.
Brain
; 145(6): 2108-2120, 2022 06 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34919635
2.
The New South Wales Sudden Cardiac Arrest Registry: A Data Linkage Cohort Study.
Heart Lung Circ
; 32(9): 1069-1075, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37419791
3.
Comparison of conventional autopsy with post-mortem magnetic resonance, computed tomography in determining the cause of unexplained death.
Forensic Sci Med Pathol
; 17(1): 10-18, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33464532
4.
Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy.
Circulation
; 139(15): 1786-1797, 2019 04 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30700137
5.
Diagnostic yield of hypertrophic cardiomyopathy in first-degree relatives of decedents with idiopathic left ventricular hypertrophy.
Europace
; 22(4): 632-642, 2020 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32011662
6.
Accuracy of the 2017 international recommendations for clinicians who interpret adolescent athletes' ECGs: a cohort study of 11 168 British white and black soccer players.
Br J Sports Med
; 54(12): 739-745, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31278087
7.
Patients With Genetic Heart Disease and COVID-19: A Cardiac Society of Australia and New Zealand (CSANZ) Consensus Statement.
Heart Lung Circ
; 29(7): e85-e87, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32418874
8.
Noncardiac genetic predisposition in sudden infant death syndrome.
Genet Med
; 21(3): 641-649, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30139991
9.
Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.
J Pediatr
; 203: 423-428.e11, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30268395
10.
NOS1AP Polymorphisms Modify QTc Interval Duration But Not Cardiac Arrest Risk in Hypertrophic Cardiomyopathy.
J Cardiovasc Electrophysiol
; 26(12): 1346-51, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26332198
11.
When do athletes benefit from cardiac genetic testing?
Br J Sports Med
; 54(15): 939-940, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32220855
12.
Genetic Testing for Inherited Cardiovascular Disease: Implications of the AHA Scientific Statement for Cardiologists.
Heart Lung Circ
; 29(11): 1581-1584, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33008731
13.
Radiation exposure during cardiac catheterisation is similar for both femoral and radial approaches.
Heart Lung Circ
; 24(3): 264-9, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25456214
14.
Brugada syndrome: a heterogeneous disease with a common ECG phenotype?
J Cardiovasc Electrophysiol
; 25(4): 450-456, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24405173
15.
Comparison of conventional autopsy and magnetic resonance imaging in determining the cause of sudden death in the young.
J Cardiovasc Magn Reson
; 16: 44, 2014 Jun 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-24947895
16.
Recurrent immunosuppressive-responsive myocarditis in a patient with desmoplakin cardiomyopathy: a case report.
Eur Heart J Case Rep
; 8(3): ytae129, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38638283
17.
Longitudinal assessment of structural phenotype in Brugada syndrome using cardiac magnetic resonance imaging.
Heart Rhythm O2
; 4(1): 34-41, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36713046
18.
The assessment of undergraduate bachelor of nursing students in the collaborative clusters education model: A qualitative descriptive design.
Nurse Educ Pract
; 70: 103675, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37329827
19.
A case series of patients with filamin-C truncating variants attending a specialized cardiac genetic clinic.
Eur Heart J Case Rep
; 7(12): ytad572, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38116480
20.
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant.
Circ Genom Precis Med
; 16(1): e003672, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36580316