Detalhe da pesquisa
1.
Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death.
Genet Med
; 23(1): 86-93, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32973354
2.
TMEM43 mutations associated with arrhythmogenic right ventricular cardiomyopathy in non-Newfoundland populations.
Hum Genet
; 132(11): 1245-52, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23812740
3.
Symptoms and signs associated with syncope in young people with primary cardiac arrhythmias.
Heart Lung Circ
; 20(9): 593-8, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21616715
4.
Digital implantable loop recorders in the investigation of syncope in children: benefits and limitations.
Heart Rhythm
; 3(11): 1306-12, 2006 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17074636
5.
Reducing sudden death in young people in Australia and New Zealand: the TRAGADY initiative.
Med J Aust
; 189(10): 539-40, 2008 Nov 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-19012547
6.
Does retrograde diastolic flow in the descending aorta signify impaired systemic perfusion in preterm infants?
Pediatr Res
; 63(1): 89-94, 2008 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18043512
7.
Long QT syndrome: not just a ventricular problem.
Heart Rhythm
; 5(5): 710-1, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18452874
8.
Guidelines for the diagnosis and management of familial long QT syndrome.
Heart Lung Circ
; 16(1): 22-4, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17194624