Detalhe da pesquisa
1.
Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications.
Int J Legal Med
; 129(1): 1-10, 2015 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-24832006
2.
An enigmatic case of cardiac death in an 18-years old girl.
Eur Rev Med Pharmacol Sci
; 25(15): 4999-5005, 2021 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-34355371
3.
High-density substrate mapping in Brugada syndrome: combined role of conduction and repolarization heterogeneities in arrhythmogenesis.
Circulation
; 120(2): 106-17, 1-4, 2009 Jul 14.
Artigo
Inglês
| MEDLINE | ID: mdl-19564561
4.
Role of genetic testing in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Clin Genet
; 77(1): 37-48, 2010 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-19863551
5.
Lamotrigine induced Brugada-pattern in a patient with genetic epilepsy associated with a novel variant in SCN9A.
Gene
; 754: 144847, 2020 Sep 05.
Artigo
Inglês
| MEDLINE | ID: mdl-32531456
6.
Dominant-negative effect of a mutant cardiac troponin T on cardiac structure and function in transgenic mice.
J Clin Invest
; 102(8): 1498-505, 1998 Oct 15.
Artigo
Inglês
| MEDLINE | ID: mdl-9788962
7.
A transgenic rabbit model for human hypertrophic cardiomyopathy.
J Clin Invest
; 104(12): 1683-92, 1999 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-10606622
8.
Familial dilated cardiomyopathy: A multidisciplinary entity, from basic screening to novel circulating biomarkers.
Int J Cardiol
; 228: 870-880, 2017 Feb 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27889554
9.
Brugada syndrome: a decade of progress.
Circ Res
; 91(12): 1114-8, 2002 Dec 13.
Artigo
Inglês
| MEDLINE | ID: mdl-12480811
10.
Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent.
Circ Res
; 85(9): 803-9, 1999 Oct 29.
Artigo
Inglês
| MEDLINE | ID: mdl-10532948
11.
Modulation of I(Kr) inactivation by mutation N588K in KCNH2: a link to arrhythmogenesis in short QT syndrome.
Cardiovasc Res
; 67(3): 498-509, 2005 Aug 15.
Artigo
Inglês
| MEDLINE | ID: mdl-16039272
12.
Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts.
Circulation
; 101(5): 510-5, 2000 Feb 08.
Artigo
Inglês
| MEDLINE | ID: mdl-10662748
13.
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy.
Circulation
; 104(18): 2188-93, 2001 Oct 30.
Artigo
Inglês
| MEDLINE | ID: mdl-11684629
14.
The Brugada Syndrome.
Arch Mal Coeur Vaiss
; 98(2): 115-22, 2005 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-15787302
15.
A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction.
Atherosclerosis
; 128(1): 107-12, 1997 Jan 03.
Artigo
Inglês
| MEDLINE | ID: mdl-9051203
16.
A prospective study of paraoxonase gene Q/R192 polymorphism and severity, progression and regression of coronary atherosclerosis, plasma lipid levels, clinical events and response to fluvastatin.
Atherosclerosis
; 154(3): 633-40, 2001 Feb 15.
Artigo
Inglês
| MEDLINE | ID: mdl-11257264
17.
Lipoprotein lipase gene mutations, plasma lipid levels, progression/regression of coronary atherosclerosis, response to therapy, and future clinical events. Lipoproteins and Coronary Atherosclerosis Study.
Atherosclerosis
; 144(2): 435-42, 1999 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-10407505
18.
Role of molecular biology in identifying individuals at risk for sudden cardiac death.
Am J Cardiol
; 86(9A): 28K-33K, 2000 Nov 02.
Artigo
Inglês
| MEDLINE | ID: mdl-11084097
19.
Sudden death in high-risk family members: Brugada syndrome.
Am J Cardiol
; 86(9A): 40K-43K, 2000 Nov 02.
Artigo
Inglês
| MEDLINE | ID: mdl-11084099
20.
Use of the prophylactic implantable cardioverter defibrillator for patients with normal hearts.
Am J Cardiol
; 83(5B): 98D-100D, 1999 Mar 11.
Artigo
Inglês
| MEDLINE | ID: mdl-10089849