Detalhe da pesquisa
1.
Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants.
Circulation
; 144(20): 1600-1611, 2021 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-34587765
2.
Ethnic differences in out-of-hospital cardiac arrest among Middle Eastern Arabs and North African populations living in Qatar.
Ethn Health
; 26(3): 460-469, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30303400
3.
Myoarchitectural disarray of hypertrophic cardiomyopathy begins pre-birth.
J Anat
; 235(5): 962-976, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31347708
4.
Classification, Epidemiology, and Global Burden of Cardiomyopathies.
Circ Res
; 121(7): 722-730, 2017 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28912179
5.
Survival After Heart Transplantation in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy.
J Card Fail
; 23(2): 107-112, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27154489
6.
Arrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy.
Europace
; 18(4): 610-6, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25825460
7.
Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing.
Europace
; 18(6): 888-96, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26498160
8.
Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosis.
Eur Heart J
; 41(14): 1414-1429, 2020 04 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31637441
9.
Fractal Analysis of Myocardial Trabeculations in 2547 Study Participants: Multi-Ethnic Study of Atherosclerosis.
Radiology
; 277(3): 707-15, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26069924
10.
Clinical Significance of Epsilon Waves in Arrhythmogenic Cardiomyopathy.
J Cardiovasc Electrophysiol
; 26(11): 1204-1210, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26183028
11.
Abnormal septal convexity into the left ventricle occurs in subclinical hypertrophic cardiomyopathy.
J Cardiovasc Magn Reson
; 17: 64, 2015 Jul 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-26219660
12.
Cellular mechanisms underlying the increased disease severity seen for patients with long QT syndrome caused by compound mutations in KCNQ1.
Biochem J
; 462(1): 133-42, 2014 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24912595
13.
Prediction of ventricular arrhythmia and sudden death in arrhythmogenic right ventricular cardiomyopathy.
Eur Heart J
; 40(23): 1859-1861, 2019 06 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30977786
14.
A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD).
Eur Heart J
; 35(30): 2010-20, 2014 Aug 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-24126876
15.
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
Hum Mol Genet
; 21(9): 2039-53, 2012 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22286171
16.
Relation between serum N-terminal pro-brain natriuretic peptide and prognosis in patients with hypertrophic cardiomyopathy.
Eur Heart J
; 34(32): 2529-37, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23455360
17.
Emerging Themes in Genetics of Hypertrophic Cardiomyopathy: Current Status and Clinical Application.
Can J Cardiol
; 40(5): 742-753, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38244984
18.
Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy.
JACC Clin Electrophysiol
; 2024 Apr 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38727660
19.
Proposed diagnostic criteria for arrhythmogenic cardiomyopathy: European Task Force consensus report.
Int J Cardiol
; 395: 131447, 2024 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37844667
20.
Disease pathways and novel therapeutic targets in hypertrophic cardiomyopathy.
Circ Res
; 109(1): 86-96, 2011 Jun 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-21700950