Detalhe da pesquisa
1.
An Alternative Mechanism of Subcellular Iron Uptake Deficiency in Cardiomyocytes.
Circ Res
; 133(2): e19-e46, 2023 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37313752
2.
Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator.
Eur Heart J
; 43(32): 3053-3067, 2022 08 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35766183
3.
International External Validation Study of the 2014 European Society of Cardiology Guidelines on Sudden Cardiac Death Prevention in Hypertrophic Cardiomyopathy (EVIDENCE-HCM).
Circulation
; 137(10): 1015-1023, 2018 03 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29191938
4.
2023 ESC Guidelines for the management of cardiomyopathies.
Eur Heart J
; 44(37): 3503-3626, 2023 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37622657
5.
Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases.
Eur Heart J
; 37(23): 1850-8, 2016 06 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-26792875
6.
The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus.
Eur Heart J
; 36(14): 872-81, 2015 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-24598986
7.
The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins.
Exp Cell Res
; 319(19): 3010-9, 2013 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24001739
8.
Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases.
Eur Heart J
; 34(19): 1448-58, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23211230
9.
Current state of knowledge on aetiology, diagnosis, management, and therapy of myocarditis: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases.
Eur Heart J
; 34(33): 2636-48, 2648a-2648d, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23824828
10.
Frequency of misdiagnosis in hypertrophic cardiomyopathy.
Eur Heart J Qual Care Clin Outcomes
; 2024 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38664062
11.
Pregnancy in women with dilated cardiomyopathy genetic variants.
Rev Esp Cardiol (Engl Ed)
; 2024 Apr 18.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-38641168
12.
Mutated desmoglein-2 proteins are incorporated into desmosomes and exhibit dominant-negative effects in arrhythmogenic right ventricular cardiomyopathy.
Hum Mutat
; 34(5): 697-705, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23381804
13.
Patients With Hypertrophic Cardiomyopathy and Normal Genetic Investigations Have Few Affected Relatives.
J Am Coll Cardiol
; 82(18): 1751-1761, 2023 10 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37879779
14.
Risks of Ventricular Arrhythmia and Heart Failure in Carriers of RBM20 Variants.
Circ Genom Precis Med
; 16(5): 434-441, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37593875
15.
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
16.
Leber's Hereditary Optic Neuropathy and Hypertrophic Cardiomyopathy.
CJC Open
; 4(9): 813-815, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-36148257
17.
Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry.
Eur Heart J Qual Care Clin Outcomes
; 9(1): 42-53, 2022 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35138368
18.
The role of the electrocardiographic phenotype in risk stratification for sudden cardiac death in childhood hypertrophic cardiomyopathy.
Eur J Prev Cardiol
; 29(4): 645-653, 2022 03 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-33772274
19.
The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the European Society of Human Genetics.
Eur Heart J
; 36(22): 1367-70, 2015 Jun 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25845928
20.
Prospective follow-up in various subtypes of cardiomyopathies: insights from the ESC EORP Cardiomyopathy Registry.
Eur Heart J Qual Care Clin Outcomes
; 7(2): 134-142, 2021 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33035297