Detalhe da pesquisa
1.
Programmed Ventricular Stimulation as an Additional Primary Prevention Risk Stratification Tool in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multinational Study.
Circulation
; 146(19): 1434-1443, 2022 11 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36205131
2.
Arrhythmic risk stratification in arrhythmogenic right ventricular cardiomyopathy.
Europace
; 25(11)2023 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37935403
3.
Role of plakophilin-2 expression on exercise-related progression of arrhythmogenic right ventricular cardiomyopathy: a translational study.
Eur Heart J
; 43(12): 1251-1264, 2022 03 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34932122
4.
A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy.
Eur Heart J
; 43(32): e1-e9, 2022 08 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35441664
5.
Arrhythmic risk prediction in arrhythmogenic right ventricular cardiomyopathy: external validation of the arrhythmogenic right ventricular cardiomyopathy risk calculator.
Eur Heart J
; 43(32): 3041-3052, 2022 08 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35766180
6.
Lack of Evidence for the Role of the p.(Ser96Ala) Polymorphism in Histidine-Rich Calcium Binding Protein as a Secondary Hit in Cardiomyopathies.
Int J Mol Sci
; 24(21)2023 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37958923
7.
Exercise does not influence development of phenotype in PLN p.(Arg14del) cardiomyopathy.
Neth Heart J
; 31(7-8): 291-299, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37474840
8.
Evidence-Based Assessment of Genes in Dilated Cardiomyopathy.
Circulation
; 144(1): 7-19, 2021 07 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33947203
9.
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
10.
The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results.
Am J Hum Genet
; 104(4): 578-595, 2019 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30951675
11.
Clinical characteristics and risk stratification of desmoplakin cardiomyopathy.
Europace
; 24(2): 268-277, 2022 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34352074
12.
Comparing clinical performance of current implantable cardioverter-defibrillator implantation recommendations in arrhythmogenic right ventricular cardiomyopathy.
Europace
; 24(2): 296-305, 2022 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34468736
13.
Strength of the genetic counselor: patient relationship is associated with extent of increased empowerment in patients with arrhythmogenic cardiomyopathy.
J Genet Couns
; 31(2): 388-397, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34672408
14.
Genotype-phenotype Correlates in Arrhythmogenic Cardiomyopathies.
Curr Cardiol Rep
; 24(11): 1557-1565, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36074218
15.
Arrhythmogenic right ventricular cardiomyopathy and sports activity: from molecular pathways in diseased hearts to new insights into the athletic heart mimicry.
Eur Heart J
; 42(13): 1231-1243, 2021 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-33200174
16.
Arrhythmogenic Right Ventricular Cardiomyopathy: Progress Toward Personalized Management.
Annu Rev Med
; 70: 1-18, 2019 01 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-30355260
17.
The genetic architecture of Plakophilin 2 cardiomyopathy.
Genet Med
; 23(10): 1961-1968, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34120153
18.
Efficacy of catheter ablation for premature ventricular contractions in arrhythmogenic right ventricular cardiomyopathy.
J Cardiovasc Electrophysiol
; 32(6): 1665-1674, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33783912
19.
Left ventricular fibro-fatty replacement in arrhythmogenic right ventricular dysplasia/cardiomyopathy: prevalence, patterns, and association with arrhythmias.
J Cardiovasc Magn Reson
; 23(1): 58, 2021 05 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34011348
20.
FLNC truncations cause arrhythmogenic right ventricular cardiomyopathy.
J Med Genet
; 57(4): 254-257, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31924696