Detalhe da pesquisa
1.
Implantable cardioverter defibrillator use in arrhythmogenic right ventricular cardiomyopathy in North America and Europe.
Eur Heart J
; 45(7): 538-548, 2024 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38195003
2.
Long-term reliability of the phospholamban (PLN) p.(Arg14del) risk model in predicting major ventricular arrhythmia: a landmark study.
Europace
; 26(4)2024 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38558121
3.
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
4.
Electrocardiographic findings in patients with arrhythmogenic cardiomyopathy and right bundle branch block ventricular tachycardia.
Europace
; 25(3): 1025-1034, 2023 03 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36635857
5.
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
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.
Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of MYBPC3 Founder Variants.
Int J Mol Sci
; 24(4)2023 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36835444
8.
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
9.
The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant.
Neth Heart J
; 31(7-8): 315-323, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37505369
10.
MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onset.
Neth Heart J
; 31(7-8): 300-307, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37488328
11.
KBTBD13 is a novel cardiomyopathy gene.
Hum Mutat
; 43(12): 1860-1865, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36335629
12.
Evidence-Based Assessment of Genes in Dilated Cardiomyopathy.
Circulation
; 144(1): 7-19, 2021 07 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33947203
13.
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
14.
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
15.
The prevalence of left and right bundle branch block morphology ventricular tachycardia amongst patients with arrhythmogenic cardiomyopathy and sustained ventricular tachycardia: insights from the European Survey on Arrhythmogenic Cardiomyopathy.
Europace
; 24(2): 285-295, 2022 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34491328
16.
Prediction of ventricular arrhythmia in phospholamban p.Arg14del mutation carriers-reaching the frontiers of individual risk prediction.
Eur Heart J
; 42(29): 2842-2850, 2021 07 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-34113975
17.
Towards a Better Understanding of Genotype-Phenotype Correlations and Therapeutic Targets for Cardiocutaneous Genes: The Importance of Functional Studies above Prediction.
Int J Mol Sci
; 23(18)2022 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36142674
18.
The genetic architecture of Plakophilin 2 cardiomyopathy.
Genet Med
; 23(10): 1961-1968, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34120153
19.
Terminal osseous dysplasia with pigmentary defects and cardiomyopathy caused by a novel FLNA variant.
Am J Med Genet A
; 185(12): 3814-3820, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34254723
20.
Homozygous damaging SOD2 variant causes lethal neonatal dilated cardiomyopathy.
J Med Genet
; 57(1): 23-30, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31494578