Detalhe da pesquisa
1.
Extracellular Kir2.1C122Y Mutant Upsets Kir2.1-PIP2 Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome.
Circ Res
; 134(8): e52-e71, 2024 Apr 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38497220
2.
Flecainide Is Associated With a Lower Incidence of Arrhythmic Events in a Large Cohort of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia.
Circulation
; 148(25): 2029-2037, 2023 12 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37886885
3.
An International Multicenter Cohort Study on ß-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia.
Circulation
; 145(5): 333-344, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34874747
4.
Impaired Binding to Junctophilin-2 and Nanostructural Alteration in CPVT Mutation.
Circ Res
; 129(3): e35-e52, 2021 07 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34111951
5.
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
6.
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
7.
Cadaveric Adipose-Derived Stem Cells for Regenerative Medicine and Research.
Int J Mol Sci
; 24(21)2023 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37958680
8.
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
9.
Titin Missense Variants as a Cause of Familial Dilated Cardiomyopathy.
Circulation
; 147(22): 1711-1713, 2023 05 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37253077
10.
Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissection.
Int J Legal Med
; 131(5): 1211-1219, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28391405
11.
Deregulated hepatic microRNAs underlie the association between non-alcoholic fatty liver disease and coronary artery disease.
Liver Int
; 36(8): 1221-9, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26901384
12.
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
13.
Pregnancy in women with dilated cardiomyopathy genetic variants.
Rev Esp Cardiol (Engl Ed)
; 2024 Apr 18.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-38641168
14.
Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy.
JACC Clin Electrophysiol
; 2024 Apr 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38727660
15.
Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives.
J Am Coll Cardiol
; 83(17): 1640-1651, 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38658103
16.
Paradoxical effect of increased diastolic Ca(2+) release and decreased sinoatrial node activity in a mouse model of catecholaminergic polymorphic ventricular tachycardia.
Circulation
; 126(4): 392-401, 2012 Jul 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-22711277
17.
Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy.
Circ J
; 77(9): 2358-65, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23782526
18.
Impact of SARS-CoV-2 infection in patients with cardiac amyloidosis: Results of a multicentre registry.
Med Clin (Barc)
; 161(11): 476-482, 2023 12 07.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-37684159
19.
Extracellular cysteine disulfide bond break at Cys122 disrupts PIP2-dependent Kir2.1 channel function and leads to arrhythmias in Andersen-Tawil Syndrome.
bioRxiv
; 2023 Jun 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37333254
20.
Non Coding RNAs as Regulators of Wnt/ß-Catenin and Hippo Pathways in Arrhythmogenic Cardiomyopathy.
Biomedicines
; 10(10)2022 Oct 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-36289882