Detalhe da pesquisa
1.
Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy.
Int J Mol Sci
; 25(7)2024 Mar 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38612618
2.
Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort.
Int J Legal Med
; 137(2): 345-351, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36693943
3.
Alterations in Calcium Handling Are a Common Feature in an Arrhythmogenic Cardiomyopathy Cell Model Triggered by Desmosome Genes Loss.
Int J Mol Sci
; 24(3)2023 Jan 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36768439
4.
Clinical impact of rare variants associated with inherited channelopathies: a 5-year update.
Hum Genet
; 141(10): 1579-1589, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34546463
5.
The Role of MicroRNAs in Dilated Cardiomyopathy: New Insights for an Old Entity.
Int J Mol Sci
; 23(21)2022 Nov 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36362356
6.
A microRNA Signature for the Diagnosis of Statins Intolerance.
Int J Mol Sci
; 23(15)2022 Jul 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35897722
7.
Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome.
Int J Mol Sci
; 23(19)2022 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36232963
8.
miR-16-5p Suppression Protects Human Cardiomyocytes against Endoplasmic Reticulum and Oxidative Stress-Induced Injury.
Int J Mol Sci
; 23(3)2022 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-35162959
9.
Unpredicted Aberrant Splicing Products Identified in Postmortem Sudden Cardiac Death Samples.
Int J Mol Sci
; 23(20)2022 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36293497
10.
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
Circulation
; 142(4): 324-338, 2020 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32429735
11.
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.
Genet Med
; 23(1): 47-58, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32893267
12.
Update on the Diagnostic Pitfalls of Autopsy and Post-Mortem Genetic Testing in Cardiomyopathies.
Int J Mol Sci
; 22(8)2021 Apr 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-33923560
13.
The role of clinical assessment and electrophysiology study in Brugada syndrome patients with syncope.
Am Heart J
; 220: 213-223, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31864099
14.
Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?
Int J Mol Sci
; 21(19)2020 Sep 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32998306
15.
Genetic interpretation and clinical translation of minor genes related to Brugada syndrome.
Hum Mutat
; 40(6): 749-764, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30821013
16.
Long-term outcome of neonates and infants with permanent junctional reciprocating tachycardia. When cardiac ablation changes natural history.
J Electrocardiol
; 56: 85-89, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31326859
17.
Update on the Genetic Basis of Sudden Unexpected Death in Epilepsy.
Int J Mol Sci
; 20(8)2019 Apr 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-31018519
18.
Molecular disturbance underlies to arrhythmogenic cardiomyopathy induced by transgene content, age and exercise in a truncated PKP2 mouse model.
Hum Mol Genet
; 25(17): 3676-3688, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27412010
19.
Update about atrial fibrillation genetics.
Curr Opin Cardiol
; 32(3): 246-252, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28169950
20.
Medico-legal perspectives on sudden cardiac death in young athletes.
Int J Legal Med
; 131(2): 393-409, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27654714