Search details
1.
Investigating cardiac genetic background in sudden infant death syndrome (SIDS).
Int J Legal Med
; 2024 Jun 07.
Article
in English
| MEDLINE | ID: mdl-38849547
2.
Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy.
Int J Mol Sci
; 25(7)2024 Mar 29.
Article
in English
| MEDLINE | ID: mdl-38612618
3.
Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort.
Int J Legal Med
; 137(2): 345-351, 2023 Mar.
Article
in English
| MEDLINE | ID: mdl-36693943
4.
Clinical impact of rare variants associated with inherited channelopathies: a 5-year update.
Hum Genet
; 141(10): 1579-1589, 2022 Oct.
Article
in English
| MEDLINE | ID: mdl-34546463
5.
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.
Article
in English
| MEDLINE | ID: mdl-36232963
6.
Unpredicted Aberrant Splicing Products Identified in Postmortem Sudden Cardiac Death Samples.
Int J Mol Sci
; 23(20)2022 Oct 20.
Article
in English
| MEDLINE | ID: mdl-36293497
7.
The role of clinical assessment and electrophysiology study in Brugada syndrome patients with syncope.
Am Heart J
; 220: 213-223, 2020 02.
Article
in English
| MEDLINE | ID: mdl-31864099
8.
Genetic interpretation and clinical translation of minor genes related to Brugada syndrome.
Hum Mutat
; 40(6): 749-764, 2019 06.
Article
in English
| MEDLINE | ID: mdl-30821013
9.
Sudden death due to catecholaminergic polymorphic ventricular tachycardia following negative stress-test outcome: genetics and clinical implications.
Forensic Sci Med Pathol
; 13(2): 217-225, 2017 Jun.
Article
in English
| MEDLINE | ID: mdl-28405885
10.
Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?
Int J Legal Med
; 130(2): 415-20, 2016 Mar.
Article
in English
| MEDLINE | ID: mdl-26872470
11.
Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing.
Int J Legal Med
; 130(2): 331-9, 2016 Mar.
Article
in English
| MEDLINE | ID: mdl-26423924
12.
A novel mutation in lamin a/c causing familial dilated cardiomyopathy associated with sudden cardiac death.
J Card Fail
; 21(3): 217-25, 2015 Mar.
Article
in English
| MEDLINE | ID: mdl-25498755
13.
Genetics of inherited arrhythmias in pediatrics.
Curr Opin Pediatr
; 27(6): 665-74, 2015 Dec.
Article
in English
| MEDLINE | ID: mdl-26371946
14.
Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death.
Int J Mol Sci
; 16(10): 25773-87, 2015 Oct 27.
Article
in English
| MEDLINE | ID: mdl-26516846
15.
Negative autopsy and sudden cardiac death.
Int J Legal Med
; 128(4): 599-606, 2014 Jul.
Article
in English
| MEDLINE | ID: mdl-24532175
16.
Genetics of arrhythmogenic right ventricular cardiomyopathy.
J Med Genet
; 50(5): 280-9, 2013 May.
Article
in English
| MEDLINE | ID: mdl-23468208
17.
The importance of variant reinterpretation in inherited cardiovascular diseases: Establishing the optimal timeframe.
PLoS One
; 19(5): e0297914, 2024.
Article
in English
| MEDLINE | ID: mdl-38691546
18.
A missense mutation in the sodium channel ß2 subunit reveals SCN2B as a new candidate gene for Brugada syndrome.
Hum Mutat
; 34(7): 961-6, 2013 Jul.
Article
in English
| MEDLINE | ID: mdl-23559163
19.
Genetics of sudden cardiac death in children and young athletes.
Cardiol Young
; 23(2): 159-73, 2013 Apr.
Article
in English
| MEDLINE | ID: mdl-22824130
20.
Postmortem diagnosis of Takotsubo syndrome on autoptic findings: is it reliable? A systematic review.
Cardiovasc Pathol
; 65: 107543, 2023.
Article
in English
| MEDLINE | ID: mdl-37169210