Theo dõi
Antonio Oliva
Antonio Oliva
Email được xác minh tại unicatt.it
Tiêu đề
Trích dẫn bởi
Trích dẫn bởi
Năm
Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death
C Antzelevitch, GD Pollevick, JM Cordeiro, O Casis, MC Sanguinetti, ...
Circulation 115 (4), 442-449, 2007
12112007
De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero
K Hong, DR Piper, A Diaz-Valdecantos, J Brugada, A Oliva, ...
Cardiovascular research 68 (3), 433-440, 2005
3872005
Amplification of spatial dispersion of repolarization underlies sudden cardiac death associated with catecholaminergic polymorphic VT, long QT, short QT and Brugada syndromes
C Antzelevitch, A Oliva
Journal of internal medicine 259 (1), 48-58, 2006
2272006
Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations
K Hong, J Brugada, A Oliva, A Berruezo-Sanchez, D Potenza, ...
Circulation 110 (19), 3023-3027, 2004
2162004
Electrocardiographic changes predicting sudden death in propofol-related infusion syndrome
K Vernooy, T Delhaas, OL Cremer, JM Di Diego, A Oliva, C Timmermans, ...
Heart Rhythm 3 (2), 131-137, 2006
2032006
Randomized double-blind placebo-controlled trial of early octreotide in patients with postoperative enterocutaneous fistula
JJ Sancho, J Di Costanzo, P Nubiola, A Larrad, A Beguiristain, F Roqueta, ...
Journal of British Surgery 82 (5), 638-641, 1995
1801995
State of the art in forensic investigation of sudden cardiac death
A Oliva, R Brugada, E D'Aloja, I Boschi, S Partemi, J Brugada, VL Pascali
The American journal of forensic medicine and pathology 32 (1), 1-16, 2011
1252011
Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation
P Parisi, A Oliva, MC Vidal, S Partemi, O Campuzano, A Iglesias, D Pisani, ...
Epilepsy research 105 (3), 415-418, 2013
1212013
Electroanatomic and pathologic right ventricular outflow tract abnormalities in patients with Brugada syndrome
M Pieroni, P Notarstefano, A Oliva, O Campuzano, P Santangeli, M Coll, ...
Journal of the American College of Cardiology 72 (22), 2747-2757, 2018
1062018
Negative autopsy and sudden cardiac death
O Campuzano, C Allegue, S Partemi, A Iglesias, A Oliva, R Brugada
International journal of legal medicine 128, 599-606, 2014
1042014
Arrhythmogenic right ventricular cardiomyopathy: severe structural alterations are associated with inflammation
O Campuzano, M Alcalde, A Iglesias, C Barahona-Dussault, ...
Journal of clinical pathology 65 (12), 1077-1083, 2012
992012
Clinical, electrocardiographic, and electrophysiologic characteristics of patients with a fasciculoventricular pathway: the role of PRKAG2 mutation
EB Sternick, A Oliva, LM Gerken, L Magalhães, R Scarpelli, FS Correia, ...
Heart Rhythm 8 (1), 58-64, 2011
862011
Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction
D Hu, S Viskin, A Oliva, T Carrier, JM Cordeiro, H Barajas-Martinez, Y Wu, ...
Heart Rhythm 4 (8), 1072-1080, 2007
862007
Molecular pathology in forensic medicine—introduction
B Madea, P Saukko, A Oliva, F Musshoff
Forensic science international 203 (1-3), 3-14, 2010
852010
Genetics of arrhythmogenic right ventricular cardiomyopathy
O Campuzano, M Alcalde, C Allegue, A Iglesias, P García-Pavía, ...
Journal of medical genetics 50 (5), 280-289, 2013
822013
Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant
C Tiron, O Campuzano, A Perez-Serra, I Mademont, M Coll, C Allegue, ...
Seizure 25, 65-67, 2015
772015
Cryptic 5′ splice site activation in SCN5A associated with Brugada syndrome
K Hong, A Guerchicoff, GD Pollevick, A Oliva, R Dumaine, M de Zutter, ...
Journal of molecular and cellular cardiology 38 (4), 555-560, 2005
762005
Genetic and biophysical basis for bupivacaine-induced ST segment elevation and VT/VF. Anesthesia unmasked Brugada syndrome
K Vernooy, S Sicouri, R Dumaine, K Hong, A Oliva, E Burashnikov, ...
Heart Rhythm 3 (9), 1074-1078, 2006
752006
Loss‐of‐function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death
S Partemi, S Cestèle, M Pezzella, O Campuzano, R Paravidino, ...
Epilepsia 54 (8), e112-e116, 2013
722013
Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing
M Coll, C Allegue, S Partemi, J Mates, B Del Olmo, O Campuzano, ...
International journal of legal medicine 130, 331-339, 2016
702016
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