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European Journal of Human Genetics : EJHG|March 21, 2013
Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11pFiorella Gurrieri, Marcella Zollino, Antonio Oliva, et al.Journal of Medical Genetics|March 8, 2013
Genetics of arrhythmogenic right ventricular cardiomyopathyOscar Campuzano, Mireia Alcalde, Catarina Allegue, et al.Seizure|February 4, 2015
Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variantColoma Tiron, Coloma Tiron de Llano, Oscar Campuzano, et al.Epilepsia|August 1, 2013
Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden deathSara Partemi, Sandrine Cestèle, Marianna Pezzella, et al.Forensic Science International|August 14, 2010
Analysis of mRNA from human heart tissue and putative applications in forensic molecular pathologySara Partemi, Paola M Berne, Montserrat Batlle, et al.Atherosclerosis|June 14, 2011
Autopsy investigation and Bayesian approach to coronary artery disease in victims of motor-vehicle accidentsAntonio Oliva, Jose Flores, Sara Merigioli, et al.Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|October 6, 2012
Analysis of the arrhythmogenic substrate in human heart failureSara Partemi, Montserrat Batlle, Paola Berne, et al.Epilepsy Research|March 30, 2013
Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutationPasquale Parisi, Antonio Oliva, Monica Coll Vidal, et al.European Journal of Human Genetics : EJHG|March 27, 2014
Genetic analysis, in silico prediction, and family segregation in long QT syndromeHelena Riuró, Oscar Campuzano, Paola Berne, et al.International Journal of Legal Medicine|August 15, 2014
Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case seriesSara Partemi, Monica Coll Vidal, Pasquale Striano, et al.Pageof 2