Sergio César Diaz
Investigador
Research group
Sergi César graduated in Medicine in 2006 from the University Rovira i Virgili. He specialized in Paediatrics in Tarragona and completed his training with a Master's Degree in Paediatric Cardiology at the University of Barcelona-SJD Barcelona Children’s Hospital between 2011 and 2013. With special interest in arrhythmias, family heart disease and neuromuscular diseases, to complete The studies completed the postgraduate course in medical genetics at the University of Valencia in 2016 and began doctoral studies in 2017 in the line of neuromuscular diseases with cardiac involvement. Along these lines, in 2016, it developed a research project on cardiac image analysis in Pennsylvania, USA, and a project on laminopathy at the National Center for Scientific Research in collaboration with the Carlos III Institute in Madrid.
Since 2013, he works in the paediatric cardiology service of the SJD Barcelona Children's Hospital and coordinates cardiological research at the Clinical Trials Unit, in addition to carrying out research tasks in the line of investigation of arrhythmias, family heart disease and sudden death.
Since 2014, he also directs and coordinates cardiac ultrasound courses at the Paediatric Classroom of the SJD Barcelona Children's Hospital.
Professional network profiles
Related websites
Last Publications
- Martínez-Barrios E, Greco A, Cruzalegui JC, César-Díaz S, Nuria Díez Escuté, Patricia Cerralbo Martín, Chipa F, Zschaeck-Luzardo I, Slanovic L, Mangas A, Toro R, Brugada-Terradellas J, Sarquella-Brugada G and Campuzano O Interpreting the actionable clinical role of rare variants associated with short QT syndrome. HUMAN GENETICS . 143(12): 1499-1508.
- Martínez-Barrios E, Greco A, Cruzalegui JC, César-Díaz S, Nuria Díez Escuté, Patricia Cerralbo Martín, Chipa F, Zschaeck-Luzardo I, Fogaça-da-Mata M, Díez-López C, Arbelo E, Grassi S, Oliva A, Toro R, Sarquella-Brugada G and Campuzano O Actionable Variants of Unknown Significance in Inherited Arrhythmogenic Syndromes: A Further Step Forward in Genetic Diagnosis. Biomedicines . 12(11): .
- de Frutos F, Ochoa JP, Webster G, Jansen M, Remior P, Rasmussen TB, Sabater-Molina M, Barriales-Villa R, Girolami F, César-Díaz S, Fuentes-Cañamero ME, Alvarez García-Rovés R, Wahbi K, Limeres J, Kubanek M, Slieker MG, Sarquella-Brugada G, Abrams DJ, Dooijes D, Domínguez F and Garcia-Pavia P Clinical Features and Outcomes of Pediatric MYH7-Related Dilated Cardiomyopathy. JOURNAL OF THE AMERICAN HEART ASSOCIATION . 13(21): .
Projects
- Project name:
- Score de daño cerebral prequirúrgico para recién nacidos con cardiopatía congénita utilizando herramientas de inteligencia artificial
- Leader
- Marta Camprubi Camprubi
- Funding entities:
- Instituto de Salud Carlos III (ISCIII), Fundació Privada per a la Recerca i la Docència Sant Joan de Déu - FSJD, Ruiz Herguido, Cristina
- Code
- PI23/00104
- Starting - finishing date:
- 2024 - 2026
- Project name:
- Monitorització remota cardíaca de pacients pediàtrics. Impacte social, mediambiental i de salut.
- Leader
- Georgia Sarquella Brugada
- Funding entities:
- ÁREA METROPOLITANA DE BARCELONA (AMB)
- Code
- 900623
- Starting - finishing date:
- 2023 - 2024
- Project name:
- Creación de un programa personalizado de actividad física dirigida para deportistas de competición diagnosticados de un síndrome hereditario asociado a muerte súbita (PAC-SAMS).
- Leader
- Georgia Sarquella Brugada
- Funding entities:
- Fundació Privada per a la Recerca i la Docència Sant Joan de Déu - FSJD, Consejo Superior de Deportes, Martínez Barrios, Estefanía
- Code
- 74742
- Starting - finishing date:
- 2023 - 2023