Zobrazeno 1 - 10
of 17
pro vyhledávání: '"José, Cruzalegui"'
Autor:
Elena Arbelo, Gonzalo Grazioli, Carles Díez-López, Oscar Campuzano, Georgia Sarquella-Brugada, Sergi Cesar, Estefanía Martínez-Barrios, Rocío Toro, José Cruzalegui, Andrea Greco, Nuria Díez-Escuté, Patricia Cerralbo, Fredy Chipa, Norma Balderrábano
Publikováno v:
BMJ Open Sport & Exercise Medicine, Vol 10, Iss 3 (2024)
Sudden cardiac death is a rare but socially devastating event, especially if occurs in young people. Usually, this unexpected lethal event occurs during or just after exercise. One of the leading causes of sudden cardiac death is inherited arrhythmog
Externí odkaz:
https://doaj.org/article/d98a2bce5c9d4002abe937027884e2b4
Akademický článek
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Autor:
Nuria Díez-Escuté, Elena Arbelo, Estefanía Martínez-Barrios, Patricia Cerralbo, Sergi Cesar, José Cruzalegui, Freddy Chipa, Victoria Fiol, Irene Zschaeck, Clara Hernández, Oscar Campuzano, Georgia Sarquella-Brugada
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
Long QT Syndrome (LQTS) is a rare, inherited channelopathy characterized by cardiac repolarization dysfunction, leading to a prolonged rate-corrected QT interval in patients who are at risk for malignant ventricular tachyarrhythmias, syncope, and eve
Externí odkaz:
https://doaj.org/article/7524962dc80d40fa8800fb7b09ba1199
Autor:
Estefanía Martínez-Barrios, Simone Grassi, María Brión, Rocío Toro, Sergi Cesar, José Cruzalegui, Mònica Coll, Mireia Alcalde, Ramon Brugada, Andrea Greco, María Luisa Ortega-Sánchez, Eneko Barberia, Antonio Oliva, Georgia Sarquella-Brugada, Oscar Campuzano
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
In the forensic medicine field, molecular autopsy is the post-mortem genetic analysis performed to attempt to unravel the cause of decease in cases remaining unexplained after a comprehensive forensic autopsy. This negative autopsy, classified as neg
Externí odkaz:
https://doaj.org/article/82adbe2de4bf4080a5976d662351f2d2
Autor:
Estefanía Martínez-Barrios, Elena Arbelo, Sergi Cesar, José Cruzalegui, Victoria Fiol, Nuria Díez-Escuté, Clara Hernández, Ramon Brugada, Josep Brugada, Oscar Campuzano, Georgia Sarquella-Brugada
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
Brugada syndrome (BrS) was initially described in 1992 by Josep and Pedro Brugada as an arrhythmogenic disease characterized by ST segment elevation in the right precordial leads and increased risk of sudden cardiac death (SCD). Alterations in the SC
Externí odkaz:
https://doaj.org/article/3bbe5daf189d4844a571c2a41cced83d
Autor:
José Cruzalegui, Sergi Cesar, Oscar Campuzano, Victoria Fiol, Josep Brugada, Georgia Sarquella-Brugada
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 9, Iss 4, p 109 (2022)
We report a pediatric patient with persistent left superior vena cava and a D-transposition of great arteries, which is an uncommon relation. It is crucial to know the anatomy of the persistent left superior vena cava and the dilated coronary sinus t
Externí odkaz:
https://doaj.org/article/50888a2be5234f1193f949e859389401
Autor:
Estefanía Martinez-Barrios, Georgia Sarquella-Brugada, Alexandra Perez-Serra, Anna Fernandez-Falgueras, Sergi Cesar, Mireia Alcalde, Mónica Coll, Marta Puigmulé, Anna Iglesias, Carles Ferrer-Costa, Bernat del Olmo, Ferran Picó, Laura Lopez, Victoria Fiol, José Cruzalegui, Clara Hernandez, Elena Arbelo, Nuria Díez-Escuté, Patricia Cerralbo, Simone Grassi, Antonio Oliva, Rocío Toro, Josep Brugada, Ramon Brugada, Oscar Campuzano
Publikováno v:
International Journal of Legal Medicine. 137:345-351
Sudden death cases in the young population remain without a conclusive cause of decease in almost 40% of cases. In these situations, cardiac arrhythmia of genetic origin is suspected as the most plausible cause of death. Molecular autopsy may reveal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17eeef65ef3b1beda2e4f99a783bb000
https://doi.org/10.1007/s00414-023-02951-0
https://doi.org/10.1007/s00414-023-02951-0
Autor:
Estefanía Martínez-Barrios, Sergi Cesar, José Cruzalegui, Clara Hernandez, Elena Arbelo, Victoria Fiol, Josep Brugada, Ramon Brugada, Oscar Campuzano, Georgia Sarquella-Brugada
Publikováno v:
Biomedicines, Vol 10, Iss 1, p 106 (2022)
Sudden death is a rare event in the pediatric population but with a social shock due to its presentation as the first symptom in previously healthy children. Comprehensive autopsy in pediatric cases identify an inconclusive cause in 40–50% of cases
Externí odkaz:
https://doaj.org/article/b8ac06423f394c39887e4909be9485ce
Autor:
Estefanía Martínez-Barrios, José Cruzalegui, Sergi Cesar, Fredy Chipa, Elena Arbelo, Victoria Fiol, Josep Brugada, Georgia Sarquella-Brugada, Oscar Campuzano
Short QT syndrome (SQTS) is an extremely rare inherited arrhythmogenic entity. Nowadays, less than 200 families affected worldwide have been reported. This syndrome is characterized by the presence of a short QT interval leading to malignant ventricu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94431c330fec524a24417e1058464277
https://mts.intechopen.com/articles/show/title/short-qt-syndrome-update-on-genetic-basis
https://mts.intechopen.com/articles/show/title/short-qt-syndrome-update-on-genetic-basis
Autor:
Antonio Oliva, Simone Grassi, Vilma Pinchi, Francesca Cazzato, Mónica Coll, Mireia Alcalde, Marta Vallverdú-Prats, Alexandra Perez-Serra, Estefanía Martínez-Barrios, Sergi Cesar, Anna Iglesias, José Cruzalegui, Clara Hernández, Victoria Fiol, Elena Arbelo, Nuria Díez-Escuté, Vincenzo Arena, Josep Brugada, Georgia Sarquella-Brugada, Ramon Brugada, Oscar Campuzano
Publikováno v:
Journal of Clinical Medicine, 2022, vol. 11, núm. 15, p. 4406
Articles publicats (IdIBGi)
Oliva, Antonio Grassi, Simone Pinchi, Vilma Cazzato, Francesca Coll Vidal, Mònica Alcalde Masegu, Mireia Vallverdú-Prats, Marta Perez-Serra, Alexandra Martínez-Barrios, Estefanía Cesar, Sergi Iglesias, Anna Cruzalegui, Jose Carlos Hernández Cera, Clara Fiol, Victoria Arbelo, Elena Díez-Escuté, Nuria Arena, Vincenzo Brugada, Josep Sarquella Brugada, Geòrgia Brugada, Ramon Campuzano Larrea, Oscar 2022 Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review Journal of Clinical Medicine 11 15 4406
DUGiDocs – Universitat de Girona
instname
Articles publicats (IdIBGi)
Oliva, Antonio Grassi, Simone Pinchi, Vilma Cazzato, Francesca Coll Vidal, Mònica Alcalde Masegu, Mireia Vallverdú-Prats, Marta Perez-Serra, Alexandra Martínez-Barrios, Estefanía Cesar, Sergi Iglesias, Anna Cruzalegui, Jose Carlos Hernández Cera, Clara Fiol, Victoria Arbelo, Elena Díez-Escuté, Nuria Arena, Vincenzo Brugada, Josep Sarquella Brugada, Geòrgia Brugada, Ramon Campuzano Larrea, Oscar 2022 Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review Journal of Clinical Medicine 11 15 4406
DUGiDocs – Universitat de Girona
instname
Brugada syndrome (BrS) is classified as an inherited cardiac channelopathy attributed to dysfunctional ion channels and/or associated proteins in cardiomyocytes rather than to structural heart alterations. However, hearts of some BrS patients exhibit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92d765b23a2d26d3c0fc1c54111c24e4
https://pubmed.ncbi.nlm.nih.gov/35956023
https://pubmed.ncbi.nlm.nih.gov/35956023