Publicacions
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Jalal, Zakaria, Galmiche, Louise, Lebeaux, David, Villemain, Olivier, Sarquella-Brugada G, Patel, Mehul, Ghigo, Jean-Marc, Beloin, Christophe and Boudjemline, Younes.
Selective propensity of bovine jugular vein material to bacterial adhesions: An in-vitro study
INTERNATIONAL JOURNAL OF CARDIOLOGY . 198: 201-205. Nº de cites: 54
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Selga E, Campuzano O, Pinsach-Abuin ML, Pérez-Serra A, Mademont-Soler I, Riuró H, Picó F, Coll M, Iglesias A, Pagans S, Sarquella-Brugada G, Berne P, Benito B, Brugada-Terradellas J, Porres JM, López Zea M, Castro-Urda V, Fernández-Lozano I and Brugada R.
Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort
PLoS One . 10(7): . Nº de cites: 16
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Sarquella-Brugada G.
Effect of p.v66m_bdnf polymorphism in heart rate recovery after maximal exercise
J APPL PHYSIOL . : .
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Sarquella-Brugada G, Campuzano O, Iglesias A, Grueso J, Bradley DJ, Kerst G, Shmorhun D, Brugada-Terradellas J and Brugada R.
Short QT and atrial fibrillation: A KCNQ1 mutation-specific disease. Late follow-up in three unrelated children
Heart Rhythm . 1(4): 193-197.
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Alcalde M, Campuzano O, Sarquella-Brugada G, Arbelo E, Allegue C, Partemi S, Iglesias A, Oliva A, Brugada-Terradellas J and Brugada R.
Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy
CLINICAL RESEARCH IN CARDIOLOGY . 104(4): 288-303. Nº de cites: 15
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Pérez-Serra A, Toro R, Campuzano O, Sarquella-Brugada G, Berne P, Iglesias A, Mangas A, Brugada-Terradellas J and Brugada R.
A Novel Mutation in Lamin A/C Causing Familial Dilated Cardiomyopathy Associated With Sudden Cardiac Death
JOURNAL OF CARDIAC FAILURE . 21(3): 217-225. Nº de cites: 19
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Sarquella-Brugada G, Rodríguez-Fanjul J, Camprubí-Camprubí M, Arango Posada CA, Moreno-Hernando J and Prada F.
Aortic thrombosis successfully treated with local recombinant tissue plasminogen activator in a newborn
JOURNAL OF THROMBOSIS AND THROMBOLYSIS . 39(2): 251-253. Nº de cites: 2
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Campuzano O, Sarquella-Brugada G, Brugada R and Brugada-Terradellas J.
Genetics of channelopathies associated with sudden cardiac death.
Global cardiology science & practice . 2015(3): 39-39. Nº de cites: 24
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Riuró H, Campuzano O, Berne P, Arbelo E, Iglesias A, Pérez-Serra A, Coll-Vidal M, Partemi S, Mademont-Soler I, Picó F, Allegue C, Oliva A, Gerstenfeld E, Sarquella-Brugada G, Castro-Urda V, Fernández-Lozano I, Mont L, Brugada-Terradellas J, Scornik FS and Brugada R.
Genetic analysis, in silico prediction, and family segregation in long QT syndrome
EUROPEAN JOURNAL OF HUMAN GENETICS . 23(1): 79-85. Nº de cites: 13
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Campuzano O, Sarquella-Brugada G, Mademont-Soler I, Allegue C, César-Díaz S, Ferrer-Costa C, Coll M, Mates J, Iglesias A, Brugada-Terradellas J and Brugada R.
Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology
PLoS One . 9(12): . Nº de cites: 30