Publicacions
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Cañizo-Vázquez D, Hadley SM, Pérez M, López-Abad M, Valls-Lafon A, Viñals ML, Moscoso BA, Benito-Fernández S, Camprubí-Camprubí M and Sanchez deToledo J.
Oxidative Stress and Indicators of Brain Damage Following Pediatric Heart Surgery
ANTIOXIDANTS . 11(3): 489. Nº de cites: 7
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Behr ER, Scrocco C, Wilde AAM, Marijon E, Crotti L, Iliodromitis KE, Remme CA, Kosiuk J, Rudaka I, Sarquella-Brugada G, Frampton K, Schulze-Bahr E, Jubele K, de Asmundis C, Hofman N, Tfelt-Hansen J, Boveda S and Conte G.
Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association Survey
Europace . 24(2): 331-339. Nº de cites: 21
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Abella L, D'Adamo E, Strozzi M, Sanchez deToledo J, Pérez-Cruz M, Gómez del Rincón O, Abella E, Cassinari M, Guaschino R, Mazzucco L, Maconi A, Testa S, Zanelli C, Perrotta M, Roberta P, Renata NC, Gasparroni G, Vitacolonna E, Chiarelli F and Gazzolo D.
S100B Maternal Blood Levels in Gestational Diabetes Mellitus Are Birthweight, Gender and Delivery Mode Dependent
INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH . 19(3): . Nº de cites: 2
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Martínez-Barrios E, Sarquella-Brugada G, Pérez-Serra A, Fernández-Falgueras A, César-Díaz S, Coll M, Puigmulé M, Iglesias A, Alcalde M, Vallverdú-Prats M, Ferrer-Costa C, Del Olmo B, Picó F, López L, Fiol JV, Cruzalegui JC, Hernández-Cera C, Arbelo E, Grassi S, Oliva A, Toro R, Brugada-Terradellas J, Brugada R and Campuzano O.
Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes
Journal of Personalized Medicine . 12(2): . Nº de cites: 4
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Escobar MC, Pérez-Cruz M, Arráez M, Cascant-Vilaplana MM, Albiach-Delgado A, Kuligowski J, Vento M, Masoller-Casas N, Gómez-Roig MD, Gómez O, Sanchez deToledo J and Camprubí-Camprubí M.
Brain Oxygen Perfusion and Oxidative Stress Biomarkers in Fetuses with Congenital Heart Disease-A Retrospective, Case-Control Pilot Study
ANTIOXIDANTS . 11(2): . Nº de cites: 4
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Toro R, Pérez-Serra A, Mangas A, Campuzano O, Sarquella-Brugada G, Quezada-Feijoo M, Ramos M, Alcalá M, Carrera E, García-Padilla C, Franco D and Bonet F.
miR-16-5p Suppression Protects Human Cardiomyocytes against Endoplasmic Reticulum and Oxidative Stress-Induced Injury
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 23(3): . Nº de cites: 22
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Peltenburg PJ, Kallas D, Bos JM, Lieve KVV, Franciosi S, Roston TM, Denjoy I, Sorensen KB, Ohno S, Roses-Noguer F, Aiba T, Maltret A, LaPage MJ, Atallah J, Giudicessi JR, Clur SB, Blom NA, Tanck M, Extramiana F, Kato K, Barc J, Borggrefe M, Behr ER, Sarquella-Brugada G, Tfelt-Hansen J, Zorio E, Swan H, Kammeraad JAE, Krahn AD, Davis A, Sacher F, Schwartz PJ, Roberts JD, Skinner JR, van den Berg MP, Kannankeril PJ, Drago F, Robyns T, Haugaa KH, Tavacova T, Semsarian C, Till J, Probst V, Brugada R, Shimizu W, Horie M, Leenhardt A, Ackerman MJ, Sanatani S, van der Werf C and Wilde AAM.
An International Multicenter Cohort Study on ß-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia
Circulation . 145(5): 333-344. Nº de cites: 30
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Martínez-Barrios E, César-Díaz S, Cruzalegui JC, Hernandez C, Arbelo E, Fiol JV, Brugada-Terradellas J, Brugada R, Campuzano O and Sarquella-Brugada G.
Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population.
Biomedicines . 10(1): . Nº de cites: 11
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Bobillo-Perez S, Girona M, Cañizo-Vázquez D, Camprubí-Camprubí M, Rodríguez-Fanjul J, Balaguer-Gargallo M, Benito-Fernández S, Valls-Lafon A, Cambra-Lasaosa FJ and Jordán-García I.
Mid-regional pro-adrenomedullin for diagnosing evolution after cardiac surgery in newborns: the PRONEW study
EUROPEAN JOURNAL OF PEDIATRICS . 181(3): 1017-1028. Nº de cites: 2
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Sarquella-Brugada G, Fernandez-Falgueras A, César-Díaz S, Arbelo E, Coll M, Perez-Serra A, Puigmulé M, Iglesias A, Alcalde M, Vallverdú-Prats M, Fiol JV, Ferrer-Costa C, Del Olmo B, Picó F, Lopez L, García-Alvarez A, Jordà P, Tiron de Llano C, Toro R, Grassi S, Oliva A, Brugada-Terradellas J, Brugada R and Campuzano O.
Clinical impact of rare variants associated with inherited channelopathies: a 5-year update
HUMAN GENETICS . 141(10): 1579-1589. Nº de cites: 18