Publicaciones
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Milman A, Behr ER, Gray B, Johnson DC, Andorin A, Hochstadt A, Gourraud JB, Maeda S, Takahashi Y, Jm Juang J, Kim SH, Kamakura T, Aiba T, Postema PG, Mizusawa Y, Denjoy I, Giustetto C, Conte G, Huang Z, Sarquella-Brugada G, Mazzanti A, Jespersen CH, Arbelo E, Brugada R, Calo L, Corrado D, Casado-Arroyo R, Allocca G, Takagi M, Delise P, Brugada-Terradellas J, Tfelt-Hansen J, Priori SG, Veltmann C, Yan GX, Brugada P, Gaita F, Leenhardt A, Wilde AAM, Kusano KF, Nam GB, Hirao K, Probst V and Belhassen B.
Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events Insights From the SABRUS in 392 Probands
Circulation-Genomic and Precision Medicine . 14(5): . Nº de citas: 7
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Barrios-Tascón A, Miura M, Domínguez-Rodríguez S, Fernández-Cooke E, Sarquella-Brugada G and Tagarro A.
Ventricular Repolarization Parameters and Coronary Involvement in Kawasaki Disease
JOURNAL OF PEDIATRICS . 236: 108.
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Sarquella-Brugada G, Algarrada L, Zambrano MD, Fernández-Falgueres A, Sailer S, César-Díaz S, Sebastiani G, Martí-Almor J, Aurensanz E, Cruzalegui JC, Merchan EF, Coll M, Pérez-Serra A, Del Olmo B, Fiol JV, Iglesias A, Ferrer-Costa C, Puigmulé M, Lopez L, Pico F, Arbelo E, Jordà P, Brugada-Terradellas J, Brugada R and Campuzano O.
Early Identification of Prolonged QT Interval for Prevention of Sudden Infant Death
Frontiers in pediatrics . 9: 704580-704580. Nº de citas: 5
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Iglesias-Gomez C, Sequeros, OG, Sarquella-Brugada G, del Rey, MLP and Martinez, DS.
Usefulness of SCT in detecting clinical reasoning deficits among pediatric professionals
Progress in Pediatric Cardiology . 61: . Nº de citas: 1
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Diz OM, Toro R, César-Díaz S, Gomez O, Sarquella-Brugada G and Campuzano O.
Personalized Genetic Diagnosis of Congenital Heart Defects in Newborns
Journal of Personalized Medicine . 11(6): 562. Nº de citas: 7
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Rodríguez-Mañero M, Jordá P, Hernandez J, Muñoz C, Grima EZ, García-Fernández A, Cañadas-Godoy MV, Jiménez-Ramos V, Oloriz T, Basterra N, Calvo D, Pérez-Álvarez L, Arias MA, Expósito V, Alemán A, Díaz-Infante E, Guerra-Ramos JM, Fernández-Armenta J, Arce-Leon Á, Sanchez-Gómez JM, Sousa P, García-Bolao I, Baluja A, Campuzano O, Sarquella-Brugada G, Martinez-Sande JL, González-Juanatey JR, Gimeno JR, Brugada-Terradellas J and Arbelo E.
Long-term prognosis of women with Brugada syndrome and electrophysiological study
Heart Rhythm . 18(5): 664-671. Nº de citas: 12
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Grassi S, Campuzano O, Coll M, Cazzato F, Sarquella-Brugada G, Rossi R, Arena V, Brugada-Terradellas J, Brugada R and Oliva A.
Update on the Diagnostic Pitfalls of Autopsy and Post-Mortem Genetic Testing in Cardiomyopathies
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 22(8): 4124. Nº de citas: 19
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Vallverdú-Prats M, Alcalde M, Sarquella-Brugada G, César-Díaz S, Arbelo E, Fernandez-Falgueras A, Coll M, Pérez-Serra A, Puigmulé M, Iglesias A, Fiol JV, Ferrer-Costa C, Olmo BD, Picó F, Lopez L, Jordà P, García-Álvarez A, Llano CT, Toro R, Grassi S, Oliva A, Brugada-Terradellas J, Brugada R and Campuzano O.
Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later
Journal of Personalized Medicine . 11(3): 162. Nº de citas: 24
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Sarquella-Brugada G, Fernandez-Falgueras A, César-Díaz S, Arbelo E, Jordà P, García-Álvarez A, Cruzalegui JC, Merchan EF, Fiol JV, Brugada-Terradellas J, Brugada R and Campuzano O.
Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in TRDN: A Comprehensive Interpretation
Frontiers in pediatrics . 8: 601708-601708. Nº de citas: 5
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Jordà P, Toro R, Diez C, Salazar-Mendiguchía J, Fernandez-Falgueras A, Perez-Serra A, Coll M, Puigmulé M, Arbelo E, García-Álvarez A, Sarquella-Brugada G, César-Díaz S, Tiron C, Iglesias A, Brugada J, Brugada R and Campuzano O.
Malignant Arrhythmogenic Role Associated with RBM20: A Comprehensive Interpretation Focused on a Personalized Approach
Journal of Personalized Medicine . 11(2): 130. Nº de citas: 8