Publications
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Alcalde M, Toro R, Bonet F, Córdoba-Caballero J, Martínez-Barrios E, Ranea JA, Vallverdú-Prats M, Brugada R, Meraviglia V, Bellin M, Sarquella-Brugada G and Campuzano O.
Role of microRNAs in arrhythmogenic cardiomyopathy: translation as biomarkers into clinical practice.
translational research : the journal of laboratory and clinical medicine . 259: 72-82.
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Grassi S, Campuzano O, Cazzato F, Coll M, Puggioni A, Zedda M, Arena V, Iglesias A, Sarquella-Brugada G, Pinchi V, Brugada R and Oliva A.
Postmortem diagnosis of Takotsubo syndrome on autoptic findings: is it reliable? A systematic review
CARDIOVASCULAR PATHOLOGY . 65: 107543-107543. Number of citations: 1
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Kaski JP, Kammeraad JAE, Blom NA, Happonen JM, Janousek J, Klaassen S, Limongelli G, Östman-Smith I, Sarquella-Brugada G and Ziolkowska L.
Indications and management of implantable cardioverter-defibrillator therapy in childhood hypertrophic cardiomyopathy.
CARDIOLOGY IN THE YOUNG . 33(5): 681-698.
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Díez-Escuté N, Arbelo E, Martínez-Barrios E, Cerralbo P, César-Díaz S, Cruzalegui JC, Chipa F, Fiol JV, Zschaeck-Luzardo I, Hernández-Cera C, Campuzano O and Sarquella-Brugada G.
Sex differences in long QT syndrome
frontiers in cardiovascular medicine . 10: 1164028-1164028.
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Landstrom, AA, Chahal, AJ, Ackerman, M, Cresci, SM, Milewicz, DA, Morris, A, Sarquella-Brugada G, Semsarian, CH, Shah, SC and Sturm, A.
Interpreting Incidentally Identified Variants in Genes Associated With Heritable Cardiovascular Disease: A Scientific Statement From the American Heart Association
Circulation-Genomic and Precision Medicine . 16(2): . Number of citations: 2
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César-Díaz S, Coll, M, Fiol JV, Fernandez-Falgueras, A, Cruzalegui JC, Iglesias, A, Moll I, Perez-Serra, A, Martínez-Barrios E, Ferrer-Costa, C, del Olmo, B, Puigmule, M, Alcalde, M, Lopez, L, Pico, F, Berrueco R, Brugada-Terradellas J, Zschaeck-Luzardo I, Natera-de Benito D, Carrera-García L, Exposito-Escudero JM, Ortez-Gonzalez CI, Nascimento-Osorio A, Brugada, R, Sarquella-Brugada G and Campuzano, O.
LMNA-related muscular dystrophy: Identification of variants in alternative genes and personalized clinical translation
Frontiers in Genetics . 14: 1135438-1135438.
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César-Díaz S, Campuzano O, Cruzalegui JC, Fiol JV, Moll I, Martínez-Barrios E, Zschaeck-Luzardo I, Natera-de Benito D, Ortez-Gonzalez CI, Carrera-García L, Exposito-Escudero JM, Berrueco R, Bautista-Rodriguez C, Dabaj I, Gómez García-de-la-Banda M, Quijano-Roy S, Brugada-Terradellas J, Nascimento-Osorio A and Sarquella-Brugada G.
Characterization of cardiac involvement in children with LMNA-related muscular dystrophy
Frontiers in Cell and Developmental Biology . 11: 1142937-1142937. Number of citations: 1
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Martínez-Barrios E, Sarquella-Brugada G, Perez-Serra A, Fernandez-Falgueras A, César-Díaz S, Alcalde M, Coll M, Puigmulé M, Iglesias A, Ferrer-Costa C, Del Olmo B, Picó F, Lopez L, Fiol JV, Cruzalegui JC, Hernández-Cera C, Arbelo E, Díez-Escuté N, Cerralbo P, Grassi S, Oliva A, Toro R, Brugada-Terradellas J, Brugada R and Campuzano O.
Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort
INTERNATIONAL JOURNAL OF LEGAL MEDICINE . 137(2): 345-351.
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Martínez-Barrios E, Grassi S, Brión M, Toro R, César-Díaz S, Cruzalegui JC, Coll M, Alcalde M, Brugada R, Greco A, Ortega-Sánchez ML, Barberia E, Oliva A, Sarquella-Brugada G and Campuzano O.
Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death
Frontiers in Medicine . 10: 1118585-1118585.
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Campuzano O and Sarquella-Brugada G.
Molecular autopsy in sudden cardiac death.
Global cardiology science & practice . 2023(1): 202308-202308.