Publications
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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): . Number of citations: 9
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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): . Number of citations: 17
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Paredes-Fuentes AJ, César-Díaz S, Montero-Sanchez R, Latre C, Genovés-Escarré J, Martorell-Sampol L, Cuadras-Palleja D, Colom H, Pineda M, O'Callaghan-Gordo M, Sarquella-Brugada G, Darling A and Artuch-Iriberri R.
Plasma idebenone monitoring in Friedreich's ataxia patients during a long-term follow-up
BIOMEDICINE & PHARMACOTHERAPY . 143: 112143-112143. Number of citations: 10
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García-Otero L, LÓpez M, GoncÉ A, Fortuny-Guasch C, Salazar L, Valenzuela-Alcaraz BI, Guirado L, César-Díaz S, Gratacós E and Crispi F.
Cardiac Remodeling and Hypertension in HIV-Uninfected Infants Exposed in utero to Antiretroviral Therapy
CLINICAL INFECTIOUS DISEASES . 73(4): 586-593. Number of citations: 13
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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. Number of citations: 10
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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. Number of citations: 14
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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. Number of citations: 26
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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. Number of citations: 9
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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. Number of citations: 12
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Natera-de Benito D, Ortez-Gonzalez CI, Jou-Munoz C, Jimenez-Mallebrera C, Codina-Bergadà A, Carrera-García L, Exposito-Escudero JM, César-Díaz S, Martorell-Sampol L, Gallano P, Gonzalez-Quereda L, Cuadras-Palleja D, Colomer J, Yubero-Siles D, Palau F and Nascimento-Osorio A.
The Phenotype and Genotype of Congenital Myopathies Based on a Large Pediatric Cohort
PEDIATRIC NEUROLOGY . 115: 50-65. Number of citations: 21