Publicacions
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Ball M, Benito-Fernández S, Caride JP, Ruiz-Herguido C, Camprubí-Camprubí M and Sanchez deToledo J.
Pediatric Animal Model of Extracorporeal Cardiopulmonary Resuscitation after Prolonged Circulatory Arrest.
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS . (195): .
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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 A position statement from the AEPC Working Group on Basic Science, Genetics and Myocardial Disease and the AEPC Working Group on Cardiac Dysrhythmias and Electrophysiology
CARDIOLOGY IN THE YOUNG . 33(5): 681-698. Nº de cites: 3
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Gómez del Rincón O, Nogué L, Soveral I, Guirado L, Izquierdo N, Pérez-Cruz M, Masoller-Casas N, Escobar MC, Sanchez deToledo J, Martínez-Crespo JM, Mar Bennasar Sans and Fàtima Crispi Brillas.
Cord blood cardiovascular biomarkers in tetralogy of fallot and D-transposition of great arteries
Frontiers in pediatrics . 11: 1151814-1151814. Nº de cites: 1
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Cassanello MP, Andreas E, Maria VS and Stanimir G.
Converting an infant with borderline left heart structures to biventricular circulation after an initial hybrid Norwood approach: a case report
EUROPEAN HEART JOURNAL-CASE REPORTS . 7(4): .
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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. Nº de cites: 2
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Neumayr TM, Alten JA, Bailly DK, Bhat PN, Brandewie KL, Diddle JW, Ghbeis M, Krawczeski CD, Mah KE, Raymond TT, Reichle G, Zang H and Selewski DT.
Assessment of fluid balance after neonatal cardiac surgery: a description of intake/output vs. weight-based methods.
PEDIATRIC NEPHROLOGY . 38(4): 1355-1364. Nº de cites: 6
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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): . Nº de cites: 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. Nº de cites: 2
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García-García AP, Pérez de Diego R, Flores C, Rinchai D, Solé-Violán J, Deyà-Martinez A, García-Solis B, Lorenzo-Salazar JM, Hernández-Brito E, Lanz AL, Moens L, Bucciol G, Almuqamam M, Domachowske JB, Colino E, Santos-Perez JL, Marco FM, Pignata C, Bousfiha A, Turvey SE, Bauer S, Haerynck F, Ocejo-Vinyals JG, Lendinez F, Prader S, Naumann-Bartsch N, Pachlopnik Schmid J, Biggs CM, Hildebrand K, Dreesman A, Cárdenes MÁ, Ailal F, Benhsaien I, Giardino G, Molina-Fuentes A, Fortuny-Guasch C, Madhavarapu S, Conway DH, Prando C, Schidlowski L, Martínez de Saavedra Álvarez MT, Alfaro R, Rodríguez de Castro F, Meyts I, Hauck F, Puel A, Bastard P, Boisson B, Jouanguy E, Abel L, Cobat A, Zhang Q, Casanova JL, Alsina L and Rodríguez-Gallego C.
Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia
JOURNAL OF EXPERIMENTAL MEDICINE . 220(5): . Nº de cites: 4