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Year Number of Results
2020 1
2021 2
2022 5
2023 5
2024 0

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12 results

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Page 1
Sex differences in long QT syndrome.
Díez-Escuté N, Arbelo E, Martínez-Barrios E, Cerralbo P, Cesar S, Cruzalegui J, Chipa F, Fiol V, Zschaeck I, Hernández C, Campuzano O, Sarquella-Brugada G. Díez-Escuté N, et al. Among authors: cruzalegui j. Front Cardiovasc Med. 2023 Apr 4;10:1164028. doi: 10.3389/fcvm.2023.1164028. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 37082456 Free PMC article. Review.
Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death.
Martínez-Barrios E, Grassi S, Brión M, Toro R, Cesar S, Cruzalegui J, Coll M, Alcalde M, Brugada R, Greco A, Ortega-Sánchez ML, Barberia E, Oliva A, Sarquella-Brugada G, Campuzano O. Martínez-Barrios E, et al. Among authors: cruzalegui j. Front Med (Lausanne). 2023 Feb 10;10:1118585. doi: 10.3389/fmed.2023.1118585. eCollection 2023. Front Med (Lausanne). 2023. PMID: 36844202 Free PMC article. Review.
Characterization of cardiac involvement in children with LMNA-related muscular dystrophy.
Cesar S, Campuzano O, Cruzalegui J, Fiol V, Moll I, Martínez-Barrios E, Zschaeck I, Natera-de Benito D, Ortez C, Carrera L, Expósito J, Berrueco R, Bautista-Rodriguez C, Dabaj I, Gómez García-de-la-Banda M, Quijano-Roy S, Brugada J, Nascimento A, Sarquella-Brugada G. Cesar S, et al. Among authors: cruzalegui j. Front Cell Dev Biol. 2023 Mar 10;11:1142937. doi: 10.3389/fcell.2023.1142937. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 36968203 Free PMC article.
Brugada Syndrome in Women: What Do We Know After 30 Years?
Martínez-Barrios E, Arbelo E, Cesar S, Cruzalegui J, Fiol V, Díez-Escuté N, Hernández C, Brugada R, Brugada J, Campuzano O, Sarquella-Brugada G. Martínez-Barrios E, et al. Among authors: cruzalegui j. Front Cardiovasc Med. 2022 Apr 11;9:874992. doi: 10.3389/fcvm.2022.874992. eCollection 2022. Front Cardiovasc Med. 2022. PMID: 35479286 Free PMC article. Review.
LMNA-related muscular dystrophy: Identification of variants in alternative genes and personalized clinical translation.
Cesar S, Coll M, Fiol V, Fernandez-Falgueras A, Cruzalegui J, Iglesias A, Moll I, Perez-Serra A, Martínez-Barrios E, Ferrer-Costa C, Del Olmo B, Puigmulè M, Alcalde M, Lopez L, Pico F, Berrueco R, Brugada J, Zschaeck I, Natera-de Benito D, Carrera-García L, Exposito-Escudero J, Ortez C, Nascimento A, Brugada R, Sarquella-Brugada G, Campuzano O. Cesar S, et al. Among authors: cruzalegui j. Front Genet. 2023 Mar 24;14:1135438. doi: 10.3389/fgene.2023.1135438. eCollection 2023. Front Genet. 2023. PMID: 37035729 Free PMC article.
Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population.
Martínez-Barrios E, Cesar S, Cruzalegui J, Hernandez C, Arbelo E, Fiol V, Brugada J, Brugada R, Campuzano O, Sarquella-Brugada G. Martínez-Barrios E, et al. Among authors: cruzalegui j. Biomedicines. 2022 Jan 5;10(1):106. doi: 10.3390/biomedicines10010106. Biomedicines. 2022. PMID: 35052786 Free PMC article. Review.
Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review.
Oliva A, Grassi S, Pinchi V, Cazzato F, Coll M, Alcalde M, Vallverdú-Prats M, Perez-Serra A, Martínez-Barrios E, Cesar S, Iglesias A, Cruzalegui J, Hernández C, Fiol V, Arbelo E, Díez-Escuté N, Arena V, Brugada J, Sarquella-Brugada G, Brugada R, Campuzano O. Oliva A, et al. Among authors: cruzalegui j. J Clin Med. 2022 Jul 28;11(15):4406. doi: 10.3390/jcm11154406. J Clin Med. 2022. PMID: 35956023 Free PMC article. Review.
Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in TRDN: A Comprehensive Interpretation.
Sarquella-Brugada G, Fernandez-Falgueras A, Cesar S, Arbelo E, Jordà P, García-Álvarez A, Cruzalegui JC, Merchan EF, Fiol V, Brugada J, Brugada R, Campuzano O. Sarquella-Brugada G, et al. Among authors: cruzalegui jc. Front Pediatr. 2021 Feb 22;8:601708. doi: 10.3389/fped.2020.601708. eCollection 2020. Front Pediatr. 2021. PMID: 33692971 Free PMC article. Review.
Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes.
Martínez-Barrios E, Sarquella-Brugada G, Pérez-Serra A, Fernández-Falgueras A, Cesar S, Coll M, Puigmulé M, Iglesias A, Alcalde M, Vallverdú-Prats M, Ferrer-Costa C, Del Olmo B, Picó F, López L, Fiol V, Cruzalegui J, Hernández C, Arbelo E, Grassi S, Oliva A, Toro R, Brugada J, Brugada R, Campuzano O. Martínez-Barrios E, et al. Among authors: cruzalegui j. J Pers Med. 2022 Feb 8;12(2):241. doi: 10.3390/jpm12020241. J Pers Med. 2022. PMID: 35207729 Free PMC article.
Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort.
Martinez-Barrios E, Sarquella-Brugada G, Perez-Serra A, Fernandez-Falgueras A, Cesar S, Alcalde M, Coll M, Puigmulé M, Iglesias A, Ferrer-Costa C, Del Olmo B, Picó F, Lopez L, Fiol V, Cruzalegui J, Hernandez C, Arbelo E, Díez-Escuté N, Cerralbo P, Grassi S, Oliva A, Toro R, Brugada J, Brugada R, Campuzano O. Martinez-Barrios E, et al. Among authors: cruzalegui j. Int J Legal Med. 2023 Mar;137(2):345-351. doi: 10.1007/s00414-023-02951-0. Epub 2023 Jan 25. Int J Legal Med. 2023. PMID: 36693943 Free PMC article.
12 results