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Year Number of Results
2019 4
2020 2
2021 4
2022 6
2023 3
2024 0

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17 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: fiol v. 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.
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: fiol v. 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: fiol v. 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: fiol v. 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: fiol v. 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: fiol v. Front Pediatr. 2021 Feb 22;8:601708. doi: 10.3389/fped.2020.601708. eCollection 2020. Front Pediatr. 2021. PMID: 33692971 Free PMC article. Review.
Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?
Mates J, Mademont-Soler I, Fernandez-Falgueras A, Sarquella-Brugada G, Cesar S, Arbelo E, García-Álvarez A, Jordà P, Toro R, Coll M, Fiol V, Iglesias A, Perez-Serra A, Olmo BD, Alcalde M, Puigmulé M, Pico F, Lopez L, Ferrer C, Tiron C, Grassi S, Oliva A, Brugada J, Brugada R, Campuzano O. Mates J, et al. Among authors: fiol v. Forensic Sci Int Genet. 2020 Jul;47:102281. doi: 10.1016/j.fsigen.2020.102281. Epub 2020 Mar 20. Forensic Sci Int Genet. 2020. PMID: 32248082 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: fiol v. J Pers Med. 2022 Feb 8;12(2):241. doi: 10.3390/jpm12020241. J Pers Med. 2022. PMID: 35207729 Free PMC article.
Clinical impact of rare variants associated with inherited channelopathies: a 5-year update.
Sarquella-Brugada G, Fernandez-Falgueras A, Cesar S, Arbelo E, Coll M, Perez-Serra A, Puigmulé M, Iglesias A, Alcalde M, Vallverdú-Prats M, Fiol V, Ferrer-Costa C, Del Olmo B, Picó F, Lopez L, García-Alvarez A, Jordà P, Tiron de Llano C, Toro R, Grassi S, Oliva A, Brugada J, Brugada R, Campuzano O. Sarquella-Brugada G, et al. Among authors: fiol v. Hum Genet. 2022 Oct;141(10):1579-1589. doi: 10.1007/s00439-021-02370-4. Epub 2021 Sep 21. Hum Genet. 2022. PMID: 34546463 Free PMC article.
17 results