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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 1
2010 1
2011 3
2012 2
2016 1
2017 2
2018 1
2019 3
2020 1
2021 5
2022 6
2023 2
2024 2

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28 results

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Page 1
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: puigmule m. Front Genet. 2023 Mar 24;14:1135438. doi: 10.3389/fgene.2023.1135438. eCollection 2023. Front Genet. 2023. PMID: 37035729 Free PMC article.
Malignant Arrhythmogenic Role Associated with RBM20: A Comprehensive Interpretation Focused on a Personalized Approach.
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, Cesar S, Tiron C, Iglesias A, Brugada J, Brugada R, Campuzano O. Jordà P, et al. Among authors: puigmule m. J Pers Med. 2021 Feb 15;11(2):130. doi: 10.3390/jpm11020130. J Pers Med. 2021. PMID: 33671899 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: puigmule m. 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.
High-quality RNA improves sensitivity of SARS-CoV-2 detection by colorimetric RT-LAMP.
Puigmulé M, Coll M, Pérez-Serra A, López L, Picó F, Neto N, Corona M, Pinsach-Abuin ML, Ferrer-Costa C, Buxó M, Queralt FX, Brugada R. Puigmulé M, et al. Exp Biol Med (Maywood). 2022 Feb;247(3):276-281. doi: 10.1177/15353702211054768. Epub 2021 Dec 14. Exp Biol Med (Maywood). 2022. PMID: 34903068 Free PMC article.
Post-mortem toxicology analysis in a young sudden cardiac death cohort.
Coll M, Fernàndez-Falgueras A, Tiron C, Iglesias A, Buxó M, Simón A, Nogué-Navarro L, Moral S, Pérez-Serra A, Puigmulé M, Del Olmo B, Campuzano O, Castellà J, Picó F, Lopez L, Neto N, Corona M, Alcalde M, Brugada R. Coll M, et al. Among authors: puigmule m. Forensic Sci Int Genet. 2022 Jul;59:102723. doi: 10.1016/j.fsigen.2022.102723. Epub 2022 May 16. Forensic Sci Int Genet. 2022. PMID: 35640313
Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later.
Vallverdú-Prats M, Alcalde M, Sarquella-Brugada G, Cesar S, Arbelo E, Fernandez-Falgueras A, Coll M, Pérez-Serra A, Puigmulé M, Iglesias A, Fiol V, Ferrer-Costa C, Olmo BD, Picó F, Lopez L, Jordà P, García-Álvarez A, Llano CT, Toro R, Grassi S, Oliva A, Brugada J, Brugada R, Campuzano O. Vallverdú-Prats M, et al. Among authors: puigmule m. J Pers Med. 2021 Feb 26;11(3):162. doi: 10.3390/jpm11030162. J Pers Med. 2021. PMID: 33652588 Free PMC article.
Unpredicted Aberrant Splicing Products Identified in Postmortem Sudden Cardiac Death Samples.
Coll M, Fernandez-Falgueras A, Iglesias A, Del Olmo B, Nogue-Navarro L, Simon A, Perez Serra A, Puigmule M, Lopez L, Pico F, Corona M, Vallverdu-Prats M, Tiron C, Campuzano O, Castella J, Brugada R, Alcalde M. Coll M, et al. Among authors: puigmule m. Int J Mol Sci. 2022 Oct 20;23(20):12640. doi: 10.3390/ijms232012640. Int J Mol Sci. 2022. PMID: 36293497 Free PMC article.
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: puigmule m. 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: puigmule m. 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.
28 results