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Gil-Ortuno C, Sebastian-Marcos P, Sabater-Molina M, Nicolas-Rocamora E, Gimeno-Blanes JR, Fernandez Del Palacio MJ. Genetics of feline hypertrophic cardiomyopathy. Clin Genet. 2020 Sep;98(3):203-214. doi: 10.1111/cge.13743. Epub 2020 Apr 1. PubMed PMID: 32215921.
AÑO: 2020; IF: 4.438
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32215921
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Olivotto I, Oreziak A, Barriales-Villa R, Abraham TP, Masri A, Garcia-Pavia P, Saberi S, Lakdawala NK, Wheeler MT, Owens A, Kubanek M, Wojakowski W, Jensen MK, Gimeno-Blanes J, Afshar K, Myers J, Hegde SM, Solomon SD, Sehnert AJ, Zhang D, Li W, Bhattacharya M, Edelberg JM, Waldman CB, Lester SJ, Wang A, Ho CY, Jacoby D; EXPLORER-HCM study investigators. Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet. 2020 Sep 12;396(10253):759-769. doi: 10.1016/S0140-6736(20)31792-X. Epub 2020 Aug 29. Erratum In: Lancet. 2020 Sep 12;396(10253):758. PubMed PMID: 32871100.
AÑO: 2020; IF: 79.321
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de la Morena-Barrio ME, Sabater M, de la Morena-Barrio B, Ruhaak RL, Minano A, Padilla J, Toderici M, Roldan V, Gimeno JR, Vicente V, Corral J. ALG12-CDG: An unusual patient without intellectual disability and facial dysmorphism, and with a novel variant. Mol Genet Genomic Med. 2020 Aug;8(8):e1304. doi: 10.1002/mgg3.1304. Epub 2020 Jun 12. PubMed PMID: 32530140; PubMed Central PMCID: PMC7434597.
AÑO: 2020; IF: 2.183
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Helio T, Elliott P, Koskenvuo JW, Gimeno JR, Tavazzi L, Tendera M, Kaski JP, Mansencal N, Bilinska Z, Carr-White G, Damy T, Frustaci A, Kindermann I, Ripoll-Vera T, Celutkiene J, Axelsson A, Lorenzini M, Saad A, Maggioni AP, Laroche C, Caforio ALP, Charron P; EORP Cardiomyopathy Registry Investigators Group. ESC EORP Cardiomyopathy Registry: real-life practice of genetic counselling and testing in adult cardiomyopathy patients. ESC Heart Fail. 2020 Oct;7(5):3013-3021. doi: 10.1002/ehf2.12925. Epub 2020 Aug 7. PubMed PMID: 32767651; PubMed Central PMCID: PMC7524128.
AÑO: 2020; IF: 4.411
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Moreno C, Oliveras A, Bartolucci C, Munoz C, de la Cruz A, Peraza DA, Gimeno JR, Martin-Martinez M, Severi S, Felipe A, Lambiase PD, Gonzalez T, Valenzuela C. Corrigendum to Supplemental Material: 'D242N, a KV7.1 LQTS mutation uncovers a key residue for IKs voltage dependence' [Journal of Molecular and Cellular Cardiology, Volume 110, September 2017, Pages 61-69]. J Mol Cell Cardiol. 2019 Mar;128:25. doi: 10.1016/j.yjmcc.2019.01.014. Epub 2019 Jan 22. No abstract available. PubMed PMID: 30682566.
AÑO: 2019; IF: 4.133
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