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Oliva-Sandoval MJ, Ruiz-Espejo F, Monserrat L, Hermida-Prieto M, Sabater M, García-Molina E, Ortiz M, Rodríguez-García MI, Núñez L, Gimeno JR, Castro-Beiras A, Valdés M. Insights into genotype-phenotype correlation in hypertrophic cardiomyopathy. Findings from 18 Spanish families with a single mutation in MYBPC3. Heart. 2010 Dec;96(24):1980-4. doi: 10.1136/hrt.2010.200402. PubMed PMID: 21088121.
AÑO: 2010; IF: 4.708
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21088121
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Sabater-Molina M, Larqué E, Torrella F, Plaza J, Ramis G, Zamora S. Effects of fructooligosaccharides on cecum polyamine concentration and gut maturation in early-weaned piglets. J Clin Biochem Nutr. 2011 May;48(3):230-6. doi: 10.3164/jcbn.10-100. Epub 2011 Apr 26. PubMed PMID: 21562644; PubMed Central PMCID: PMC3082079.
AÑO: 2011; IF: 1.975
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García-Molina E, Lacunza J, Ruiz-Espejo F, Sabater M, García-Alberola A, Gimeno JR, Cañizares F, García A, Martínez P, Valdés M, Tovar I. A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome. Clin Genet. 2013 Jun;83(6):530-8. doi: 10.1111/cge.12017. PubMed PMID: 22984773.
AÑO: 2013; IF: 3.652
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Sabater-Molina M, Guillén-Navarro E, García-Molina E, Ballesta-Martínez MJ, Escudero F, Ruiz-Espejo F. Barth syndrome in adulthood: a clinical case. Rev Esp Cardiol (Engl Ed). 2013 Jan;66(1):68-70. doi: 10.1016/j.recesp.2012.05.015. English, Spanish. PubMed PMID: 22999963.
AÑO: 2013; IF: 3.342
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Luxán G, Casanova JC, Martínez-Poveda B, Prados B, D'Amato G, MacGrogan D, Gonzalez-Rajal A, Dobarro D, Torroja C, Martinez F, Izquierdo-García JL, Fernández-Friera L, Sabater-Molina M, Kong YY, Pizarro G, Ibañez B, Medrano C, García-Pavía P, Gimeno JR, Monserrat L, Jiménez-Borreguero LJ, de la Pompa JL. Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy. Nat Med. 2013 Feb;19(2):193-201. doi: 10.1038/nm.3046. PubMed PMID: 23314057.
AÑO: 2013; IF: 28.054
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