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Page 1
Genetic basis of short stature.
Castro-Feijóo L, Quinteiro C, Loidi L, Barreiro J, Cabanas P, Arévalo T, Diéguez C, Casanueva FF, Pombo M. Castro-Feijóo L, et al. Among authors: cabanas p. J Endocrinol Invest. 2005;28(5 Suppl):30-7. J Endocrinol Invest. 2005. PMID: 16114273 Review.
Genetic diagnosis of X-linked dominant Hypophosphatemic Rickets in a cohort study: tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation type.
Morey M, Castro-Feijóo L, Barreiro J, Cabanas P, Pombo M, Gil M, Bernabeu I, Díaz-Grande JM, Rey-Cordo L, Ariceta G, Rica I, Nieto J, Vilalta R, Martorell L, Vila-Cots J, Aleixandre F, Fontalba A, Soriano-Guillén L, García-Sagredo JM, García-Miñaur S, Rodríguez B, Juaristi S, García-Pardos C, Martínez-Peinado A, Millán JM, Medeira A, Moldovan O, Fernandez A, Loidi L. Morey M, et al. Among authors: cabanas p. BMC Med Genet. 2011 Sep 8;12:116. doi: 10.1186/1471-2350-12-116. BMC Med Genet. 2011. PMID: 21902834 Free PMC article.
Evolutionary analyses of entire genomes do not support the association of mtDNA mutations with Ras/MAPK pathway syndromes.
Gómez-Carballa A, Cerezo M, Balboa E, Heredia C, Castro-Feijóo L, Rica I, Barreiro J, Eirís J, Cabanas P, Martínez-Soto I, Fernández-Toral J, Castro-Gago M, Pombo M, Carracedo Á, Barros F, Salas A. Gómez-Carballa A, et al. Among authors: cabanas p. PLoS One. 2011 Apr 19;6(4):e18348. doi: 10.1371/journal.pone.0018348. PLoS One. 2011. PMID: 21526175 Free PMC article.
Design and deployment of the STEEER-AF trial to evaluate and improve guideline adherence: a cluster-randomized trial by the European Society of Cardiology and European Heart Rhythm Association.
Sterliński M, Bunting KV, Boriani G, Boveda S, Guasch E, Mont L, Rajappan K, Sommer P, Mehta S, Sun Y, Gale CP, van Deutekom C, Van Gelder IC, Kotecha D; STEEER-AF Trial Team. Sterliński M, et al. Europace. 2024 Jul 2;26(7):euae178. doi: 10.1093/europace/euae178. Europace. 2024. PMID: 38940494 Free PMC article. Clinical Trial.
19 results