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Page 1
Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease.
Requena T, Gazquez I, Moreno A, Batuecas A, Aran I, Soto-Varela A, Santos-Perez S, Perez N, Perez-Garrigues H, Lopez-Nevot A, Martin E, Sanz R, Perez P, Trinidad G, Alarcon-Riquelme ME, Teggi R, Zagato L, Lopez-Nevot MA, Lopez-Escamez JA. Requena T, et al. Immunogenetics. 2013 May;65(5):345-55. doi: 10.1007/s00251-013-0683-z. Epub 2013 Feb 1. Immunogenetics. 2013. PMID: 23370977
Influence of age and gender in the sensory analysis of balance control.
Faraldo-García A, Santos-Pérez S, Crujeiras-Casais R, Labella-Caballero T, Soto-Varela A. Faraldo-García A, et al. Eur Arch Otorhinolaryngol. 2012 Feb;269(2):673-7. doi: 10.1007/s00405-011-1707-7. Epub 2011 Jul 26. Eur Arch Otorhinolaryngol. 2012. PMID: 21789678
[Peripheral vertigo classification of the Otoneurology Committee of the Spanish Otorhinolaryngology Society: diagnostic agreement and update (version 2-2011)].
Soto-Varela A, Arán-González I, López-Escámez JA, Morera-Pérez C, Oliva-Domínguez M, Pérez-Fernández N, Pérez-Garrigues H, Pérez-Vázquez P, Rossi-Izquierdo M, Santos-Pérez S. Soto-Varela A, et al. Acta Otorrinolaringol Esp. 2012 Mar-Apr;63(2):125-31. doi: 10.1016/j.otorri.2011.10.004. Epub 2011 Dec 14. Acta Otorrinolaringol Esp. 2012. PMID: 22169589 Free article. Spanish.
Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.
Gázquez I, Moreno A, Requena T, Ohmen J, Santos-Perez S, Aran I, Soto-Varela A, Pérez-Garrigues H, López-Nevot A, Batuecas A, Friedman RA, López-Nevot MA, López-Escamez JA. Gázquez I, et al. Eur Arch Otorhinolaryngol. 2013 Mar;270(4):1521-9. doi: 10.1007/s00405-012-2268-0. Epub 2012 Nov 21. Eur Arch Otorhinolaryngol. 2013. PMID: 23179933
Familial clustering and genetic heterogeneity in Meniere's disease.
Requena T, Espinosa-Sanchez JM, Cabrera S, Trinidad G, Soto-Varela A, Santos-Perez S, Teggi R, Perez P, Batuecas-Caletrio A, Fraile J, Aran I, Martin E, Benitez J, Pérez-Fernández N, Lopez-Escamez JA. Requena T, et al. Clin Genet. 2014 Mar;85(3):245-52. doi: 10.1111/cge.12150. Epub 2013 Apr 9. Clin Genet. 2014. PMID: 23521103
76 results