José Antonio López Escámez-rekin lankidetzan egindako argitalpenak (10)

2022

  1. Defective α‐tectorin may involve tectorial membrane in familial Meniere disease

    Clinical and Translational Medicine

2018

  1. Analysis of scientific production in otolaryngology in Spain in the period 2011-2015

    Acta Otorrinolaringologica Espanola, Vol. 69, Núm. 5, pp. 275-282

2017

  1. Extended phenotype and clinical subgroups in unilateral Meniere disease: A cross-sectional study with cluster analysis

    Clinical Otolaryngology, Vol. 42, Núm. 6, pp. 1172-1180

  2. Regulation of Fn14 receptor and NF-κB underlies inflammation in Meniere's disease

    Frontiers in Immunology, Vol. 8, Núm. DEC

2016

  1. Clinical subgroups in bilateral meniere disease

    Frontiers in Neurology, Vol. 7, Núm. OCT

2014

  1. Familial clustering and genetic heterogeneity in Meniere's disease

    Clinical Genetics, Vol. 85, Núm. 3, pp. 245-252

  2. Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in meniere's disease

    PLoS ONE, Vol. 9, Núm. 11

2013

  1. Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease

    Immunogenetics, Vol. 65, Núm. 5, pp. 345-355

2012

  1. Clasificación de los vértigos periféricos de la Comisión de Otoneurología de la Sociedad Española de Otorrinolaringología: Concordancia diagnóstica y actualización (versión 2, año 2011)

    Acta Otorrinolaringologica Espanola, Vol. 63, Núm. 2, pp. 125-131

2008

  1. Time course of episodes of definitive vertigo in Ménière's disease

    Archives of Otolaryngology - Head and Neck Surgery, Vol. 134, Núm. 11, pp. 1149-1154