Publicacións en colaboración con investigadores/as de Universidad de Granada (10)

2019

  1. Differential proinflammatory signature in vestibular migraine and meniere disease

    Frontiers in Immunology, Vol. 10, Núm. JUN

2018

  1. Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease

    Scientific Reports, Vol. 8, Núm. 1

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. A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease

    Human Molecular Genetics, Vol. 25, Núm. 16, pp. 3407-3415

  2. 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

  2. Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.

    European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery, Vol. 270, Núm. 4, pp. 1521-1529