Publicacións nas que colabora con José Antonio López Escámez (25)

2023

  1. Single-cell immune profiling of Meniere Disease patients

    Clinical Immunology, Vol. 252

2022

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

    Clinical and Translational Medicine

2021

  1. Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study

    EBioMedicine, Vol. 66

  2. Clinical and cytokine profile in patients with early and late onset meniere disease

    Journal of Clinical Medicine, Vol. 10, Núm. 18

  3. Dna methylation signature in mononuclear cells and proinflammatory cytokines may define molecular subtypes in sporadic meniere disease

    Biomedicines, Vol. 9, Núm. 11

  4. Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease

    Hearing Research, Vol. 409

2020

  1. Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease

    Ear and Hearing, Vol. 41, Núm. 6, pp. 1598-1605

2019

  1. Differential proinflammatory signature in vestibular migraine and meniere disease

    Frontiers in Immunology, Vol. 10, Núm. JUN

2018

  1. Practice Guidelines for the Diagnosis and Management of Benign Paroxysmal Positional Vertigo Otoneurology Committee of Spanish Otorhinolaryngology and Head and Neck Surgery Consensus Document

    Acta Otorrinolaringologica Espanola, Vol. 69, Núm. 6, pp. 345-366

  2. 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

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

  2. MICA-STR A.4 is associated with slower hearing loss progression in patients with Ménière's disease

    Otology and Neurotology, Vol. 33, Núm. 2, pp. 223-229