Publicaciones en las que colabora con José Antonio López Escámez (27)

2023

  1. Single-cell immune profiling of Meniere Disease patients

    Clinical Immunology, Vol. 252

2022

  1. Acúfenos

    Manual de otorrinolaringología (Avicam), pp. 123-132

  2. Bases genéticas de la hipoacusia. Hipoacusia infantil

    Manual de otorrinolaringología (Avicam), pp. 83-98

  3. Manual de otorrinolaringología

    Avicam

2021

  1. A Predictive Model of Bilateral Sensorineural Hearing Loss in Meniere Disease Using Clinical Data

    Ear and hearing, Vol. 43, Núm. 3, pp. 1079-1085

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

    EBioMedicine, Vol. 66

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

  2. Corrigendum: Clinical Features of Headache in Patients With Diagnosis of Definite Vestibular Migraine: The VM-Phenotypes Projects (Frontiers in Neurology, (2018), 9, 10.3389/fneur.2018.00395)

    Frontiers in Neurology

2019

  1. A tinnitus symphony in 100 patients with Meniere's disease

    Clinical Otolaryngology

  2. Differential proinflammatory signature in vestibular migraine and meniere disease

    Frontiers in Immunology, Vol. 10, Núm. JUN

2018

  1. Clinical Features, Familial History, and Migraine Precursors in Patients With Definite Vestibular Migraine: The VM-Phenotypes Projects

    Headache, Vol. 58, Núm. 4, pp. 534-544

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

    Scientific Reports, Vol. 8, Núm. 1

  3. Towards personalized medicine in Ménière's disease

    F1000Research, Vol. 7

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

  3. Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease

    European Journal of Human Genetics, Vol. 25, Núm. 2, pp. 200-207

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