Publicacións en colaboración con investigadores/as de Hospital Universitario de Salamanca (18)

2023

  1. Presbycusis and balance disorders in the elderly. Bibliographical review of ethiopathogenic aspects, consequences on quality of life and positive effects of its treatment

    Acta Otorrinolaringologica Espanola, Vol. 74, Núm. 2, pp. 124-132

  2. Single-cell immune profiling of Meniere Disease patients

    Clinical Immunology, Vol. 252

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

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. Compensación vestibular

    Revista ORL, Vol. 11, Vol. 1, pp. 19-28

2019

  1. Differential proinflammatory signature in vestibular migraine and meniere disease

    Frontiers in Immunology, Vol. 10, Núm. JUN

  2. Normative data for static balance testing in healthy individuals using open source computerized posturography

    European Archives of Oto-Rhino-Laryngology, Vol. 276, Núm. 1, pp. 41-48

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

2011

  1. Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in ménière's disease in a European Caucasian Population

    DNA and Cell Biology, Vol. 30, Núm. 9, pp. 699-708

  2. High prevalence of systemic autoimmune diseases in patients with menière's disease

    PLoS ONE, Vol. 6, Núm. 10