Publicacións en colaboración con investigadores/as de Hospital Universitario Virgen de las Nieves (16)

2024

  1. Clinical practice guideline on the management of vestibular schwannoma

    Acta Otorrinolaringologica Espanola, Vol. 75, Núm. 2, pp. 108-128

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

  2. Smell and taste dysfunction in covid-19 is associated with younger age in ambulatory settings: A multicenter cross-sectional study

    Journal of Investigational Allergology and Clinical Immunology, Vol. 30, Núm. 5, pp. 346-357

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

    Frontiers in Immunology, Vol. 8, Núm. DEC

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. 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

2011

  1. Polymorphisms of CD16A and CD32 Fcγ receptors and circulating immune complexes in Ménière's disease: A case-control study

    BMC Medical Genetics, Vol. 12

2009

  1. Poly(ADP-ribose) polymerase-1 (PARP-1) longer alleles spanning the promoter region may confer protection to bilateral Meniere's disease

    Acta Oto-Laryngologica, Vol. 129, Núm. 11, pp. 1222-1225

2007

  1. HLA-DRB1*1101 allele may be associated with bilateral Ménière's disease in southern European population

    Otology and Neurotology, Vol. 28, Núm. 7, pp. 891-895