Publicacións en colaboración con investigadores/as de Hospital Universitario La Fe (12)

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. Clinical subgroups in bilateral meniere disease

    Frontiers in Neurology, Vol. 7, Núm. OCT

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. 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

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

  3. 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

2008

  1. Clasificación de los vértigos periféricos. Documento de Consenso de la Comisión de Otoneurología de la Sociedad Española de Otorrinolaringología (2003-2006)

    Acta Otorrinolaringologica Espanola, Vol. 59, Núm. 2, pp. 76-79

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