Publications en collaboration avec des chercheurs de Hospital de Poniente (10)

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

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. 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

2010

  1. Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral meniere's disease

    Laryngoscope, Vol. 120, Núm. 1, pp. 103-107

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. Time course of episodes of definitive vertigo in Ménière's disease

    Archives of Otolaryngology - Head and Neck Surgery, Vol. 134, Núm. 11, pp. 1149-1154

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