Publicaciones en colaboración con investigadores/as de Hospital de Poniente (9)

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. 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

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

2004

  1. Absence of COCH mutations in patients with Meniere disease

    European Journal of Human Genetics, Vol. 12, Núm. 1, pp. 75-78

2002

  1. Expression of A, B, C and DR antigens in definite Meniere's disease in a Spanish population

    European Archives of Oto-Rhino-Laryngology, Vol. 259, Núm. 7, pp. 347-350