Publicaciones en las que colabora con MIGUEL ÁNGEL LÓPEZ NEVOT (11)

2023

  1. Human adipose tissue as a major reservoir of cytomegalovirus-reactive T cells

    Frontiers in Immunology, Vol. 14

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

  2. Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.

    European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery, Vol. 270, Núm. 4, pp. 1521-1529

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

  2. Reduction of false-negative papillary thyroid carcinomas by the routine analysis of BRAFT1799A mutation on fine-needle aspiration biopsy specimens: A prospective study of 814 thyroid FNAB patients

    Annals of Surgery, Vol. 255, Núm. 5, pp. 986-992

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. Presencia de la mutación BRAFT1799A en el tumor primario como indicador de riesgo, recidiva o persistencia de carcinoma papilar de tiroides

    Endocrinología y nutrición: órgano de la Sociedad Española de Endocrinología y Nutrición, Vol. 58, Núm. 4, pp. 175-184

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

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