Publikationen in Zusammenarbeit mit Forschern von Hospital San Agustin (6)

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

2016

  1. Clinical subgroups in bilateral meniere disease

    Frontiers in Neurology, Vol. 7, Núm. OCT

2015

  1. Common variants of NFE2L2 gene predisposes to acute respiratory distress syndrome in patients with severe sepsis

    Critical Care, Vol. 19, Núm. 1

2014

  1. Familial clustering and genetic heterogeneity in Meniere's disease

    Clinical Genetics, Vol. 85, Núm. 3, pp. 245-252

  2. Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in meniere's disease

    PLoS ONE, Vol. 9, Núm. 11

2006

  1. Utilidad del NT-proBNP para el diagnóstico de insuficiencia cardiaca en una población heterogénea de pacientes con disnea. Estudio multicéntrico español

    Revista Espanola de Cardiologia, Vol. 59, Núm. 5, pp. 465-472