Publikationen in Zusammenarbeit mit Forschern von Hospital Universitario de Salamanca (27)

2023

  1. Single-cell immune profiling of Meniere Disease patients

    Clinical Immunology, Vol. 252

2022

  1. Synaptophysin is a selective marker for axons in human cutaneous end organ complexes

    Annals of Anatomy, Vol. 243

  2. The acquisition of mechanoreceptive competence by human digital Merkel cells and sensory corpuscles during development: An immunohistochemical study of PIEZO2

    Annals of Anatomy, Vol. 243

2021

  1. Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study

    EBioMedicine, Vol. 66

  2. Clinical and cytokine profile in patients with early and late onset meniere disease

    Journal of Clinical Medicine, Vol. 10, Núm. 18

  3. Hydroxyethyl starch and acute kidney injury in high-risk patients undergoing cardiac surgery: A prospective multicenter study

    Journal of Clinical Anesthesia, Vol. 73

2020

  1. Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease

    Ear and Hearing, Vol. 41, Núm. 6, pp. 1598-1605

  2. Heparan sulfate in human cutaneous Meissner's and Pacinian corpuscles

    Anatomical Record, Vol. 303, Núm. 8, pp. 2262-2273

2019

  1. Ageing of the somatosensory system at the periphery: age-related changes in cutaneous mechanoreceptors

    Journal of Anatomy, Vol. 234, Núm. 6, pp. 839-852

  2. Class I and Class II small leucine-rich proteoglycans in human cutaneous pacinian corpuscles

    Annals of Anatomy, Vol. 224, pp. 62-72

  3. Differential proinflammatory signature in vestibular migraine and meniere disease

    Frontiers in Immunology, Vol. 10, Núm. JUN

  4. Multicentric study on total pancreatectomies

    Cirugia Espanola, Vol. 97, Núm. 7, pp. 377-384

2018

  1. Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease

    Scientific Reports, Vol. 8, Núm. 1

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. A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease

    Human Molecular Genetics, Vol. 25, Núm. 16, pp. 3407-3415

  2. 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