Publicaciones en colaboración con investigadores/as de Hospital Universitario Virgen de las Nieves (54)

2024

  1. A Systematic Review on Heritability of Sudden Sensorineural Hearing Loss

    Laryngoscope, Vol. 134, Núm. 8, pp. 3447-3457

  2. A Systematic Review on the Genetic Contribution to Tinnitus

    JARO - Journal of the Association for Research in Otolaryngology, Vol. 25, Núm. 1, pp. 13-33

  3. Cajal’s contributions to vestibular research

    Frontiers in Neuroanatomy , Vol. 18

  4. Clinical practice guideline on the management of vestibular schwannoma

    Acta Otorrinolaringologica Espanola, Vol. 75, Núm. 2, pp. 108-128

  5. Cognitive Screening and Hearing Assessment in Patients With Chronic Tinnitus

    Clinical and Experimental Otorhinolaryngology, Vol. 17, Núm. 1, pp. 15-25

  6. Cytokine profiling and transcriptomics in mononuclear cells define immune variants in Meniere Disease

    Genes and Immunity, Vol. 25, Núm. 2, pp. 124-131

  7. Phenotypic spectrum of tinnitus patients bearing rare ANK2 gene variants

    European Archives of Oto-Rhino-Laryngology, Vol. 281, Núm. 8, pp. 4071-4080

  8. Rafael Lorente de Nó (1902–1990)

    Journal of Neurology, Vol. 271, Núm. 7, pp. 4727-4729

  9. Rare Deletions or Large Duplications Contribute to Genetic Variation in Patients with Severe Tinnitus and Meniere Disease

    Genes, Vol. 15, Núm. 1

2023

  1. Domingo Sánchez y Sánchez (1860–1947): Cajal’s man on the nervous system of invertebrates

    Frontiers in Neuroanatomy, Vol. 17

  2. The Importance of Cajal’s and Lorente de Nó’s Neuroscience to the Birth of Cybernetics

    Neuroscientist

  3. The statistical analysis plan for the unification of treatments and interventions for tinnitus patients randomized clinical trial (UNITI-RCT)

    Trials, Vol. 24, Núm. 1

  4. The vestibular system: Contributions of Lorente de Nó

    Journal of Vestibular Research: Equilibrium and Orientation, Vol. 33, Núm. 5, pp. 287-297

2022

  1. A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss

    European Journal of Human Genetics, Vol. 30, Núm. 11, pp. 1301-1305

  2. Balance Disorders Including Ménière’s Disease

    Comprehensive Pharmacology (Elsevier), pp. 770-782

  3. Presbyvestibulopathy: A new challenge for Otoneurology

    Acta Otorrinolaringologica Espanola

  4. Standardized Clinical Profiling in Spanish Patients with Chronic Tinnitus

    Journal of Clinical Medicine, Vol. 11, Núm. 4

  5. Technological Advances in the Diagnosis and Management of Tinnitus

    Journal of Clinical Medicine

  6. Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus

    npj Genomic Medicine, Vol. 7, Núm. 1

2021

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

    EBioMedicine, Vol. 66