OTN
OTOLOGIA Y OTONEUROLOGIA
Publicaciones (13) Publicaciones en las que ha participado algún/a investigador/a
2024
-
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
-
An overload of missense variants in the OTOG gene may drive a higher prevalence of familial Meniere disease in the European population
Human Genetics, Vol. 143, Núm. 3, pp. 423-435
-
Clinical practice guideline on the management of vestibular schwannoma
Acta Otorrinolaringologica Espanola, Vol. 75, Núm. 2, pp. 108-128
-
Cytokine profiling and transcriptomics in mononuclear cells define immune variants in Meniere Disease
Genes and Immunity, Vol. 25, Núm. 2, pp. 124-131
-
Rafael Lorente de Nó (1902–1990)
Journal of Neurology, Vol. 271, Núm. 7, pp. 4727-4729
-
Rare Deletions or Large Duplications Contribute to Genetic Variation in Patients with Severe Tinnitus and Meniere Disease
Genes, Vol. 15, Núm. 1
2023
-
A systematic review on machine learning approaches in the diagnosis and prognosis of rare genetic diseases
Journal of Biomedical Informatics, Vol. 143
-
Rare Coding Variants in Patients with Non-Syndromic Vestibular Dysfunction
Genes, Vol. 14, Núm. 4
-
Types of Inheritance and Genes Associated with Familial Meniere Disease
JARO - Journal of the Association for Research in Otolaryngology, Vol. 24, Núm. 3, pp. 269-279
2022
-
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
-
Defective α‐tectorin may involve tectorial membrane in familial Meniere disease
Clinical and Translational Medicine
-
Involvement of the PI3K/AKT Intracellular Signaling Pathway in the AntiCancer Activity of Hydroxytyrosol, a Polyphenol from Olea europaea, in Hematological Cells and Implication of HSP60 Levels in Its Anti-Inflammatory Activity
International Journal of Molecular Sciences, Vol. 23, Núm. 13
-
Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus
npj Genomic Medicine, Vol. 7, Núm. 1