Rocio Aguado-Gonzalez

Enhanced Exome Sequencing Improves the Genetic Diagnosis of Deafblindness.

Journal: Genes

Published: January 27, 2026

Burden of novel and ultra-rare missense variants in the NF-κB pathway genes associated to Ménière's disease.

Journal: Frontiers in immunology

Published: January 16, 2026

First episode of "probable benign paroxysmal positional vertigo, spontaneously resolved": a comparative and follow-up study.

Journal: 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

Published: July 20, 2025

Ménière's Disease With a Prior Diagnosis of Idiopathic Sudden Hearing Loss.

Journal: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology

Published: May 01, 2025

Characteristics of Hearing Loss in Patients with COL2A1 Gene Variants (Sticker Syndrome Type 1).

Journal: Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India

Published: March 06, 2025

Exploring DIAPH1 gene mutations in patients with sensorineural hearing loss of unknown etiology in Northern Spain.

Journal: Acta otorrinolaringologica espanola

Published: February 27, 2025

Hearing Loss Secondary to TECTA Gene Mutations.

Journal: The Annals of otology, rhinology, and laryngology

Published: February 05, 2025

Hearing loss secondary to novel variants of the KCNQ4 gene.

Journal: 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

Published: November 14, 2024

Life after benign paroxysmal positional vertigo: one-year analysis of recurrence, headaches, neck pain, falls, and functional vestibular symptoms.

Journal: 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

Published: September 28, 2024

Enhanced Exome Sequencing Improves the Genetic Diagnosis of Deafblindness.

Enhanced Exome Sequencing Improves the Genetic Diagnosis of Deafblindness.

Burden of novel and ultra-rare missense variants in the NF-κB pathway genes associated to Ménière's disease.

Burden of novel and ultra-rare missense variants in the NF-κB pathway genes associated to Ménière's disease.

First episode of "probable benign paroxysmal positional vertigo, spontaneously resolved": a comparative and follow-up study.

First episode of "probable benign paroxysmal positional vertigo, spontaneously resolved": a comparative and follow-up study.

Ménière's Disease With a Prior Diagnosis of Idiopathic Sudden Hearing Loss.

Ménière's Disease With a Prior Diagnosis of Idiopathic Sudden Hearing Loss.

Characteristics of Hearing Loss in Patients with COL2A1 Gene Variants (Sticker Syndrome Type 1).

Characteristics of Hearing Loss in Patients with COL2A1 Gene Variants (Sticker Syndrome Type 1).

Exploring DIAPH1 gene mutations in patients with sensorineural hearing loss of unknown etiology in Northern Spain.

Exploring DIAPH1 gene mutations in patients with sensorineural hearing loss of unknown etiology in Northern Spain.

Hearing Loss Secondary to TECTA Gene Mutations.

Hearing Loss Secondary to TECTA Gene Mutations.

Hearing loss secondary to novel variants of the KCNQ4 gene.

Hearing loss secondary to novel variants of the KCNQ4 gene.

Life after benign paroxysmal positional vertigo: one-year analysis of recurrence, headaches, neck pain, falls, and functional vestibular symptoms.

Life after benign paroxysmal positional vertigo: one-year analysis of recurrence, headaches, neck pain, falls, and functional vestibular symptoms.

Cochleo-vestibular phenotype in patients with pathogenic variations in the ACTG1 gene.

Cochleo-vestibular phenotype in patients with pathogenic variations in the ACTG1 gene.

Sensorineural Hearing Loss in Patients With the m.1555A>G Mutation in the MTRNR1 Gene.

Sensorineural Hearing Loss in Patients With the m.1555A>G Mutation in the MTRNR1 Gene.

Hearing loss secondary to variants in the OTOF gene.

Hearing loss secondary to variants in the OTOF gene.