Paula Bolivar-Robles

Madrid, MD, Spain

Last Updated: 09/26/2026

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Found 15 publications

Association of PHEX Gene Dosage With Meniere Disease and Related Audiovestibular Phenotypes in X-Linked Hypophosphatemia.

Association of PHEX Gene Dosage With Meniere Disease and Related Audiovestibular Phenotypes in X-Linked Hypophosphatemia.

Journal: JAMA otolaryngology-- head & neck surgery

Published: April 16, 2026

Prevalence of the endolymphatic sac hypoplasia in a cohort of individuals without Meniere disease.

Prevalence of the endolymphatic sac hypoplasia in a cohort of individuals without Meniere disease.

Journal: Journal of vestibular research : equilibrium & orientation

Published: August 25, 2025

Hyperplastic growth, not hydrostatic distension, in endolymphatic hydrops in humans challenges the classic view of Meniere's disease.

Hyperplastic growth, not hydrostatic distension, in endolymphatic hydrops in humans challenges the classic view of Meniere's disease.

Journal: Scientific reports

Published: May 15, 2025

A modern conceptual framework for study and treatment of Meniere's disease.

A modern conceptual framework for study and treatment of Meniere's disease.

Journal: Frontiers in neurology

Published: April 07, 2025

Different Contribution of Missense and Loss-of-Function Variants to the Genetic Structure of Familial and Sporadic Meniere Disease.

Different Contribution of Missense and Loss-of-Function Variants to the Genetic Structure of Familial and Sporadic Meniere Disease.

Journal: MedComm

Published: November 11, 2024

Single versus combination treatment in tinnitus: an international, multicentre, parallel-arm, superiority, randomised controlled trial.

Single versus combination treatment in tinnitus: an international, multicentre, parallel-arm, superiority, randomised controlled trial.

Journal: Nature communications

Published: August 23, 2024

Allergy and autoinflammation drive persistent systemic inflammatory response in Meniere Disease: A longitudinal study.

Allergy and autoinflammation drive persistent systemic inflammatory response in Meniere Disease: A longitudinal study.

Journal: Clinical immunology (Orlando, Fla.)

Published: July 25, 2024

A rare haplotype of the GJD3 gene segregating in familial Meniere's disease interferes with connexin assembly.

A rare haplotype of the GJD3 gene segregating in familial Meniere's disease interferes with connexin assembly.

Journal: Genome medicine

Published: January 09, 2024

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

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

Journal: Trials

Published: December 02, 2022

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

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

Journal: NPJ genomic medicine

Published: May 25, 2022

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

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

Journal: European journal of human genetics : EJHG

Published: May 14, 2022

Unification of Treatments and Interventions for Tinnitus Patients (UNITI): a study protocol for a multi-center randomized clinical trial.

Unification of Treatments and Interventions for Tinnitus Patients (UNITI): a study protocol for a multi-center randomized clinical trial.

Journal: Trials

Published: May 28, 2021

Showing 1-12 of 15

Last Updated: 09/26/2026