Sage Journals: Discover world-class research

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Research article

First published 2026

Hearing Loss in Sagittal Versus Metopic Non-syndromic Craniosynostosis

Sammy Othman, Jason Cohn, Jeewanjot S. Grewal [...]

FACE

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Case report

First published 2023-11

A Novel Exon 2 Deletion Mutation in the GRXCR1 Gene Associated With Non-Syndromic Hearing Loss: A Case Report and Review of Literatures

Hadith Rastad, Parham Samimisedeh, Shahram Savad [...]

Annals of Otology,Rhinology & Laryngology

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Research article

First published 2015-5

Non-ocular Stickler Syndrome With a Novel Mutation in COL11A2 Diagnosed by Massively Parallel Sequencing in Japanese Hearing Loss Patients

Yoh-ichiro Iwasa, Hideaki Moteki, Mitsuru Hattori [...]

Annals of Otology,Rhinology & Laryngology

Open access

Case report

First published 2019

Report of a Novel Splicing Mutation in the MYO15A Gene in a Patient With Sensorineural Hearing Loss and Spectrum of the MYO15A Mutations

Elinaz Akbariazar, Ali Vahabi, Isa Abdi Rad

Clinical Medicine Insights: Case Reports

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Research article

First published 2025-6

Hearing Loss Secondary to TECTA Gene Mutations

Rocío González-Aguado, Esther Onecha, Jaime Gallo-Terán [...]

Annals of Otology,Rhinology & Laryngology

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Research article

First published 2025-2

A Preliminary Study of Hearing Loss in Children With Craniosynostosis

Eric Min, John Munday, Josh Bricker [...]

The Cleft Palate Craniofacial Journal

Open access

Case report

First published 2017

Delayed diagnosis of a patient with Usher syndrome 1C in a Louisiana Acadian family highlights the necessity of timely genetic testing for the diagnosis and management of congenital hearing loss

Ayesha Umrigar, Amanda Musso, Danielle Mercer [...]

Sage Open Medical Case Reports

Open access

Case report

First published 2024

Syndromic Association of Depigmentation With Congenital Hearing Loss: A Review of Three Children With Auditory Pigmentary Disorders

Shabari Ghosh, Mainak Dutta, Diptanshu Mukherjee [...]

Ear,Nose & Throat Journal

Open access

Review article

First published 2020

Usher syndrome: clinical features,molecular genetics and advancing therapeutics

Maria Toms, Waheeda Pagarkar, Mariya Moosajee

Therapeutic Advances in Ophthalmology

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Other

First published 2012-8

Mining Immune Epitopes in Ménière’s Disease and Sudden Sensorineural Hearing Loss

Michael P. Platt, Alphi P. Elackattu, Sonam Dilwali [...]

Otolaryngology–Head and Neck Surgery

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