OpenAlex topic

Ear Surgery and Otitis Media

This page lists works and academicians tagged with an OpenAlex topic. It is not a YÖKSİS primary or secondary field.

OpenAlex 3,433 works 218 author topics

Works

3,433 works

Hearing loss prevalence and years lived with disability, 1990–2019: findings from the Global Burden of Disease Study 2019 2021
YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 100.0%
BACKGROUND: Hearing loss affects access to spoken language, which can affect cognition and development, and can negatively affect social wellbeing. We present updated estimates from the Global Burden of Disease (GBD) study on the prevalence of hearing loss in 2019, as well as the condition's associated disability. MET…
- VAHİT YİĞİT
Anatomy of the superficial temporal artery and its branches its importance for surgery 2006
YÖKSİS SJR Q2 JCR Q4 OpenAlex top 10% OpenAlex 98.1%
No abstract yet.
- YELDA PINAR
Complications of chronic suppurative otitis media: a retrospective review 2012
OpenAlex top 10% OpenAlex 95.0%
No abstract yet.
Complications of chronic suppurative otitis media a retrospective review 2013
YÖKSİS SJR Q1 JCR Q2 OpenAlex top 10% OpenAlex 95.0%
No abstract yet.
- RECEP TEKİN
Mutations in OTOGL Encoding the Inner Ear Protein Otogelin like Cause Moderate Sensorineural Hearing Loss 2012
YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.6%
Identification of the pathogenic mutations underlying autosomal recessive nonsyndromic hearing loss (ARNSHL) is difficult, since causative mutations in 39 different genes have so far been reported. After excluding mutations in the most common ARNSHL gene, GJB2, via Sanger sequencing, we performed whole-exome sequencin…
- DUYGU DUMAN
Whole Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss 2012
YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.6%
Identification of the pathogenic mutations underlying autosomal recessive nonsyndromic hearing loss (ARNSHL) is difficult, since causative mutations in 39 different genes have so far been reported. After excluding mutations in the most common ARNSHL gene, GJB2, via Sanger sequencing, we performed whole-exome sequencin…
- DUYGU DUMAN
Preservation of hearing in patients undergoing microsurgery for vestibular schwannoma: degree of meatal filling 2005
OpenAlex top 10% OpenAlex 92.4%
OBJECT: Preservation of hearing has become a standard goal in selected patients undergoing surgery for a vestibular schwannoma (VS). This study was aimed at analyzing the role played by filling of the internal auditory canal (IAC) as well as those played by preoperative hearing quality, and tumor size in the postopera…
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents 2016
YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.6%
No abstract yet.
- DUYGU DUMAN
The role of topical nasal steroids in the treatment of children with otitis media with effusion and/or adenoid hypertrophy 2006
YÖKSİS SJR Q1 JCR Q3 OpenAlex top 10% OpenAlex 92.6%
No abstract yet.
- MEHMET UMUT AKYOL
- SENEM ÇENGEL KURNAZ
Morphometry of the External Ear in Our Adult Population 2006
OpenAlex 83.7%
No abstract yet.
Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss 2012
YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 97.1%
No abstract yet.
- DUYGU DUMAN
Morphometric examination of the paranasal sinuses and mastoid air cells using computed tomography 2005
OpenAlex 87.0%
BACKGROUND: The paranasal sinuses and mastoid air cells vary considerably in size and shape from person to person. The main structures are pneumatic. In this study, we investigated the relationship between right and left sides and evaluated the volume changes according to age and sex. METHODS: Of all patients attendin…

Academicians

218 academicians