Results 171 to 180 of about 39,146 (298)

Cochlear Implantation in Patient with Arnold-Chiari Malformation. [PDF]

J Int Adv Otol
Podlawska-Nowak P, Bartochowska A, Balcerowiak A, Gawecki W.   +3 more
europepmc   +1 more source

COCHLEAR IMPLANTS FOR ADULT PRELINGUALLY DEAF PATIENTS

, 1994
Juichi Ito, Kiyohiro Fujino, Yosaku Shiomi, Akira Takagi, Haruo Takahashi, Michio Kawano, Iwao Honjo   +6 more
openalex   +2 more sources

Cochlear implantation in the presence of chronic suppurative otitis media [PDF]

, 1997
Patrick Axon, Deborah Mawman, T. Upile, R. T. Ramsden   +3 more
openalex   +1 more source

Understanding hearing health‐care access in Australia: Users' perspectives

Australasian Journal on Ageing, Volume 44, Issue 2, June 2025.
Abstract Objective The aim of this qualitative study was to evaluate the barriers and enablers to current hearing health‐care services in Australia for middle‐aged and older adults who use cochlear implants (CI) and/or hearing aids. Methods Adults aged 40 years and older from the Hearing impairment Adults: a Longitudinal Outcomes Study (HALOS), with ...
Shermin Lim, Jessica Turner, Diana Tang, Kerry Sherman, Kompal Sinha, Sharad Chawla, Simon Carney, Giriraj Singh Shekhawat, Bamini Gopinath   +8 more
wiley   +1 more source

Cochlear Implantation in the United Arab Emirates: Otolaryngologists' Knowledge, Attitudes, and Practices. [PDF]

Audiol Res
Ayas M, Al Amadi A, Al Shamsi A, Muzaffar J, Bance M.   +4 more
europepmc   +1 more source

Cochlear Implantation

, 1994
Chong Sun Kim, Byeong Ho Song, Mi Sun Yoon   +2 more
openalex   +2 more sources

YME1L1 Dysfunction Associated With 3‐Methylglutaconic Aciduria

Journal of Inherited Metabolic Disease, Volume 48, Issue 3, May 2025.
YME1L1 dysfunction is a new type of secondary 3‐methylglutaconic aciduria, observed in two siblings with a novel homozygous YME1L1 variant. ABSTRACT 3‐methylglutaconic aciduria (3‐MGCA) is a biochemical finding in a diverse group of inherited metabolic disorders.
Anthi Demetriadou, Olga Grafakou, Theodoros Georgiou, Daniela Burska, Anna Malekkou, Jana Krizova, Efstathia Paramera, Gavriella Mavrikiou, Maria Dionysiou, Athina Theodosiou, Carolina Sismani, Violetta Anastasiadou, Ioannis Ioannou, Evangelos Papakonstantinou, Hana Hansikova, Anthi Drousiotou, Petros P. Petrou   +16 more
wiley   +1 more source

Timing of cochlear implantation in large vestibular aqueduct syndrome-a retrospective cohort analysis. [PDF]

Front Neurol
Liu X, Huang W, Wang Y, Xu J, Xie L, Liu L, Chen J.   +6 more
europepmc   +1 more source

Performance of prelingually and postlingually deaf patients using single‐channel or multichanel cochlear implants [PDF]

, 1995
Johannes B. Hinderink, Lucas H. M. Mens, Paul Van Der Broek, J.P.L. Brokx   +3 more
openalex   +1 more source

Prevalence of Molecular Diagnoses for Usher Syndrome and the Need for Coordinated Care

The Laryngoscope, Volume 135, Issue 5, Page 1777-1780, May 2025.
Usher syndrome (USH) is a rare, autosomal‐recessive genetic disorder and a leading cause of early onset deaf‐blindness. Molecular testing is able to distinguish USH subtypes by causative gene. Molecular testing and diagnosis should be part of the routine care of USH individuals to facilitate earlier interventions and coordinated care between ...
Brett M. Colbert, Molly Smeal, Zachary J. Cromar, Potyra Rosa, Susan H. Blanton, Byron L. Lam, Xue Z. Liu   +6 more
wiley   +1 more source