ALLMedicine™ Auditory Neuropathy Center
Research & Reviews 206 results
https://doi.org/10.1016/j.ijporl.2021.110967
International Journal of Pediatric Otorhinolaryngology; Laurent C, Fayad G et. al.
Nov 18th, 2021 - Auditory neuropathy spectrum disorders (ANSD) are defined by the association of a preserved outer hair cell function and an impaired auditory nerve neural response, and present mostly bilaterally. Unilateral ANSD are consequently only seldom descr...
https://doi.org/10.1097/AUD.0000000000001122
Ear and Hearing; White-Schwoch T, Anderson S et. al.
Oct 8th, 2021 - The role of subcortical synchrony in speech-in-noise (SIN) recognition and the frequency-following response (FFR) was examined in multiple listeners with auditory neuropathy. Although an absent FFR has been documented in one listener with idiopath...
https://doi.org/10.1016/j.amjoto.2021.103250
American Journal of Otolaryngology; Lyle W, Sajjad A et. al.
Oct 4th, 2021 - There have been previous case reports suggesting the resolution of both sensorineural hearing loss and retrocochlear involvement through the management of hydrocephalus with shunt placement. This is a case report of a patient with Auditory Neuropa...
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Human Genetics; Batissoco AC, Pedroso-Campos V et. al.
Oct 3rd, 2021 - Hearing loss is one of the most common sensory defects, affecting 5.5% of the worldwide population and significantly impacting health and social life. It is mainly attributed to genetic causes, but their relative contribution reflects the geograph...
https://doi.org/10.1007/s00439-021-02351-7 10.1073/pnas.1817537116 10.1038/gim.2017.143 10.15252/emmm.201809396 10.1038/s41436-019-0655-2 10.1159/000293992 10.1111/j.1399-0004.2008.01128.x 10.2147/TACG.S113828 10.1371/journal.pone.0215932 10.1186/s12967-018-1708-z 10.1097/AUD.0000000000000586 10.1016/j.ijporl.2012.07.030 10.1016/j.bbrc.2010.03.062 10.1111/j.1399-0004.2012.01897.x 10.1136/jmg.39.7.502 10.1097/MAO.0000000000000936 10.1038/nrneurol.2016.10 10.1002/humu.23630 10.1002/humu.20708 10.1016/j.ijporl.2005.09.006 10.1016/j.cell.2006.08.040 10.1007/s10162-009-0181-z 10.1002/lio2.288 10.1093/brain/119.3.741 10.15252/embj.201694564 10.1002/ajmg.a.30907 10.1136/jmg.2005.038612 10.3390/genes11121411 10.1186/1471-2350-11-79 10.1093/nar/gkq603 10.1080/00016489.2018.1476777 10.1038/pr.2016.250 10.3390/genes10100772 10.1016/j.ijporl.2014.03.022 10.1016/j.ijporl.2010.02.004 10.1111/cge.12744 10.3389/fnins.2020.00447
Human Genetics; Iwasa YI, Nishio SY et. al.
Sep 19th, 2021 - Mutations in the OTOF gene are a common cause of hereditary hearing loss and the main cause of auditory neuropathy spectrum disorder (ANSD). Although it is reported that most of the patients with OTOF mutations have stable, congenital or prelingua...
Clinicaltrials.gov 1 results
https://clinicaltrials.gov/ct2/show/NCT04202185
Aug 3rd, 2021 - ANAD is not a rare type of hearing loss. Nevertheless, its profile is heterogeneous and the pathology remain underdiagnosed. The investigators will screen all new patients with bilateral severe to profound HL, looking for DFNB9. They will analyse ...
