ALLMedicine™ Auditory Neuropathy Center
Research & Reviews 198 results
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...
https://doi.org/10.1016/j.otc.2021.07.004
Otolaryngologic Clinics of North America; Hood LJ
Sep 19th, 2021 - Patients with auditory neuropathy (AN)/auditory synaptopathy (AS) present unique evaluation and management challenges. Communication ability using auditory stimuli varies among patients, with particular difficulty understanding speech in noise. Au...
https://doi.org/10.1017/S0022215121002395
The Journal of Laryngology and Otology; Omar R, Rajput K et. al.
Sep 10th, 2021 - Brown-Vialetto-Van Laere syndrome, a rare disorder associated with motor, sensory and cranial nerve neuropathy, is caused by mutations in riboflavin transporter genes SLC52A2 and SLC52A3. Hearing loss is a characteristic feature of Brown-Vialetto-...
https://doi.org/10.1007/s00439-021-02340-w 10.1038/sj.ejhg.5200489 10.1002/humu.20084 10.1016/j.ajhg.2018.08.006 10.3390/ijms21113951 10.3389/fnsys.2013.00092 10.1159/000293992 10.1111/j.1399-0004.2008.01128.x 10.1073/pnas.1703240114 10.1186/1471-2350-14-95 10.1016/j.ijporl.2014.03.033 10.1038/s41586-020-2308-7 10.1097/AUD.0000000000000586 10.1016/j.ijporl.2012.07.030 10.1111/j.1399-0004.2012.01897.x 10.1136/jmg.39.7.502 10.1093/hmg/ddz129 10.1002/humu.10274 10.1002/humu.20708 10.1038/jhg.2009.45 10.1016/j.ijporl.2005.09.006 10.1007/s10162-009-0181-z 10.1097/01.AUD.0000120361.87401.C8 10.1002/lio2.288 10.1016/S0140-6736(05)71047-3 10.1086/497996 10.15252/embj.201694564 10.1136/bmjopen-2014-007506 10.1002/humu.22268 10.1097/AUD.0b013e3181ce693b 10.1136/jmg.40.1.45 10.1136/jmg.2005.038612 10.1038/s41592-019-0686-2 10.1007/s00439-020-02174-y 10.2147/TACG.S113828 10.1038/7693 10.1086/303049 10.1016/j.ijporl.2014.03.022 10.1016/j.ijporl.2010.02.004 10.3389/fnins.2020.00447
Human Genetics; Thorpe RK, Azaiez H et. al.
Aug 24th, 2021 - Pathogenic variations in the OTOF gene are a common cause of hearing loss. To refine the natural history and genotype-phenotype correlations of OTOF-related auditory neuropathy spectrum disorders (ANSD), audiograms and distortion product otoacoust...
https://doi.org/10.1177/01945998211029836
Otolaryngology--head and Neck Surgery : Official Journal ... Mahomva C, Liu YC et. al.
Jul 28th, 2021 - To determine the incidence of auditory neuropathy spectrum disorder (ANSD) and its risk factors among the neonatal intensive care unit (NICU) population from 2009 to 2018 in the Pediatric Health Information System database. Retrospective national ...
