scholarly journals Investigation Of Outer Hair Cell Function Of The Cochlea in Psoriasis Patients

Author(s):  
Ozlem YAGİZ AGHAYAROV ◽  
Esra İNAN DOĞAN
2014 ◽  
Vol 44 ◽  
pp. 150-156 ◽  
Author(s):  
Hayriye KARABULUT ◽  
İsmail KARABULUT ◽  
Muharrem DAĞLI ◽  
Yıldırım Ahmet BAYAZIT ◽  
Şule BİLEN ◽  
...  

2017 ◽  
Vol 38 (1) ◽  
pp. e1-e12 ◽  
Author(s):  
Naomi F. Bramhall ◽  
Dawn Konrad-Martin ◽  
Garnett P. McMillan ◽  
Susan E. Griest

2018 ◽  
Vol 32 (2) ◽  
pp. 52
Author(s):  
VikasMysore Dwarakanath ◽  
Pavana Mohan ◽  
Sapthami Patel

2011 ◽  
Vol 125 (8) ◽  
pp. 786-794 ◽  
Author(s):  
I de Almeida-Silva ◽  
J A A de Oliveira ◽  
M Rossato ◽  
F Fiacadori Salata ◽  
M A Hyppolito

AbstractBackground:High sodium salicylate doses can cause reversible hearing loss and tinnitus, possibly due to reduced outer hair cell electromotility. Sodium salicylate is known to alter outer hair cell structure and function. This study determined the reversibility and cochlear recovery time after administration of an ototoxic sodium salicylate dose to guinea pigs with normal cochlear function.Study design:Prospective experimental investigation.Methods:All animals received a single 500 mg sodium salicylate dose, but with different durations of action. Function was evaluated before drug administration and immediately before sacrifice. Cochleae were processed and viewed using scanning electron microscopy.Results:Changes in outer hair cell function were observed to be present 2 hours after drug administration, with recovery of normal anatomy beginning after 24 hours. Subsequently, derangement and distortion of cilia reduced, with effects predominantly in row three. At 168 hours, cilia were near-normal but with mild distortions which interfered with normal cochlear physiology.Conclusions:Ciliary changes persisted for up to 168 hours after ototoxic sodium salicylate administration.


2014 ◽  
Vol 40 (12) ◽  
pp. 3785-3792 ◽  
Author(s):  
Sridhar Srinivasan ◽  
Andreas Keil ◽  
Kyle Stratis ◽  
Aaron F. Osborne ◽  
Colin Cerwonka ◽  
...  

2016 ◽  
Vol 337 ◽  
pp. 25-34 ◽  
Author(s):  
Julia Dlugaiczyk ◽  
Dietmar Hecker ◽  
Christian Neubert ◽  
Stefanie Buerbank ◽  
Dario Campanelli ◽  
...  

1980 ◽  
Vol 2 (3-4) ◽  
pp. 423-430 ◽  
Author(s):  
R. Pujol ◽  
E. Carlier ◽  
M. Lenoir

1994 ◽  
Vol 95 (1) ◽  
pp. 350-354 ◽  
Author(s):  
David C. Mountain ◽  
Allyn E. Hubbard

2021 ◽  
pp. 1-5
Author(s):  
Soukaina Elrharchi ◽  
Zied Riahi ◽  
Sara Salime ◽  
Hicham Charoute ◽  
Lamiae Elkhattabi ◽  
...  

<b><i>Introduction:</i></b> Auditory neuropathy is a hearing disorder where outer hair cell function within the cochlea is normal, but inner hair cell and/or the auditory nerve function is disrupted. It is a heterogeneous disorder, which can have either congenital or acquired causes. <b><i>Methods:</i></b> We found a disease-segregating mutation in the X-linked <i>AIFM1</i> gene through whole-exome sequencing, encoding the apoptosis-inducing factor mitochondrion-associated 1. <b><i>Results:</i></b> The impact of the c.1045A&#x3e;G; p.(Ser349Gly) mutation on the AIFM1 protein was predicted using different bioinformatics tools. The pedigree analysis in the examined family was consistent with X-linked dominant inheritance. <b><i>Discussion/Conclusion:</i></b> To our knowledge, this is the first study that identifies a mutation in the <i>AIFM1</i> gene in Moroccan patients suffering from X-linked auditory neuropathy.


Sign in / Sign up

Export Citation Format

Share Document