Search details
1.
Validity and reliability of the ERSA questionnaire in Turkish.
J Deaf Stud Deaf Educ
; 29(2): 258-264, 2024 Mar 17.
Article
in English
| MEDLINE | ID: mdl-38215790
2.
Outcomes of Treatment of Multicanal Benign Paroxysmal Positional Vertigo by Means of TRV Chair.
Audiol Neurootol
; 28(1): 1-5, 2023.
Article
in English
| MEDLINE | ID: mdl-36316006
3.
Processes of Emotion Idioms Comprehension of Turkish-Speaking People with Wernice's Aphasia.
Folia Phoniatr Logop
; 2023 Oct 05.
Article
in English
| MEDLINE | ID: mdl-37797595
4.
Does glutaric aciduria type 1 affect hearing function?
Metab Brain Dis
; 37(6): 2121-2132, 2022 08.
Article
in English
| MEDLINE | ID: mdl-35488943
5.
Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss.
Proc Natl Acad Sci U S A
; 116(4): 1347-1352, 2019 01 22.
Article
in English
| MEDLINE | ID: mdl-30610177
6.
Transcutaneous Electric Nerve Stimulation in Chronic Subjective Tinnitus.
Am J Otolaryngol
; 43(5): 103521, 2022.
Article
in English
| MEDLINE | ID: mdl-35691053
7.
Audiological involvement in patients with systemic sclerosis.
Mod Rheumatol
; 32(6): 1094-1101, 2022 Oct 15.
Article
in English
| MEDLINE | ID: mdl-34850918
8.
A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss.
Hum Genet
; 138(10): 1071-1075, 2019 Oct.
Article
in English
| MEDLINE | ID: mdl-31175426
9.
Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing loss.
Clin Genet
; 96(6): 575-578, 2019 12.
Article
in English
| MEDLINE | ID: mdl-31432506
10.
ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice.
Proc Natl Acad Sci U S A
; 113(21): 5993-8, 2016 May 24.
Article
in English
| MEDLINE | ID: mdl-27162350
11.
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing.
Proc Natl Acad Sci U S A
; 111(27): 9864-8, 2014 Jul 08.
Article
in English
| MEDLINE | ID: mdl-24958875
12.
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort.
Genet Med
; 18(4): 364-71, 2016 Apr.
Article
in English
| MEDLINE | ID: mdl-26226137
13.
Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss.
Am J Hum Genet
; 91(5): 872-82, 2012 11 02.
Article
in English
| MEDLINE | ID: mdl-23122586
14.
Validity and Reliability of the Turkish Version of the Glottal Function Index.
J Voice
; 2024 May 06.
Article
in English
| MEDLINE | ID: mdl-38714439
15.
The effect of having a child with hearing impairment on parents.
Int J Pediatr Otorhinolaryngol
; 177: 111864, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-38237356
16.
A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss.
Am J Hum Genet
; 86(5): 797-804, 2010 May 14.
Article
in English
| MEDLINE | ID: mdl-20451170
17.
The effects of dietary and physical activity interventions on tinnitus symptoms: An RCT.
Auris Nasus Larynx
; 50(1): 40-47, 2023 Feb.
Article
in English
| MEDLINE | ID: mdl-35568580
18.
The effect of screen time on hearing and balance in 6-16 aged children.
Acta Otolaryngol
; 143(11-12): 965-970, 2023.
Article
in English
| MEDLINE | ID: mdl-38197860
19.
The Effect of Repositioning Maneuver Applied with the TRV Chair on Residual Dizziness after Benign Paroxysmal Positional Vertigo.
Otol Neurotol
; 44(8): e596-e601, 2023 09 01.
Article
in English
| MEDLINE | ID: mdl-37550882
20.
Does Chronic Subjective Tinnitus Affect Cognitive Performance in Normal Hearing Adults?
J Am Acad Audiol
; 2023 Nov 21.
Article
in English
| MEDLINE | ID: mdl-37989231