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207 related items for PubMed ID: 23946138
21. Auditory and optic neuropathy in Kjer's disease: case report. Haaksma-Schaafsma SC, van Dijk P, Dikkers FG. J Laryngol Otol; 2012 Mar; 126(3):309-12. PubMed ID: 22017926 [Abstract] [Full Text] [Related]
22. Cochlear Microphonic and Summating Potential Responses from Click-Evoked Auditory Brain Stem Responses in High-Risk and Normal Infants. Hunter LL, Blankenship CM, Gunter RG, Keefe DH, Feeney MP, Brown DK, Baroch K. J Am Acad Audiol; 2018 May; 29(5):427-442. PubMed ID: 29708492 [Abstract] [Full Text] [Related]
23. [Analyses of audiological examination in children without auditory brainstem response]. Zhang H, Geng MY, Mi YF, Shan ZL, Tang JF, Guo XY. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 Jul 07; 54(7):540-543. PubMed ID: 31315363 [Abstract] [Full Text] [Related]
24. Auditory neuropathy in Brown-Vialetto-Van Laere syndrome due to riboflavin transporter RFVT2 deficiency. Menezes MP, O'Brien K, Hill M, Webster R, Antony J, Ouvrier R, Birman C, Gardner-Berry K. Dev Med Child Neurol; 2016 Aug 07; 58(8):848-54. PubMed ID: 26918385 [Abstract] [Full Text] [Related]
25. The effects of a connexin 26 mutation--35delG--on oto-acoustic emissions and brainstem evoked potentials: homozygotes and carriers. Engel-Yeger B, Zaaroura S, Zlotogora J, Shalev S, Hujeirat Y, Carrasquillo M, Barges S, Pratt H. Hear Res; 2002 Jan 07; 163(1-2):93-100. PubMed ID: 11788203 [Abstract] [Full Text] [Related]
26. Auditory and vestibular phenotypes associated with GATA3 mutation. Chien WW, Leiding JW, Hsu AP, Zalewski C, King K, Holland SM, Brewer C. Otol Neurotol; 2014 Apr 07; 35(4):577-81. PubMed ID: 24622013 [Abstract] [Full Text] [Related]
27. A homozygous MYO7A mutation associated to Usher syndrome and unilateral auditory neuropathy spectrum disorder. Xia H, Hu P, Yuan L, Xiong W, Xu H, Yi J, Yang Z, Deng X, Guo Y, Deng H. Mol Med Rep; 2017 Oct 07; 16(4):4241-4246. PubMed ID: 28731162 [Abstract] [Full Text] [Related]
28. Clinical characteristics of patients with unilateral auditory neuropathy. Song M, Li J, Lan L, Xie L, Xiong F, Yu L, Shi W, Wang D, Guan J, Wang H, Wang Q. Am J Otolaryngol; 2021 Oct 07; 42(5):103143. PubMed ID: 34175691 [Abstract] [Full Text] [Related]
29. Auditory neuropathy with preserved cochlear microphonics and secondary loss of otoacoustic emissions. Deltenre P, Mansbach AL, Bozet C, Christiaens F, Barthelemy P, Paulissen D, Renglet T. Audiology; 1999 Oct 07; 38(4):187-95. PubMed ID: 10431904 [Abstract] [Full Text] [Related]
30. Unilateral auditory neuropathy spectrum disorder. Zhang QJ, Lan L, Shi W, Wang DY, Qi Y, Zong L, Li Q, Wang H, Ding HN, Li N, Han B, Wang QJ. Acta Otolaryngol; 2012 Jan 07; 132(1):72-9. PubMed ID: 22073929 [Abstract] [Full Text] [Related]
31. Auditory neuropathy in childhood. Doyle KJ, Sininger Y, Starr A. Laryngoscope; 1998 Sep 07; 108(9):1374-7. PubMed ID: 9738760 [Abstract] [Full Text] [Related]
32. [Transitory evoked and distortion products of otoacoustic emissions in absent auditory evoked potentials]. Schöler C, Schönweiler R, Ptok M. HNO; 1997 Dec 07; 45(12):1008-15. PubMed ID: 9486382 [Abstract] [Full Text] [Related]
33. Diverse etiologies manifesting auditory neuropathy characteristics from infants with profound hearing loss and clinical implications. Kim SH, Choi HS, Han YE, Choi BY. Int J Pediatr Otorhinolaryngol; 2016 Jul 07; 86():63-7. PubMed ID: 27260582 [Abstract] [Full Text] [Related]
34. The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management. Tranebjærg L, Strenzke N, Lindholm S, Rendtorff ND, Poulsen H, Khandelia H, Kopec W, Lyngbye TJB, Hamel C, Delettre C, Bocquet B, Bille M, Owen HH, Bek T, Jensen H, Østergaard K, Möller C, Luxon L, Carr L, Wilson L, Rajput K, Sirimanna T, Harrop-Griffiths K, Rahman S, Vona B, Doll J, Haaf T, Bartsch O, Rosewich H, Moser T, Bitner-Glindzicz M. Hum Genet; 2018 Feb 07; 137(2):111-127. PubMed ID: 29305691 [Abstract] [Full Text] [Related]