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Items: 1 to 20 of 103

1.

Cochlear implantation in children with congenital X-linked deafness due to novel mutations in POU3F4 gene.

Stankovic KM, Hennessey AM, Herrmann B, Mankarious LA.

Ann Otol Rhinol Laryngol. 2010 Dec;119(12):815-22.

PMID:
21250553
2.

Positive Outcomes and Surgical Strategies for Bilateral Cochlear Implantation in a Child With X-Linked Deafness.

Kim L, Wisely CE, Lucius S, Weingarten J, Dodson EE.

Ann Otol Rhinol Laryngol. 2016 Feb;125(2):173-6. doi: 10.1177/0003489415604167. Epub 2015 Sep 7.

PMID:
26346280
3.

Clinical and molecular characterizations of novel POU3F4 mutations reveal that DFN3 is due to null function of POU3F4 protein.

Lee HK, Song MH, Kang M, Lee JT, Kong KA, Choi SJ, Lee KY, Venselaar H, Vriend G, Lee WS, Park HJ, Kwon TK, Bok J, Kim UK.

Physiol Genomics. 2009 Nov 6;39(3):195-201. doi: 10.1152/physiolgenomics.00100.2009. Epub 2009 Aug 11.

PMID:
19671658
4.

Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafness.

Vore AP, Chang EH, Hoppe JE, Butler MG, Forrester S, Schneider MC, Smith LL, Burke DW, Campbell CA, Smith RJ.

Arch Otolaryngol Head Neck Surg. 2005 Dec;131(12):1057-63.

PMID:
16365218
5.

Clinical evaluation of DFN3 patients with deletions in the POU3F4 locus and detection of carrier female using MLPA.

Song MH, Lee HK, Choi JY, Kim S, Bok J, Kim UK.

Clin Genet. 2010 Dec;78(6):524-32. doi: 10.1111/j.1399-0004.2010.01426.x.

PMID:
20412083
6.

Clinical observations and molecular variables of patients with hearing loss and incomplete partition type III.

Choi BY, An YH, Song JJ, Koo JW, Lee JH, Oh SH, Chang SO, Kim CS, Park JH.

Laryngoscope. 2016 Mar;126(3):E123-8. doi: 10.1002/lary.25573. Epub 2015 Nov 24.

PMID:
26600195
7.

X-linked Malformation and Cochlear Implantation.

Smeds H, Wales J, Asp F, Löfkvist U, Falahat B, Anderlid BM, Anmyr L, Karltorp E.

Otol Neurotol. 2017 Jan;38(1):38-46.

PMID:
27779564
8.

Novel POU3F4 mutations and clinical features of DFN3 patients with cochlear implants.

Lee HK, Lee SH, Lee KY, Lim EJ, Choi SY, Park RK, Kim UK.

Clin Genet. 2009 Jun;75(6):572-5. doi: 10.1111/j.1399-0004.2009.01181.x. Epub 2009 May 5. No abstract available.

PMID:
19438930
9.

Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations.

Bademci G, Lasisi A, Yariz KO, Montenegro P, Menendez I, Vinueza R, Paredes R, Moreta G, Subasioglu A, Blanton S, Fitoz S, Incesulu A, Sennaroglu L, Tekin M.

BMC Med Genet. 2015 Feb 25;16:9. doi: 10.1186/s12881-015-0149-2.

10.

Novel mutation in the homeobox domain of transcription factor POU3F4 associated with profound sensorineural hearing loss.

Schild C, Prera E, Lüblinghoff N, Arndt S, Aschendorff A, Birkenhäger R.

Otol Neurotol. 2011 Jun;32(4):690-4. doi: 10.1097/MAO.0b013e318210b749.

PMID:
21555964
11.

X-linked deafness-2 (DFNX2) phenotype associated with a paracentric inversion upstream of POU3F4.

Anger GJ, Crocker S, McKenzie K, Brown KK, Morton CC, Harrison K, MacKenzie JJ.

Am J Audiol. 2014 Mar;23(1):1-6. doi: 10.1044/1059-0889(2013/13-0018).

12.

HRCT and MRI findings in X-linked non-syndromic deafness patients with a POU3F4 mutation.

Gong WX, Gong RZ, Zhao B.

Int J Pediatr Otorhinolaryngol. 2014 Oct;78(10):1756-62. doi: 10.1016/j.ijporl.2014.08.013. Epub 2014 Aug 17.

PMID:
25175280
13.

Successful cochlear implantation in prelingual profound deafness resulting from the common 233delC mutation of the GJB2 gene in the Japanese.

Matsushiro N, Doi K, Fuse Y, Nagai K, Yamamoto K, Iwaki T, Kawashima T, Sawada A, Hibino H, Kubo T.

Laryngoscope. 2002 Feb;112(2):255-61.

PMID:
11889380
14.

Cochlear implantation effect on deaf children with gap junction protein beta 2 gene mutation.

Kong Y, Liu S, Wang SJ, Li SJ, Liang S.

Chin Med J (Engl). 2013 Apr;126(7):1298-301.

PMID:
23557562
15.

Audiological and surgical evidence for the presence of a third window effect for the conductive hearing loss in DFNX2 deafness irrespective of types of mutations.

Choi BY, An YH, Park JH, Jang JH, Chung HC, Kim AR, Lee JH, Kim CS, Oh SH, Chang SO.

Eur Arch Otorhinolaryngol. 2013 Nov;270(12):3057-62. doi: 10.1007/s00405-013-2386-3. Epub 2013 Feb 12.

PMID:
23400403
16.

Cochlear implantation in individuals with Usher type 1 syndrome.

Liu XZ, Angeli SI, Rajput K, Yan D, Hodges AV, Eshraghi A, Telischi FF, Balkany TJ.

Int J Pediatr Otorhinolaryngol. 2008 Jun;72(6):841-7. doi: 10.1016/j.ijporl.2008.02.013. Epub 2008 Apr 18.

PMID:
18395802
17.

Cochlear implantation in X-linked deafness - How to manage the surgical challenges.

Saeed H, Powell HR, Saeed SR.

Cochlear Implants Int. 2016 Jul;17(4):178-183. Epub 2016 May 3.

PMID:
27142359
18.
19.

De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing loss.

Moteki H, Shearer AE, Izumi S, Kubota Y, Azaiez H, Booth KT, Sloan CM, Kolbe DL, Smith RJ, Usami S.

Ann Otol Rhinol Laryngol. 2015 May;124 Suppl 1:169S-76S. doi: 10.1177/0003489415575042. Epub 2015 Mar 19.

20.

Facial nerve stimulation following cochlear implantation for X-linked stapes gusher syndrome leading to identification of a novel POU3F4 mutation.

Wester JL, Merna C, Peng KA, Lewis R, Sepahdari AR, Ishiyama G, Hosokawa K, Kumakawa K, Ishiyama A.

Int J Pediatr Otorhinolaryngol. 2016 Dec;91:121-123. doi: 10.1016/j.ijporl.2016.10.003. Epub 2016 Oct 6.

PMID:
27863625

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