PubMed for id: 355880

Year	Number of Results
2005	1
2007	1
2010	1
2011	2
2012	1
2013	2
2014	1
2015	1
2016	4
2017	1
2018	1
2019	2
2020	1
2021	2
2022	1
2023	1
2024	0

1

Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts.

Nakano A, Arimoto Y, Mutai H, Nara K, Inoue S, Matsunaga T. Nakano A, et al. Int J Pediatr Otorhinolaryngol. 2022 Jan;152:110975. doi: 10.1016/j.ijporl.2021.110975. Epub 2021 Nov 14. Int J Pediatr Otorhinolaryngol. 2022. PMID: 34801268

2

Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane.

Avan P, Le Gal S, Michel V, Dupont T, Hardelin JP, Petit C, Verpy E. Avan P, et al. Proc Natl Acad Sci U S A. 2019 Dec 17;116(51):25948-25957. doi: 10.1073/pnas.1902781116. Epub 2019 Nov 27. Proc Natl Acad Sci U S A. 2019. PMID: 31776257 Free PMC article.

3

The Natural History of Hearing Loss in Pendred Syndrome and Non-Syndromic Enlarged Vestibular Aqueduct.

Mey K, Bille M, Rye Rasmussen SH, Tranebjærg L, Cayé-Thomasen P. Mey K, et al. Otol Neurotol. 2019 Mar;40(3):e178-e185. doi: 10.1097/MAO.0000000000002140. Otol Neurotol. 2019. PMID: 30741891

4

Molecular characterization of autosomal recessive non syndromic hearing loss in selected families from District Mardan, Pakistan.

Hussain S, Khattak JZ, Ismail M, Mansoor Q, Khan MH. Hussain S, et al. Pak J Pharm Sci. 2018 Jan;31(1):51-56. Pak J Pharm Sci. 2018. PMID: 29348084

5

Cochlear Cell Modeling Using Disease-Specific iPSCs Unveils a Degenerative Phenotype and Suggests Treatments for Congenital Progressive Hearing Loss.

Hosoya M, Fujioka M, Sone T, Okamoto S, Akamatsu W, Ukai H, Ueda HR, Ogawa K, Matsunaga T, Okano H. Hosoya M, et al. Cell Rep. 2017 Jan 3;18(1):68-81. doi: 10.1016/j.celrep.2016.12.020. Cell Rep. 2017. PMID: 28052261 Free article.

6

Mutations in eight small DFNB genes are not a frequent cause of non-syndromic hereditary hearing loss in Czech patients.

Marková S, Šafka Brožková D, Mészárosová A, Neupauerová J, Groh D, Křečková G, Laššuthová P, Seeman P. Marková S, et al. Int J Pediatr Otorhinolaryngol. 2016 Jul;86:27-33. doi: 10.1016/j.ijporl.2016.04.005. Epub 2016 Apr 7. Int J Pediatr Otorhinolaryngol. 2016. PMID: 27260575

7

[Advances in hereditary hearing loss caused by TMC1 mutations].

Wu K, Wang H, Wang Q. Wu K, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016 Mar;51(3):224-9. doi: 10.3760/cma.j.issn.1673-0860.2016.03.016. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016. PMID: 27033582 Chinese.

8

Clinical characteristics of a Japanese family with hearing loss accompanied by compound heterozygous mutations in LOXHD1.

Minami SB, Mutai H, Namba K, Sakamoto H, Matsunaga T. Minami SB, et al. Auris Nasus Larynx. 2016 Dec;43(6):609-13. doi: 10.1016/j.anl.2016.02.010. Epub 2016 Mar 10. Auris Nasus Larynx. 2016. PMID: 26973026

9

High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss.

Mizutari K, Mutai H, Namba K, Miyanaga Y, Nakano A, Arimoto Y, Masuda S, Morimoto N, Sakamoto H, Kaga K, Matsunaga T. Mizutari K, et al. Orphanet J Rare Dis. 2015 May 13;10:60. doi: 10.1186/s13023-015-0276-z. Orphanet J Rare Dis. 2015. PMID: 25963016 Free PMC article.

10

A novel DFNA36 mutation in TMC1 orthologous to the Beethoven (Bth) mouse associated with autosomal dominant hearing loss in a Chinese family.

Zhao Y, Wang D, Zong L, Zhao F, Guan L, Zhang P, Shi W, Lan L, Wang H, Li Q, Han B, Yang L, Jin X, Wang J, Wang J, Wang Q. Zhao Y, et al. PLoS One. 2014 May 14;9(5):e97064. doi: 10.1371/journal.pone.0097064. eCollection 2014. PLoS One. 2014. PMID: 24827932 Free PMC article.

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