Han B - Search Results

1

[The study of clinical characteristics of sudden sensorineural hearing loss patients with tinnitus].

Li Q, Ma X, Wang D, Su Q, Wang H, Lan L, Han B, Qi Y, Yin Z, Wu Z, Xue X, Wang Q. Li Q, et al. Among authors: han b. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2015 Jan;29(1):57-60. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2015. PMID: 25966557 Chinese.

2

[Clinical analysis of sudden sensorineural hearing loss in patients with different ages].

Wang DY, Hou ZQ, Liu Y, Gao Y, Li Q, Lan L, Zhao FF, Han B, Wang QJ. Wang DY, et al. Among authors: han b. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 May;48(5):385-8. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013. PMID: 24016562 Chinese.

3

[Clinical analysis of in-patients with large vestibular aqueduct syndrome].

Wang D, Zhao Y, Zhao F, Zong L, Han B, Lan L, Zhang Q, Qi Y, Wang Q. Wang D, et al. Among authors: han b. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Oct;27(19):1063-7. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013. PMID: 24417164 Chinese.

4

[The study of the pure tone audiometry characteristics and curative effect in sudden hearing loss patients with hypertension].

Li Q, Wang D, Wang H, Lan L, Han B, Qi Y, Guan J, Yin Z, Wu Z, Wang Q. Li Q, et al. Among authors: han b. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2014 Apr;29(8):748-52. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2014. PMID: 26248453 Chinese.

5

Comparative study of mutation spectrums of MT-RNR1 m.1555A>G, GJB2, and SLC26A4 between familial and sporadic patients with nonsyndromic sensorineural hearing loss in Chinese Han.

Li Q, Ji Y, Han B, Zong L, Lan L, Zhao Y, Wang H, Wang D, Wang Q. Li Q, et al. Among authors: han b. Chin Med J (Engl). 2014;127(18):3233-7. Chin Med J (Engl). 2014. PMID: 25266519

6

Correlation analysis of genotypes, auditory function, and vestibular size in Chinese children with enlarged vestibular aqueduct syndrome.

Zhao FF, Lan L, Wang DY, Han B, Qi Y, Zhao Y, Zong L, Li Q, Wang QJ. Zhao FF, et al. Among authors: han b. Acta Otolaryngol. 2013 Dec;133(12):1242-9. doi: 10.3109/00016489.2013.822555. Acta Otolaryngol. 2013. PMID: 24245694

7

Targeted high-throughput sequencing identifies pathogenic mutations in KCNQ4 in two large Chinese families with autosomal dominant hearing loss.

Wang H, Zhao Y, Yi Y, Gao Y, Liu Q, Wang D, Li Q, Lan L, Li N, Guan J, Yin Z, Han B, Zhao F, Zong L, Xiong W, Yu L, Song L, Yi X, Yang L, Petit C, Wang Q. Wang H, et al. Among authors: han b. PLoS One. 2014 Aug 12;9(8):e103133. doi: 10.1371/journal.pone.0103133. eCollection 2014. PLoS One. 2014. PMID: 25116015 Free PMC article.

8

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. Zhang QJ, et al. Among authors: han b. Acta Otolaryngol. 2012 Jan;132(1):72-9. doi: 10.3109/00016489.2011.629630. Epub 2011 Nov 10. Acta Otolaryngol. 2012. PMID: 22073929

9

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. Among authors: han b. PLoS One. 2014 May 14;9(5):e97064. doi: 10.1371/journal.pone.0097064. eCollection 2014. PLoS One. 2014. PMID: 24827932 Free PMC article.

10

Identification of a novel mutation of PJVK in the Chinese non-syndromic hearing loss population with low prevalence of the PJVK mutations.

Zhang QJ, Lan L, Li N, Qi Y, Zong L, Shi W, Yu L, Wang H, Yang J, Xie LY, Zhao F, Wang DY, Han B, Wang QJ. Zhang QJ, et al. Among authors: han b. Acta Otolaryngol. 2015 Mar;135(3):211-6. doi: 10.3109/00016489.2014.985799. Epub 2015 Jan 28. Acta Otolaryngol. 2015. PMID: 25631766

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