Wang D - 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: wang h, wang d, wang q. 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

[Correlation between phonetically balanced maximum and pure tone auditory threshold among 106 auditory neuropathy patients].

Lan L, Han DY, Shi W, Han MK, Liu Q, Ding HN, Chen ZH, Wang DY, Li SH, Guo ML, Rao SQ, Wang QJ. Lan L, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2008 May;43(5):341-6. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2008. PMID: 18717308 Chinese.

3

[Audiological characteristics of young children with otitis media with effusion].

Wang QJ, Shi W, Lan L, Wang DY, Zhang YM. Wang QJ, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2008 Dec;43(12):891-5. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2008. PMID: 19141237 Chinese.

4

[Audiological and genetic studies on 130 infants with hearing loss].

Wang DY, Wang QJ, Lan L, Shi W, Zhao C, Hui PL, Rao SQ, Han DY. Wang DY, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009 Mar;44(3):177-81. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009. PMID: 19558853 Chinese.

5

[Evaluation of deaf-mute patients with sensitive deafness gene screening in Shandong province].

Ji YB, Han DY, Wang DY, Zhou Y, Zhao C, Wang H, Lan L, Wang QJ. Ji YB, et al. Zhonghua Yi Xue Za Zhi. 2009 Sep 29;89(36):2531-5. Zhonghua Yi Xue Za Zhi. 2009. PMID: 20137612 Chinese.

6

Identification of two novel mutations, c.232T>C and c.2006A>T, in SLC26A4 in a Chinese family associated with enlarged vestibular aqueduct.

Guo YF, Wang YL, Xu BC, Liu XW, Zhu YM, Zhao FF, Ji YB, Zhou Y, Li JQ, Li Q, Wang DY, Wang QJ. Guo YF, et al. Int J Pediatr Otorhinolaryngol. 2010 Jul;74(7):831-5. doi: 10.1016/j.ijporl.2010.04.005. Epub 2010 May 18. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20483489

7

Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China.

Ji YB, Han DY, Lan L, Wang DY, Zong L, Zhao FF, Liu Q, Benedict-Alderfer C, Zheng QY, Wang QJ. Ji YB, et al. Acta Otolaryngol. 2011 Feb;131(2):124-9. doi: 10.3109/00016489.2010.483479. Epub 2010 Dec 16. Acta Otolaryngol. 2011. PMID: 21162657 Free PMC article.

8

Phenotype-genotype correlation in 295 Chinese deaf subjects with biallelic causative mutations in the GJB2 gene.

Zhao FF, Ji YB, Wang DY, Lan L, Han MK, Li Q, Zhao Y, Rao S, Han D, Wang QJ. Zhao FF, et al. Among authors: wang dy, wang qj. Genet Test Mol Biomarkers. 2011 Sep;15(9):619-25. doi: 10.1089/gtmb.2010.0192. Epub 2011 Apr 13. Genet Test Mol Biomarkers. 2011. PMID: 21488715

9

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. Acta Otolaryngol. 2012 Jan;132(1):72-9. doi: 10.3109/00016489.2011.629630. Epub 2011 Nov 10. Acta Otolaryngol. 2012. PMID: 22073929

10

Newborn genetic screening for high risk deafness-associated mutations with a new Tetra-primer ARMS PCR kit.

Han B, Zong L, Li Q, Zhang Z, Wang D, Lan L, Zhang J, Zhao Y, Wang Q. Han B, et al. Among authors: wang d, wang q. Int J Pediatr Otorhinolaryngol. 2013 Sep;77(9):1440-5. doi: 10.1016/j.ijporl.2013.05.040. Epub 2013 Jun 29. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23815884

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

63,323 results

Search Page

Filters