Bian P - Search Results

1

Analysis between phenotypes and genotypes of inner ear malformation.

Wang S, Ding W, Chen C, Xu B, Liu X, Bian P, Guo Y. Wang S, et al. Among authors: bian p. Acta Otolaryngol. 2019 Mar;139(3):223-232. doi: 10.1080/00016489.2018.1554262. Epub 2019 Feb 14. Acta Otolaryngol. 2019. PMID: 30762457 Review.

2

Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China.

Xu BC, Bian PP, Liu XW, Zhu YM, Yang XL, Ma JL, Chen XJ, Wang YL, Guo YF. Xu BC, et al. Acta Otolaryngol. 2014 Sep;134(9):924-9. doi: 10.3109/00016489.2014.927588. Epub 2014 Jun 18. Acta Otolaryngol. 2014. PMID: 24941117

3

The deafness-causing mutation c.508_511dup in the GJB2 gene and a literature review.

Zhu YM, Li Y, Wang YL, Bian PP, Xu BC, Liu XW, Chen XJ, Liu F, Guo YF, Wang QJ. Zhu YM, et al. Acta Otolaryngol. 2015 Sep;135(9):914-8. doi: 10.3109/00016489.2015.1035796. Epub 2015 Apr 20. Acta Otolaryngol. 2015. PMID: 25891447 Review.

4

Pharyngeal Ectopic Thymus: A Case Report.

Chen C, Liu BB, Bian PP, Xu BC, Guo YF. Chen C, et al. Ear Nose Throat J. 2021 Sep;100(8):NP354-NP356. doi: 10.1177/0145561320918434. Epub 2020 Apr 22. Ear Nose Throat J. 2021. PMID: 32320300 Free article.

5

[Computer tomography demonstrations of single-sided deafness].

Hu J, Zhao X, Wu Q, Liu B, Chen C, Bian P, Guo Y, Xu B. Hu J, et al. Among authors: bian p. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2020 Nov;34(11):981-986. doi: 10.13201/j.issn.2096-7993.2020.11.005. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2020. PMID: 33254314 Free PMC article. Chinese.

6

Analysis of GJB2 Gene Mutations in 1330 Deafness Cases of Major Ethnic Groups in Northwest China.

Bian P, Xu B, Zhao X, Zhu Y, Chen C, Chen X, Liu X, Wang Y, Guo Y. Bian P, et al. Inquiry. 2022 Jan-Dec;59:469580211055571. doi: 10.1177/00469580211055571. Inquiry. 2022. PMID: 35212567 Free PMC article.

7

The value of nonverbal intelligence in cochlear implant.

Dang J, Bian PP, Chen C, Bai SJ, Guo Y, Xu BC. Dang J, et al. Acta Otolaryngol. 2023 Jan;143(1):24-27. doi: 10.1080/00016489.2022.2161624. Epub 2023 Jan 5. Acta Otolaryngol. 2023. PMID: 36602408 Review.

8

The effect of SLC26A4 gene mutations on long-term rehabilitative outcomes in cochlear implant patients.

Wang Q, Hu J, Bian P, Chen C, Wang Y, Cheng S, Guo Y, Xu B. Wang Q, et al. Among authors: bian p. Acta Otolaryngol. 2023 Feb;143(2):156-162. doi: 10.1080/00016489.2023.2174592. Epub 2023 Feb 13. Acta Otolaryngol. 2023. PMID: 36780306

9

Research on congenital severe-to-profound sensorineural hearing loss associated with central lucency of the bony island of the lateral semicircular canal.

Wang Q, Bian P, Bai S, Chen C, Wang Y, Guo Y, Xu B. Wang Q, et al. Among authors: bian p. Acta Otolaryngol. 2023 Feb;143(2):134-140. doi: 10.1080/00016489.2023.2179661. Epub 2023 Feb 25. Acta Otolaryngol. 2023. PMID: 36840650

10

Research Advances on Deafness Genes Associated with Mitochondrial tRNA-37 Modifications.

Bian P, Chai J, Xu B. Bian P, et al. J Int Adv Otol. 2023 Oct;19(5):414-419. doi: 10.5152/iao.2023.231107. J Int Adv Otol. 2023. PMID: 37789629 Free PMC article. Review.

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