Chen GH - Search Results

1

Clinical characteristics of sudden hearing loss during pregnancy.

Wu XN, Wang HY, Zhang XL, Chen GH, Guan J, Gao Y, Wang DY, Wang QJ. Wu XN, et al. Among authors: chen gh. World J Otorhinolaryngol Head Neck Surg. 2023 Oct 8;10(3):165-172. doi: 10.1002/wjo2.135. eCollection 2024 Sep. World J Otorhinolaryngol Head Neck Surg. 2023. PMID: 39233853 Free PMC article.

2

Comparison between Bilateral and Unilateral Sudden Sensorineural Hearing Loss.

Bing D, Wang DY, Lan L, Zhao LD, Yin ZF, Yu L, Chen GH, Guan J, Wang QJ. Bing D, et al. Among authors: chen gh. Chin Med J (Engl). 2018 Feb 5;131(3):307-315. doi: 10.4103/0366-6999.223843. Chin Med J (Engl). 2018. PMID: 29363646 Free PMC article.

3

Sudden sensorineural hearing loss as the initial symptom in patients with acoustic neuroma.

Song M, Wang D, Li J, Chen G, Zhang X, Wang H, Wang Q. Song M, et al. Front Neurol. 2022 Aug 17;13:953265. doi: 10.3389/fneur.2022.953265. eCollection 2022. Front Neurol. 2022. PMID: 36061993 Free PMC article.

4

Novel de novo interstitial deletion in 2q36.1q36.3 causes syndromic hearing loss and further delineation of the 2q36 deletion syndrome.

Guan J, Yin L, Wang H, Chen G, Zhao C, Wang D, Wang QJ. Guan J, et al. Acta Otolaryngol. 2019 Oct;139(10):870-875. doi: 10.1080/00016489.2019.1592219. Epub 2019 Aug 12. Acta Otolaryngol. 2019. PMID: 31403828

5

Recurrent de novo WFS1 pathogenic variants in Chinese sporadic patients with nonsyndromic sensorineural hearing loss.

Guan J, Wang H, Lan L, Wu Y, Chen G, Zhao C, Wang D, Wang Q. Guan J, et al. Mol Genet Genomic Med. 2020 Aug;8(8):e1367. doi: 10.1002/mgg3.1367. Epub 2020 Jun 22. Mol Genet Genomic Med. 2020. PMID: 32567228 Free PMC article.

6

Family trio-based sequencing in 404 sporadic bilateral hearing loss patients discovers recessive and De novo genetic variants in multiple ways.

Guan J, Li J, Chen G, Shi T, Lan L, Wu X, Zhao C, Wang D, Wang H, Wang Q. Guan J, et al. Eur J Med Genet. 2021 Oct;64(10):104311. doi: 10.1016/j.ejmg.2021.104311. Epub 2021 Aug 17. Eur J Med Genet. 2021. PMID: 34416374

7

[Application of behavioral audiometry in subjective hearing assessment of children].

Chen G, Ding H, Shi W, Xie L, Xiong F, Lan L, Zhang J, Wang Q. Chen G, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2023 Mar;37(3):173-176. doi: 10.13201/j.issn.2096-7993.2023.03.003. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2023. PMID: 36843513 Free PMC article. Chinese.

8

[Clinical features of CAPOS syndrome caused by maternal ATP1A3 gene variation: a case report].

Gao Y, Li F, Luo R, Chen G, Li D, Wang D, Wang Q. Gao Y, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2024 Jan;38(1):73-76. doi: 10.13201/j.issn.2096-7993.2024.01.012. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2024. PMID: 38297853 Free PMC article. Chinese.

9

Discovery of sensorineural hearing loss and ossicle deformity in a Chinese Li nationality family with spondyloepiphyseal dysplasia congenita caused by p.G504S mutation of COL2A1.

Wu K, Li Z, Zhu Y, Wang X, Chen G, Hou Z, Zhang Q. Wu K, et al. BMC Med Genomics. 2021 Jun 28;14(1):170. doi: 10.1186/s12920-021-01020-y. BMC Med Genomics. 2021. PMID: 34182999 Free PMC article.

10

Therapeutic evaluation of lumbar tender point deep massage for chronic non-specific low back pain.

Zheng Z, Wang J, Gao Q, Hou J, Ma L, Jiang C, Chen G. Zheng Z, et al. J Tradit Chin Med. 2012 Dec;32(4):534-7. doi: 10.1016/s0254-6272(13)60066-7. J Tradit Chin Med. 2012. PMID: 23427384 Free article. Clinical Trial.

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