Guo YF - Search Results

1

Analysis of quality of clinical practice guidelines for otorhinolaryngology in China.

Zhang ZW, Liu XW, Xu BC, Wang SY, Li L, Kang YY, Guo YF. Zhang ZW, et al. Among authors: guo yf. PLoS One. 2013;8(1):e53566. doi: 10.1371/journal.pone.0053566. Epub 2013 Jan 18. PLoS One. 2013. PMID: 23349719 Free PMC article. Review.

2

[Clinical analysis of sphenoid disease manifesting orbital apex syndrome].

Guo YF, Yuan YM, Liu ZP, Xu BC, Guan J. Guo YF, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005 Sep;40(9):688-90. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005. PMID: 16335404 Chinese.

3

[Mitochondrial DNA A1555G mutation analysis in 802 nonsyndromic hearing impairment patients].

Liu XW, Guo YF, Han DY, Zhao YL, Lan L, Zhao C, Wang QJ. Liu XW, et al. Among authors: guo yf. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Oct;42(10):739-42. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 18229583 Chinese.

4

GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.

Guo YF, Liu XW, Guan J, Han MK, Wang DY, Zhao YL, Rao SQ, Wang QJ. Guo YF, et al. Acta Otolaryngol. 2008 Mar;128(3):297-303. doi: 10.1080/00016480701767382. Acta Otolaryngol. 2008. PMID: 18274916

5

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

6

Analysis of a large-scale screening of mitochondrial DNA m.1555A>G mutation in 2417 deaf-mute students in northwest of China.

Guo YF, Liu XW, Xu BC, Zhu YM, Wang YL, Zhao FF, Wang DY, Zhao YL, Ji YB, Wang QJ. Guo YF, et al. Genet Test Mol Biomarkers. 2010 Aug;14(4):527-31. doi: 10.1089/gtmb.2010.0020. Genet Test Mol Biomarkers. 2010. PMID: 20662562

7

Auditory screening concurrent deafness predisposing genes screening in 10,043 neonates in Gansu province, China.

Zhang Z, Ding W, Liu X, Xu B, Du W, Nan S, Guo Y. Zhang Z, et al. Int J Pediatr Otorhinolaryngol. 2012 Jul;76(7):984-8. doi: 10.1016/j.ijporl.2012.03.016. Epub 2012 Apr 15. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22510577

8

[Analysis of the hereditary etiology of 336 patients with non-syndromic sensorineural hearing loss from Ningxia Hui Autonomous Region of China].

Wang YL, Zhu YM, Liu XW, Xu BC, Guo YF, Wang QJ. Wang YL, et al. Among authors: guo yf. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Sep;47(9):760-3. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 23141447 Chinese.

9

Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China.

Yang XL, Bai-Cheng X, Chen XJ, Pan-Pan B, Jian-Li M, Xiao-Wen L, Zhang ZW, Wan D, Zhu YM, Guo YF. Yang XL, et al. Among authors: guo yf. Acta Otolaryngol. 2013 Sep;133(9):930-4. doi: 10.3109/00016489.2013.795288. Epub 2013 Jul 9. Acta Otolaryngol. 2013. PMID: 23834103

10

A systematic review and meta-analysis of common mutations of SLC26A4 gene in Asian populations.

Du W, Guo Y, Wang C, Wang Y, Liu X. Du W, et al. Int J Pediatr Otorhinolaryngol. 2013 Oct;77(10):1670-6. doi: 10.1016/j.ijporl.2013.07.023. Epub 2013 Aug 17. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23958391 Review.

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