Guo Y - Search Results

1

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. Among authors: guo y. 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

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. 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

Microdebrider vs. electrocautery for tonsillectomy: a meta-analysis.

Du W, Ma B, Guo Y, Yang K. Du W, et al. Among authors: guo y. Int J Pediatr Otorhinolaryngol. 2010 Dec;74(12):1379-83. doi: 10.1016/j.ijporl.2010.09.007. Epub 2010 Oct 8. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20934756

8

Newborn hearing concurrent gene screening can improve care for hearing loss: a study on 14,913 Chinese newborns.

Wang QJ, Zhao YL, Rao SQ, Guo YF, He Y, Lan L, Yang WY, Zheng QY, Ruben RJ, Han DY, Shen Y. Wang QJ, et al. Among authors: guo yf. Int J Pediatr Otorhinolaryngol. 2011 Apr;75(4):535-42. doi: 10.1016/j.ijporl.2011.01.016. Epub 2011 Feb 17. Int J Pediatr Otorhinolaryngol. 2011. PMID: 21329993

9

[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. 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.

10

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. 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.

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