Han D - Search Results

1

Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches.

Lu Y, Zhou X, Jin Z, Cheng J, Shen W, Ji F, Liu L, Zhang X, Zhang M, Cao Y, Han D, Choy K, Yuan H. Lu Y, et al. Among authors: han d. J Hum Genet. 2014 Nov;59(11):599-607. doi: 10.1038/jhg.2014.78. Epub 2014 Sep 18. J Hum Genet. 2014. PMID: 25231367 Free PMC article.

2

[Screening for mitochondrial DNA mutation in two pedigrees with nonsyndromic inherited sensorineural hearing loss].

Li W, Han D, Yuan H, Wang Y, Cao J, Yang W, Jiang S. Li W, et al. Among authors: han d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Feb;19(1):64-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 11836692 Chinese.

3

Correlation of cochlear blood supply with mitochondrial DNA common deletion in presbyacusis.

Dai P, Yang W, Jiang S, Gu R, Yuan H, Han D, Guo W, Cao J. Dai P, et al. Among authors: han d. Acta Otolaryngol. 2004 Mar;124(2):130-6. doi: 10.1080/00016480410016586. Acta Otolaryngol. 2004. PMID: 15072414

4

[Refractory recovery function of electrical auditory on the survival auditory nerve in cochlear implant recipients].

Xi X, Ji F, Han DY, Huang DL, Hong MD, Yang WY. Xi X, et al. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2004 Feb;39(2):77-80. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2004. PMID: 15195587 Chinese.

5

[Pedigree analysis and sequence analysis of mtDNA 12srRNA, tRNA(Leu(UUR)), tRNA(Ser(UCN)) gene in nonsyndromic inherited deafness pedigrees].

Li W, Han D, Yuan H, Cao J. Li W, et al. Among authors: han d. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2004 Oct;18(10):582-5, 589. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2004. PMID: 15620132 Chinese.

6

[The expression pattern of L-type voltage-gated Ca2+ channel in rat cochlea].

Shen W, Hu Y, Yang W, Han D. Shen W, et al. Among authors: han d. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2004 Oct;18(10):613-5. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2004. PMID: 15620144 Chinese.

7

Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.

Wang Q, Li R, Zhao H, Peters JL, Liu Q, Yang L, Han D, Greinwald JH Jr, Young WY, Guan MX. Wang Q, et al. Among authors: han d. Am J Med Genet A. 2005 Feb 15;133A(1):27-30. doi: 10.1002/ajmg.a.30424. Am J Med Genet A. 2005. PMID: 15637703 Free PMC article.

8

[Rating evaluation of the effect of pre-lingual cochlear implanted's aural/oral rehabilitation by questionnaires].

Ji F, Xi X, Hong MD, Han DY, Huang DL, Wu WM. Ji F, et al. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2004 Oct;39(10):584-8. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2004. PMID: 15696914 Chinese.

9

[The significance of the interaural latency difference of VEMP].

Wu Z, Zhang S, Ji F, Zhou N, Guo W, Yang W, Han D. Wu Z, et al. Among authors: han d. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2005 May;19(10):433-5. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2005. PMID: 16108316 Chinese.

10

Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.

Yuan H, Qian Y, Xu Y, Cao J, Bai L, Shen W, Ji F, Zhang X, Kang D, Mo JQ, Greinwald JH, Han D, Zhai S, Young WY, Guan MX. Yuan H, et al. Among authors: han d. Am J Med Genet A. 2005 Oct 1;138A(2):133-40. doi: 10.1002/ajmg.a.30952. Am J Med Genet A. 2005. PMID: 16152638 Free PMC article.

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