Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 16

1.

[Modifier factors influencing the phenotypic manifestation of the deafness associated mitochondrial DNA mutations].

YANG AF, ZHENG J, LV JX, GUAN MX.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Apr;28(2):165-71. doi: 10.3760/cma.j.issn.1003-9406.2011.02.010. Review. Chinese.

PMID:
21462128
2.

The role of mitochondrial DNA mutations in hearing loss.

Ding Y, Leng J, Fan F, Xia B, Xu P.

Biochem Genet. 2013 Aug;51(7-8):588-602. doi: 10.1007/s10528-013-9589-6. Epub 2013 Apr 21. Review.

PMID:
23605717
3.

Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity.

Guan MX.

Mitochondrion. 2011 Mar;11(2):237-45. doi: 10.1016/j.mito.2010.10.006. Epub 2010 Nov 1. Review.

PMID:
21047563
4.

[Mitochondrial DNA mutations and aminoglycoside antibiotics and hearing loss].

Qu J, Wang J, Xu S.

Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2015 Nov;29(22):1936-40. Review. Chinese.

PMID:
26911053
5.

Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.

Bindu LH, Reddy PP.

Int J Audiol. 2008 Nov;47(11):702-7. doi: 10.1080/14992020802215862. Review.

PMID:
19031229
6.

Maternally inherited hearing impairment.

Van Camp G, Smith RJ.

Clin Genet. 2000 Jun;57(6):409-14. Review.

PMID:
10905659
7.

Sensorineural hearing loss caused by mitochondrial DNA mutations: special reference to the A1555G mutation.

Usami S, Abe S, Shinkawa H, Kimberling WJ.

J Commun Disord. 1998 Sep-Oct;31(5):423-34; quiz 434-5. Review.

PMID:
9777488
8.

Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature.

Berrettini S, Forli F, Passetti S, Rocchi A, Pollina L, Cecchetti D, Mancuso M, Siciliano G.

Biosci Rep. 2008 Feb;28(1):49-59. doi: 10.1042/BSR20070027. Review.

PMID:
18215147
9.

Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness?

Kokotas H, Grigoriadou M, Korres GS, Ferekidou E, Giannoulia-Karantana A, Kandiloros D, Korres S, Petersen MB.

J Hum Genet. 2010 May;55(5):265-9. doi: 10.1038/jhg.2010.23. Epub 2010 Mar 19. Review.

PMID:
20300122
10.

Nuclear factors: roles related to mitochondrial deafness.

Luo LF, Hou CC, Yang WX.

Gene. 2013 May 15;520(2):79-89. doi: 10.1016/j.gene.2013.03.041. Epub 2013 Mar 17. Review.

PMID:
23510774
11.

[Epigenetics--a new perspective for the study of deafness].

Xu F, Wang HJ, Ma D.

Yi Chuan. 2012 Mar;34(3):253-9. Review. Chinese.

PMID:
22425943
12.

The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations.

Yan D, Kannan-Sundhari A, Vishwanath S, Qing J, Mittal R, Kameswaran M, Liu XZ.

Genet Test Mol Biomarkers. 2015 Sep;19(9):512-27. doi: 10.1089/gtmb.2015.0023. Epub 2015 Jul 17. Review.

13.

Human nonsyndromic sensorineural deafness.

Friedman TB, Griffith AJ.

Annu Rev Genomics Hum Genet. 2003;4:341-402. Review.

PMID:
14527306
14.

[Mitochondrial DNA secondary mutation associated with deafness].

Tang XW, Guan MX.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Dec;47(12):1050-3. Review. Chinese. No abstract available.

PMID:
23328056
15.

[Mitochondrial mutation and nonsyndromic hereditary deafness].

Bai YH, Ren CC.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Nov;42(11):873-6. Review. Chinese. No abstract available.

PMID:
18300461
16.

Science, medicine, and the future: New interventions in hearing impairment.

Steel KP.

BMJ. 2000 Mar 4;320(7235):622-5. Review. No abstract available.

Supplemental Content

Support Center