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Results: 1 to 20 of 103

1.

Mitochondrial DNA mutation screening in an ethnically diverse nonsyndromic deafness cohort.

Vivero RJ, Ouyang X, Yan D, Du L, Liu W, Angeli SI, Liu XZ.

Genet Test Mol Biomarkers. 2012 Sep;16(9):1146-8. doi: 10.1089/gtmb.2011.0365. Epub 2012 Aug 1.

PMID:
22853457
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Large-scale screening of mitochondrial DNA mutations among Iranian patients with prelingual nonsyndromic hearing impairment.

Montazer Zohour M, Tabatabaiefar MA, Dehkordi FA, Farrokhi E, Akbari MT, Chaleshtori MH.

Genet Test Mol Biomarkers. 2012 Apr;16(4):271-8. doi: 10.1089/gtmb.2011.0176. Epub 2011 Nov 11.

PMID:
22077646
[PubMed - indexed for MEDLINE]
3.

Genetic mutations in non-syndromic deafness patients of Uyghur and Han Chinese ethnicities in Xinjiang, China: a comparative study.

Chen Y, Tudi M, Sun J, He C, Lu HL, Shang Q, Jiang D, Kuyaxi P, Hu B, Zhang H.

J Transl Med. 2011 Sep 14;9:154. doi: 10.1186/1479-5876-9-154.

PMID:
21917135
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population.

Kabahuma RI, Ouyang X, Du LL, Yan D, Hutchin T, Ramsay M, Penn C, Liu XZ.

Int J Pediatr Otorhinolaryngol. 2011 May;75(5):611-7. doi: 10.1016/j.ijporl.2011.01.029. Epub 2011 Mar 9.

PMID:
21392827
[PubMed - indexed for MEDLINE]
5.

Audiological and genetic features of the mtDNA mutations.

Liu XZ, Angeli S, Ouyang XM, Liu W, Ke XM, Liu YH, Liu SX, Du LL, Deng XW, Yuan H, Yan D.

Acta Otolaryngol. 2008 Jul;128(7):732-8. doi: 10.1080/00016480701719011.

PMID:
18568513
[PubMed - indexed for MEDLINE]
6.

Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss.

Maniglia LP, Moreira BC, Silva MA, Piatto VB, Maniglia JV.

Braz J Otorhinolaryngol. 2008 Sep-Oct;74(5):731-6.

PMID:
19082356
[PubMed - indexed for MEDLINE]
Free Article
7.

[Prevalence of common genetic mutations and clinical characteristics analysis in patients at different ages with nonsyndromic hearing impairment].

Zhang CQ, Chen BB, Chen YY, Liu XJ, Zheng J, Gao JJ, Huang SY, Nan BY, Zhang YY, Yu X, Guan MX.

Yi Chuan. 2013 Mar;35(3):352-8. Chinese.

PMID:
23575541
[PubMed - indexed for MEDLINE]
8.

Screening of the general Polish population for deafness-associated mutations in mitochondrial 12S rRNA and tRNA Ser(UCN) genes.

Rydzanicz M, Wróbel M, Cywińska K, Froehlich D, Gawecki W, Szyfter W, Szyfter K.

Genet Test Mol Biomarkers. 2009 Apr;13(2):167-72. doi: 10.1089/gtmb.2008.0098.

PMID:
19371214
[PubMed - indexed for MEDLINE]
9.

[Incidence of A1555G mutations in the mitochondrial DNA and 35delG in the GJB2 gene (connexin-26) in families with late onset non-syndromic sensorineural hearing loss from Cantabria].

Gallo-Terán J, Morales-Angulo C, del Castillo I, Villamar M, Moreno-Pelayo MA, García-Mantilla J, Moreno F.

Acta Otorrinolaringol Esp. 2002 Oct;53(8):563-71. Spanish.

PMID:
12530196
[PubMed - indexed for MEDLINE]
Free Article
10.

Phenotype/genotype correlations in a DFNB1 cohort with ethnical diversity.

Angeli SI.

Laryngoscope. 2008 Nov;118(11):2014-23. doi: 10.1097/MLG.0b013e31817fb7ad.

PMID:
18758381
[PubMed - indexed for MEDLINE]
11.

The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss.

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

Biochem Biophys Res Commun. 2009 Dec 18;390(3):755-7. doi: 10.1016/j.bbrc.2009.10.044. Epub 2009 Oct 14.

PMID:
19835846
[PubMed - indexed for MEDLINE]
12.

Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides.

Estivill X, Govea N, Barceló E, Badenas C, Romero E, Moral L, Scozzri R, D'Urbano L, Zeviani M, Torroni A.

Am J Hum Genet. 1998 Jan;62(1):27-35.

PMID:
9490575
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

[Mitochondrial DNA A1555G mutation of seven families with nonsyndromic hearing loss].

Ou QS, Cheng ZJ, Yang B, Jiang L, Chen J.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):550-4. doi: 10.3760/cma.j.issn.1003-9406.2009.05.017. Chinese.

PMID:
19806580
[PubMed - indexed for MEDLINE]
15.

Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia.

Malik SG, Pieter N, Sudoyo H, Kadir A, Marzuki S.

J Hum Genet. 2003;48(9):480-3. Epub 2003 Sep 3.

PMID:
12955586
[PubMed - indexed for MEDLINE]
16.

A maternal hereditary deafness pedigree of the A1555G mitochondrial mutation, causing aminoglycoside ototoxicity predisposition.

Bai YH, Ren CC, Gong XR, Meng LP.

J Laryngol Otol. 2008 Oct;122(10):1037-41. doi: 10.1017/S0022215107001648. Epub 2008 Feb 19.

PMID:
18282333
[PubMed - indexed for MEDLINE]
17.

[Mitochondrial DNA G7444A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation].

Yang AF, Zhu Y, Lu JX, Yang L, Zhao JY, Sun DM.

Yi Chuan. 2008 Jun;30(6):728-34. Chinese.

PMID:
18550495
[PubMed - indexed for MEDLINE]
18.

[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.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Sep;47(9):760-3. Chinese.

PMID:
23141447
[PubMed - indexed for MEDLINE]
19.

Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor.

Chapiro E, Feldmann D, Denoyelle F, Sternberg D, Jardel C, Eliot MM, Bouccara D, Weil D, Garabédian EN, Couderc R, Petit C, Marlin S.

Eur J Hum Genet. 2002 Dec;10(12):851-6.

PMID:
12461693
[PubMed - indexed for MEDLINE]
Free Article
20.

Etiologic diagnosis of nonsyndromic genetic hearing loss in adult vs pediatric populations.

King PJ, Ouyang X, Du L, Yan D, Angeli SI, Liu XZ.

Otolaryngol Head Neck Surg. 2012 Nov;147(5):932-6. doi: 10.1177/0194599812453553. Epub 2012 Jul 11.

PMID:
22785241
[PubMed - indexed for MEDLINE]

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