158 related articles for article (PubMed ID: 12882732)
1. [Familial susceptibility to aminoglycoside ototoxicity due to the A1555G mutation in the mitochondrial DNA].
Gallo-Terán J; Morales-Angulo C; del Castillo I; Moreno-Pelayo MA; Mazón A; Moreno F
Med Clin (Barc); 2003 Jul; 121(6):216-8. PubMed ID: 12882732
[TBL] [Abstract][Full Text] [Related]
2. [Prevalence of the A1555G mutation in the mitochondrial DNA in patients with cochlear or vestibular damage due to aminoglycoside-induced ototoxicity].
Gallo-Terán J; Arellano B; Morales-Angulo C; Modamio-Høybjør S; Moreno-Pelayo MA; Ramírez-Camacho R; del Castillo I; Moreno F
Acta Otorrinolaringol Esp; 2004 May; 55(5):212-7. PubMed ID: 15461317
[TBL] [Abstract][Full Text] [Related]
3. 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
Am J Med Genet A; 2005 Oct; 138A(2):133-40. PubMed ID: 16152638
[TBL] [Abstract][Full Text] [Related]
4. Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree.
Chen T; Liu Q; Jiang L; Liu C; Ou Q
Genet Test Mol Biomarkers; 2013 Feb; 17(2):122-30. PubMed ID: 23256547
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 9490575
[TBL] [Abstract][Full Text] [Related]
6. [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. PubMed ID: 18550495
[TBL] [Abstract][Full Text] [Related]
7. Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications.
Casano RA; Johnson DF; Bykhovskaya Y; Torricelli F; Bigozzi M; Fischel-Ghodsian N
Am J Otolaryngol; 1999; 20(3):151-6. PubMed ID: 10326749
[TBL] [Abstract][Full Text] [Related]
8. [Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness].
Liu X; Dai P; Huang DL; Yuan HJ; Li WM; Cao JY; Yu F; Zhang RN; Lin HY; Zhu XH; He Y; Yu YJ; Yao K
Zhonghua Yi Xue Za Zhi; 2006 May; 86(19):1318-22. PubMed ID: 16796900
[TBL] [Abstract][Full Text] [Related]
9. Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.
Zhao L; Wang Q; Qian Y; Li R; Cao J; Hart LC; Zhai S; Han D; Young WY; Guan MX
Biochem Biophys Res Commun; 2005 Oct; 336(3):967-73. PubMed ID: 16168391
[TBL] [Abstract][Full Text] [Related]
10. [Audiometric features of familial hearing impairment transmitted by mitochondrial inheritance (A1555G)].
Morales Angulo C; Gallo Terán J; del Castillo I; Moreno Pelayo MA; García-Mantilla J; Moreno Herrero F
Acta Otorrinolaringol Esp; 2002 Nov; 53(9):641-8. PubMed ID: 12584878
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 19031229
[TBL] [Abstract][Full Text] [Related]
12. Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation.
Wang Q; Li QZ; Han D; Zhao Y; Zhao L; Qian Y; Yuan H; Li R; Zhai S; Young WY; Guan MX
Biochem Biophys Res Commun; 2006 Feb; 340(2):583-8. PubMed ID: 16380089
[TBL] [Abstract][Full Text] [Related]
13. [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. PubMed ID: 19806580
[TBL] [Abstract][Full Text] [Related]
14. Deafness due to A1555G mitochondrial mutation without use of aminoglycoside.
Matsunaga T; Kumanomido H; Shiroma M; Ohtsuka A; Asamura K; Usami S
Laryngoscope; 2004 Jun; 114(6):1085-91. PubMed ID: 15179218
[TBL] [Abstract][Full Text] [Related]
15. [Analysis of mtDNA 12SrRNA A1555G mutations of Uigur patients with nonsyndromic hereditary hearing loss in Xinjiang].
Jiang H; Li Y; Sheng G; Yang L; Li H; Li H; Luo Y; Wang C
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2010 May; 24(10):439-41, 446. PubMed ID: 20669656
[TBL] [Abstract][Full Text] [Related]
16. 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; 390(3):755-7. PubMed ID: 19835846
[TBL] [Abstract][Full Text] [Related]
17. Pharmacogenomic testing to prevent aminoglycoside-induced hearing loss in cystic fibrosis patients: potential impact on clinical, patient, and economic outcomes.
Veenstra DL; Harris J; Gibson RL; Rosenfeld M; Burke W; Watts C
Genet Med; 2007 Oct; 9(10):695-704. PubMed ID: 18073583
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 18282333
[TBL] [Abstract][Full Text] [Related]
19. Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity.
Scrimshaw BJ; Faed JM; Tate WP; Yun K
J Hum Genet; 1999; 44(6):388-90. PubMed ID: 10570910
[TBL] [Abstract][Full Text] [Related]
20. Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycoside.
Matsunaga T; Kumanomido H; Shiroma M; Goto Y; Usami S
Ann Otol Rhinol Laryngol; 2005 Feb; 114(2):153-60. PubMed ID: 15757197
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
