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1993 1
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Page 1
Aminoglycoside-induced deafness during treatment of acute leukaemia.
Bitner-Glindzicz M, Osei-Lah V, Colvin I, Sirimanna T, Lucas D, Mac Ardle B, Webb D, Shankar A, Kingston J, Jenkins L, Rahman S. Bitner-Glindzicz M, et al. Arch Dis Child. 2010 Feb;95(2):153-5. doi: 10.1136/adc.2009.158220. Arch Dis Child. 2010. PMID: 20172897
Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics.
Shen Z, Zheng J, Chen B, Peng G, Zhang T, Gong S, Zhu Y, Zhang C, Li R, Yang L, Zhou J, Cai T, Jin L, Lu J, Guan MX. Shen Z, et al. J Transl Med. 2011 Jan 4;9:4. doi: 10.1186/1479-5876-9-4. J Transl Med. 2011. PMID: 21205314 Free PMC article.
CONCLUSIONS: Mutations in mitochondrial 12S rRNA accounted for ~30% cases of aminoglycoside-induced deafness in this cohort. Our data strongly support the idea that the mitochondrial 12S rRNA is the hot spot for mutations associated with aminoglycoside ototox …
CONCLUSIONS: Mutations in mitochondrial 12S rRNA accounted for ~30% cases of aminoglycoside-induced deafness in this co …
Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity.
Fischel-Ghodsian N, Prezant TR, Chaltraw WE, Wendt KA, Nelson RA, Arnos KS, Falk RE. Fischel-Ghodsian N, et al. Am J Otolaryngol. 1997 May-Jun;18(3):173-8. doi: 10.1016/s0196-0709(97)90078-8. Am J Otolaryngol. 1997. PMID: 9164619
PURPOSE: Aminoglycoside-induced deafness caused by mutations in the mitochondrial 12S ribosomal RNA gene has been described in a number of Asian patients. ...
PURPOSE: Aminoglycoside-induced deafness caused by mutations in the mitochondrial 12S ribosomal RNA gene has been descr …
A South African family with the mitochondrial A1555G mutation on haplogroup L0d.
Human H, Lombard D, de Jong G, Bardien S. Human H, et al. Biochem Biophys Res Commun. 2009 May 1;382(2):390-4. doi: 10.1016/j.bbrc.2009.03.032. Epub 2009 Mar 12. Biochem Biophys Res Commun. 2009. PMID: 19285484
The most common mutation associated with aminoglycoside-induced deafness is A1555G and it has been found in diverse populations worldwide. ...It is important to identify mutation-positive individuals and inform them of their increased risk of developing am …
The most common mutation associated with aminoglycoside-induced deafness is A1555G and it has been found in diverse pop …
The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population.
Ealy M, Lynch KA, Meyer NC, Smith RJ. Ealy M, et al. Laryngoscope. 2011 Jun;121(6):1184-6. doi: 10.1002/lary.21778. Epub 2011 Apr 14. Laryngoscope. 2011. PMID: 21495045
Although no hearing loss was detected by newborn hearing screens in the at-risk patients, these neonatal intensive care unit graduates have an increased life-time risk for developing aminoglycoside-induced deafness....
Although no hearing loss was detected by newborn hearing screens in the at-risk patients, these neonatal intensive care unit graduates have …
A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity.
Guan MX, Fischel-Ghodsian N, Attardi G. Guan MX, et al. Hum Mol Genet. 2000 Jul 22;9(12):1787-93. doi: 10.1093/hmg/9.12.1787. Hum Mol Genet. 2000. PMID: 10915767
The A1555 G mutation in mitochondrial 12S rRNA has been found to be associated with non-syndromic deafness and aminoglycoside-induced deafness. The sensitivity to the aminoglycoside paromomycin has been analyzed in lymphoblastoid cell lines derived from five …
The A1555 G mutation in mitochondrial 12S rRNA has been found to be associated with non-syndromic deafness and aminoglycoside-indu …
Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss.
Maniglia LP, Moreira BCL, da Silva MAOM, Piatto VB, Maniglia JV. Maniglia LP, et al. Braz J Otorhinolaryngol. 2008 Sep-Oct;74(5):731-736. doi: 10.1016/S1808-8694(15)31384-7. Braz J Otorhinolaryngol. 2008. PMID: 19082356 Free PMC article.
The A1555G mitochondrial mutation is the main alteration associated with aminoglycoside-induced deafness. AIM: to investigate the prevalence of the A1555G mutation in patients sensorineural hearing loss patients with and without aminoglycosides antibiotic use …
The A1555G mitochondrial mutation is the main alteration associated with aminoglycoside-induced deafness. AIM: to inves …
Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity.
Fischel-Ghodsian N, Prezant TR, Bu X, Oztas S. Fischel-Ghodsian N, et al. Am J Otolaryngol. 1993 Nov-Dec;14(6):399-403. doi: 10.1016/0196-0709(93)90113-l. Am J Otolaryngol. 1993. PMID: 8285309
PURPOSE: Aminoglycoside-induced deafness has been described in a number of Chinese pedigrees. ...
PURPOSE: Aminoglycoside-induced deafness has been described in a number of Chinese pedigrees. ...
12 results