These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
139 related articles for article (PubMed ID: 10842587)
1. Genetic factors in aminoglycoside toxicity. Fischel-Ghodsian N Ann N Y Acad Sci; 1999 Nov; 884():99-109. PubMed ID: 10842587 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity. Fischel-Ghodsian N; Prezant TR; Bu X; Oztas S Am J Otolaryngol; 1993; 14(6):399-403. PubMed ID: 8285309 [TBL] [Abstract][Full Text] [Related]
4. Genetic factors in aminoglycoside toxicity. Fischel-Ghodsian N Pharmacogenomics; 2005 Jan; 6(1):27-36. PubMed ID: 15723603 [TBL] [Abstract][Full Text] [Related]
5. Genetic susceptibility to aminoglycoside ototoxicity. Nguyen T; Jeyakumar A Int J Pediatr Otorhinolaryngol; 2019 May; 120():15-19. PubMed ID: 30743189 [TBL] [Abstract][Full Text] [Related]
6. [Aminoglycoside ototoxicity associated with mitochondrial DNA mutation]. Ke X; Qi Y; Gu Z; Zhang Z; Zhang W; Jiang S; Liu J Lin Chuang Er Bi Yan Hou Ke Za Zhi; 1999 May; 13(5):195-7. PubMed ID: 12563999 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. [Progress in genetic susceptibility to aminoglycoside-induced deafness]. Tian Y; Chen Z Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2021 Apr; 35(4):375-379. PubMed ID: 33794642 [No Abstract] [Full Text] [Related]
10. Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity. Pandya A; Xia X; Radnaabazar J; Batsuuri J; Dangaansuren B; Fischel-Ghodsian N; Nance WE J Med Genet; 1997 Feb; 34(2):169-72. PubMed ID: 9039999 [TBL] [Abstract][Full Text] [Related]
11. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Prezant TR; Agapian JV; Bohlman MC; Bu X; Oztas S; Qiu WQ; Arnos KS; Cortopassi GA; Jaber L; Rotter JI Nat Genet; 1993 Jul; 4(3):289-94. PubMed ID: 7689389 [TBL] [Abstract][Full Text] [Related]
12. Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness. Bacino C; Prezant TR; Bu X; Fournier P; Fischel-Ghodsian N Pharmacogenetics; 1995 Jun; 5(3):165-72. PubMed ID: 7550368 [TBL] [Abstract][Full Text] [Related]
13. Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk? Tang HY; Hutcheson E; Neill S; Drummond-Borg M; Speer M; Alford RL Genet Med; 2002; 4(5):336-45. PubMed ID: 12394346 [TBL] [Abstract][Full Text] [Related]
14. Interaction of aminoglycosides with human mitochondrial 12S rRNA carrying the deafness-associated mutation. Qian Y; Guan MX Antimicrob Agents Chemother; 2009 Nov; 53(11):4612-8. PubMed ID: 19687236 [TBL] [Abstract][Full Text] [Related]
15. [The relation between mitochondrial DNA mutation and aminogly- coside antibiotics-induced deafness]. Zhang L; Lu M; Huang Y; Zhou X; Qiu D; Wang W Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Jun; 16(3):138-40. PubMed ID: 10359860 [TBL] [Abstract][Full Text] [Related]
19. Familial streptomycin ototoxicity in a South African family: a mitochondrial disorder. Gardner JC; Goliath R; Viljoen D; Sellars S; Cortopassi G; Hutchin T; Greenberg J; Beighton P J Med Genet; 1997 Nov; 34(11):904-6. PubMed ID: 9391883 [TBL] [Abstract][Full Text] [Related]
20. Aminoglycoside-associated nonsyndromic deafness and speech disorder in mitochondrial A1555G mutation in a family: A case report. Ou YH; Chen AW; Fan JY; Cheng WL; Lin TT; Chen MK; Liu CS Medicine (Baltimore); 2018 Oct; 97(42):e12878. PubMed ID: 30335006 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]