288 related articles for article (PubMed ID: 34032273)
1. Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT-RNR1 Genotype.
McDermott JH; Wolf J; Hoshitsuki K; Huddart R; Caudle KE; Whirl-Carrillo M; Steyger PS; Smith RJH; Cody N; Rodriguez-Antona C; Klein TE; Newman WG
Clin Pharmacol Ther; 2022 Feb; 111(2):366-372. PubMed ID: 34032273
[TBL] [Abstract][Full Text] [Related]
2. Clinical Pharmacogenomic MT-RNR1 Screening for Aminoglycoside-Induced Ototoxicity and the Post-Test Counseling Conundrum.
Rigobello R; Shaw J; Ilg D; Zimmerman R; Edelmann L; Kornreich R; Scott SA; Cody N
Clin Pharmacol Ther; 2023 Aug; 114(2):262-265. PubMed ID: 37314952
[TBL] [Abstract][Full Text] [Related]
3. [Pharmacogenetics of aminoglycoside ototoxicity: State of knowledge and practices - Recommendations of the Francophone Network of Pharmacogenetics (RNPGx)].
Lebreton L; Hennart B; Baklouti S; Trimouille A; Boyer JC; Becquemont L; Dhaenens CM; Picard N
Therapie; 2024 Jun; ():. PubMed ID: 38876950
[TBL] [Abstract][Full Text] [Related]
4. Pharmacogenetics of aminoglycoside-related ototoxicity: a systematic review.
Gaafar D; Baxter N; Cranswick N; Christodoulou J; Gwee A
J Antimicrob Chemother; 2024 Jul; 79(7):1508-1528. PubMed ID: 38629462
[TBL] [Abstract][Full Text] [Related]
5. The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence.
Igumnova V; Veidemane L; Vīksna A; Capligina V; Zole E; Ranka R
J Hum Genet; 2019 Mar; 64(3):199-206. PubMed ID: 30523288
[TBL] [Abstract][Full Text] [Related]
6. The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population.
Ealy M; Lynch KA; Meyer NC; Smith RJ
Laryngoscope; 2011 Jun; 121(6):1184-6. PubMed ID: 21495045
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Audiologic testing and molecular analysis of 12S rRNA in patients receiving aminoglycosides.
Gürtler N; Schmuziger N; Kim Y; Mhatre AN; Jungi M; Lalwani AK
Laryngoscope; 2005 Apr; 115(4):640-4. PubMed ID: 15805873
[TBL] [Abstract][Full Text] [Related]
9. Allele-specific PCR for detecting the deafness-associated mitochondrial 12S rRNA mutations.
Ding Y; Xia BH; Liu Q; Li MY; Huang SX; Zhuo GC
Gene; 2016 Oct; 591(1):148-152. PubMed ID: 27397648
[TBL] [Abstract][Full Text] [Related]
10. Increased risk of hearing loss associated with MT-RNR1 gene mutations: a real-world investigation among Han Taiwanese Population.
Chen HK; Hsieh YW; Hsu HY; Liu TY; Zhang YT; Lin CD; Tsai FJ
BMC Med Genomics; 2024 Jun; 17(1):155. PubMed ID: 38840095
[TBL] [Abstract][Full Text] [Related]
11. [Mitochondrial DNA mutations and aminoglycoside antibiotics and hearing loss].
Qu J; Wang J; Xu S
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 29(22):1936-40. PubMed ID: 26911053
[TBL] [Abstract][Full Text] [Related]
12. Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families.
Wei Q; Xu D; Chen Z; Li H; Lu Y; Liu C; Bu X; Xing G; Cao X
Int J Audiol; 2013 Feb; 52(2):98-103. PubMed ID: 23237192
[TBL] [Abstract][Full Text] [Related]
13. C1494T mitochondrial DNA mutation, hearing loss, and aminoglycosides antibiotics.
Postal M; Palodeto B; Sartorato EL; Oliveira CA
Braz J Otorhinolaryngol; 2009; 75(6):884-7. PubMed ID: 20209292
[TBL] [Abstract][Full Text] [Related]
14. Rapid Point-of-Care Genotyping to Avoid Aminoglycoside-Induced Ototoxicity in Neonatal Intensive Care.
McDermott JH; Mahaveer A; James RA; Booth N; Turner M; Harvey KE; Miele G; Beaman GM; Stoddard DC; Tricker K; Corry RJ; Garlick J; Ainsworth S; Beevers T; Bruce IA; Body R; Ulph F; MacLeod R; Roberts PL; Wilson PM; Newman WG;
JAMA Pediatr; 2022 May; 176(5):486-492. PubMed ID: 35311942
[TBL] [Abstract][Full Text] [Related]
15. Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C->T mutation in the mitochondrial 12S rRNA gene.
Rodríguez-Ballesteros M; Olarte M; Aguirre LA; Galán F; Galán R; Vallejo LA; Navas C; Villamar M; Moreno-Pelayo MA; Moreno F; del Castillo I
J Med Genet; 2006 Nov; 43(11):e54. PubMed ID: 17085680
[TBL] [Abstract][Full Text] [Related]
16. A mutation in mitochondrial 12S rRNA, A827G, in Argentinean family with hearing loss after aminoglycoside treatment.
Chaig MR; Zernotti ME; Soria NW; Romero OF; Romero MF; Gerez NM
Biochem Biophys Res Commun; 2008 Apr; 368(3):631-6. PubMed ID: 18261986
[TBL] [Abstract][Full Text] [Related]
17. 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
J Transl Med; 2011 Jan; 9():4. PubMed ID: 21205314
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity.
Guan MX
Mitochondrion; 2011 Mar; 11(2):237-45. PubMed ID: 21047563
[TBL] [Abstract][Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]