111 related articles for article (PubMed ID: 20172897)
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
Arch Dis Child; 2010 Feb; 95(2):153-5. PubMed ID: 20172897
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. [Screening for mitochondrial 1555(G) mutation in patients with aminoglycoside antibiotic-induced deafness].
Yuan H; Jiang S; Yang W; Guo W; Cao J; Dai P
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Jun; 16(3):141-4. PubMed ID: 10359861
[TBL] [Abstract][Full Text] [Related]
4. [Screening for the 1555G mutation in mitochondrial DNA in pedigrees with aminoglycoside antibiotic induced deafness].
Yuan H; Jiang S; Yang W
Zhonghua Er Bi Yan Hou Ke Za Zhi; 1998 Apr; 33(2):67-70. PubMed ID: 11498854
[TBL] [Abstract][Full Text] [Related]
5. 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]
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. [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]
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. [Determination of the point of gene mutation in two types of tissue from the aminoglycoside antibiotics induced deaf patients].
Xu L; Chen W; Xing C
Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2001 Apr; 15(4):149-51. PubMed ID: 12541634
[TBL] [Abstract][Full Text] [Related]
10. Different clinical characteristics of aminoglycoside-induced profound deafness with and without the 1555 A-->G mitochondrial mutation.
Tono T; Kiyomizu K; Matsuda K; Komune S; Usami S; Abe S; Shinkawa H
ORL J Otorhinolaryngol Relat Spec; 2001; 63(1):25-30. PubMed ID: 11174059
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness.
Hamasaki K; Rando RR
Biochemistry; 1997 Oct; 36(40):12323-8. PubMed ID: 9315872
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [Pathogenetic heterogenicity of ototoxic complications caused by aminoglycoside antibiotics].
Zhuravskiĭ SG; Setkhiiaasiilan T; Dekhtiareva IuA
Vestn Otorinolaringol; 2005; (1):62-5. PubMed ID: 15700018
[No Abstract] [Full Text] [Related]
15. Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G.
Shohat M; Fischel-Ghodsian N; Legum C; Halpern GJ
Am J Otolaryngol; 1999; 20(1):64-7. PubMed ID: 9950117
[No Abstract] [Full Text] [Related]
16. 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]
17. Sequence analysis of the mitochondrial genome from a large family with maternally inherited nonsyndromic deafness.
Zhang HJ; Xu CH; Zhan YJ; Zhao SY; Shan YF; Geng XX; Shan XN
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):368-71. PubMed ID: 16086269
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.
Wu CC; Chiu YH; Chen PJ; Hsu CJ
Ear Hear; 2007 Jun; 28(3):332-42. PubMed ID: 17485982
[TBL] [Abstract][Full Text] [Related]
20. Prevalence of mitochondrial 1555A-->G mutation in European children.
Bitner-Glindzicz M; Pembrey M; Duncan A; Heron J; Ring SM; Hall A; Rahman S
N Engl J Med; 2009 Feb; 360(6):640-2. PubMed ID: 19196684
[No Abstract] [Full Text] [Related]
[Next] [New Search]
