共 14 条
Ototoxicity caused by aminoglycosides
被引:41
作者:

Bitner-Glindzicz, Maria
论文数: 0 引用数: 0
h-index: 0
机构:
UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England

Rahman, Shamima
论文数: 0 引用数: 0
h-index: 0
机构:
UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
机构:
[1] UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
来源:
BMJ-BRITISH MEDICAL JOURNAL
|
2007年
/
335卷
/
7624期
关键词:
D O I:
10.1136/bmj.39301.680266.AE
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
引用
收藏
页码:784 / 785
页数:2
相关论文
共 14 条
[11]
Genetic susceptibility to aminoglycoside ototoxicity: How many are at risk?
[J].
Tang, HY
;
Hutcheson, E
;
Neill, S
;
Drummond-Borg, M
;
Speer, M
;
Alford, RL
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GENETICS IN MEDICINE,
2002, 4 (05)
:336-345

Tang, HY
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Bobby R Alford Dept Otorhinolaryngol & Communica, Houston, TX 77030 USA

Hutcheson, E
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Bobby R Alford Dept Otorhinolaryngol & Communica, Houston, TX 77030 USA

Neill, S
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Bobby R Alford Dept Otorhinolaryngol & Communica, Houston, TX 77030 USA

Drummond-Borg, M
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Bobby R Alford Dept Otorhinolaryngol & Communica, Houston, TX 77030 USA

Speer, M
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Bobby R Alford Dept Otorhinolaryngol & Communica, Houston, TX 77030 USA

Alford, RL
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Bobby R Alford Dept Otorhinolaryngol & Communica, Houston, TX 77030 USA
[12]
Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation
[J].
Tang, Xiaowen
;
Yang, Li
;
Zhu, Yi
;
Liao, Zhisu
;
Wang, Jindan
;
Qian, Yaping
;
Tao, Zhihua
;
Hue, Lenong
;
Wu, Guomin
;
Lan, Jinshan
;
Wang, Xinjian
;
Ji, Jingzhang
;
Wu, Jian
;
Ji, Yu
;
Feng, Jinbao
;
Chen, Jianfu
;
Li, Zhiyuan
;
Zhang, Xue
;
Lu, Jianxin
;
Guan, Min-Xin
.
GENE,
2007, 393 (1-2)
:11-19

Tang, Xiaowen
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Yang, Li
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Zhu, Yi
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Liao, Zhisu
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Wang, Jindan
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Qian, Yaping
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Tao, Zhihua
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Hue, Lenong
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Wu, Guomin
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Lan, Jinshan
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Wang, Xinjian
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Ji, Jingzhang
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Wu, Jian
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Ji, Yu
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Feng, Jinbao
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Chen, Jianfu
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Li, Zhiyuan
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Zhang, Xue
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Lu, Jianxin
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA

Guan, Min-Xin
论文数: 0 引用数: 0
h-index: 0
机构: Childrens Hosp, Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA
[13]
Prevalence of mitochondrial gene mutations among hearing impaired patients
[J].
Usami, S
;
Abe, S
;
Akita, J
;
Namba, A
;
Shinkawa, H
;
Ishii, M
;
Iwasaki, S
;
Hoshino, T
;
Ito, J
;
Doi, K
;
Kubo, T
;
Nakagawa, T
;
Komiyama, S
;
Tono, T
;
Komune, S
.
JOURNAL OF MEDICAL GENETICS,
2000, 37 (01)
:38-40

Usami, S
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Abe, S
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Akita, J
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Namba, A
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Shinkawa, H
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Ishii, M
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Iwasaki, S
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Hoshino, T
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Ito, J
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Doi, K
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Kubo, T
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Nakagawa, T
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Komiyama, S
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Tono, T
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan

Komune, S
论文数: 0 引用数: 0
h-index: 0
机构: Miyazaki Med Coll, Dept Otorhinolaryngol, Miyazaki 88916, Japan
[14]
Sensorineural hearing loss caused by mitochondrial DNA mutations: Special reference to the A1555G mutation
[J].
Usami, SI
;
Abe, S
;
Shinkawa, H
;
Kimberling, WJ
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JOURNAL OF COMMUNICATION DISORDERS,
1998, 31 (05)
:423-435

Usami, SI
论文数: 0 引用数: 0
h-index: 0
机构: Hirosaki Univ, Sch Med, Dept Otorhinolaryngol, Hirosaki, Aomori 0368562, Japan

Abe, S
论文数: 0 引用数: 0
h-index: 0
机构: Hirosaki Univ, Sch Med, Dept Otorhinolaryngol, Hirosaki, Aomori 0368562, Japan

Shinkawa, H
论文数: 0 引用数: 0
h-index: 0
机构: Hirosaki Univ, Sch Med, Dept Otorhinolaryngol, Hirosaki, Aomori 0368562, Japan

Kimberling, WJ
论文数: 0 引用数: 0
h-index: 0
机构: Hirosaki Univ, Sch Med, Dept Otorhinolaryngol, Hirosaki, Aomori 0368562, Japan