(Q46171060)

20 December 2017

title

Aminoglycoside ototoxicity in Nicaraguan children: patient risk factors and mitochondrial DNA results (English)

1 reference

20 December 2017

0 references

0 references

1 reference

James E Saunders

1

1 reference

20 December 2017

John H Greinwald

series ordinal

2

1 reference

20 December 2017

Sharon Vaz

series ordinal

3

1 reference

20 December 2017

Yinshi Guo

series ordinal

4

1 reference

20 December 2017

publication date

1 January 2009

1 reference

20 December 2017

Otolaryngology—Head and Neck Surgery

published in

1 reference

20 December 2017

volume

140

1 reference

20 December 2017

issue

1

1 reference

20 December 2017

page(s)

103-107

1 reference

20 December 2017

Systematic review of the etiology of bilateral sensorineural hearing loss in children.

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk?

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

Deafness due to A1555G mitochondrial mutation without use of aminoglycoside

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

Prevalence and etiology of hearing loss in rural Nicaraguan children

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

Risk factors for the development of auditory toxicity in patients receiving aminoglycosides.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.OTOHNS.2008.09.027

10.1016/J.OTOHNS.2008.09.027

21 January 2018

Identifiers

DOI

1 reference

20 December 2017

1 reference

20 December 2017