Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk? (Q46500420)

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scientific article published in September 2002

Language	Label	Description	Also known as
English	Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk?	scientific article published in September 2002

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

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

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

1 reference

based on heuristic

inferred from title

author name string

Hsiao-Yuan Tang

1

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

Eldridge Hutcheson

2

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

Susan Neill

3

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

Margaret Drummond-Borg

4

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

Michael Speer

5

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

Raye Lynn Alford

6

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

language of work or name

0 references

publication date

1 September 2002

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

Genetics in Medicine

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

4

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

5

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

336-345

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

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

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

Familial streptomycin ototoxicity in a South African family: a mitochondrial disorder

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

Prevalence of mitochondrial gene mutations among hearing impaired patients

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafness

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

Human mtDNA haplogroups associated with high or reduced spermatozoa motility

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

Mitochondrial DNA and human evolution

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

U.S. newborn screening policy dilemmas for the twenty-first century

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

21 January 2018

Identifiers

10.1097/00125817-200209000-00004

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/12394346

ResearchGate publication ID

0 references

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