(Q34538375)

2 August 2017

Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants (English)

1 reference

2 August 2017

0 references

0 references

Ursula Felderhoff-Müser

6

Ursula Felderhoff-Müser

1 reference

2 August 2017

German Neonatal Network

11

German Neonatal Network

0 references

Michael Preuss

Michael Preuss

3

0 references

Andreas Ziegler

Andreas Ziegler

4

0 references

Wolfgang Göpel

1

Wolfgang Göpel

1 reference

2 August 2017

8

Michael Mögel

1 reference

2 August 2017

10

Egbert Herting

1 reference

2 August 2017

9

Christoph Härtel

1 reference

2 August 2017

German Neonatal Network

11

German Neonatal Network

1 reference

2 August 2017

5

Helmut Küster

1 reference

2 August 2017

Sandra Berkowski

2

1 reference

2 August 2017

Ludwig Gortner

7

1 reference

2 August 2017

26 August 2014

1 reference

2 August 2017

1 reference

2 August 2017

14

1 reference

2 August 2017

210

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2431-14-210

2 August 2017

0 references

cites work

The future role of genetic screening to detect newborns at risk of childhood-onset hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4236616

Antibiotic use and misuse in the neonatal intensive care unit

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4236616

Hearing in 44-45 year olds with m.1555A>G, a genetic mutation predisposing to aminoglycoside-induced deafness: a population based cohort study

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4236616

Are gentamicin and/or vancomycin associated with ototoxicity in the neonate? A retrospective audit.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4236616

Hearing loss in children with very low birth weight: current review of epidemiology and pathophysiology

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4236616

Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4236616

Low prevalence of hearing impairment among very low birthweight infants as detected by universal neonatal hearing screening

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4236616

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4236616

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4236616

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4236616

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

7 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2431-14-210

Empiric use of ampicillin and cefotaxime, compared with ampicillin and gentamicin, for neonates at risk for sepsis is associated with an increased risk of neonatal death

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2431-14-210

The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2431-14-210

Genetic mutations and aminoglycoside-induced ototoxicity in neonates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2431-14-210

Prevalence of Mitochondrial 1555A→G Mutation in European Children

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25155176

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Audiological follow-up of children with the m.1555A>G mutation in mitochondrial DNA

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25155176

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2431-14-210

1 reference

Dimensions Publication ID

2 August 2017

0 references

1 reference

2 August 2017

1 reference