Accurate consent for insertion and later removal of grommets (Q44068983)

29 November 2017

Accurate consent for insertion and later removal of grommets (English)

1 reference

29 November 2017

0 references

Sood S

1

1 reference

PubMed ID

17403263

29 November 2017

Waddell A

series ordinal

2

1 reference

29 November 2017

1 April 2007

1 reference

Journal of Laryngology and Otology

29 November 2017

1 reference

29 November 2017

121

1 reference

29 November 2017

4

1 reference

29 November 2017

338-340

1 reference

Cochlear implantation in maternal inherited diabetes and deafness syndrome.

29 November 2017

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

Cochlear implantation of a patient with a previously undescribed mitochondrial DNA defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

Cochlear implantation in a profoundly deaf patient with MELAS syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

Maternally inherited diabetes and deafness: a multicenter study

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

Hearing impairment in patients with 3243A-->G mtDNA mutation: phenotype and rate of progression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

Cochlear histopathology associated with mitochondrial transfer RNA(Leu(UUR)) gene mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

Bilateral sensorineural hearing loss associated with the point mutation in mitochondrial genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

Auditory findings in patients with maternally inherited diabetes and deafness harboring a point mutation in the mitochondrial transfer RNA(Leu) (UUR) gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

Prevalence of mitochondrial gene mutations among hearing impaired patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

Measuring patient benefit from otorhinolaryngological surgery and therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

A 3-year clinical follow-up of adult patients with 3243A>G in mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

inferred from DOI database lookup

7 January 2021

based on heuristic

A molecular and cellular hypothesis for aminoglycoside-induced deafness

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

inferred from DOI database lookup

7 January 2021

based on heuristic

Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001508

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1017/S0022215107001508

1 reference

29 November 2017

1 reference

PubMed ID

17403263