(Q28255026)

25 June 2017

OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation (English)

1 reference

25 June 2017

1 reference

Elona Cama

4

0 references

Pietro Scimemi

Pietro Scimemi

3

0 references

Chiara La Morgia

Chiara La Morgia

6

0 references

Leonardo Caporali

Leonardo Caporali

7

0 references

Maria Lucia Valentino

Maria Lucia Valentino

5

0 references

Rocco Liguori

Rocco Liguori

8

0 references

Valerio Carelli

Valerio Carelli

13

0 references

author name string

Rosamaria Santarelli

1

1 reference

25 June 2017

Roberta Rossi

2

1 reference

25 June 2017

Vincenzo Magnavita

9

1 reference

25 June 2017

Anna Monteleone

10

1 reference

25 June 2017

Ariella Biscaro

11

1 reference

25 June 2017

Edoardo Arslan

12

1 reference

25 June 2017

language of work or name

English

0 references

publication date

5 January 2015

1 reference

25 June 2017

1 reference

25 June 2017

138

1 reference

25 June 2017

Pt 3

1 reference

25 June 2017

563-576

1 reference

Multi-system neurological disease is common in patients with OPA1 mutations

25 June 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

Mitochondrial dynamics and disease, OPA1

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

Mitochondrial dysfunction as a cause of optic neuropathies

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

Infantile optic atrophy with dominant mode of inheritance: a clinical and genetic study of 19 Danish families

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

Information from cochlear potentials and genetic mutations helps localize the lesion site in auditory neuropathy

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

Perceptual consequences of disrupted auditory nerve activity.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

An Introduction to the Genetics of Normal and Defective Hearing

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

OPA1, the disease gene for optic atrophy type Kjer, is expressed in the inner ear.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

A comparison of extratympanic versus transtympanic recordings in electrocochleography.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

Are inner or outer hair cells the source of summating potentials recorded from the round window?

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

Dominant optic nerve atrophy with progressive hearing loss and chronic progressive external ophthalmoplegia (CPEO).

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

Maturation of the traveling-wave delay in the human cochlea

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

Auditory brainstem recovery processes from birth to adulthood

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

OPA1 R445H mutation in optic atrophy associated with sensorineural deafness.

2 June 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Neurophysiology of cochlear implant users I: effects of stimulus current level and electrode site on the electrical ABR, MLR, and N1-P2 response.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Vestibular neuropathy accompanying auditory and peripheral neuropathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Mutation of OPA1 gene causes deafness by affecting function of auditory nerve terminals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Sustained depression of brainstem auditory electrophysiology during the first months in term infants after perinatal asphyxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Absent auditory brain stem response: peripheral hearing loss or brain stem dysfunction?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Sensorineural hearing loss in OPA1-linked disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Frequency-specific electrocochleography indicates that presynaptic and postsynaptic mechanisms of auditory neuropathy exist.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Intracochlear and extracochlear ECAPs suggest antidromic action potentials.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Vestibular dysfunction in a Japanese patient with a mutation in the gene OPA1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Electrocochleography in auditory neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Neural and receptor cochlear potentials obtained by transtympanic electrocochleography in auditory neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Involvement of peripheral vestibular nerve in individuals with auditory neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Opa1 deficiency in a mouse model of dominant optic atrophy leads to retinal ganglion cell dendropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

Reply: Sensorineural hearing loss in OPA1-linked disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU378

[Statistical study of the phonetic composition of the Italian language and its practical application to audiometry of words.]

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

Application of maximum length sequence analysis to auditory brainstem response testing of premature newborns.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4339771

Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy

27 November 2018

1 reference

12 December 2020

Depressed brainstem auditory function in children with cerebral palsy

1 reference

12 December 2020

Cochlear implantation in cochlear otosclerosis

1 reference

12 December 2020

Action Potentials and Summating Potentials in the Normal Human Cochlea

1 reference

12 December 2020

Identifiers

DOI

10.1093/BRAIN/AWU378

1 reference

OpenCitations bibliographic resource ID

25 June 2017

5051291

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference