(Q35027846)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12487079%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

review article

1 reference

title

Medical evaluation of pediatric hearing loss. Laboratory, radiographic, and genetic testing (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12487079%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12487079%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

author name string

Stephen W Hone

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12487079%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

publication date

1 August 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12487079%20AND%20SRC:MED&resulttype=core&format=json

Otolaryngologic Clinics of North America

15 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12487079%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

volume

35

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12487079%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12487079%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

page(s)

751-764

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12487079%20AND%20SRC:MED&resulttype=core&format=json

Universal infant hearing screening by automated auditory brainstem response measurement

15 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Aetiology of bilateral sensorineural hearing impairment in children: a 10 year study

7 January 2021

1 reference

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Absence of Sensorineural Hearing Loss in Treated Infants and Children with Congenital Toxoplasmosis

7 January 2021

1 reference

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Subclinical Maternal Rubella and Congenital Deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Cytomegalovirus urinary excretion and long term outcome in children with congenital cytomegalovirus infection. Congenital CMV Longitudinal Study Group.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Ganciclovir treatment of symptomatic congenital cytomegalovirus infection: results of a phase II study. National Institute of Allergy and Infectious Diseases Collaborative Antiviral Study Group

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Hearing loss and herpes simplex.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Risk factors for childhood sensorineural hearing loss in the Oxford region.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Aetiological investigations of hearing loss in childhood: a review

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

The epidemiology of childhood hearing impairment: factor relevant to planning of services

7 January 2021

1 reference

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Dexamethasone as adjunctive therapy in bacterial meningitis. A meta-analysis of randomized clinical trials since 1988

7 January 2021

1 reference

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Prevalence of sensorineural hearing loss in Asian children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Visual impairment in severe and profound sensorineural deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

A stepwise approach to the diagnosis and treatment of hereditary hearing loss

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Mild impairment of neuro-otological function in early treated congenital hypothyroidism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

The Pendred syndrome gene encodes a chloride-iodide transport protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Pendred syndrome--100 years of underascertainment?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Otologic and laryngologic manifestations of mucopolysaccharidoses after bone marrow transplantation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Progressive sensorineural hearing loss in association with distal renal tubular acidosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Low penetrance in the long-QT syndrome: clinical impact

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Value of CT scan in the diagnosis of temporal bone diseases in children.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Temporal bone computed tomography findings in bilateral sensorineural hearing loss

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Usefulness of computed tomographic scan in the evaluation of sensorineural hearing loss in children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Clinical course of pediatric congenital inner ear malformations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Diagnostic yield of high-resolution computed tomography for pediatric sensorineural hearing loss

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Radiological malformations of the ear in Pendred syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Phenotypic manifestations of branchio-oto-renal syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Ear-nose-throat abnormalities in the CHARGE association.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Cochlear implant failure due to unexpected absence of the eighth nerve--a cautionary tale.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Connexin-26 mutations in sporadic non-syndromal sensorineural deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Connexin 26 studies in patients with sensorineural hearing loss.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Prevalent connexin 26 gene (GJB2) mutations in Japanese

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

Otological manifestations of thalassaemia intermedia: evidence of temporal bone involvement and report of a unique cholesteatoma-like lesion

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2802%2900048-8

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0030-6665(02)00048-8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12487079%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

1 reference