Value of systematic aetiological investigation in children with sensorineural hearing loss-Reference-Cited by-同舟云学术

Value of systematic aetiological investigation in children with sensorineural hearing loss

Published:2012-08 Issue:4 Volume:129 Page:185-189
ISSN:1879-7296
Container-title:European Annals of Otorhinolaryngology, Head and Neck Diseases
language:en
Short-container-title:European Annals of Otorhinolaryngology, Head and Neck Diseases

Author:

Elziere M.,Roman S.,Nicollas R.,Triglia J.-M.

Publisher

Elsevier BV

Subject

Otorhinolaryngology,Surgery

Reference17 articles.

1. The false-positive in universal newborn hearing screening;Clemens;Pediatrics,2000

2. American Academy of Pediatrics, Joint Committee on Infant Hearing. Year 2007 Position Statement: principles and guidelines for early hearing detection and intervention programs. Pediatrics 2007;120(4):898–921.

3. Treatment of symptomatic congenital cytomegalovirus infection with intravenous ganciclovir followed by long-term oral valganciclovir;Amir;Eur J Pediatr,2010

4. British Association of Audiovestibular Physicians and British Association of Paediatricians in Audiology. Aetiological investigation into severe to profound permanent hearing loss in children; October 2008. http://www.baap.org.uk/docs/Severe%20to%20Profound%20Permanent%20Hearing%20Loss%20in%20Children%20Aetiological%20Investigation%20BAAP%20BAPA%20Guideline%202008.pdf.

5. Audit of local performance compared with standards recommended by the national guidelines for aetiologic investigation of permanent childhood hearing impairment;Yoong;Child: Care Dev,2005

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3. Bilateral congenital deafness: What investigations should be performed?;Swiss Medical Weekly;2017-03-03

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