Alport's syndrome: can carriers be identified by audiometry?
Author:
Publisher
Wiley
Subject
Otorhinolaryngology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2273.1995.tb00035.x/fullpdf
Reference20 articles.
1. HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS
2. ALPORT'S SYNDROME OF HEREDITARY NEPHRITIS WITH DEAFNESS
3. 3C.L. Atkin, M.C. Gregory, W.A. Border, R.W. Schrier, and Gottschalk (1988 ) In Diseases of the Kidney , 4th Ed , Little Brown, Boston, pp617 -641 .
4. GENETICS OF CLASSIC ALPORT'S SYNDROME
5. OUTCOME OF THIRTY PATIENTS WITH ALPORTʼS SYNDROME AFTER RENAL TRANSPLANTATION
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1. Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss;Scientific Reports;2021-11-18
2. Severe to profound hearing loss in patients with progressed Alport's syndrome;Acta Oto-Laryngologica;2009-01
3. Revisão sobre a perda auditiva na Síndrome de Alport, analisando os aspectos clínicos, genéticos e biomoleculares;Revista Brasileira de Otorrinolaringologia;2005-12
4. Revision about hearing loss in the Alport's syndrome, analyzing the clinical, genetic and bio-molecular aspects;Brazilian Journal of Otorhinolaryngology;2005-11
5. The Audioscan: a high frequency resolution audiometric technique and its clinical applications;Clinical Otolaryngology and Allied Sciences;2002-01
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