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Usher’s Syndrome

  • Published:2015-09 Issue:8 Volume:36 Page:1421-1427
  • ISSN:1531-7129
  • Container-title:Otology & Neurotology
  • language:en
  • Short-container-title:

Author:

Magliulo Giuseppe,Iannella Giannicola,Gagliardi Silvia,Iozzo Nicola,Plateroti Rocco,Plateroti Pasquale,Re Massimo,Vingolo Enzo Maria

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Sensory Systems,Otorhinolaryngology

Reference33 articles.

1. Histopathologic features of the temporal bone in usher syndrome type I.;Wagenaar;Arch Otolaryngol Head Neck Surg,2000

2. On the inheritance of retinitis pigmentosa, with notes of cases.;Usher;R Lond Ophthalmol Hosp Rep,1916

3. Variable clinical features in patients with CDH23 mutations (USH1D-DFNB12).;Pennings;Otol Neurotol,2004

4. Usher syndrome: hearing loss, retinal degeneration and associated abnormalities.;Mathur;Biochim Biophys Acta,2015

5. Recent advances in the understanding of syndromic forms of hearing loss.;Friedman;Ear Hear,2003
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