Vestibular Nerve Compression in Camurati-Engelmann Disease
Author:
Affiliation:
1. Adrian, Michigan
2. London, Canada
Publisher
SAGE Publications
Subject
General Medicine,Otorhinolaryngology
Link
http://journals.sagepub.com/doi/pdf/10.1177/000348949510401013
Reference13 articles.
1. Engelmann's Disease
2. Camurati-Engelmann disease (progressive hereditary craniodiaphyseal dysplasia)
3. Ocular Findings in Hereditary Diaphyseal Dysplasia
4. Facial-skeletal manifestations of Engelmann's disease
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1. A family with Camurati-Engelman disease: the role of the missense p.R218C mutation in TGFbeta1 in bones and endocrine glands;Journal of Pediatric Endocrinology and Metabolism;2013-01-01
2. A family with Camurati-Engelman disease. The role of the missense p.R218C mutation in TGFB1 in bones and endocrine glands;Journal of Pediatric Endocrinology and Metabolism;2013-01-01
3. Camurati-engelmann disease: Unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand;Journal of Bone and Mineral Research;2011-05
4. Comparative Case Series of Exostoses and Osteomas of the Internal Auditory Canal;Annals of Otology, Rhinology & Laryngology;2011-04
5. Skull Base Manifestations of Camurati-Engelmann Disease;Archives of Otolaryngology–Head & Neck Surgery;2010-06-21
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