Camurati–Engelmann disease: imaging, clinical features and differential diagnosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Radiology Nuclear Medicine and imaging
Link
http://link.springer.com/content/pdf/10.1007/s00256-008-0642-1.pdf
Reference30 articles.
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2. Greenfield GB. Radiology of bone diseases, (fourth edition). Philadelphia: Lippincott; 1986.
3. Vanhoenacker FM, De Beuckeleer LH, Van Hul W, et al. Sclerosing bone dysplasias: genetic and radioclinical features. Eur Radiol. 2000; 10: 1423–1433.
4. Janssens K, Gershoni-Baruch R, Van Hul E, et al. Localisation of the gene causing diaphyseal dysplasia Camurati–Engelmann to chromosome 19q13. J Med Genet. 2000; 37: 245–249.
5. Janssens K, Vanhoenacker F, Bonduelle M, et al. Camurati–Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment. J Med Genet. 2006; 43: 1–11.
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