Camurati-Engelmann Disease. Review of radioclinical features-Reference-Cited by-同舟云学术

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Camurati-Engelmann Disease. Review of radioclinical features

Published:2003-07 Issue:4 Volume:44 Page:430-434
ISSN:0284-1851
Container-title:Acta Radiologica
language:en
Short-container-title:Acta Radiologica

Author:

Vanhoenacker F. M.,Janssens K.,Van Hul W.,Gershoni-Baruch R.,Brik R.,De Schepper A. M.

Publisher

SAGE Publications

Subject

Radiology Nuclear Medicine and imaging,General Medicine,Radiological and Ultrasound Technology

Link

http://journals.sagepub.com/doi/pdf/10.1034/j.1600-0455.2003.00088.x

Reference8 articles.

1. Genetic Mapping of the Camurati-Engelmann Disease Locus to Chromosome 19q13.1-q13.3

2. Sclerosing bone dysplasias ? a target-site approach

3. Mutations in the gene encoding the latency-associated peptide of TGF-β1 cause Camurati-Engelmann disease

4. Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13

5. Progressive diaphyseal dysplasia (Camurati-Engelmann): radiographic follow-up and CT findings.

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1. Anterior Total Hip Arthroplasty With Bulk Femoral Head Autograft in a Patient With Camurati-Engelmann Disease;Arthroplasty Today;2021-04

2. Osteopetrosis, a potential mimicker of sclerotic metastatic bone lesions in breast cancer;Current Problems in Cancer: Case Reports;2021-03

3. A new LRP6 variant and Camurati-Engelmann-like disease;Bone;2021-02

4. Van Buchem Disease: First Case Report from the Indian Subcontinent with an Early Presentation;Journal of Child Science;2021-01

5. A patient with Camurati-Engelmann disease presenting bilateral TMJ ankylosis: A case report;International Journal of Surgery Case Reports;2020

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