Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Endosteal thickening"'
Autor:
Richard M. Dell, Erin S. LeBlanc, David L. Boardman, Dennis M. Black, A. G. Rosales, Arthur C. Santora, Harry K. Genant, A. E. de Papp, Douglas C. Bauer, Eric S. Orwoll, Darin Friess
Publikováno v:
Osteoporosis International. 30:1287-1295
The paper focuses on the identification of atypical fractures (AFFs). This paper examines the concordance between objective classification and expert subjective review. We believe the paper adds critical information about how to apply the American So
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7ff7e24b213ba0ec26effd41aa56779
https://doi.org/10.1007/s00198-019-04869-z
https://doi.org/10.1007/s00198-019-04869-z
Publikováno v:
European Radiology. 23:222-227
To describe the characteristics of multifocal endosteal thickening in patients on bisphosphonate therapy.A retrospective study of 68 patients with atypical femoral fractures (as defined by ASBMR) whilst on bisphosphonate therapy was performed. Femora
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9cf0f105810d5c914385d9b69e8c1d7
https://doi.org/10.1007/s00330-012-2587-y
https://doi.org/10.1007/s00330-012-2587-y
Publikováno v:
Clinical nuclear medicine. 38(5)
A 69-year-old woman presented with a spontaneous right subtrochanteric hip fracture. Pan-imaging following orthopedic repair failed to identify a primary malignancy to explain the presumed pathologic basis for this fracture. The patient then underwen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c14fb7837780e3a62a502ac7bac50f49
https://pubmed.ncbi.nlm.nih.gov/23478849
https://pubmed.ncbi.nlm.nih.gov/23478849
Publikováno v:
Journal of Clinical Medicine Research
We report on a 5-year-old girl who presented with the full clinical criteria of Hallermann-Streiff syndrome (HSS). Classically, overtubulation (thin and gracile) bones are the characteristic and constant features in HSS. Interestingly, our present pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d67047a9ff195a6b64315f7da5c416df
https://doi.org/10.4021/jocmr704e
https://doi.org/10.4021/jocmr704e
Akademický článek
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Akademický článek
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Publikováno v:
Radiology. 164(3)
Sixteen patients with progressive diaphyseal dysplasia (PDD) and aged six months to 76 years were examined. Fourteen cases were hereditary, two were not. The progression of the radiologic manifestations in 13 patients who were followed up from 1 to 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e6857fa02225a728edc895866c8c954
https://pubmed.ncbi.nlm.nih.gov/3615880
https://pubmed.ncbi.nlm.nih.gov/3615880