scholarly journals Use of Denosumab in Children With Osteoclast Bone Dysplasias: Report of Three Cases

JBMR Plus ◽  
2019 ◽  
Vol 3 (10) ◽  
Author(s):  
Alexander Upfill‐Brown ◽  
Susan Bukata ◽  
Nicholas M Bernthal ◽  
Alan L Felsenfeld ◽  
Scott D Nelson ◽  
...  
Keyword(s):  
2012 ◽  
Vol 82 (1) ◽  
pp. 12-21 ◽  
Author(s):  
N A Akawi ◽  
B R Ali ◽  
L Al-Gazali
Keyword(s):  

1967 ◽  
Vol 34 (4) ◽  
pp. 136-141
Author(s):  
G. B. Mahapatra
Keyword(s):  

2019 ◽  
Vol 62 (12) ◽  
pp. 103603 ◽  
Author(s):  
Santiago Pablo Duarte ◽  
María Eugenia Rocha ◽  
María Paz Bidondo ◽  
Rosa Liascovich ◽  
Pablo Barbero ◽  
...  
Keyword(s):  

PEDIATRICS ◽  
1965 ◽  
Vol 35 (4) ◽  
pp. 640-640
Author(s):  
JONATHAN COHEN

With the exception of the skill, the bones have more varieties of lesions about which little or nothing is known than do any other tissues of the body. While mast of these lesions, known largely through their roentgenological appearance and empirical course, are rare, the total group is numerous enough to engage the interest of many. Any approach to useful classification or increased understanding of etiology or pathogenesis would be welcome. Whether Rubin's novel approach fulfils this need in any measure is problematic.


1978 ◽  
pp. 101-107 ◽  
Author(s):  
Bryan J. Cremin ◽  
Peter Beighton
Keyword(s):  

2018 ◽  
pp. 757-794
Author(s):  
Jürgen W. Spranger ◽  
Paula W. Brill ◽  
Christine Hall ◽  
Gen Nishimura ◽  
Andrea Superti-Furga ◽  
...  

This chapter further discusses bone dysplasias and includes discussion on campomelic dysplasia, cousin dysplasia, spondylo-megaepiphyseal-metaphyseal dysplasia, cleidocranial dysplasia, Yunis-Varon syndrome, CDAGS, nail-patella syndrome, ischio-pubic-patellar dysplasia, ischiospinal dysostosis, and cerebro-costo-mandibular syndrome. Each discussion includes major radiographic features, major clinical findings, genetics, major differential diagnoses, and a bibliography.


2018 ◽  
pp. 245-306
Author(s):  
Jürgen W. Spranger ◽  
Paula W. Brill ◽  
Christine Hall ◽  
Gen Nishimura ◽  
Andrea Superti-Furga ◽  
...  

This chapter further discusses bone dysplasias and includes discussion on achondrogenesis (type IB), atelosteogenesis type 2, diastrophic dysplasia, multiple epiphyseal dysplasia (recessive type [rMED]), Desbuquois dysplasia, chondrodysplasia with joint dislocations (IMPAD1/gPAPP type), Catel-Manzke syndrome, chondrodysplasia with congenital joint dislocations (CHST3-type), temtamy preaxial brachydactyly syndrome (TPBS), B4GALT7 deficiency, B3GAT3 deficiency, XYLT1 deficiency, spondyloepimetaphyseal dysplasia with joint laxity Beighton type, spondyloepimetaphyseal dysplasia with joint laxity (leptodactylic type), pseudodiastrophic dysplasia, and Steel syndrome. Each discussion includes major radiographic features, major clinical findings, genetics, major differential diagnoses, and a bibliography.


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