Coalescing expansile skeletal disease: Delineation of an extraordinary osteopathy involving the IFITM5 mutation of osteogenesis imperfecta type V

Author:

Whyte Michael P.,Aronson James,McAlister William H.,Weinstein Robert S.,Wenkert Deborah,Clements Karen L.,Gottesman Gary S.,Madson Katherine L.,Stolina Marina,Bijanki Vinieth N.,Plotkin Horacio,Huskey Margaret,Duan Shenghui,Mumm Steven

Funder

Foundation for Barnes-Jewish Hospital

National Institutes of Health

Shriners Hospitals for Children

Amgen

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference51 articles.

1. Reeder and Felson’s Gamuts in Bone, Joint and Spine Radiology;Reeder,1993

2. Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFß1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand;Whyte;J. Bone Miner. Res.,2011

3. Chapter 35: Gsα, pseudohypoparathyroidism, fibrous dysplasia, and McCune–Albright syndrome;Weinstein,2018

4. Pathophysiology and Treatment of Paget’s Disease of Bone;Kanis,1998

5. Chapter 26: Mendelian disorders of RANKL/OPG/RANK/NF-κB signaling;Whyte,2018

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