Osteogenesis imperfecta (OI) refers to a group of rare genetic bone disorders that results in the formation of fragile bones. In patients with OI, the matrix that makes up the bone has been found to ...
Scientists have successfully restored hearing in animal models of ENPP1 deficiency, a genetic disease in which individuals lack an enzyme essential for bone and blood vessel health. The rare disorder ...
Aligned with our mission, the Comprehensive Arthritis, Musculoskeletal, Bone, and Autoimmunity Center is hosting a one-day regional symposium on the Genetics of Musculoskeletal Diseases. Featuring ...
The MarketWatch News Department was not involved in the creation of this content. CHEO Research Institute and Shriners Hospitals for Children Canada Collaborate to Launch First-of-its-kind Joint ...
"This work is a copublication of: Urban & Fischer Verlag, München, Jena; and Oxford University Press, Oxford, New York ..."--Verso of title page. SCDIRB copy 39088019623156 not included in the ...
Ipsen’s oral small molecule has failed to reduce the progression of a genetic disease that gradually turns tendons and ...
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