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Two years’ experience with denosumab for children with Osteogenesis imperfecta type VI

BACKGROUND: Osteogenesis imperfecta (OI) is a hereditary disease causing reduced bone mass, increased fracture rate, long bone deformities and vertebral compressions. Additional non skeletal findings are caused by impaired collagen function and include hyperlaxity of joints and blue sclera. Most OI...

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Detalhes bibliográficos
Main Authors: Hoyer-Kuhn, Heike, Netzer, Christian, Koerber, Friederike, Schoenau, Eckhard, Semler, Oliver
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4180531/
https://ncbi.nlm.nih.gov/pubmed/25257953
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-014-0145-1
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