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A standard set of outcome measures for the comprehensive assessment of osteogenesis imperfecta
BACKGROUND: Osteogenesis Imperfecta (OI) is a genetic disorder also known as ‘brittle bone disease’. The clinical manifestation of OI shows a wide variation. Therefore, care for patients with OI requires an interdisciplinary approach. The effectiveness of particular interventions and treatment proto...
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| Publié dans: | Orphanet J Rare Dis |
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| Auteurs principaux: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BioMed Central
2021
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7980586/ https://ncbi.nlm.nih.gov/pubmed/33743784 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-021-01682-y |
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