Osteogenesis Imperfecta: A study of the patient journey in 13 European countries
There is an urgent need for increased awareness about OI and its wide range of symptoms. In particular, there is a need for consensus guidelines outlining the optimum care throughout the duration of the OI patient's life.
Authors
- Valérie Cormier‐Daire (ORCID: https://orcid.org/0000-0002-2839-9856)
- Sean M. O’Malley (ORCID: https://orcid.org/0000-0003-1039-0033)
- Richard Keen (ORCID: https://orcid.org/0009-0001-8216-3828)
- Scott F. Gilbert (ORCID: https://orcid.org/0000-0002-5071-8876)
- Ingunn Westerheim
Institutions
- Hôpital Necker-Enfants Malades (FR)
- Inserm (FR)
- Université Paris Cité (FR)
- Royal National Orthopaedic Hospital (GB)
- More Associates (GB)
- Royal National Orthopaedic Hospital NHS Trust (GB)
- Heifer International (US)
- University College London (GB)
Publication Details
- Journal
- Orphanet Journal of Rare Diseases
- Published
- 2024-09-09
- DOI
- https://doi.org/10.1186/s13023-024-03345-0
- Citations
- 4
- Primary Topic
- Connective tissue disorders research
- Type
- article
- Field-Weighted Citation Impact
- 2.20
Funders
- Mereo BioPharma