Carregant...
Teriparatide in the treatment of recurrent fractures in a Rett patient
Rett syndrome is a common X-linked neurodevelopmental disorder caused by mutations in the MECP2 gene. Patients with Rett syndrome have a low bone mineral density and increased risk of fracture. The present case report describes a successful novel therapeutic intervention with teriparatide with one p...
Guardat en:
| Publicat a: | Clin Cases Miner Bone Metab |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
CIC Edizioni Internazionali
2015
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4708971/ https://ncbi.nlm.nih.gov/pubmed/26811706 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11138/ccmbm/2015.12.3.253 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|