Mostra el registre parcial de l'element
dc.contributor.author | Gandra, Thaygla-Cristhina-Araujo | es |
dc.contributor.author | Tavares, Isabella-Caroline-Fonseca | es |
dc.contributor.author | Carlos, Ana-Luiza-Farnese-Morais | es |
dc.contributor.author | Rodrigues, Lizandra-Gonzaga | es |
dc.contributor.author | Lima, Izabella-Lucas de Abreu | es |
dc.contributor.author | Manzi, Flávio Ricardo | es |
dc.date.accessioned | 2023-05-31T12:29:35Z | |
dc.date.available | 2023-05-31T12:29:35Z | |
dc.date.issued | 2023 | es |
dc.identifier.citation | Gandra, T. C., Tavares, I. C., Carlos, A. L., Rodrigues, L. G., Lima, I. A., & Manzi, F. R. (2023). Patient with McCune albright syndrome: Case report and 10 Years of follow-up imaging examination. Journal of clinical and experimental dentistry, 15(3), e264–e268. | es |
dc.identifier.uri | https://hdl.handle.net/10550/87571 | |
dc.description.abstract | The McCune Albright syndrome (MAS) is a rare, multi-system disease composed of the triad of polyostotic fibrous dysplasia of bone (PFDB), café-au-lait skin hyperpigmentation, and endocrine disorders. The diagnosis involves clinical, biochemical and imagin | es |
dc.title | Patient with McCune albright syndrome : case report and 10 Years of follow-up imaging examination | es |
dc.type | journal article | es_ES |
dc.subject.unesco | UNESCO:CIENCIAS MÉDICAS | es |
dc.identifier.doi | 10.4317/jced.60161 | es |
dc.type.hasVersion | VoR | es_ES |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10062463/ |