A carregar...
Current and Emerging Therapies for Pancreatic Neuroendocrine Tumours in Patients with or without Multiple Endocrine Neoplasia Type 1
Pancreatic neuroendocrine tumours (PNETs) may occur as a non-familial isolated endocrinopathy or as part of a complex hereditary syndrome, such as multiple endocrine neoplasia type 1 (MEN1), which is an autosomal dominant disorder characterised by the combined occurrence of PNETs with tumours of the...
Na minha lista:
| Publicado no: | Nat Rev Endocrinol |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6538535/ https://ncbi.nlm.nih.gov/pubmed/29449689 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nrendo.2018.3 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|