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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...
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| Publicat a: | Nat Rev Endocrinol |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2018
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| Matèries: | |
| Accés en línia: | 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 |
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