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Pancreatic neuroendocrine tumors: approach to treatment with focus on sunitinib
Pancreatic neuroendocrine tumors (pNETs) are relatively rare malignancies. With secretory tumors such as insulinomas, vasoactive intestinal peptideomas, and gastrinomas, the hormone produced causes the symptom complex (e.g. hypoglycemia, peptic ulcer disease). With nonsecretory NETs, the clinical co...
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| Main Authors: | , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
SAGE Publications
2013
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3756637/ https://ncbi.nlm.nih.gov/pubmed/24003340 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1756283X13493878 |
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