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Published in 2018 at "Nature Reviews Endocrinology"
DOI: 10.1038/nrendo.2018.3
Abstract: Pancreatic neuroendocrine tumours (PNETs) might occur as a non-familial isolated endocrinopathy or as part of a complex hereditary syndrome, such as multiple endocrine neoplasia type 1 (MEN1). MEN1 is an autosomal dominant disorder characterized by…
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Keywords:
without men1;
current emerging;
pnets patients;
emerging therapies ... See more keywords