Current and emerging therapies for PNETs in patients with or without MEN1
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 the combined occurrence of PNETs with tumours of th...
Main Authors: | Frost, M, Lines, K, Thakker, R |
---|---|
Format: | Journal article |
Published: |
Nature Publishing Group
2018
|
Similar Items
-
A MEN1 pancreatic neuroendocrine tumour mouse model, under temporal control
by: Lines, K, et al.
Published: (2017) -
Preclinical drug studies in MEN1-related neuroendocrine neoplasms (MEN1-NENs)
by: Grozinsky-Glasberg, S, et al.
Published: (2020) -
Bilateral Spontaneous Hemothorax with PNET: case report and review
by: Ali Ghasemi, et al.
Published: (2014-07-01) -
Optimized hybrid YOLOu‐Quasi‐ProtoPNet for insulators classification
by: Stefano Frizzo Stefenon, et al.
Published: (2023-08-01) -
A Peripheral Primitive Neuro-ectodermal Tumor (pPNET) of Larynx
by: Raman Wadhera, et al.
Published: (2018-04-01)