Pancreatic neuroendocrine tumors (pNETs) are frequently malignant (50-80%, except for insulinoma) and may show an aggressive course with metastases to the liver as well as more distant sites. These heterogeneous neoplasms include functioning tumors, which secrete a variety of peptide hormones, and non-functioning tumors (up to 90% of pNETs), which often show metastases at the time of diagnosis
Treatment of the clinically and prognostically heterogeneous neuroendocrine neoplasms (NEN) should b...
Pancreatic neuroendocrine tumors (pNETs) are unique, slow-growing malignancies whose molecular patho...
Pancreatic neuroendocrine tumors (pNETs) are a vast growing disease. Over 50% of these tumors are re...
Pancreatic neuroendocrine tumor (pNET) is a rare type of pancreatic tumors. The incidence of pNET sh...
Abstract. Pancreatic neuroendocrine tumors (PNETs) are a rare group of neoplasms originating from th...
Abstract Background Pancreatic neuroendocrine tumors (PNETs) are rare pancreatic neoplasms. About 40...
The management of pancreatic neuroendocrine tumors (PanNETs) involves classification into non-functi...
Pancreatic neuroendocrine tumors (PNETs) are rare pancreatic neoplasms. About 40-80% of patients wit...
Pancreatic neuroendocrine tumors (pNETs) are rare neoplasms arising from the pancreatic islet of Lan...
Pancreatic neuroendocrine tumors (pNETs) are rare and heterogenous tumors and surgery to remove the ...
Simple Summary Pancreatic neuroendocrine tumors (pNET) are a heterogeneous and challenging entity, ...
Neuroendocrine tumors (NETs) in general and specifically these gastroenteropancreatic-neuroendocrine...
BACKGROUND: Pancreatic neuroendocrine tumors (PNET) are rare malignancies frequently diagnosed at a ...
Background: Liver metastases are a strong prognostic indicator in patients with gastro-entero-pancre...
In this article, we aimed to review the literature on the clinics and management of nonfunctional pa...
Treatment of the clinically and prognostically heterogeneous neuroendocrine neoplasms (NEN) should b...
Pancreatic neuroendocrine tumors (pNETs) are unique, slow-growing malignancies whose molecular patho...
Pancreatic neuroendocrine tumors (pNETs) are a vast growing disease. Over 50% of these tumors are re...
Pancreatic neuroendocrine tumor (pNET) is a rare type of pancreatic tumors. The incidence of pNET sh...
Abstract. Pancreatic neuroendocrine tumors (PNETs) are a rare group of neoplasms originating from th...
Abstract Background Pancreatic neuroendocrine tumors (PNETs) are rare pancreatic neoplasms. About 40...
The management of pancreatic neuroendocrine tumors (PanNETs) involves classification into non-functi...
Pancreatic neuroendocrine tumors (PNETs) are rare pancreatic neoplasms. About 40-80% of patients wit...
Pancreatic neuroendocrine tumors (pNETs) are rare neoplasms arising from the pancreatic islet of Lan...
Pancreatic neuroendocrine tumors (pNETs) are rare and heterogenous tumors and surgery to remove the ...
Simple Summary Pancreatic neuroendocrine tumors (pNET) are a heterogeneous and challenging entity, ...
Neuroendocrine tumors (NETs) in general and specifically these gastroenteropancreatic-neuroendocrine...
BACKGROUND: Pancreatic neuroendocrine tumors (PNET) are rare malignancies frequently diagnosed at a ...
Background: Liver metastases are a strong prognostic indicator in patients with gastro-entero-pancre...
In this article, we aimed to review the literature on the clinics and management of nonfunctional pa...
Treatment of the clinically and prognostically heterogeneous neuroendocrine neoplasms (NEN) should b...
Pancreatic neuroendocrine tumors (pNETs) are unique, slow-growing malignancies whose molecular patho...
Pancreatic neuroendocrine tumors (pNETs) are a vast growing disease. Over 50% of these tumors are re...