Challenges and controversies in management of pancreatic neuroendocrine tumours in patients with MEN1
CJ Yates, PJ Newey, RV Thakker - The Lancet Diabetes & …, 2015 - thelancet.com
Multiple endocrine neoplasia type 1 (MEN1), an autosomal dominant disorder, is
characterised by the occurrence of pancreatic neuroendocrine tumours (P-NETs) in …
characterised by the occurrence of pancreatic neuroendocrine tumours (P-NETs) in …
Current and emerging therapies for PNETs in patients with or without MEN1
M Frost, KE Lines, RV Thakker - Nature Reviews Endocrinology, 2018 - nature.com
Pancreatic neuroendocrine tumours (PNETs) might occur as a non-familial isolated
endocrinopathy or as part of a complex hereditary syndrome, such as multiple endocrine …
endocrinopathy or as part of a complex hereditary syndrome, such as multiple endocrine …
[HTML][HTML] Management of pancreatic neuroendocrine tumors in patients with MEN 1
SM Sadowski, F Triponez - Gland surgery, 2015 - ncbi.nlm.nih.gov
Pancreatic neuroendocrine tumors (PNETs) are frequent and can be non-functional (NF) in
patients with multiple endocrine neoplasia type 1 (MEN1). Their identification is of clinical …
patients with multiple endocrine neoplasia type 1 (MEN1). Their identification is of clinical …
Utility of FDG-PET imaging for risk stratification of pancreatic neuroendocrine tumors in MEN1
ER Kornaczewski Jackson, OP Pointon… - The Journal of …, 2017 - academic.oup.com
Context: Patients with multiple endocrine neoplasia type 1 (MEN1) are at high risk of
malignant pancreatic neuroendocrine tumors (pNETs). Structural imaging is typically used to …
malignant pancreatic neuroendocrine tumors (pNETs). Structural imaging is typically used to …
Treatment of pancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1: some clarity but continued controversy
RT Jensen, JA Norton - Pancreas, 2017 - journals.lww.com
Multiple endocrine neoplasia type 1 (MEN1)(prevalence, 1-10/100,000) is the most
important inherited pancreatic neuroendocrine tumor (pNET) syndrome causing up to 10 …
important inherited pancreatic neuroendocrine tumor (pNET) syndrome causing up to 10 …
Recent topics around multiple endocrine neoplasia type 1
SJ Marx - The Journal of Clinical Endocrinology & Metabolism, 2018 - academic.oup.com
Introduction Multiple endocrine neoplasia type 1 (MEN1) is complex with regard to clinical
expressions, management, and molecular pathways. Advances are being made broadly and …
expressions, management, and molecular pathways. Advances are being made broadly and …
Diagnosing nonfunctional pancreatic NETs in MEN1: the evidence base
MJC van Treijen, DJ van Beek… - Journal of the …, 2018 - academic.oup.com
In multiple endocrine neoplasia type 1 (MEN1), nonfunctional pancreatic neuroendocrine
tumors (NF-pNETs) are the most frequently diagnosed NETs and a leading cause of MEN1 …
tumors (NF-pNETs) are the most frequently diagnosed NETs and a leading cause of MEN1 …
Multiple endocrine neoplasia type 1 and the pancreas: diagnosis and treatment of functioning and non-functioning pancreatic and duodenal neuroendocrine …
B Niederle, A Selberherr, DK Bartsch, ML Brandi… - …, 2021 - karger.com
The better understanding of the biological behavior of multiple endocrine neoplasia type 1
(MEN1) organ manifestations and the increase in clinical experience warrant a revision of …
(MEN1) organ manifestations and the increase in clinical experience warrant a revision of …
[HTML][HTML] The current strategy for managing pancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1
Y Niina, N Fujimori, T Nakamura, H Igarashi, T Oono… - Gut and liver, 2012 - ncbi.nlm.nih.gov
Multiple endocrine neoplasia type 1 (MEN1) is an inherited autosomal dominant disease
presenting with pancreatic neuroendocrine tumors (pNETs), parathyroid tumors, or pituitary …
presenting with pancreatic neuroendocrine tumors (pNETs), parathyroid tumors, or pituitary …
Lanreotide therapy vs active surveillance in MEN1-related pancreatic neuroendocrine tumors< 2 centimeters
A Faggiano, R Modica, F Lo Calzo… - The Journal of …, 2020 - academic.oup.com
Purpose Pancreatic neuroendocrine tumors (pNETs) are frequent in multiple endocrine
neoplasia type 1 (MEN1) syndrome. They are usually not surgically treated unless larger …
neoplasia type 1 (MEN1) syndrome. They are usually not surgically treated unless larger …
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