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 …

Outcome of duodenopancreatic resections in patients with multiple endocrine neoplasia type 1

DK Bartsch, V Fendrich, P Langer, I Celik… - Annals of …, 2005 - journals.lww.com
Objective: To evaluate the outcome of an aggressive surgical approach for
duodenopancreatic neuroendocrine tumors (PETs) associated with multiple endocrine …

Clinical aspects of multiple endocrine neoplasia type 1

A Al-Salameh, G Cadiot, A Calender… - Nature Reviews …, 2021 - nature.com
Multiple endocrine neoplasia type 1 (MEN1) is a rare syndrome characterized by the co-
occurrence of primary hyperparathyroidism, duodenopancreatic neuroendocrine tumours …

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 …

[HTML][HTML] Phenotypes associated with MEN1 syndrome: a focus on genotype-phenotype correlations

C Mele, M Mencarelli, M Caputo, S Mai… - Frontiers in …, 2020 - frontiersin.org
Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant inherited tumor
syndrome, associated with parathyroid, pituitary, and gastro-entero-pancreatic (GEP) …

Clinical genetic testing and early surgical intervention in patients with multiple endocrine neoplasia type 1 (MEN 1)

TC Lairmore, LD Piersall, MK DeBenedetti… - Annals of …, 2004 - journals.lww.com
Objective: We sought to develop a comprehensive program for clinical genetic testing in a
large group of extended families with multiple endocrine neoplasia type 1 (MEN 1), with the …

Prospective evaluation of imaging procedures for the detection of pancreaticoduodenal endocrine tumors in patients with multiple endocrine neoplasia type 1

P Langer, PH Kann, V Fendrich, G Richter, S Diehl… - World journal of …, 2004 - Springer
Early identification of pancreaticoduodenal endocrine tumors (PETs) in multiple endocrine
neoplasia type 1 (MEN-1) is mandatory, because these tumors represent the most common …

Timing and extent of surgery in symptomatic and asymptomatic neuroendocrine tumors of the pancreas in MEN 1

G Åkerström, O Hessman, B Skogseid - Langenbeck's archives of surgery, 2002 - Springer
Pancreaticoduodenal tumors develop in a majority of patients with multiple endocrine
neoplasia type 1 (MEN 1) and have a pronounced effect on life expectancy as the principal …

Causes of death and prognostic factors in multiple endocrine neoplasia type 1: a prospective study: comparison of 106 MEN1/Zollinger-Ellison syndrome patients with …

T Ito, H Igarashi, H Uehara, MJ Berna, RT Jensen - Medicine, 2013 - journals.lww.com
Multiple endocrine neoplasia type 1 (MEN1) is classically characterized by the development
of functional or nonfunctional hyperplasia or tumors in endocrine tissues (parathyroid …

Multiple endocrine neoplasia type 1: new clinical and basic findings

DH Schussheim, MC Skarulis, SK Agarwal… - Trends in Endocrinology …, 2001 - cell.com
Multiple endocrine neoplasia type 1 (MEN1) provides a prime example of how a rare
disease can advance our understanding of basic cell biology, neoplasia and common …