Multiple endocrine neoplasia type 1 (MEN1), a rare tumor syndrome that is inherited in an
autosomal dominant pattern, is continuing to raise great interest for endocrinology …

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 …

Parathyroid carcinoma (PC) is an extremely rare disease. Although it may occasionally
occur in genetic syndromes, it is more often sporadic. It is usually associated with a …

Context Duodenopancreatic neuroendocrine tumors (dpNETs) frequently occur in patients
with multiple endocrine neoplasia type 1 (MEN1), and metastatic dpNET is the primary …

ABSTRACT Multiple Endocrine Neoplasia Type 1 (MEN1) is a rare autosomal dominantly
inherited endocrine tumor predisposition syndrome, caused by mutations in the MEN1 gene …

Background Metastasized pancreatic neuroendocrine tumors are the leading cause of death
in patients with multiple endocrine neoplasia type 1. Aside from tumor size, prognostic …

Multiple endocrine neoplasia type 1 (MEN1) is an inherited tumor endocrine syndrome
caused by pathogenic variants of the MEN1 gene, mainly involving the parathyroids, anterior …

Neuroendocrine neoplasms (NENs) occur usually as sporadic tumours; however, rarely,
they may arise in the context of a hereditary syndrome, such as multiple endocrine …

The clinical use of nuclear medicine imaging and therapy in pancreatic neuroendocrine
tumors has been greatly strengthened since the approval of 68Ga-DOTATATE and 177Lu …

Understanding cell behavior within the cellular microenvironment is a chief goal of
multicellular systems biology. My dissertation approaches multicellular systems biology …