Over the past few decades, the number of available structural bioinformatics pipelines,
libraries, plugins, web resources and software has increased exponentially and become …

Multiple endocrine neoplasia type 1 (MEN1) is a rare hereditary tumor syndrome inherited in
an autosomal dominant manner and characterized by a predisposition to a multitude of …

Gastrinomas are neuroendocrine neoplasms, usually located in the duodenum or pancreas,
that secrete gastrin and cause a clinical syndrome known as Zollinger-Ellison syndrome …

Pituitary adenomas are usually benign monoclonal tumours presenting either due to
hypersecretion of pituitary hormones, and/or due to local space occupying effects and …

Multiple endocrine neoplasia type 1 (MEN1) is classically characterized by the development
of functional or nonfunctional hyperplasia or tumors in endocrine tissues (parathyroid …

Objective Limited data regarding adrenal involvement in multiple endocrine neoplasia type
1 (MEN1) is available. We describe the characteristics of MEN1-associated adrenal lesions …

Abstract Multiple Endocrine Neoplasia type 1 (MEN1) is a rare autosomal dominant
hereditary cancer syndrome presented mostly by tumours of the parathyroids, endocrine …

Parathyroid carcinoma (PC) may occur as part of a complex hereditary syndrome or an
isolated (ie, non‐syndromic) non‐hereditary (ie, sporadic) endocrinopathy. Studies of …

Purpose Neuroendocrine neoplasms can occur as part of inherited disorders, usually in the
form of well-differentiated, slow-growing tumors (NET). The main predisposing syndromes …

Gastrinomas are neuroendocrine neoplasms (NENs), that occur primarily in the duodenum
and pancreas, which ectopically secrete gastrin, resulting in the Zollinger-Ellison syndrome …