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 …

This review provides an overview of novel insights in the clinical management of patients
with Multiple Endocrine Neoplasia Type 1, focusing on the last decade since the last update …

Recent data suggest an increase in the overall incidence of parathyroid disorders, with
primary hyperparathyroidism (PHPT) being the most prevalent parathyroid disorder. PHPT is …

Guidelines French guidelines from the GTE, AFCE and ENDOCAN-RENATEN (Groupe
d'étude des Tumeurs Endocrines/Association Francophone de Chirurgie Endocrinienne …

Introduction Multiple endocrine neoplasia type 1 (MEN1)-related neuroendocrine tumors
(NETs) of the lung are mostly indolent, with a good prognosis. Nevertheless, cases of …

BACKGROUND: The differences between sporadic and multiple endocrine neoplasia type 1
(MEN-1)–associated insulinoma are not well described. Herein, we compared …

Abstract Multiple Endocrine Neoplasia type 1 (MEN1) Clinical Practice Guidelines (2012)
are predominantly based on expert opinion due to limited available evidence at the time …

The co-occurrence of primary hyperparathyroidism (PHPT) and pituitary adenomas (PAs) is
often indicative of underlying genetic syndromes such as Multiple Endocrine Neoplasia type …

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 Protein-truncating germline pathogenic variants in the N-and C-terminal exons
(2, 9, and 10) of the MEN1 gene may be associated with aggressive pancreatic …