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 …

Multiple endocrine neoplasia type 1 (MEN1) is a rare disease caused by mutations in the
MEN1 gene on chromosome 11. It is characterized by the occurrence of primary …

Multiple endocrine neoplasia type 1 (MEN1) is a rare syndrome characterized by the co-
occurrence of primary hyperparathyroidism, duodenopancreatic neuroendocrine tumours …

Objective: The aim was to provide guidelines for evaluation, treatment, and genetic testing
for multiple endocrine neoplasia type 1 (MEN1). Participants: The group, which comprised …

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 …

Introduction Multiple endocrine neoplasia type 1 (MEN1) is complex with regard to clinical
expressions, management, and molecular pathways. Advances are being made broadly and …

Objective The aim of this study was to integrate European epidemiological data on patients
with multiple endocrine neoplasia type 1 by creating an Italian registry of this syndrome …

Key points Multiple endocrine neoplasia type 1 is a rare genetic syndrome, characterized by
the co-occurrence, in the same individual or in related individuals of the same family, of …

Context Early genetic association studies yielded too high risk estimates for multiple
endocrine neoplasia (MEN2A), suggesting a need for extended surgery. Objective The …

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 …