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 …

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 …

PURPOSE: To perform clinical and genetic screening for multiple endocrine neoplasia type
1 (MEN1) in patients at the Academic Hospital of the University of São Paulo School of …

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder
characterized by the occurrence of tumors of the parathyroids, pancreas, and anterior …

Multiple Endocrine Neoplasia type 1 (MEN1) is an autosomal-dominant disorder
characterised by the occurrence of tumours of the parathyroids, pancreas and anterior …

Objective Effect of genetic screening on outcome in multiple endocrine neoplasia type 1
(MEN1) remains unclear. Expression of MEN1 is described using currently available …

Abstract Background Multiple Endocrine Neoplasia type 1 (MEN1) is diagnosed when two
out of the three primary MEN1-associated endocrine tumors occur in a patient. Up to 10 …

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 …

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

Multiple endocrine neoplasia type 1 (MEN1) is a rare but informative syndrome for
endocrine tumorigenesis. Since its isolation, several groups have begun to determine the …