Multiple endocrine neoplasia type 1 (MEN-1) is an interesting genetic syndrome of
polyendocrinopathies. Clinical knowledge about MEN-1 is essential as it appears to be …

Abstract Multiple endocrine neoplasia‐1 (MEN‐1) is an autosomal dominant inherited
syndrome that occurs due to inactivating mutations of the MEN1 gene locus, coding for a …

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

M ultiple endocrine neoplasia type 1 (MEN1) is inherited in an autosomal dominant fashion
and predisposes to the development of hyperplastic or neoplastic changes in the …

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 …

Multiple endocrine neoplasia type 1 (MEN1; formerly known as Wermer syndrome) is a rare
disorder characterized by the combined occurrence of two or more tumors involving …

Multiple Endocrine Neoplasia type 1 (MEN1) is a rare hereditary endocrine cancer
syndrome characterized primarily by tumors of the parathyroid glands (95% of cases) …

Multiple endocrine neoplasia (MEN) are clinical inherited syndromes affecting different
endocrine glands. Three different patterns of MEN syndromes can occur (MEN 1, MEN 2A …

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

Multiple endocrine neoplasia type 1 (MEN-1) is a familial cancer syndrome with parathyroid,
pituitary and enteropancreatic tumors. The disease phenotype segregates with markers on …