More than 50% of patients with typical MEN-2B have a de novo M918T germline mutation of
the RET protooncogene. However, even in typical MEN-2B, extrathyroidal manifestations of …

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 …

Objective Multiple endocrine neoplasia type 1 (MEN1) is less well recognized in Asian
countries, including Japan, than in the West. The clinical features and optimal management …

Background & Aims: The identification of precursor lesions has a great impact on the
understanding of tumorigenesis. Precursor lesions of endocrine tumors are known to occur …

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 …

Zollinger‐Ellison syndrome (ZES) can occur without an accompanying inherited syndrome
(ie, sporadic ZES) or as part of the multiple endocrine neoplasia type 1 syndrome (MEN1) …

Zollinger-Ellison Syndrome: Classical Considerations and Current Controversies | The
Oncologist | Oxford Academic Skip to Main Content Advertisement Oxford Academic …