Αποτελέσματα Αναζήτησης
1 Σεπ 2012 · Patients with multiple endocrine neoplasia (MEN) type 1 (MEN1) and their families should be managed by a multidisciplinary team (MDT) consisting of relevant specialists with experience in the management of endocrine tumors (2|⊕⊕ ).
31 Αυγ 2005 · Multiple endocrine neoplasia type 1 (MEN1) is characterized by varying combinations of more than 20 endocrine and non-endocrine tumors. Endocrine tumors occurring in individuals with MEN1 are shown in Table 2.
21 Οκτ 2022 · Multiple endocrine neoplasia type 1 (MEN1), also known as Wermer syndrome, is an autosomal dominant genetic disease that results in proliferative lesions in multiple endocrine organs, particularly the pituitary gland, pancreas, and parathyroid glands.
10 Ιουλ 2023 · Multiple endocrine neoplasia type 1 (MEN1) is a rare endocrine tumor syndrome with high penetrance. This syndrome is also known as Wermer syndrome. It primarily causes neoplasia of the parathyroid glands, the anterior pituitary gland, and the neuroendocrine tissue of gastro-entero-pancreatic organ systems.
6 Αυγ 2019 · The multiple endocrine neoplasia (MEN) syndromes include MEN1, MEN2 (formerly MEN2A), MEN3 (formerly MEN2B) and the recently identified MEN4. Clinical presentations are varied and often relate to the overproduction of specific hormones. Understanding the genetics of each syndrome assists in determining screening timelines.
Multiple endocrine neoplasia type 1 (MEN-1) is one of a group of disorders, the multiple endocrine neoplasias, that affect the endocrine system through development of neoplastic lesions in pituitary, parathyroid gland and pancreas. [1]
Overview of multiple endocrine neoplasia type 1 (MEN1), an inherited disorder that causes tumors to develop in two or more endocrine glands.
