Multiple endocrine neoplasia type 1 (MEN1): an update and the significance of early genetic and clinical diagnosis

CDC Kamilaris, CA Stratakis - Frontiers in endocrinology, 2019 - frontiersin.org
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 …

[HTML][HTML] The clinical practice guidelines for primary hyperparathyroidism, short version

NG Mokrysheva, AK Eremkina… - Problems of …, 2021 - probl-endojournals.ru
Primary hyperparathyroidism (PHPT) is an endocrine disorder of parathyroid glands
characterized by excessive secretion of parathyroid hormone (PTH) with an upper normal or …

The North American Neuroendocrine Tumor Society consensus paper on the surgical management of pancreatic neuroendocrine tumors

JR Howe, NB Merchant, C Conrad, XM Keutgen… - Pancreas, 2020 - journals.lww.com
This manuscript is the result of the North American Neuroendocrine Tumor Society
consensus conference on the surgical management of pancreatic neuroendocrine tumors …

MEN1 disease occurring before 21 years old: a 160-patient cohort study from the Groupe d'étude des Tumeurs Endocrines

P Goudet, A Dalac, M Le Bras… - The Journal of …, 2015 - academic.oup.com
Context: Multiple endocrine neoplasia Type-1 (MEN1) in young patients is only described by
case reports. Objective: To improve the knowledge of MEN1 natural history before 21 years …

Multiple endocrine neoplasia syndrome type 1: institution, management, and data analysis of a nationwide multicenter patient database

F Giusti, L Cianferotti, F Boaretto, F Cetani, F Cioppi… - Endocrine, 2017 - Springer
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 …

[HTML][HTML] Клинические рекомендации по первичному гиперпаратиреозу, краткая версия

НГ Мокрышева, АК Еремкина, СС Мирная… - Проблемы …, 2021 - cyberleninka.ru
Первичный гиперпаратиреоз (ПГПТ)-эндокринное заболевание, характеризующееся
избыточной секрецией паратиреоидного гормона (ПТГ) при верхненормальном или …

Challenges and controversies in management of pancreatic neuroendocrine tumours in patients with MEN1

CJ Yates, PJ Newey, RV Thakker - The Lancet Diabetes & …, 2015 - thelancet.com
Multiple endocrine neoplasia type 1 (MEN1), an autosomal dominant disorder, is
characterised by the occurrence of pancreatic neuroendocrine tumours (P-NETs) in …

[HTML][HTML] Multiple endocrine neoplasia type 1 (MEN1): not only inherited endocrine tumors

A Falchetti, F Marini, E Luzi, F Giusti, L Cavalli… - Genetics in …, 2009 - Elsevier
MEN 1 is a rare hereditary cancer syndrome which manifests a variety of endocrine and non-
endocrine neoplasms and lesions. Growing knowledge of this condition in both its molecular …

[HTML][HTML] Biochemically curative surgery for gastrinoma in multiple endocrine neoplasia type 1 patients

M Imamura, I Komoto, S Ota, T Hiratsuka… - World Journal of …, 2011 - ncbi.nlm.nih.gov
AIM: To search for the optimal surgery for gastrinoma and duodenopancreatic
neuroendocrine tumors in patients with multiple endocrine neoplasia type 1. METHODS …

Multiple endocrine neoplasia syndromes

GG Callender, TA Rich, ND Perrier - Surgical Clinics of North America, 2008 - Elsevier
The multiple endocrine neoplasia (MEN) syndromes are rare autosomal-dominant
conditions that predispose affected individuals to benign and malignant tumors of the …