Familial multiple endocrine neoplasia type I: a new look at pathophysiology
ML Brandi, SJ Marx, GD Aurbach… - Endocrine …, 1987 - academic.oup.com
I. Introduction F AMILIAL multiple endocrine endocrine neoplasia type I (FMENI) is a
complex hereditary disorder encompassing pancreatic and pituitary tumors and hyperplasia …
complex hereditary disorder encompassing pancreatic and pituitary tumors and hyperplasia …
Mutation of the Multiple Endocrine Neoplasia Type 1 Gene in Nonfamilial, Malignant Tumors of the Endocrine Pancreas
O Hessman, D Lindberg, B Skogseid, T Carling… - Cancer research, 1998 - AACR
Endocrine pancreatic tumors are rare neoplasms that occur sporadically or as part of a
multiple endocrine neoplasia type 1 (MEN1) syndrome. Germ-line mutations of the MEN1 …
multiple endocrine neoplasia type 1 (MEN1) syndrome. Germ-line mutations of the MEN1 …
[PDF][PDF] Current concepts in the surgical management of multiple endocrine neoplasia type 1 pancreatic-duodenal disease. Results in the treatment of 40 patients with …
NW Thompson - Journal of internal medicine, 1998 - deepblue.lib.umich.edu
Thompson NW (University of Michigan, Ann Arbor, MI, USA). Current concepts in the
surgical management of multiple endocrine neoplasia type 1 pancreatic-duodenal disease …
surgical management of multiple endocrine neoplasia type 1 pancreatic-duodenal disease …
Clinical genetic testing and early surgical intervention in patients with multiple endocrine neoplasia type 1 (MEN 1)
TC Lairmore, LD Piersall, MK DeBenedetti… - Annals of …, 2004 - journals.lww.com
Objective: We sought to develop a comprehensive program for clinical genetic testing in a
large group of extended families with multiple endocrine neoplasia type 1 (MEN 1), with the …
large group of extended families with multiple endocrine neoplasia type 1 (MEN 1), with the …
Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with …
N Hai, N Aoki, A Shlmatsu, T Mod… - Clinical …, 2000 - Wiley Online Library
OBJECTIVE Multiple endocrine neoplasia type 1 (MEN1) is a familial tumour syndrome of
endocrine tumours involving parathyroids, anterior pituitary and enteropancreatic …
endocrine tumours involving parathyroids, anterior pituitary and enteropancreatic …
Multiple endocrine neoplasia type 1
GM Doherty - Journal of surgical oncology, 2005 - Wiley Online Library
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 …
syndrome that occurs due to inactivating mutations of the MEN1 gene locus, coding for a …
Prospective endoscopic ultrasonographic evaluation of the frequency of nonfunctioning pancreaticoduodenal endocrine tumors in patients with multiple endocrine …
L Thomas-Marques, A Murat, B Delemer… - Official journal of the …, 2006 - journals.lww.com
Prospective Endoscopic Ultrasonographic Evaluation of the Fr... : Official journal of the
American College of Gastroenterology | ACG Prospective Endoscopic Ultrasonographic …
American College of Gastroenterology | ACG Prospective Endoscopic Ultrasonographic …
[HTML][HTML] Characterization of mutations in patients with multiple endocrine neoplasia type 1
JHD Bassett, SA Forbes, AAJ Pannett, SE Lloyd… - The American Journal of …, 1998 - cell.com
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder
characterized by tumors of the parathyroids, pancreatic islets, and anterior pituitary. The …
characterized by tumors of the parathyroids, pancreatic islets, and anterior pituitary. The …
Multiple endocrine neoplasia 2B syndrome due to codon 918 mutation: clinical manifestation and course in early and late onset disease
M Brauckhoff, O Gimm, CL Weiss, J Ukkat… - World journal of …, 2004 - Springer
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 …
the RET protooncogene. However, even in typical MEN-2B, extrathyroidal manifestations of …
Multiple endocrine neoplasia type 1: latest insights
ML Brandi, SK Agarwal, ND Perrier, KE Lines… - Endocrine …, 2021 - academic.oup.com
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 …
autosomal dominant pattern, is continuing to raise great interest for endocrinology …