P Soczomski, B Jurecka-Lubieniecka… - Frontiers in …, 2021 - frontiersin.org
Introduction Pancreatic neuroendocrine tumors (PNETs) in hereditary syndromes pose a significant challenge to clinicians. The rarity of these syndromes and PNETs itself make it …
D Lorenzo, F Maire, O Hentic, F Prat… - Current Opinion in …, 2021 - Elsevier
The incidence of nonmetastatic digestive neuroendocrine tumors (NETs) is increasing. Conventional endoscopy and endoscopic ultrasonography are key examinations for the …
CH Ma, HB Guo, XY Pan, WX Zhang - World Journal of Clinical …, 2020 - ncbi.nlm.nih.gov
BACKGROUND Multiple endocrine neoplasia type 1 (MEN1) is a rare hereditary disorder caused by mutations of the MEN1 gene. It is characterized by hyperparathyroidism and …
W Spindelböck, PK Kump, A Püspök… - Zeitschrift für …, 2019 - thieme-connect.com
Neuroendokrine Tumoren des Gastrointestinaltrakts (GI-NET) sind selten. Die im Vergleich zu den mit hormonellen Syndromen assoziierten funktionellen Tumoren (Insulinom …
FH Ma, H Liu, S Ma, Y Li, YT Tian, S Georgiadou… - World, 2019 - researchgate.net
AIMS AND SCOPE The primary aim of World Journal of Clinical Cases (WJCC, World J Clin Cases) is to provide scholars and readers from various fields of clinical medicine with a …