Results 71 to 80 of about 15,083 (188)

NUP153 immunoreactivity in neuroendocrine neoplasms supports the diagnosis of NET versus NEC and is modulated by post‐translational modifications

Journal of Neuroendocrinology, Volume 38, Issue 8, August 2026.
Abstract Nucleoporins (NUPs) constitute the nuclear pore complex (NPC) and are essentially involved in nuclear transport, chromatin organization, and context‐dependent gene regulation. However, the role of NUPs in neuroendocrine (tumor)biology and related diagnostic potential is poorly defined.
Sven Mattern, Arslan Ali, Vanessa Hollfoth, Eyyub Bag, Katharina Kluthe, Esther Herpel, Frank Bergmann, Thomas Muley, Michael Meister, Judith Lehmann‐Koch, Benjamin Goeppert, Arne Warth, Kai Breuhahn, Irina Bonzheim, Stephan Singer, Kerstin Singer   +15 more
wiley   +1 more source

Cognitive Impairment in Insulinoma, Consequence of a Delayed Diagnosis: A Case Report

Endocrinology Research and Practice, 2007
The diagnosis of insulinoma is often delayed and this usually results with complications such as cognitive impairment. A 60 year old man who had history of aggressive behaviour and attacks of unconciousness was evaluated for hypoglycemia.
Dilek Soysal, Özlem Kabayeğit, Gonca Oruk, Bahar Ustaoglu, Umut Koşan, Arzu Avcı, Çiğdem Özdemir   +6 more
doaj   +2 more sources

Procedure‐specific morbidity and pathologic assessment after resection of small (≤20 mm) pancreatic neuroendocrine tumors

Journal of Neuroendocrinology, Volume 38, Issue 8, August 2026.
Abstract Pancreatic neuroendocrine tumors (PanNETs) are increasingly detected, and the optimal extent of resection remains uncertain because perioperative burden and oncologic assessment may differ by procedure. Enucleation (EN) and central pancreatectomy (CP) are often grouped together as parenchyma‐sparing resections (PSRs) despite substantial ...
Aya Maekawa, Giampaolo Perri, Stefano Partelli, Charles de Ponthaud, Safi Dokmak, Carsten Jäger, Maria Lavinia Luzietti, Alessio Marchetti, Valentina Andreasi, Anna Battistella, Bengi Su Yilmaz, Andrea Sheel, Kunal Rajput, Haiyi Hu, Umberto Cillo, Alain Sauvanet, Helmut Friess, Ryan D. Baron, Sébastien Gaujoux, Massimo Falconi, Giovanni Marchegiani   +20 more
wiley   +1 more source

Clinical characteristics and treatment outcomes of patients with insulinoma–a single center's experience of 76 cases over a 10-year period

Heliyon
Objective: Insulinoma is a rare pancreatic neuroendocrine neoplasm caused by pancreatic beta cell tumor or beta cell proliferation resulting in excessive insulin secretion.
Wei Li, Yali Cheng, Qingyong Ma, Zheng Wu, Zheng Wang   +4 more
doaj   +1 more source

Differential Pathophysiological Drivers of Susceptibility to Type 2 Diabetes and Metabolic Dysfunction–Associated Steatotic Liver Disease: Ethnic Differences in Insulin Dynamics, Whole‐Body Fat Metabolism, and Organ‐Specific Lipid Deposition

Obesity Reviews, Volume 27, Issue 8, August 2026.
ABSTRACT Introduction This narrative review explores the epidemiological evidence and potential underlying pathophysiological defects underlying the disproportionately greater risk of Type 2 diabetes (T2D) and cardiometabolic disease in people of South Asian and African Caribbean ancestry compared with White Europeans.
Daniel J. Cuthbertson, Martin Whyte, Alex E. Henney, Uazman Alam, Louise Goff, Barbara A. Fielding, A. Margot Umpleby   +6 more
wiley   +1 more source

Five Advances in Benign Pancreatic Surgery in the Last 50 Years

World Journal of Surgery, Volume 50, Issue 8, Page 2102-2105, August 2026.
Stephan B. Dreyer, Rowan W. Parks
wiley   +1 more source

Varied presentation of hyperinsulinaemic hypoglycaemia [PDF]

Journal of Clinical and Scientific Research, 2012
Hypoglycaemia is a fairly common clinical entity, mainly due to its high prevalence as a complication of therapy for diabetes. Spontaneous hypoglycemia with unsuppressed plasma insulin is a relatively uncommon endocrine disorder.
K.V. Sreedhar Babu, M.N. Pawan, C.V. Harinarayan, V. Suresh, P. Satish, P. Amaresh Reddy, G. Rajagopal, A.Y. Lakshmi, Alok Sachan   +8 more
doaj  

Insulinoma Associated with MEN1 Syndrome: A Case of Persistent Hypoglycemia in a School-aged Child

JCRPE
Insulinoma is a rare cause of non-ketotic hypoglycemia, both in adults and in children. Pediatric patients account for approximately 5% of all cases, mostly due to isolated benign lesions, but insulinoma may also be part of a multiple endocrine neoplasia
Rodrigo Lemus-Zepeda, Aura María Salazar-Solarte, Diana Marcela Vasquez-Forero, Mario Jr. Angulo-Mosquera, Liliana Mejía-Zapata   +4 more
doaj   +1 more source

Insulinoma in Iran : A 20-year review.

Annals of Saudi Medicine, 2005
Background: The time between onset of symptoms of insulinoma to diagnosis ranges from 10 days to more than 20 years. To help physicians make an earlier diagnosis, we defined the clinical, imaging and paraclinical characteristics of insulinoma in cases ...
Larijani Bagher, Aghakhani Shahriar, Lor Shams Sadat, Zahedi Farzaneh, Pajouhi Mohammad, Bastanhagh Mohammad   +5 more
doaj  

Sporadic Insulinoma as a Rare Cause of Recurrent Hypoglycemia in Children

Case Reports in Pediatrics, 2017
Insulinoma is a rare pancreatic tumor in children and adolescents. As a result of insulin hypersecretion, signs and symptoms are more commonly consequences of the pathophysiologic responses to hypoglycemia.
Hedyeh Saneifard, Ahmad Khaleghnejad Tabari, Maryam Kazemi Aghdam, Mohadese Musavi Khorshidi, Ali Sheikhy   +4 more
doaj   +1 more source