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Year Number of Results
1981 1
1982 6
1984 4
1985 5
1986 4
1987 6
1988 6
1989 7
1990 6
1991 6
1992 2
1993 5
1994 8
1995 7
1996 4
1997 5
1999 5
2000 2
2001 1
2002 1
2003 1
2004 7
2005 6
2006 3
2007 4
2008 3
2009 4
2010 3
2011 4
2012 7
2013 3
2014 1
2015 4
2016 4
2017 1
2018 4
2019 3
2020 2
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2023 1
2024 0

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152 results

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Page 1
Pancreatic neuroendocrine tumors: clinical features, diagnosis and medical treatment: advances.
Ito T, Igarashi H, Jensen RT. Ito T, et al. Best Pract Res Clin Gastroenterol. 2012 Dec;26(6):737-53. doi: 10.1016/j.bpg.2012.12.003. Best Pract Res Clin Gastroenterol. 2012. PMID: 23582916 Free PMC article. Review.
Pancreatic neuroendocrine tumors (pNETs) comprise with gastrointestinal carcinoids, the main groups of gastrointestinal neuroendocrine tumors (GI-NETs). ...The other aspects of the management of these tumors (surgery, treatment of advanced disease, tumor localizatio
Pancreatic neuroendocrine tumors (pNETs) comprise with gastrointestinal carcinoids, the main groups of gastrointestinal neuroendocrin
Vasoactive Intestinal Peptide-Secreting Tumors: A Review.
Siddappa PK, Vege SS. Siddappa PK, et al. Pancreas. 2019 Oct;48(9):1119-1125. doi: 10.1097/MPA.0000000000001402. Pancreas. 2019. PMID: 31609932 Review.
Vasoactive intestinal peptide-secreting tumors (VIPomas) are a group of rare neuroendocrine tumors, which cause a typical syndrome of watery diarrhea. Most of these tumors are found in the pancreas and are usually detected at a later stage. Although cu
Vasoactive intestinal peptide-secreting tumors (VIPomas) are a group of rare neuroendocrine tumors, which cause a typic
Pancreatic neuroendocrine tumors.
Batcher E, Madaj P, Gianoukakis AG. Batcher E, et al. Endocr Res. 2011;36(1):35-43. doi: 10.3109/07435800.2010.525085. Endocr Res. 2011. PMID: 21226566 Review.
Pancreatic neuroendocrine tumors (PNETs) are rare neoplasms representing <5% of all pancreatic malignancies with an estimated incidence of 1-1.5 cases/100,000. PNETs are broadly classified as either functional or nonfunctional. Functional PNETs include insulinoma
Pancreatic neuroendocrine tumors (PNETs) are rare neoplasms representing <5% of all pancreatic malignancies with an estimat
Pancreatic VIPomas from China: Case reports and literature review.
Chen C, Zheng Z, Li B, Zhou L, Pang J, Wu W, Zheng C, Zhao Y. Chen C, et al. Pancreatology. 2019 Jan;19(1):44-49. doi: 10.1016/j.pan.2018.10.007. Epub 2018 Oct 26. Pancreatology. 2019. PMID: 30391116 Review.
Vasoactive intestinal polypeptide-secreting tumors (VIPomas) are rare neuroendocrine tumors that often present as watery diarrhea, hypokalemia, and achlorhydria or hypochlorhydria. ...Comprehensive review of 41 cases allows evaluation of clinical characteristics, tr
Vasoactive intestinal polypeptide-secreting tumors (VIPomas) are rare neuroendocrine tumors that often present as watery diarr
Diarrhoea due to pancreatic diseases.
Brelian D, Tenner S. Brelian D, et al. Best Pract Res Clin Gastroenterol. 2012 Oct;26(5):623-31. doi: 10.1016/j.bpg.2012.11.010. Best Pract Res Clin Gastroenterol. 2012. PMID: 23384807 Review.
Any disruption of this process can lead to malabsorption and resultant diarrhoea. Typically, disruption of over 90 percent of the pancreatic parenchyma is needed to result in diarrhoea. This disruption can result from widespread pancreatic necrosis in acute pancr
Any disruption of this process can lead to malabsorption and resultant diarrhoea. Typically, disruption of over 90 percent of the pancrea
Verner-Morrison syndrome. Literature review.
Belei OA, Heredea ER, Boeriu E, Marcovici TM, Cerbu S, Mărginean O, Iacob ER, Iacob D, Motoc AGM, Boia ES. Belei OA, et al. Rom J Morphol Embryol. 2017;58(2):371-376. Rom J Morphol Embryol. 2017. PMID: 28730220 Free article. Review.
VIPomas are neuroendocrine tumors that autonomously secrete vasoactive intestinal peptide (VIP). Watery diarrhea, hypokalemia and achlorhydria (WDHA) syndrome caused by VIP-producing tumors only rarely occurs in adult patients with non-pancreatic
VIPomas are neuroendocrine tumors that autonomously secrete vasoactive intestinal peptide (VIP). Watery diarrhea, hypok …
Synchronous Insulinoma and Glucagonoma: A Review of the Literature.
Damaskos C, Dimitroulis D, Garmpi A, Antoniou EA, Kouraklis G, Psilopatis I, Mavri M, Diamantis E, Marinos G, Kyriakos G, Farmaki P, Patsouras A, Kontzoglou K, Garmpis N. Damaskos C, et al. In Vivo. 2023 Nov-Dec;37(6):2402-2408. doi: 10.21873/invivo.13345. In Vivo. 2023. PMID: 37905620 Free PMC article. Review.
BACKGROUND/AIM: Pancreatic neuroendocrine tumors (PNETs) are pancreatic neoplasms with neuroendocrine features, divided into functioning and non-functioning. ...MATERIALS AND METHODS: A review of the literature was performed using the PubMed database and Cochrane li …
BACKGROUND/AIM: Pancreatic neuroendocrine tumors (PNETs) are pancreatic neoplasms with neuroendocrine features, divided into f …
Pancreatic VIPomas: subject review and one institutional experience.
Ghaferi AA, Chojnacki KA, Long WD, Cameron JL, Yeo CJ. Ghaferi AA, et al. J Gastrointest Surg. 2008 Feb;12(2):382-93. doi: 10.1007/s11605-007-0177-0. J Gastrointest Surg. 2008. PMID: 17510774 Review.
All patients had no family history of multiple endocrine neoplasia. Computed tomography revealed the primary pancreatic tumor in all patients, with three tumors located in the tail of the pancreas. ...Mean serum vasoactive intestinal polypeptide …
All patients had no family history of multiple endocrine neoplasia. Computed tomography revealed the primary pancreatic tumor
Clinical Presentation and Diagnosis of Pancreatic Neuroendocrine Tumors.
Anderson CW, Bennett JJ. Anderson CW, et al. Surg Oncol Clin N Am. 2016 Apr;25(2):363-74. doi: 10.1016/j.soc.2015.12.003. Epub 2016 Feb 18. Surg Oncol Clin N Am. 2016. PMID: 27013370 Review.
Pancreatic neuroendocrine tumors are a rare group of neoplasms that arise from multipotent stem cells in the pancreatic ductal epithelium. Although they comprise only 1% to 2% of pancreatic neoplasms, their incidence is increasing. Most pancreatic neur
Pancreatic neuroendocrine tumors are a rare group of neoplasms that arise from multipotent stem cells in the pancreatic ductal
Pancreatic neuroendocrine tumors: contemporary diagnosis and management.
Parbhu SK, Adler DG. Parbhu SK, et al. Hosp Pract (1995). 2016 Aug;44(3):109-19. doi: 10.1080/21548331.2016.1210474. Epub 2016 Jul 18. Hosp Pract (1995). 2016. PMID: 27404266 Review.
Pancreatic neuroendocrine tumors (PNETs) are neoplasms that arise from the hormone producing cells of the islets of Langerhans, also known as pancreatic islet cells. ...This manuscript will review pancreatic neuroendocrine tumor subtypes, syndro
Pancreatic neuroendocrine tumors (PNETs) are neoplasms that arise from the hormone producing cells of the islets of Langerhans
152 results