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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1964 1
1965 1
1966 1
1969 1
1970 4
1971 2
1972 1
1973 4
1974 5
1975 4
1976 2
1977 1
1978 2
1979 5
1980 2
1981 3
1982 4
1983 4
1984 6
1985 3
1986 13
1987 12
1988 5
1989 7
1990 7
1991 9
1992 7
1993 15
1994 6
1995 13
1996 10
1997 8
1998 18
1999 16
2000 5
2001 12
2002 11
2003 8
2004 8
2005 10
2006 8
2007 8
2008 4
2009 9
2010 9
2011 10
2012 7
2013 7
2014 1
2015 3
2016 1
2017 3
2018 3
2019 4
2020 3
2021 3
2022 2
2023 4
2024 2

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337 results

Results by year

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Page 1
Incidence and Prognosis of Primary Gastrinomas in the Hepatobiliary Tract.
Norton JA, Foster DS, Blumgart LH, Poultsides GA, Visser BC, Fraker DL, Alexander HR, Jensen RT. Norton JA, et al. JAMA Surg. 2018 Mar 1;153(3):e175083. doi: 10.1001/jamasurg.2017.5083. JAMA Surg. 2018. PMID: 29365025 Free PMC article.
Gastrinomas typically occur in the pancreas or the duodenum. OBJECTIVE: To describe the incidence and prognosis of very unusual gastrinomas originating in the hepatobiliary tract. ...In addition, their discovery dictates that lymph nodes in the porta hepatis should be rout …
Gastrinomas typically occur in the pancreas or the duodenum. OBJECTIVE: To describe the incidence and prognosis of very unusual gastr …
Zollinger-Ellison syndrome: recent advances and controversies.
Ito T, Igarashi H, Jensen RT. Ito T, et al. Curr Opin Gastroenterol. 2013 Nov;29(6):650-61. doi: 10.1097/MOG.0b013e328365efb1. Curr Opin Gastroenterol. 2013. PMID: 24100728 Free PMC article. Review.
RECENT FINDINGS: Recent advances in the management of ZES include: improved understanding of the pathogenesis of gastrinoma and pancreatic neuroendocrine tumors, new prognostic classification systems, new diagnostic algorithms, more sensitive localization studies, new trea …
RECENT FINDINGS: Recent advances in the management of ZES include: improved understanding of the pathogenesis of gastrinoma and pancreatic n …
Causes of death and prognostic factors in multiple endocrine neoplasia type 1: a prospective study: comparison of 106 MEN1/Zollinger-Ellison syndrome patients with 1613 literature MEN1 patients with or without pancreatic endocrine tumors.
Ito T, Igarashi H, Uehara H, Berna MJ, Jensen RT. Ito T, et al. Medicine (Baltimore). 2013 May;92(3):135-181. doi: 10.1097/MD.0b013e3182954af1. Medicine (Baltimore). 2013. PMID: 23645327 Free PMC article.
Because effective treatments have been developed for the hormone excess state, which was a major cause of death in these patients in the past, coupled with the recognition that nonendocrine tumors increasingly develop late in the disease course, the natural history of the …
Because effective treatments have been developed for the hormone excess state, which was a major cause of death in these patients in the pas …
Diagnosis and management of Zollinger-Ellison syndrome in 2018.
De Angelis C, Cortegoso Valdivia P, Venezia L, Bruno M, Pellicano R. De Angelis C, et al. Minerva Endocrinol. 2018 Jun;43(2):212-220. doi: 10.23736/S0391-1977.17.02745-6. Epub 2017 Sep 25. Minerva Endocrinol. 2018. PMID: 28949124 Review.
Gastrinoma--morphological aspects.
Klöppel G, Anlauf M. Klöppel G, et al. Wien Klin Wochenschr. 2007;119(19-20):579-84. doi: 10.1007/s00508-007-0885-1. Wien Klin Wochenschr. 2007. PMID: 17985091 Review.
The duodenal gastrinomas are small, and when they occur in association with the genetic syndrome of multiple endocrine neoplasia type 1 (MEN1), they are multicentric and originate from precursor lesions. The prognosis of duodenal gastrinomas is better than that of pancreat …
The duodenal gastrinomas are small, and when they occur in association with the genetic syndrome of multiple endocrine neoplasia type 1 (MEN …
Neuroendocrine Tumors of the Stomach.
Corey B, Chen H. Corey B, et al. Surg Clin North Am. 2017 Apr;97(2):333-343. doi: 10.1016/j.suc.2016.11.008. Epub 2017 Mar 3. Surg Clin North Am. 2017. PMID: 28325190 Review.
Type I gastric NETs are associated with chronic atrophic gastritis. They have a good prognosis and endoscopic resection is the mainstay of treatment. Type II gastric NETs are caused by hypergastrinemia. They have a poorer prognosis, and resection is required to cont …
Type I gastric NETs are associated with chronic atrophic gastritis. They have a good prognosis and endoscopic resection is the mainst …
Gastric neuroendocrine tumours.
Crosby DA, Donohoe CL, Fitzgerald L, Muldoon C, Hayes B, O'Toole D, Reynolds JV. Crosby DA, et al. Dig Surg. 2012;29(4):331-48. doi: 10.1159/000342988. Epub 2012 Oct 17. Dig Surg. 2012. PMID: 23075625 Free article. Review.
Selection of articles was based on peer review, journal and relevance. RESULTS: Gastric NETs may be divided into three clinical prognostic groups: type I is associated with autoimmune atrophic gastritis and hypergastrinaemia, type II is associated with Zollinger-Ellison sy …
Selection of articles was based on peer review, journal and relevance. RESULTS: Gastric NETs may be divided into three clinical prognosti …
Gastric neuroendocrine tumors.
Delle Fave G, Capurso G, Annibale B, Panzuto F. Delle Fave G, et al. Neuroendocrinology. 2004;80 Suppl 1:16-9. doi: 10.1159/000080734. Neuroendocrinology. 2004. PMID: 15477710 Review.
Gastric carcinoids are rare neuroendocrine tumors, usually classified as type I, if associated with atrophic body gastritis; type II, if associated with Zollinger-Ellison syndrome and multiple endocrine neoplasia type I, and type III, in the absence of any gastric pathology (spor …
Gastric carcinoids are rare neuroendocrine tumors, usually classified as type I, if associated with atrophic body gastritis; type II, if ass …
Pancreatic endocrine tumors.
Oberg K. Oberg K. Semin Oncol. 2010 Dec;37(6):594-618. doi: 10.1053/j.seminoncol.2010.10.014. Semin Oncol. 2010. PMID: 21167379 Review.
They represent a heterogeneous group with very varying tumor biology and prognosis. About half of the patients present clinical symptoms and syndromes related to substances released from the tumors (Zollinger-Ellison syndrome, insulinoma, glucagonoma, etc) and the other ha …
They represent a heterogeneous group with very varying tumor biology and prognosis. About half of the patients present clinical sympt …
337 results