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Article: Pancreatic neuroendocrine tumours

TitlePancreatic neuroendocrine tumours
Authors
KeywordsNeuroendocrine tumors
Pancreatic neoplasms
Issue Date2017
Citation
Hong Kong Journal of Radiology, 2017, v. 20, n. 4, p. 292-302 How to Cite?
Abstract© 2017 Hong Kong College of Radiologists. Neuroendocrine tumours (NETs) are a heterogeneous group of malignancies that can arise in different organs. Although NETs account for only 0.5% of all malignancies, their incidence has significantly increased in recent years. In the Asia Pacific region, the most common site of primary NETs is the pancreas. Many new treatment modalities have been shown to be effective in treating NETs. This study re views the diagnosis, management, and prognosis of pancreatic NETs.
Persistent Identifierhttp://hdl.handle.net/10722/251709
ISSN
2020 SCImago Journal Rankings: 0.104
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLam, M. H.C.-
dc.contributor.authorCheuk, W.-
dc.contributor.authorAu Yong, T. K.-
dc.contributor.authorCheng, H. C.-
dc.contributor.authorNgan, R. K.C.-
dc.date.accessioned2018-03-08T05:00:44Z-
dc.date.available2018-03-08T05:00:44Z-
dc.date.issued2017-
dc.identifier.citationHong Kong Journal of Radiology, 2017, v. 20, n. 4, p. 292-302-
dc.identifier.issn2223-6619-
dc.identifier.urihttp://hdl.handle.net/10722/251709-
dc.description.abstract© 2017 Hong Kong College of Radiologists. Neuroendocrine tumours (NETs) are a heterogeneous group of malignancies that can arise in different organs. Although NETs account for only 0.5% of all malignancies, their incidence has significantly increased in recent years. In the Asia Pacific region, the most common site of primary NETs is the pancreas. Many new treatment modalities have been shown to be effective in treating NETs. This study re views the diagnosis, management, and prognosis of pancreatic NETs.-
dc.languageeng-
dc.relation.ispartofHong Kong Journal of Radiology-
dc.subjectNeuroendocrine tumors-
dc.subjectPancreatic neoplasms-
dc.titlePancreatic neuroendocrine tumours-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.12809/hkjr1716443-
dc.identifier.scopuseid_2-s2.0-85041456368-
dc.identifier.volume20-
dc.identifier.issue4-
dc.identifier.spage292-
dc.identifier.epage302-
dc.identifier.isiWOS:000436691500006-
dc.identifier.issnl2223-6619-

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