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[Comparison of clinical characteristics between sporadic gastrinoma and multiple endocrine neoplasia type 1-related gastrinoma].
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A Novel Pathogenic Gene Variant Identified in a Family With Multiple Pancreatic Neuroendocrine Tumors.
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Epidemiological trends of pancreatic and gastrointestinal neuroendocrine tumors in Japan: a nationwide survey analysis.
J Gastroenterol. 2015 Jan;50(1):58-64. doi: 10.1007/s00535-014-0934-2. Epub 2014 Feb 6.
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Multiple endocrine neoplasia type 1 in Japan: establishment and analysis of a multicentre database.
Clin Endocrinol (Oxf). 2012 Apr;76(4):533-9. doi: 10.1111/j.1365-2265.2011.04227.x.
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Completion pancreatectomy and duodenectomy for recurrent MEN-1 pancreaticoduodenal endocrine neoplasms.
Surgery. 2009 Oct;146(4):801-6; discussion 807-8. doi: 10.1016/j.surg.2009.06.038.
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Management of pancreatic endocrine tumors in multiple endocrine neoplasia type 1.
World J Surg. 2006 May;30(5):643-53. doi: 10.1007/s00268-006-0360-y.
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Pituitary disease in MEN type 1 (MEN1): data from the France-Belgium MEN1 multicenter study.
J Clin Endocrinol Metab. 2002 Feb;87(2):457-65. doi: 10.1210/jcem.87.2.8145.
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MEN1 gene mutations in sporadic neuroendocrine tumors of foregut derivation.
Pathol Int. 1999 Nov;49(11):968-73. doi: 10.1046/j.1440-1827.1999.00971.x.
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Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases.
Hum Mutat. 1999;13(1):54-60. doi: 10.1002/(SICI)1098-1004(1999)13:1<54::AID-HUMU6>3.0.CO;2-K.

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