- Scintigraphic evaluation of multiple endocrine neoplasia type 2 (MEN type 2)
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Lee JT, Lee KB, Whang KS, Kim BW, Lee IK
- KMID: 1686044
- Korean J Nucl Med.
- 1991 May;25(1):122-128.
No abstract available. -
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- Multiple Endocrine Neoplasia and Familial Medullary Thyroid Carcinoma
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Choi YS
- KMID: 2095101
- J Korean Thyroid Assoc.
- 2012 Nov;5(2):124-131.
- doi: 10.11106/jkta.2012.5.2.124
Multiple endocrine neoplasia (MEN) is defined as a disorder with neoplasms in two or more different hormonal tissues in several members of a family. MEN1, or Wermer's syndrome, is inherited... -
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- Imaging Finding of Multiple Endocrine Neoplasia Type 1: Case Report
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Yum TJ, Cho HW
- KMID: 1427220
- J Korean Soc Ultrasound Med.
- 2012 Dec;31(4):247-249.
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant inherited syndrome with characteristic clinical and radiological manifestations. Many reports on MEN1 have been published; however, no cases of radiologically... -
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- A Case of Multiple Endocrine Neoplasia type 3 With Multiple Mucosal Neuroma
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Lee CW, Oh CK, Jang HS, Kwon KS, Chung TA
- KMID: 2303400
- Korean J Dermatol.
- 1999 Apr;37(4):505-509.
Multiple endocrine neoplasi~a type 3 is a rare, heritable or sporadic, multiple neoplastic disorder that is charracterized by thyroid medullary careinoma, pheochromocytoma, multiple mucosal neuroma, and marfanoid habitus. The most... -
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- A Case of Insulinoma Combined with Pheochromocytoma
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Lee SH, Youn YH, Lim SK, Cha BS, Lee HC, Noh TW, Huh KB
- KMID: 2199752
- J Korean Soc Endocrinol.
- 2000 Oct;15(4-5):640-647.
Multiple endocrine neoplasia (MEN) is a combination of endocrine tumor associations and consists of 3 types: 1, 2A and 2B. Herein, we report a case of insulinoma which is combined... -
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- A Case of Multiple Endocrine Neoplasia Type I with Atypical Clinical Course
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Choi YS, Bai YS, Ku BJ, Jo YS, Kim YK, Ro HK, Shong M
- KMID: 2333264
- J Korean Endocr Soc.
- 2008 Aug;23(4):266-271.
Multiple endocrine neoplasia type 1 (MEN 1) is characterized by the combined occurrence of primary hyperparathyroidism, enteropancreatic tumors and anterior pituitary adenoma. Yet carcinoid tumors, adrenal adenoma and lipoma might... -
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- Genetic diagnosis of multiple endocrine neoplasia 2A with linkage analysis
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Lee MS, Lee JO, Kang TW, Lee JH
- KMID: 1698150
- Korean J Intern Med.
- 1992 Jun;42(6):809-815.
No abstract available. -
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- Partial adrenalectomy for bilateral pheochromocytoma in multiple endocrine neoplasia type IIa with maintenance of adrenocortical function: a case report
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Jeong HS, Kim KR, Moon YH
- KMID: 1939962
- J Korean Surg Soc.
- 1992 Apr;42(4):568-574.
No abstract available. -
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- Multiple Endocrine Neoplasia Type 2B Diagnosed Early by Conjunctival Neuroma: a Case Report
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Kim DH, Jang YS, Kang SR, Lim DM
- KMID: 2362360
- Int J Thyroidol.
- 2016 Nov;9(2):204-209.
- doi: 10.11106/ijt.2016.9.2.204
Multiple endocrine neoplasia type 2B (MEN 2B) is an autosomal dominant disorder characterized by medullary thyroid cancer, pheochromocytoma, neuroma and Marfanoid feature. Medullary thyroid cancer occurs in more than 95%... -
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- A case of multiple endocrine neoplasia type 3
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Yoon KH, Yoo SJ, Son HS, Kang MI, Hong KS, Lee KW, Son HY, Kang SK
- KMID: 1686665
- J Korean Soc Endocrinol.
- 1991 Sep;6(3):282-286.
No abstract available. -
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- A new type of multiple endocrine adenopathy
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Oh SK, Yoo HY
- KMID: 1939857
- J Korean Surg Soc.
- 1993 Dec;45(6):1034-1041.
No abstract available. -
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- A case of multiple endocrine neoplasia type IIa with family history
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Chun SB, Kim SE, Chung YS, Ahn KJ, Lee HC, Huh KB, Choi YJ, Lee YB
- KMID: 1698155
- Korean J Intern Med.
- 1992 Jun;42(6):842-850.
No abstract available. -
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- A Case of Familial Multiple Endocrine Neoplasia with MEN1 Gene Mutation
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Sung HY, Chun YJ, Lee H, Kwon BJ, Park KW, Lee JM, Moon SD, Chang SA, Han JH
- KMID: 2391913
- J Korean Endocr Soc.
- 2006 Dec;21(6):560-566.
Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal dominant disorder that's characterized by the combined occurrence of primary hyperparathyroidism, endocrine pancreatic tumors and anterior pituitary adenomas, but such... -
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- Multiple Neuroendocrine Tumors in Stomach and Duodenum in a Multiple Endocrine Neoplasia Type 1 Patient
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Kim B, Yang HK, Kim WH
- KMID: 2408514
- J Pathol Transl Med.
- 2018 Mar;52(2):126-129.
- doi: 10.4132/jptm.2017.09.16
A 67-year-old woman with a history of subtotal parathyroidectomy, distal pancreatectomy, and total splenectomy 23 years prior underwent surgical gastric resection for neuroendocrine tumors of the stomach and duodenum. Meticulous... -
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- Endoscopic Ultrasonography-Guided Ethanol Injection for a Pancreatic Neuroendocrine Tumor with Multiple Endocrine Neoplasia Type 1
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An S, Lee JY, Hwang SH, Park DH, Lee SK
- KMID: 2448580
- Korean J Pancreas Biliary Tract.
- 2016 Oct;21(4):202-208.
- doi: 10.15279/kpba.2016.21.4.202
Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited disorder caused by mutations in the MEN1 gene on chromosome 1. Clinical diagnostic criteria for MEN1 include the presence of... -
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- Ectopic ACTH Syndrome with Bilateral Pheochromocytoma in Multiple Endocrine Neoplasia Type 2A
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Moon JM, Kim YJ, Seo YJ, Choi HY, Kim JH, Park JR, Lee YJ, Kim HY, Kim SG, Choi DS
- KMID: 1468546
- J Korean Endocr Soc.
- 2009 Dec;24(4):265-271.
- doi: 10.3803/jkes.2009.24.4.265
Multiple endocrine neoplasia type 2A (MEN 2A) is an autosomal dominant syndrome characterized by the presence of medullary thyroid carcinoma, pheochromocytoma, and hyperparathyroidism. MEN 2A arises due to a germline... -
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- Hereditary Aspect of Isolated Familial Acromegaly
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Lee WC, Shin MS, Lee KS, Jung N, Huh SK
- KMID: 1694193
- J Korean Neurosurg Soc.
- 1993 Dec;22(12):1309-1318.
Acromegaly is classically considered a sporadic nonfamilial condition. The familial occurance of pituitary adenomas is encountered as a manifestation of the Multiple Endocrine Neoplasia Type I(MEN 1). Moreover in MEN... -
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- A family of multiple endocrine neoplasia type 2A associated with a C618R mutation in RET proto-oncogene
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Kim NH, Kim JH, Nam JH, Park JP, Park JE, Choi YS, Park YH
- KMID: 1833332
- Korean J Med.
- 2006 Apr;70(4):448-454.
Medullary thyroid carcinoma (MTC) is a relatively rare malignant thyroid disease that accounts for approximately 1% to 5% of all thyroid carcinomas. MTC occurs as a sporadic disease and as... -
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- A Case of Multiple endocrine neoplasia type 2a
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Hong SJ, Yang IM, Woo JT, Kim JW, Kim YS, Choi YK, Yun YS, Lee CH, Lee SH, Kim DY, Kim SW
- KMID: 2331074
- J Korean Soc Endocrinol.
- 1997 Jun;12(2):328-337.
Multiple endocrine neoplasia type2a (MEN type2a) is a dominantly inherited cancer syndrome which is characterized by medullary thyroid carcinoma, pheochromocytoma and parathyroid hyperplasia or adenoma. Recent reports show that DNA... -
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- A case of multiple endocrine neoplasia, type 3
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Kim YL, Yoo SJ, Son HS, Yoon KH, Kang MI, Hong KS, Jun SS, Lee KW, Son HY, Kang SK, Park SM, Kim YH
- KMID: 1698010
- Korean J Intern Med.
- 1991 Nov;41(5):703-709.
No abstract available. -
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