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Medullary thyroid carcinoma, genes, and the prevention of cancer.

作者信息

Utiger R D

出版信息

N Engl J Med. 1994 Sep 29;331(13):870-1. doi: 10.1056/NEJM199409293311309.

DOI:10.1056/NEJM199409293311309
PMID:7915823
Abstract
摘要

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Medullary thyroid carcinoma, genes, and the prevention of cancer.甲状腺髓样癌、基因与癌症预防
N Engl J Med. 1994 Sep 29;331(13):870-1. doi: 10.1056/NEJM199409293311309.
2
Impact of prospective screening for multiple endocrine neoplasia type 2.2型多发性内分泌腺瘤病前瞻性筛查的影响
Henry Ford Hosp Med J. 1987;35(2-3):94-8.
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Clinical screening as compared with DNA analysis in families with multiple endocrine neoplasia type 2A.2A型多发性内分泌腺瘤病家族中临床筛查与DNA分析的比较
N Engl J Med. 1994 Sep 29;331(13):828-35. doi: 10.1056/NEJM199409293311302.
4
Pheochromocytoma and medullary carcinoma of thyroid.嗜铬细胞瘤与甲状腺髓样癌。
Cancer. 1968 Feb;21(2):302-11. doi: 10.1002/1097-0142(196802)21:2<302::aid-cncr2820210220>3.0.co;2-r.
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MEN-2 syndrome: the value of screening and central registration; a study of six kindreds in The Netherlands.多发性内分泌腺瘤2型综合征:筛查及中央登记的价值;荷兰六个家族的研究
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6
One hundred and seven family members with the rearranged during transfection V804M proto-oncogene mutation presenting with simultaneous medullary and papillary thyroid carcinomas, rare primary hyperparathyroidism, and no pheochromocytomas: is this a new syndrome--MEN 2C?107名家庭成员存在转染期间重排的V804M原癌基因突变,表现为同时患有甲状腺髓样癌和乳头状癌、罕见的原发性甲状旁腺功能亢进,且无嗜铬细胞瘤:这是一种新的综合征——MEN 2C吗?
Surgery. 2009 Dec;146(6):998-1005. doi: 10.1016/j.surg.2009.09.021.
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[Multiple endocrine neoplasm type II-A].[II型多发性内分泌腺瘤病A]
Med Clin (Barc). 1985 Nov 30;85(18):756-8.
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Molecular abnormalities in tumors associated with multiple endocrine neoplasia type 2.与2型多发性内分泌肿瘤相关的肿瘤中的分子异常
Endocrinol Metab Clin North Am. 1994 Mar;23(1):187-213.
9
[Multiple endocrine neoplasm syndrome (MEN-2a) or Sipple syndrome. Report of 2 cases].[多发性内分泌肿瘤综合征(MEN - 2a)或西普尔综合征。2例报告]
Rev Clin Esp. 1983;170(1-2):45-9.
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[Usefulness of calcitonin measurement for the diagnosis of medullary cancer of the thyroid in a family with multiple endocrine adenoma syndrome of type IIB].[降钙素测定在IIB型多发性内分泌腺瘤综合征家族性甲状腺髓样癌诊断中的应用]
Rev Med Chil. 1984 Jul;112(7):675-80.

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Carcinoembryonic antigen levels correlated with advanced disease in medullary thyroid cancer.癌胚抗原水平与甲状腺髓样癌的晚期疾病相关。
J Otolaryngol Head Neck Surg. 2018 Sep 17;47(1):55. doi: 10.1186/s40463-018-0303-x.
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Can Medullary Thyroid Carcinoma Arise in Thyroglossal Duct Cysts? A Search for Parafollicular C-cells in 41 Resected Cases.甲状腺髓样癌会在甲状舌管囊肿中发生吗?对41例切除病例中滤泡旁C细胞的研究。
Head Neck Pathol. 2018 Mar;12(1):71-74. doi: 10.1007/s12105-017-0826-x. Epub 2017 May 23.
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Different RET gene mutation-induced multiple endocrine neoplasia type 2A in 3 Chinese families.3个中国家系中不同RET基因突变诱发的2A型多发性内分泌肿瘤
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Metastatic lymph node ratio can further stratify risk for mortality in medullary thyroid cancer patients: A population-based analysis.转移性淋巴结比率可进一步对甲状腺髓样癌患者的死亡风险进行分层:一项基于人群的分析。
Oncotarget. 2016 Oct 4;7(40):65937-65945. doi: 10.18632/oncotarget.11725.
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Prognostic significance and optimal cutoff of age in medullary thyroid cancer.甲状腺髓样癌中年龄的预后意义及最佳临界值
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Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome).2B型多发性内分泌肿瘤(黏膜神经瘤综合征,瓦根曼-弗勒布斯综合征)
J Med Genet. 1996 Sep;33(9):779-82. doi: 10.1136/jmg.33.9.779.