WordNet

any of various organs that synthesize substances needed by the body and release it through ducts or directly into the bloodstream (同)secretory organ, secretor, secreter
an abnormal new mass of tissue that serves no purpose (同)tumour, neoplasm

PrepTutorEJDIC

《所有・所属》…『の』,…のものである,…に属する・《材料・要素》…『でできた』,から成る・《部分》…『の』[『中の』] ・《数量・単位・種類を表す名詞に付いて》…の・《原因・動機》…『で』,のために(because of) ・《主格関係》…『の』,による,によって・《目的格関係》…『を』,の・《同格関係》…『という』・《関係・関連》…『についての』[『の』],の点で・《抽象名詞などと共に》…の[性質をもつ] ・《『It is』+『形』+『of』+『名』+『to』 doの形で,ofの後の名詞を意味上の主語として》・《分離》…『から』・《起原・出所》…『から』[『の』](out of) ・《『名』+『of』+『a』(『an』)+『名』の形で》…のような・《『名』+『of』+『mine』(『yours, his』など独立所有格)の形で》…の…・《時》(1)《副詞句を作って》…に《形容詞句を作って》…の・《時刻》《米》…前(to,《米》before)
(生物体内の)腺(せん)
副甲状腺の,上皮小体の
OLD French古[代]フランス語

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

Early-onset, severe, and recurrent primary hyperparathyroidism associated with a novel CDC73 mutation.

Shibata Y1, Yamazaki M, Takei M, Uchino S, Sakurai A, Komatsu M.
Endocrine journal.Endocr J.2015 May 8. [Epub ahead of print]
Hyperparathyroidism-jaw tumor syndrome (HPT-JT) is a rare autosomal dominant hereditary tumor syndrome characterized by synchronous or metachronous occurrence of primary hyperparathyroidism (PHPT), ossifying fibroma of the maxilla and/or mandible, renal tumor and uterine tumors. Early diagnosis of t
PMID 25959515

Complication rates of central compartment dissection in papillary thyroid cancer.

Kwan WY1, Chow TL, Choi CY, Lam SH.
ANZ journal of surgery.ANZ J Surg.2015 Apr;85(4):274-8. doi: 10.1111/ans.12343. Epub 2013 Jul 26.
BACKGROUND: The benefits of central compartment dissection (CCD) in papillary thyroid carcinoma (PTC) are still debatable and should be weighed against its potential risks. We aim to compare the complication rates in total thyroidectomy with and without CCD for patients with PTC.METHODS: This is a r
PMID 23890372

Corrado KR1, Andrade SC, Bellizzi J, D'Souza-Li L, Arnold A.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.J Bone Miner Res.2015 Mar 31. doi: 10.1002/jbmr.2516. [Epub ahead of print]
Neonatal severe hyperparathyroidism (NSHPT) is a rare disorder characterized by major hypercalcemia, elevated parathyroid hormone levels, and marked enlargement of multiple parathyroid glands, usually associated with germline mutations in the calcium receptor gene CASR. However, little is known abou
PMID 25828954

Early-onset, severe, and recurrent primary hyperparathyroidism associated with a novel CDC73 mutation

Shibata Yusuke,Yamazaki Masanori,Takei Masahiro,Uchino Shinya,Sakurai Akihiro,Komatsu Mitsuhisa
Endocrine Journal advpub(0), 2015
… Hyperparathyroidism-jaw tumor syndrome (HPT-JT) is a rare autosomal dominant hereditary tumor syndrome characterized by synchronous or metachronous occurrence of primary hyperparathyroidism (PHPT), ossifying fibroma of the maxilla and/or mandible, renal tumor and uterine tumors. …
NAID 130005066950

A newly identified missense mutation in RET codon 666 is associated with the development of medullary thyroid carcinoma [Rapid Communication]

Yamazaki Masanori,Hanamura Toru,Ito Ken-ichi,Uchino Shinya,Sakurai Akihiro,Komatsu Mitsuhisa
Endocrine Journal 61(11), 1141-1144, 2014
… A 38-year-old woman with a thyroid nodule measuring approximately 2 cm was suspected to have medullary thyroid carcinoma (MTC) because of markedly elevated serum calcitonin and carcinoembryonic antigen levels. …
NAID 130004699221

佐藤伸也,橘正剛,横井忠郎,山下弘幸,廣田伊千夫,江口徹
日本臨床外科学会雑誌 74(9), 2389-2393, 2013
症例は39歳，女性．尿路結石の検査時に高カルシウム血症が判明した．カルシウム11.1mg/dl，無機リン2.6mg/dl，intact-PTH 148pg/mlより原発性副甲状腺機能亢進症が疑われたが，頸部では腫大副甲状腺を同定できなかった．<SUP>99m</SUP>Tc-MIBIシンチにて中縦隔に淡い集積を認め，胸部CTで肺動脈と大動脈弓に囲まれる位置に1.5cmの腫瘍 …
NAID 130004901158