WordNet
- write by means of a keyboard with types; "type the acceptance letter, please" (同)typewrite
- a small metal block bearing a raised character on one end; produces a printed character when inked and pressed on paper; "he dropped a case of type, so they made him pick them up"
- (biology) the taxonomic group whose characteristics are used to define the next higher taxon
- a subdivision of a particular kind of thing; "what type of sculpture do you prefer?"
- all of the tokens of the same symbol; "the word `element contains five different types of character"
- printed characters; "small type is hard to read"
- identify as belonging to a certain type; "Such people can practically be typed" (同)typecast
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- writing done with a typewriter (同)typewriting
- of or relating to the immune response of the body against substance normally present in the body
PrepTutorEJDIC
- 〈C〉(…の)『型』,タイプ,類型,種類(kind)《+of+名》 / 〈C〉(その種類の特質を最もよく表している)『典型』,手本,模範《+of+名》 / 〈U〉《集合的に》活字;〈C〉(1個の)活字 / 〈U〉(印刷された)字体,活字 / 〈C〉(貨幣・メダルなどの)模様,図柄 / 〈C〉血液型(blood group) / …‘を'タイプに打つ / (…として)…‘を'分類する《+名+as+名(doing)》 / …‘の'型を決める / タイプライターを打つ
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
UpToDate Contents
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- 1. 原発性副腎不全（アジソン病）の原因 causes of primary adrenal insufficiency addisons disease
- 2. 慢性粘膜皮膚カンジダ症 chronic mucocutaneous candidiasis
- 3. 自己免疫性副腎不全の病因 pathogenesis of autoimmune adrenal insufficiency
- 4. 副甲状腺機能低下症 hypoparathyroidism
- 5. 幼児および小児における低カルシウム血症の病因 etiology of hypocalcemia in infants and children
English Journal
- Polyglandular autoimmune syndrome type I - a novel AIRE mutation in a North American patient.
- Huibregtse KE, Wolfgram P, Winer KK, Connor EL.
- Journal of pediatric endocrinology & metabolism : JPEM.J Pediatr Endocrinol Metab.2014 Jun 19. pii: /j/jpem.ahead-of-print/jpem-2013-0328/jpem-2013-0328.xml. doi: 10.1515/jpem-2013-0328. [Epub ahead of print]
- Abstract Autoimmune polyglandular syndrome type 1 (APS-1), also referred to as autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), is a rare autoimmune disease that results from autosomal recessive mutations of the human autoimmune regulatory (AIRE) gene. We present the case of
- PMID 24945421
- A Case of Non-Ischaemic Cardiomyopathy Associated with Autoimmune Polyglandular Syndrome Type III.
- Hadwen TI1, Foster K2, Buchanan J2, Sutcliffe S2, Sinha AK1.
- Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.Endocr Pract.2014 Jun 16:1-10. [Epub ahead of print]
- Objective: To report a case of non-ischaemic dilated cardiomyopathy associated with Autoimmune Polyglandular Syndrome type III.Methods: A review of our patient's medical records was undertaken and her clinical history, investigations, and outcome have been described. In addition a literature review
- PMID 24936552
- Effects of Pump versus Twice-Daily Injection Delivery of Synthetic Parathyroid Hormone 1-34 in Children with Severe Congenital Hypoparathyroidism.
- Winer KK1, Fulton KA2, Albert PS2, Cutler GB Jr2.
- The Journal of pediatrics.J Pediatr.2014 Jun 16. pii: S0022-3476(14)00418-1. doi: 10.1016/j.jpeds.2014.04.060. [Epub ahead of print]
- OBJECTIVE: To compare the response with synthetic human parathyroid hormone (PTH) 1-34 delivered by twice-daily injection vs insulin pump in children with severe congenital hypoparathyroidism due to calcium receptor mutation or autoimmune polyglandular syndrome type 1.STUDY DESIGN: Children and youn
- PMID 24948345
Japanese Journal
- Type 1 Diabetes Mellitus and Isolated Adrenocorticotropin Deficiency Manifested by Parkinsonism: A Case Report and Literature Review
- Internal Medicine 54(20), 2629-2635, 2015
- NAID 130005103195
- 重症筋無力症，バセドウ病合併自己免疫性1型糖尿病の1例
- 糖尿病 58(3), 198-204, 2015
- NAID 130005063318
- 抗GAD抗体，抗glycine受容体抗体，抗GM1抗体が陽性のprogressive encephalomyelitis with rigidity and myoclonusの1例
- 臨床神経学 55(2), 111-114, 2015
- NAID 130004921314
Related Links
- Autoimmune polyglandular syndrome, type 1 is an inherited condition that affects many of the body's organs. It is one of many autoimmune diseases, which are disorders that occur when the immune system ...
- The Counsyl Test: a simple DNA test before pregnancy can screen for birth defects associated with over 100 genetic diseases. ... What is the Prognosis for a Person With Polyglandular Autoimmune Syndrome Type 1? The ...
Related Pictures
★リンクテーブル★
| リンク元 | 「HAM症候群」「APS-1」 |
| 関連記事 | 「type」「typed」「typing」「syndrome」 |
「HAM症候群」
- 英
- HAM syndrome
- 同
- 多腺性自己免疫症候群1型 autoimmune polyglandular syndrome type 1、hypoparathyroidism-Addison-moniliasis syndrome
- ≠HAM HTLV-1関連脊髄症
- 関
- アジソン病、多発性内分泌腺不全症、副甲状腺機能低下症、モニリア症
「APS-1」
[★] 多腺性自己免疫症候群1型 autoimmune polyglandular syndrome type 1
「type」
- n.
- (windows)ファイル内容表示(linux -> cat])
- ex. type report_20111118.jp.htm | php a.php > report_20111118.jp.jp.jp.html
「typed」
- adj.
- 型の
「typing」
- n.
- タイプで打つこと、タイピング。分類
「syndrome」
- n.