多腺性自己免疫症候群1型
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"
- the 9th letter of the Roman alphabet (同)i
- 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
- 『私は』私が
- iodineの化学記号
UpToDate Contents
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.
English Journal
- Associated autoimmune diseases in children and adolescents with type 1 diabetes mellitus (T1DM).
- Kakleas K1, Soldatou A1, Karachaliou F2, Karavanaki K3.
- Autoimmunity reviews.Autoimmun Rev.2015 Sep;14(9):781-97. doi: 10.1016/j.autrev.2015.05.002. Epub 2015 May 20.
- Type 1 diabetes (T1DM) is an autoimmune disease with aberrant immune responses to specific β-cell autoantigens, resulting in insulin deficiency. Children and adolescents with T1DM may also develop organ-specific multiple autoimmunity in the context of APS (autoimmune polyendocrine syndrome) type 1,
- PMID 26001590
- Transglutaminase 4 as a prostate autoantigen in male subfertility.
- Landegren N1, Sharon D2, Shum AK3, Khan IS4, Fasano KJ4, Hallgren Å5, Kampf C6, Freyhult E7, Ardesjö-Lundgren B8, Alimohammadi M9, Rathsman S10, Ludvigsson JF11, Lundh D12, Motrich R13, Rivero V13, Fong L14, Giwercman A15, Gustafsson J16, Perheentupa J17, Husebye ES18, Anderson MS4, Snyder M19, Kämpe O5.
- Science translational medicine.Sci Transl Med.2015 Jun 17;7(292):292ra101. doi: 10.1126/scitranslmed.aaa9186.
- Autoimmune polyendocrine syndrome type 1 (APS1), a monogenic disorder caused by AIRE gene mutations, features multiple autoimmune disease components. Infertility is common in both males and females with APS1. Although female infertility can be explained by autoimmune ovarian failure, the mechanisms
- PMID 26084804
- Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases.
- Oftedal BE1, Hellesen A2, Erichsen MM3, Bratland E1, Vardi A4, Perheentupa J5, Kemp EH6, Fiskerstrand T7, Viken MK8, Weetman AP6, Fleishman SJ9, Banka S10, Newman WG10, Sewell WA11, Sozaeva LS12, Zayats T13, Haugarvoll K14, Orlova EM12, Haavik J13, Johansson S7, Knappskog PM7, Løvås K2, Wolff AS1, Abramson J4, Husebye ES15.
- Immunity.Immunity.2015 Jun 16;42(6):1185-96. doi: 10.1016/j.immuni.2015.04.021.
- The autoimmune regulator (AIRE) gene is crucial for establishing central immunological tolerance and preventing autoimmunity. Mutations in AIRE cause a rare autosomal-recessive disease, autoimmune polyendocrine syndrome type 1 (APS-1), distinguished by multi-organ autoimmunity. We have identified m
- PMID 26084028
Japanese Journal
- Reversible Cardiomyopathy Associated with Autoimmune Polyendocrine Syndrome Type II
- Hashimoto's Thyroiditis Concomitant with Sequential Autoimmune Hepatitis, Chorea and Polyserositis: A New Entity of Autoimmune Polyendocrine Syndrome?
Related Links
- APECED APECED Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. A subtype of mucocutaneous candidiasis characterised by increased immunoglobulins and decreased IgA, with progressive decline in ...
- Autoimmune polyendocrine syndrome type 1 (APS-1) (Online Mendelian Inheritance in Man number 240300) is a rare autosomal recessive disorder that develops in early childhood and results in tissue-specific multiorgan ...
★リンクテーブル★
[★]
- 英
- autoimmune polyendocrine syndrome type 1, autoimmune polyendocrine syndrome type I, polyglandular autoimmune syndrome type 1, polyglandular autoimmune syndrome type I, APS1, APS-1
- 関
- 自己免疫性多腺性内分泌不全症、シュミット症候群、多腺性自己免疫症候群2型、HAM症候群
- autoimmune polyendocrinopathycandidiasis-ectodermal dystrophy, APECED
[show details]
概念
参考
- 1. AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I; APS1 - OMIM
- http://omim.org/240300
- 2. 多腺性自己免疫症候群 1 型と副甲状腺自己抗原 NALP5
- http://www.nankodo.co.jp/yosyo/xforeign/nejm/358/358mar/xf358-10-1018.htm
[★]
- (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
- 関
- form、mode、pattern、type specimen、typed
[★]
[★]
[★]
- 関
- form、mode、pattern、type
[★]