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
- any degenerative disorder resulting from inadequate or faulty nutrition
- of or relating to or consisting of muscle; "muscular contraction"
- having or suggesting great physical power or force; "the muscular and passionate Fifth Symphony"
- present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
- writing done with a typewriter (同)typewriting
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
- 栄養障害 / 筋萎縮症,筋ジストロフィー(筋肉の退化・萎縮・運動障害などが起こる病気)
- 『助肉の』,筋肉でできた / 筋肉による / 筋肉の発達した
- (病気・身体的欠陥など)生まれつきの,先天的な
UpToDate Contents
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English Journal
- ISPD gene homozygous deletion identified by SNP array confirms prenatal manifestation of Walker-Warburg syndrome.
- Trkova M1, Krutilkova V2, Smetanova D2, Becvarova V2, Hlavova E2, Jencikova N2, Hodacova J2, Hnykova L2, Hroncova H2, Horacek J2, Stejskal D2.
- European journal of medical genetics.Eur J Med Genet.2015 Aug;58(8):372-5. doi: 10.1016/j.ejmg.2015.05.004. Epub 2015 Jun 16.
- Walker-Warburg syndrome (WWS) is a rare form of autosomal recessive, congenital muscular dystrophy that is associated with brain and eye anomalies. Several genes encoding proteins involved in abnormal α-dystroglycan glycosylation have been implicated in the aetiology of WWS, most recently the ISPD
- PMID 26087224
- Cochlear malformation and sensorineural hearing loss in the Walker-Warburg Syndrome.
- Aimoni C1, Malagò M, Bianchini C, Borgatti L, Ciorba A.
- Minerva pediatrica.Minerva Pediatr.2015 Aug;67(4):380-1. Epub 2015 Jan 16.
- PMID 25592765
Japanese Journal
- 臨床研究・症例報告 頭蓋内出血によるけいれん発作を契機に発見された横紋筋融解症合併の福山型先天性筋ジストロフィーの1例
Related Links
- Fukuyama congenital muscular dystrophy is an inherited condition that predominantly affects the muscles, brain, and .... Fukuyama syndrome; Fukuyama type congenital muscular dystrophy; Muscular dystrophy, congenital, Fukuyama type ...
★リンクテーブル★
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- 英
- Fukuyama congenital muscular dystrophy FCMD, Fukuyama type congenital muscular dystrophy
- 同
- 福山型筋ジストロフィー
- 関
- 福山症候群、先天性筋ジストロフィー
[show details]
- fukutin遺伝子異常による中枢神経症状を伴う筋変性疾患
参考
- Fukuyama congenital muscular dystrophy
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- 同
- Fukuyama type congenital muscular dystrophy
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- (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
[★]
- (医)栄養失調、栄養失調症。(医)異栄養、異栄養症、ジフトロフィー
- 栄養障害。細胞や組織の物質代謝障害によって変性・萎縮などの起こること。
[★]
- 関
- congenital、congenitally
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- 関
- muscle、muscularis、musculus、myo
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- 関
- form、mode、pattern、type