- 関
- neurofibromatosis 1、neurofibromatosis I、neurofibromatosis type 1、neurofibromatosis type I、type I neurofibromatosis、von Recklinghausen disease、von Recklinghausen's disease、Watson syndrome
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
- autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities (同)von Recklinghausen''s disease
- 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
UpToDate Contents
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- 1. 神経線維腫症I型（NF1）：病因、臨床的特徴、および診断 neurofibromatosis type 1 nf1 pathogenesis clinical features and diagnosis
- 2. 神経線維腫症I型（NF1）：マネージメントおよび予後 neurofibromatosis type 1 nf1 management and prognosis
- 3. 色素沈着過剰を有する患者へのアプローチ approach to the patient with hyperpigmentation disorders
- 4. 神経線維腫症2型 neurofibromatosis type 2
- 5. 末梢神経腫瘍 peripheral nerve tumors
English Journal
- Effect of posterior multilevel vertebral osteotomies on coronal and sagittal balance in fused scoliosis deformity caused by previous surgery: preliminary results.
- Yang JH1, Suh SW, Cho WT, Hwang JH, Hong JY, Modi HN.
- Spine.Spine (Phila Pa 1976).2014 Oct 15;39(22):1840-9. doi: 10.1097/BRS.0000000000000555.
- STUDY DESIGN: Prospective case series study.OBJECTIVE: To study the effect of posterior multilevel vertebral osteotomy (posterior crack osteotomy) on coronal and sagittal balance in patients with the fusion mass over the spine caused by previous surgery.SUMMARY OF BACKGROUND DATA: Few studies have i
- PMID 25299167
- Somatic mutations of SUZ12 in malignant peripheral nerve sheath tumors.
- Zhang M1, Wang Y1, Jones S2, Sausen M2, McMahon K1, Sharma R3, Wang Q1, Belzberg AJ4, Chaichana K4, Gallia GL4, Gokaslan ZL4, Riggins GJ4, Wolinksy JP4, Wood LD3, Montgomery EA3, Hruban RH3, Kinzler KW1, Papadopoulos N1, Vogelstein B1, Bettegowda C5.
- Nature genetics.Nat Genet.2014 Oct 12. doi: 10.1038/ng.3116. [Epub ahead of print]
- Neurofibromatosis 1 is a hereditary syndrome characterized by the development of numerous benign neurofibromas, a small subset of which progress to malignant peripheral nerve sheath tumors (MPNSTs). To better understand the genetic basis for MPNSTs, we performed genome-wide or targeted sequencing on
- PMID 25305755
- Combination of tracheal bronchus and partial anomalous pulmonary venous return in a patient with type 1 neurofibromatosis and ipsilateral vagal nerve neurofibroma.
- Gorospe Sarasúa L1, Saldaña Garrido D2, Ayala Carbonero AM3.
- Archivos de bronconeumologia.Arch Bronconeumol.2014 Oct 6. pii: S0300-2896(14)00334-2. doi: 10.1016/j.arbres.2014.07.013. [Epub ahead of print]
- PMID 25301412
Japanese Journal
- Development of a practical NF1 genetic testing method through the pilot analysis of five Japanese families with neurofibromatosis type 1
- Okumura Akiko,Ozaki Mamoru,Niida Yo
- Brain and Development 37(7), 677-689, 2015-08-01
- … Objective: Mutation analysis of NF1, the responsible gene for neurofibromatosis type 1 (NF1), is still difficult due to its large size, lack of mutational hotspots, the presence of many pseudogenes, and its wide spectrum of mutations. … In the other two families, type-1 and unique NF1 microdeletions were detected by DNA microarray analysis. …
- NAID 120005593951
- 症例報告 神経線維腫症1型に合併した縦隔原発胚細胞腫の1例
- 嘉島 相輝,齋藤 満,土谷 順彦 [他]
- 日本泌尿器科学会雑誌 = The Japanese journal of urology 106(3), 178-184, 2015-07
- NAID 40020532427
- 症例 神経線維腫症Ⅰ型に合併した肺MALTリンパ腫の1手術例
- 本村 文宏,田中 明彦,山口 圭介 [他]
- 日本呼吸器学会誌 = Annals of the Japanese Respiratory Society 4(3), 231-234, 2015-05-10
- NAID 40020473772
Related Links
- neurofibromatosis type 1, neurofibromatosis type 2 親から子に遺伝（常染色体優性遺伝疾患）することもありますが，半分以上の患者さんは遺伝ではありません 1型は全身の皮膚にたくさんの小さな腫瘍（末梢神経線維腫）と茶色のシミ ...
- Neurofibromatosis is the name for a number of genetic conditions that cause tumours to grow along your nerves. ... The Neuro Foundation If you or someone you know has neurofibromatosis (both type 1 and type 2), The Neuro ...
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★リンクテーブル★
| リンク元 | 「neurofibromatosis type 1」 |
| 関連記事 | 「type」「typed」「typing」「neurofibromatosis」 |
「neurofibromatosis type 1」
- 関
- neurofibromatosis 1、neurofibromatosis I、neurofibromatosis type I、type 1 neurofibromatosis、type I neurofibromatosis、von Recklinghausen disease、von Recklinghausen's disease、Watson syndrome
「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