フィンランド型アミロイドーシス
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
- republic in northern Europe; achieved independence from Russia in 1917 (同)Republic of Finland, Suomi
- a disorder characterized by deposit of amyloid in organs or tissues; often secondary to chronic rheumatoid arthritis or tuberculosis or multiple myeloma
- 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
- フィンランド(北欧の共和国;首都はHelsinki)
UpToDate Contents
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English Journal
- Penetrating keratoplasty for corneal amyloidosis in familial amyloidosis, Finnish type.
- Mattila JS1, Krootila K1, Kivelä T1, Holopainen JM2.
- Ophthalmology.Ophthalmology.2015 Mar;122(3):457-63. doi: 10.1016/j.ophtha.2014.09.035. Epub 2014 Nov 13.
- PURPOSE: To analyze the outcome of penetrating keratoplasty (PK) to the first eye for corneal amyloidosis in familial amyloidosis, Finnish type (FAF).DESIGN: Single-center, retrospective, nonrandomized, interventional, noncomparative case series.PARTICIPANTS: Thirty-one eyes of 31 patients with FAF.
- PMID 25444639
- Hereditary renal amyloidosis caused by a heterozygous G654A gelsolin mutation: a report of two cases.
- Yamanaka S1, Miyazaki Y2, Kasai K3, Ikeda S4, Kiuru-Enari S5, Hosoya T2.
- Clinical kidney journal.Clin Kidney J.2013 Apr;6(2):189-93. doi: 10.1093/ckj/sft007.
- Finnish-type familial amyloidosis (FAF) is a rare hereditary systemic amyloidosis that mainly exhibits cranial neuropathy. We describe a Japanese family with FAF manifested predominantly as renal amyloidosis. The proband was a 42-year-old woman with a 21-year history of proteinuria due to renal amyl
- PMID 26019848
- Familial amyloidotic polyneuropathy type IV--gelsolin amyloidosis.
- Pihlamaa T1, Suominen S, Kiuru-Enari S.
- Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.Amyloid.2012 Jun;19 Suppl 1:30-3. doi: 10.3109/13506129.2012.674076. Epub 2012 Apr 18.
- Familial amyloidotic polyneuropathy type IV, or Gelsolin amyloidosis (GA), is a rare condition caused by G654A or G654T mutation in gelsolin gene at 9q32-34. Gelsolin seems essential in many processes, including inflammation, cell motility, neural recovery, apoptosis and even carcinogenesis. So far
- PMID 22512621
Related Links
- Finland type amyloidosis symptoms, causes, diagnosis, and treatment information for Finland type amyloidosis (Meretoja syndrome) with alternative diagnoses, full-text book chapters, misdiagnosis, research treatments, prevention ...
- While this is considered an autosomal dominant disorder, presumed homozygous cases have been reported in Finland where the first cases were described. These cases seem to have more severe disease with an earlier onset than ...
★リンクテーブル★
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- 英
- Meretoja syndrome
- 同
- アミロイドーシスV型 amyloidosis type V、フィンランド型アミロイドーシス Finland type amyloidosis
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- 英
- Finland type amyloidosis
- 関
- メレトヤ症候群
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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
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- 関
- form、mode、pattern、type
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アミロイドーシス アミロイド症
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- 関
- Finnish