H因子欠損症
WordNet
- be a contributing factor; "make things factor into a companys profitability"
- any of the numbers (or symbols) that form a product when multiplied together
- an independent variable in statistics
- anything that contributes causally to a result; "a number of factors determined the outcome"
- consider as relevant when making a decision; "You must factor in the recent developments" (同)factor in, factor out
- resolve into factors; "a quantum computer can factor the number 15" (同)factor in, factor out
- an event known to have happened or something known to have existed; "your fears have no basis in fact"; "how much of the story is fact and how much fiction is hard to tell"
- a concept whose truth can be proved; "scientific hypotheses are not facts"
- a piece of information about circumstances that exist or events that have occurred; "first you must collect all the facts of the case"
- a statement or assertion of verified information about something that is the case or has happened; "he supported his argument with an impressive array of facts"
- the 8th letter of the Roman alphabet (同)h
PrepTutorEJDIC
- (…の)『要因』,(…を生み出す)要素《+『in』+『名』(do『ing』)》 / 囲数,約数 / 代理人,《おもに英》仲買人 / =factorize
- 〈C〉『事実』,実際にある(あった)事 / 〈U〉真相,真実(truth) / 《the~》(法律用語で)犯行
- 〈U〉〈C〉(…の)(量・額などの)不足,欠乏《+『of』(『in』)+『名』》 / 〈C〉不足分,不足量,不足額 / 〈C〉(精神・肉体などの)欠陥
- hydrogenの化学記号
- 鉛筆の硬度 / 《俗》heroin
UpToDate Contents
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English Journal
- Novel factor H mutation associated with familial membranoproliferative glomerulonephritis type I.
- Alfandary H1, Davidovits M2,3.
- Pediatric nephrology (Berlin, Germany).Pediatr Nephrol.2015 Dec;30(12):2129-34. doi: 10.1007/s00467-015-3166-7. Epub 2015 Aug 20.
- BACKGROUND: Idiopathic membranoproliferative glomerulonephritis (MPGN) is a rare disease, accounting for 3-5 % of all cases of primary nephritic syndrome. We report an uncommon case of familial MPGN type I associated with a new mutation in the complement factor H gene (CFH).METHODS: Clinical data w
- PMID 26289290
- Partial Complement Factor H Deficiency Associates with C3 Glomerulopathy and Thrombotic Microangiopathy.
- Vernon KA1, Ruseva MM1, Cook HT1, Botto M1, Malik TH1, Pickering MC2.
- Journal of the American Society of Nephrology : JASN.J Am Soc Nephrol.2015 Sep 15. pii: ASN.2015030295. [Epub ahead of print]
- The complement-mediated renal diseases C3 glomerulopathy (C3G) and atypical hemolytic uremic syndrome (aHUS) strongly associate with inherited and acquired abnormalities in the regulation of the complement alternative pathway (AP). The major negative regulator of the AP is the plasma protein complem
- PMID 26374608
- Eculizumab in neonatal hemolytic uremic syndrome with homozygous factor H deficiency.
- Michaux K1, Bacchetta J, Javouhey E, Cochat P, Frémaux-Bacchi V, Sellier-Leclerc AL.
- Pediatric nephrology (Berlin, Germany).Pediatr Nephrol.2014 Dec;29(12):2415-9. doi: 10.1007/s00467-014-2933-1. Epub 2014 Aug 23.
- BACKGROUND: Neonatal atypical hemolytic uremic syndrome (aHUS) is a rare but severe disease that is mainly due to methylmalonic aciduria or genetic complement abnormalities. Traditional management of aHUS includes plasma infusion/exchange, but in small or unstable infants, plasma exchange can be cha
- PMID 25149852
Japanese Journal
- Hepatic stellate cells relay inflammation signaling from sinusoids to parenchyma in mouse models of immune-mediated hepatitis.
- 低リン血症性くる病・骨軟化症 (特集 分子メカニズム解明がすすむ内分泌疾患)
- 内分泌・糖尿病・代謝内科 = Endocrinology, diabetology & metabolism 42(3), 179-184, 2016-03
- NAID 40020789790
- 臨床免疫・アレルギー科 = Clinical immunology & allergology 65(1), 94-98, 2016-01
- NAID 40020720028
Related Links
- Dense deposit disease (DDD)/membranoproliferative glomerulonephritis type II (MPGNII) is characterized by onset of hematuria and/or proteinuria, acute nephritic syndrome, or nephrotic syndrome. It most frequently affects children ...
- Factor H deficiency information including symptoms, causes, diseases, symptoms, treatments, and other medical and health issues. ... Factor H deficiency: Related Topics These medical condition or symptom topics may be ...
★リンクテーブル★
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- 不足、欠乏、欠失、欠如、欠損、不十分。栄養不足、栄養素欠乏、欠乏症。(遺伝子)(染色体内の)遺伝子欠失
- 欠けているもの、不足している物。不足分。不完全なもの、欠点のあるもの
- 関
- absence, agenesis, dearth, defect, defective, deficient, deficit, delete, deletion, deletional, depletion, deprivation, deprive, lack, miss, missing, morphological defect, paucity, scarce, scarcity, starve
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- 関
- complement-regulatory protein
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- 関
- actual、actually、in fact、in practice、indeed、practically
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- 関
- element、elementary、factorial、parameter
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