後天性腎性尿崩症
- 関
- congenital nephrogenic diabetes insipidus、nephrogenic diabetes insipidus
WordNet
- locate (a moving entity) by means of a tracking system such as radar
- win something through ones efforts; "I acquired a passing knowledge of Chinese"; "Gain an understanding of international finance" (同)win, gain
- lacking interest or significance or impact; "an insipid personality"; "jejune novel" (同)jejune
- a polygenic disease characterized by abnormally high glucose levels in the blood; any of several metabolic disorders marked by excessive urination and persistent thirst
- gotten through environmental forces; "acquired characteristics (such as a suntan or a broken nose) cannot be passed on"
PrepTutorEJDIC
- (不断の努力・習慣などで)…'を'『習得する』,身につける / 〈財産・権利など〉'を'手に入れる,取得する
- (飲食物が)味のない,まずい / (人・話などが)味気ない,無味乾燥な
- 糖尿病(尿に糖が異常に出る病気)
UpToDate Contents
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- 1. 腎性尿崩症の臨床症状および原因 clinical manifestations and causes of nephrogenic diabetes insipidus
- 2. 腎性尿崩症の治療 treatment of nephrogenic diabetes insipidus
- 3. 多尿および尿崩症の診断 diagnosis of polyuria and diabetes insipidus
- 4. 腎アミロイドーシス renal amyloidosis
- 5. 高ナトリウム血症の病因および評価 etiology and evaluation of hypernatremia
English Journal
- Two new large deletions of the AVPR2 gene causing nephrogenic diabetes insipidus and a review of previously published deletions.
- Anesi L, de Gemmis P, Galla D, Hladnik U.SourceMedical Genetics Unit, ' Mauro Baschirotto' Institute for Rare Diseases, Vicenza, Italy.
- Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.Nephrol Dial Transplant.2012 Aug 9. [Epub ahead of print]
- BackgroundIn this paper, we report two new original deletions and present an extended review of the previously characterized AVPR2 gene deletions to better understand the underlying deletion mechanisms.MethodsThe two novel deletions were defined using polymerase chain reaction mapping and junction f
- PMID 22879391
- A urine-concentrating defect in 11β-hydroxysteroid dehydrogenase type 2 null mice.
- Evans LC, Livingstone DE, Kenyon CJ, Jansen MA, Dear JW, Mullins JJ, Bailey MA.SourceBHF Centre for Cardiovascular Science, The Queen's Medical Research Institute, The Univ. of Edinburgh, 47, Little France Crescent, Edinburgh, UK EH16 4TJ. matthew.bailey@ed.ac.uk.
- American journal of physiology. Renal physiology.Am J Physiol Renal Physiol.2012 Aug;303(4):F494-502. Epub 2012 May 23.
- In aldosterone target tissues, 11β-hydroxysteroid dehydrogenase type 2 (11βHSD2) is coexpressed with mineralocorticoid receptors (MR) and protects the receptor from activation by glucocorticoids. Null mutations in the encoding gene, HSD11B2, cause apparent mineralocorticoid excess, in which hypert
- PMID 22622456
Related Links
- Nephrogenic DI (NDI) is most common in its acquired forms, meaning that the defect was not present at birth. These acquired forms have numerous potential causes. The most obvious cause is a kidney or systemic ...
★リンクテーブル★
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- 英
- acquired nephrogenic diabetes insipidus
- 関
- 腎性尿崩症、先天性腎性尿崩症
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- 関
- acquisition、gain、get、obtain、procure、procurement、yield
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- 関
- insipidly, insipidness, insipidity
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- 関
- insipid
- diabetes insipidus
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- 関
- nephrogenesis
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- 関
- 糖尿病 diabetes mellitus DM