- 塩喪失性の、塩喪失の
WordNet
- sprinkle as if with salt; "the rebels had salted the fields with mines and traps"
- a compound formed by replacing hydrogen in an acid by a metal (or a radical that acts like a metal)
- preserve with salt; "people used to salt meats on ships"
- the taste experience when common salt is taken into the mouth (同)saltiness, salinity
- white crystalline form of especially sodium chloride used to season and preserve food (同)table_salt, common salt
- (of speech) painful or bitter; "salt scorn"- Shakespeare; "a salt apology"
- add salt to
- add zest or liveliness to; "She salts her lectures with jokes"
- (used especially of meats) preserved in salt (同)salt-cured, brine-cured
- the act of adding salt to food
PrepTutorEJDIC
- 〈U〉『塩』食塩 / 〈U〉(化学で)塩 / 《複数形で》薬用塩類(Epsom salt[s],smelling salts) / 〈U〉生気(刺激,興趣)を与えるもの / 〈C〉《話》(特に老練な)水夫 / 塩の,塩を含んでいる;塩気のある,塩辛い / 塩漬けにした / (土地が)塩につかった / 塩信でできた,塩水の中で育つ / 〈食べ物〉‘を'塩で味をつける;〈肉・魚など〉‘を'塩漬けにして保存する《+『名』+『down』,+『down』+『名』》 / 《受動態で》(…で)〈言葉・話なで〉‘を'ぴりっとさせる,‘に'味をつける《+『名』+『with』+『名』》
- 衰弱(荒廃)させる
- 塩で味をつけて,塩味の;塩漬けの
- Strategic Arms Limitation Talks戦略兵器制限交渉
UpToDate Contents
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- 1. 中枢性塩類喪失 cerebral salt wasting
- 2. 低ナトリウム血症を有する成人の評価 evaluation of adults with hyponatremia
- 3. 多尿および尿崩症の診断 diagnosis of polyuria and diabetes insipidus
- 4. 小児における低ナトリウム血症 hyponatremia in children
- 5. 抗利尿ホルモン不適合分泌（SIADH）症候群の病態生理および病因 pathophysiology and etiology of the syndrome of inappropriate antidiuretic hormone secretion siadh
English Journal
- Growth and development in children with classic congenital adrenal hyperplasia.
- Bonfig W1.
- Current opinion in endocrinology, diabetes, and obesity.Curr Opin Endocrinol Diabetes Obes.2017 Feb;24(1):39-42. doi: 10.1097/MED.0000000000000308.
- PURPOSE OF REVIEW: Final height outcome in classic congenital adrenal hyperplasia (CAH) has been of interest for many years. With analysis of growth patterns and used glucocorticoid regimens, enhanced treatment strategies have been developed and are still under development.RECENT FINDINGS: Most of t
- PMID 27898585
- Role and mechanisms of regulation of the basolateral Kir 4.1/Kir 5.1K+ channels in the distal tubules.
- Palygin O1, Pochynyuk O2, Staruschenko A1.
- Acta physiologica (Oxford, England).Acta Physiol (Oxf).2017 Jan;219(1):260-273. doi: 10.1111/apha.12703. Epub 2016 May 20.
- Epithelial K+ channels are essential for maintaining electrolyte and fluid homeostasis in the kidney. It is recognized that basolateral inward-rectifying K+ (Kir ) channels play an important role in the control of resting membrane potential and transepithelial voltage, thereby modulating water and e
- PMID 27129733
- Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia.
- Dumic KK1, Grubic Z2, Yuen T3, Wilson RC4, Kusec V5, Barisic I6, Stingl K2, Sansovic I6, Skrabic V7, Dumic M8, New MI3.
- The Journal of steroid biochemistry and molecular biology.J Steroid Biochem Mol Biol.2017 Jan;165(Pt A):51-56. doi: 10.1016/j.jsbmb.2016.03.035. Epub 2016 Mar 31.
- Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency is caused by mutation in the CYP21A2 gene. The frequency and spectrum of CYP21A2 mutations and genotype-phenotype correlations among different populations are variable. Aim of this study was to define mutation frequency and spectrum o
- PMID 27041116
Japanese Journal
- 中枢性塩類喪失症候群を呈した急性辺縁系脳炎の1例
- 西尾 元伸,西谷 信之,田中 惠子
- 臨床神経学 = Clinical neurology 54(8), 657-659, 2014-08
- NAID 40020180971
- A rare CYP 21 mutation (p.E431K) induced deactivation of CYP 21A2 and resulted in congenital adrenal hyperplasia
- Kawashima Yuki,Usui Takeshi,Fujimoto Masanobu,Miyahara Naoki,Nishimura Rei,Hanaki Keiichi,Kanzaki Susumu
- Endocrine Journal, 2014
- … The compound heterozygous mutations (IVS2-13 A/C>G, and p.E431K) in CYP21A2 were identified at 2 months old, and we diagnosed non-classical CAH, since he did not have significant physical signs (pigmentation and salt-wasting). …
- NAID 130004699222
- A pedigree analysis of two homozygous mutant Gitelman Syndrome cases
- Luo Jiewei,Yang Xiao,Liang Jixing,Li Weihua
- Endocrine Journal, 2014
- … Gitelman Syndrome (GS) is a salt-wasting tubulointerstitial disease of autosomal recessive inheritance (OMIM613395) caused by genic mutation of SLC12A3, which codes thiazide-sensitive Na-Cl cotransporter (NCCT) gene. …
- NAID 130004694064
Related Links
- salt wasting n. A condition in which there is an inappropriately large renal excretion of salt despite the body's apparent need to retain it. salt wasting, inappropriate sodium excretion in the urine (natriuresis) with hyponatremia and ...
- Salt wasting definition at Dictionary.com, a free online dictionary with pronunciation, synonyms and translation. Look it up now! Added to Favorites Dictionary Thesaurus Word Dynamo Quotes Reference Translator Spanish Log In ...
Related Pictures
★リンクテーブル★
| リンク元 | 「塩喪失」「塩喪失性」 |
| 拡張検索 | 「cerebral salt-wasting syndrome」 |
| 関連記事 | 「wasting」「salt」 |
「塩喪失」
- 英
- salt-wasting
- 関
- 塩喪失性
「塩喪失性」
- 英
- salt-wasting
- 関
- 塩喪失
「cerebral salt-wasting syndrome」
「wasting」
- adj.
- 荒廃させる、破壊的な。消耗性の
- n.
「salt」
- n.
- 関
- saline