氨氯吡咪（一种保钾利尿剂）的临床评估。 - Suppr

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超能文献

Clinical evaluation of amiloride, a potassium-sparing diuretic.

作者信息

Lant A F, Smith A J, Wilson G M

出版信息

Clin Pharmacol Ther. 1969 Jan-Feb;10(1):50-63. doi: 10.1002/cpt196910150.

DOI:10.1002/cpt196910150

PMID:4884296

Abstract

摘要

相似文献

Clinical evaluation of amiloride, a potassium-sparing diuretic.氨氯吡咪（一种保钾利尿剂）的临床评估。

Clin Pharmacol Ther. 1969 Jan-Feb;10(1):50-63. doi: 10.1002/cpt196910150.

Amiloride (MK-870), a new antikaluretic diuretic. Comparison to other antikaluretic diuretics in patients with liver disease and ascites.氨氯吡咪（MK-870），一种新型抗利钾性利尿剂。与其他抗利钾性利尿剂在肝病和腹水患者中的比较。

Gastroenterology. 1970 Dec;59(6):833-41.

[Course of diuresis in heart failure during ethacrynic acid and amiloride therapy].

Munch Med Wochenschr. 1971 Dec 3;113(49):1660-3.

Combinations of diuretics in the treatment of edema.利尿剂联合用药治疗水肿

Am Heart J. 1970 Sep;80(3):422-6. doi: 10.1016/0002-8703(70)90107-9.

High doses of spironolactone (Aldactone, SC-14266, Verospirone) alone and in combination with triamterene and-or diuretics in the treatment of refractory edema associated with secondary hyperaldosteronism.高剂量螺内酯（安体舒通、SC - 14266、维螺酮）单独使用以及与氨苯蝶啶和/或利尿剂联合使用治疗与继发性醛固酮增多症相关的难治性水肿。

Endokrinologie. 1970;57(1):46-62.

[Diuretics in cirrhosis. Accidents. Indications].[肝硬化中的利尿剂。不良反应。适应证]

Presse Med (1893). 1969 Mar 29;77(16):575-8.

Usefulness of amiloride hydrochloride (MK-870) as an adjuvant in long-term treatment of hepatic cirrhosis.

J Clin Pharmacol New Drugs. 1971 Mar-Apr;11(2):146-51. doi: 10.1177/009127007101100210.

Extrarenal effects of diuretic agents.

Int Z Klin Pharmakol Ther Toxikol. 1970 Dec;4(1):106-10.

[Treatment of cirrhotic edemas with triamterene, amiloride and spirolactone. New clinical and biological facts].

Schweiz Med Wochenschr. 1971 Mar 20;101(11):398-401.

[Antikaliuretic agents].

Internist (Berl). 1971 Aug;12:Suppl:352-6.

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6-Substituted Hexamethylene Amiloride (HMA) Derivatives as Potent and Selective Inhibitors of the Human Urokinase Plasminogen Activator for Use in Cancer.6-取代己二烯基氨甲酰基密胺衍生物作为人尿激酶型纤溶酶原激活物的高效和选择性抑制剂在癌症中的应用。

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The small molecule phenamil is a modulator of adipocyte differentiation and PPARgamma expression.小分子苯甲酰胺是脂肪细胞分化和过氧化物酶体增殖物激活受体γ表达的调节剂。

J Lipid Res. 2010 Sep;51(9):2775-84. doi: 10.1194/jlr.M008490. Epub 2010 Jun 2.

The small molecule phenamil induces osteoblast differentiation and mineralization.小分子苯那明诱导成骨细胞分化和矿化。

Mol Cell Biol. 2009 Jul;29(14):3905-14. doi: 10.1128/MCB.00002-09. Epub 2009 May 11.

Amiloride pharmacokinetics in rat.氨氯吡咪在大鼠体内的药代动力学

Eur J Drug Metab Pharmacokinet. 1998 Apr-Jun;23(2):218-22. doi: 10.1007/BF03189343.

Metabolic effects of high dose amiloride and spironolactone: a comparative study in normal subjects.高剂量阿米洛利和螺内酯的代谢效应：一项在正常受试者中的对比研究。

Br J Clin Pharmacol. 1984 Sep;18(3):369-75. doi: 10.1111/j.1365-2125.1984.tb02478.x.

Use of amiloride as a potassium conserving agent in severe cardiac disease.

Br Heart J. 1973 Apr;35(4):456-61. doi: 10.1136/hrt.35.4.456.

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