Apparent mineralocorticoid excess syndrome: an overview - Wikidata - thesis-toulmin - TriplyDB

Apparent mineralocorticoid excess syndrome: an overview

Apparent mineralocorticoid excess syndrome: an overview

http://www.wikidata.org/entity/Q28239329

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Sambucus nigra extracts inhibit infectious bronchitis virus at an early point during replication The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders Steroidogenesis in the skin: implications for local immune functions Pseudohyperaldosteronism, liquorice, and hypertension Licorice induced hypokalemia, edema, and thrombocytopenia.11β-Hydroxysteroid dehydrogenase type 1: relevance of its modulation in the pathophysiology of obesity, the metabolic syndrome and type 2 diabetes mellitus.Liquorice: a root cause of secondary hypertension.The Diagnostics of Human Steroid Hormone Disorders.Citosine-Adenine-Repeat Microsatellite of 11β-hydroxysteroid dehydrogenase 2 Gene in Hypertensive Children.

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Apparent mineralocorticoid excess syndrome: an overview

http://www.wikidata.org/entity/Q28239329

description

2004 nî lūn-bûn

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2004 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2004 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年论文

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Apparent mineralocorticoid excess syndrome: an overview

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Apparent mineralocorticoid excess syndrome: an overview

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S0004-27302004000500015

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Arquivos Brasileiros de Endocrinologia e Metabologia

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Apparent mineralocorticoid excess syndrome: an overview

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Mario Palermo

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P2860

Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor

Molecular basis for hypertension in the "type II variant" of apparent mineralocorticoid excess

A genetic defect resulting in mild low-renin hypertension

Cloning and tissue distribution of the human 11 beta-hydroxysteroid dehydrogenase type 2 enzyme

Hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the 11 beta-hydroxysteroid dehydrogenase type 2 gene

Gene structure and chromosomal localization of the human HSD11K gene encoding the kidney (type 2) isozyme of 11 beta-hydroxysteroid dehydrogenase

Mineralocorticoid action: target tissue specificity is enzyme, not receptor, mediated

Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase

Reduced activity of 11 beta-hydroxysteroid dehydrogenase in patients with cholestasis

Congenital deficiency of 11beta-hydroxysteroid dehydrogenase (apparent mineralocorticoid excess syndrome): diagnostic value of urinary free cortisol and cortisone.

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687-96

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scholarly article

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10.1590/S0004-27302004000500015

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5

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48

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Marcus Quinkler

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2004-10-01T00:00:00Z

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15761540

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apparent mineralocorticoid excess syndrome

mineralocorticoid