Primary aldosteronism: hypertension with a genetic basis

Author:

Gordon R.D.,Klemm S.A.,Tunny T.J.,Stowasser M.

Publisher

Elsevier BV

Subject

General Medicine

Reference17 articles.

1. A chimaeric 11 β-hydroxylase/ aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension;Lifton;Nature,1992

2. Hypertension, increased aldosterone secretion and low plasma renin activity relieved by dexamethasone;Sutherland;Can Med Assoc J,1966

3. Glucocorticoid-suppressible hyperaldosteronism: ultrastructural observation of a case;Matsuo;Acta Pathol Jpn,1985

4. A case of glucocorticoid-responsive hyperaldosteronism;Miura;J Clin Endocrinol,1968

5. Clinical and pathlogical diversity of primary aldosteronism including a new familial variety;Gordon;Clin Exp Pharmacol Physiol,1991

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1. Pathophysiology and histopathology of primary aldosteronism;Trends in Endocrinology & Metabolism;2022-01

2. International Histopathology Consensus for Unilateral Primary Aldosteronism;The Journal of Clinical Endocrinology & Metabolism;2020-07-27

3. Molecular Basis of Primary Aldosteronism and Adrenal Cushing Syndrome;Journal of the Endocrine Society;2020-06-29

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