Familial or Genetic Primary Aldosteronism and Gordon Syndrome
- 1 June 2011
- journal article
- Published by Elsevier BV in Endocrinology and Metabolism Clinics of North America
- Vol. 40 (2), 343-368
- https://doi.org/10.1016/j.ecl.2011.01.007
Abstract
No abstract availableKeywords
This publication has 100 references indexed in Scilit:
- K + Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary HypertensionScience, 2011
- Hypertension of Kcnmb1 −/− is linked to deficient K secretion and aldosteronismProceedings of the National Academy of Sciences of the United States of America, 2009
- An adrenal β-arrestin 1-mediated signaling pathway underlies angiotensin II-induced aldosterone production in vitro and in vivoProceedings of the National Academy of Sciences of the United States of America, 2009
- TASK channel deletion in mice causes primary hyperaldosteronismProceedings of the National Academy of Sciences of the United States of America, 2008
- Primary Aldosteronism: Update on Diagnosis and TreatmentThe Endocrinologist, 1997
- PCR‐SSCP ANALYSIS OF THE ANGIOTENSIN II TYPE 1: RECEPTOR GENE IN PATIENTS WITH ALDOSTERONE‐PRODUCING ADENOMASClinical and Experimental Pharmacology and Physiology, 1995
- A New Genetic Test for Familial Hyperaldosteronism Type I Aids in the Detection of Curable HypertensionBiochemical and Biophysical Research Communications, 1995
- Indomethacin and Atrial Natriuretic Peptide in Bartter's SyndromeThe New England Journal of Medicine, 1986
- A rapid and potent natriuretic response to intravenous injection of atrial myocardial extract in ratsLife Sciences, 1981
- Hyperkalemia, acidosis, and short stature associated with a defect in renal potassium excretionThe Journal of Pediatrics, 1974