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Year Number of Results
1995 4
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2006 1
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70 results

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Page 1
Diagnosis and treatment of primary aldosteronism.
Reincke M, Bancos I, Mulatero P, Scholl UI, Stowasser M, Williams TA. Reincke M, et al. Lancet Diabetes Endocrinol. 2021 Dec;9(12):876-892. doi: 10.1016/S2213-8587(21)00210-2. Lancet Diabetes Endocrinol. 2021. PMID: 34798068 Free article. Review.
In addition, germline mutations cause rare familial forms of aldosteronism (familial hyperaldosteronism types 1-4). Genetic testing for inherited forms in suspected cases of familial hyperaldosteronism avoids the burdensome diagnostic investigation in …
In addition, germline mutations cause rare familial forms of aldosteronism (familial hyperaldosteronism types 1-4). Genetic te …
Pathophysiology of bilateral hyperaldosteronism.
Nanba K, Rainey WE. Nanba K, et al. Curr Opin Endocrinol Diabetes Obes. 2022 Jun 1;29(3):233-242. doi: 10.1097/MED.0000000000000729. Curr Opin Endocrinol Diabetes Obes. 2022. PMID: 35621175 Free PMC article. Review.
In this review, we aimed to summarize recent findings regarding pathophysiology of bilateral forms of PA, including sporadic bilateral hyperaldosteronism (BHA) and rare familial hyperaldosteronism. RECENT FINDINGS: The presence of subcapsular aldosterone synthase (C …
In this review, we aimed to summarize recent findings regarding pathophysiology of bilateral forms of PA, including sporadic bilateral hyper …
Familial hyperaldosteronism.
Stowasser M, Gordon RD. Stowasser M, et al. J Steroid Biochem Mol Biol. 2001 Sep;78(3):215-29. doi: 10.1016/s0960-0760(01)00097-8. J Steroid Biochem Mol Biol. 2001. PMID: 11595502 Review.
The study of familial varieties has facilitated a fuller appreciation of the nature and diversity of its clinical, biochemical, morphological and molecular aspects. In familial hyperaldosteronism type I (FH-I), glucocorticoid-remediable PAL is caused by inheritance …
The study of familial varieties has facilitated a fuller appreciation of the nature and diversity of its clinical, biochemical, morphologica …
Familial hyperaldosteronism.
Torpy DJ, Stratakis CA, Chrousos GP. Torpy DJ, et al. Braz J Med Biol Res. 2000 Oct;33(10):1149-55. doi: 10.1590/s0100-879x2000001000004. Braz J Med Biol Res. 2000. PMID: 11004715 Free article. Review.
This autosomal dominant disorder has been shown to be caused by a hybrid gene mutation formed by a crossover of genetic material between the ACTH-responsive regulatory portion of the 11ss-hydroxylase (CYP11B1) gene and the coding region of the aldosterone synthase (CYP11B2) gene. …
This autosomal dominant disorder has been shown to be caused by a hybrid gene mutation formed by a crossover of genetic material between the …
Genetic causes of primary aldosteronism.
Seidel E, Schewe J, Scholl UI. Seidel E, et al. Exp Mol Med. 2019 Nov 6;51(11):1-12. doi: 10.1038/s12276-019-0337-9. Exp Mol Med. 2019. PMID: 31695023 Free PMC article. Review.
Rare causes include unilateral hyperplasia, adrenocortical carcinoma and Mendelian forms (familial hyperaldosteronism). Studies conducted in the last eight years have identified somatic driver mutations in a substantial portion of aldosterone-producing adenomas, inc …
Rare causes include unilateral hyperplasia, adrenocortical carcinoma and Mendelian forms (familial hyperaldosteronism). Studie …
Therapeutic management of congenital forms of endocrine hypertension.
Charoensri S, Auchus RJ. Charoensri S, et al. Eur J Endocrinol. 2023 Nov 8;189(5):R11-R22. doi: 10.1093/ejendo/lvad140. Eur J Endocrinol. 2023. PMID: 37847213 Review.
This review article summarizes the current state of knowledge on the therapeutic management of congenital forms of endocrine hypertension, focusing on familial hyperaldosteronism (FH), congenital adrenal hyperplasia, apparent mineralocorticoid excess, and Liddle syn …
This review article summarizes the current state of knowledge on the therapeutic management of congenital forms of endocrine hypertension, f …
Familial hyperaldosteronism type III.
Monticone S, Tetti M, Burrello J, Buffolo F, De Giovanni R, Veglio F, Williams TA, Mulatero P. Monticone S, et al. J Hum Hypertens. 2017 Dec;31(12):776-781. doi: 10.1038/jhh.2017.34. Epub 2017 Apr 27. J Hum Hypertens. 2017. PMID: 28447626 Review.
Pathophysiologic approach in genetic hypokalemia: An update.
Blanchard A. Blanchard A. Ann Endocrinol (Paris). 2023 Apr;84(2):298-307. doi: 10.1016/j.ando.2022.11.005. Epub 2023 Jan 10. Ann Endocrinol (Paris). 2023. PMID: 36639120 Review.
Clinical analysis distinguishes hypertension-associated hypokalemia, due to hypermineralocorticism or related disorders. Genetic hypertensive hypokalemia is rare. It includes familial hyperaldosteronism, Liddle syndrome, apparent mineralocorticoid excess,11beta hydr …
Clinical analysis distinguishes hypertension-associated hypokalemia, due to hypermineralocorticism or related disorders. Genetic hypertensiv …
What We Know about and What Is New in Primary Aldosteronism.
Ekman N, Grossman AB, Dworakowska D. Ekman N, et al. Int J Mol Sci. 2024 Jan 11;25(2):900. doi: 10.3390/ijms25020900. Int J Mol Sci. 2024. PMID: 38255973 Free PMC article. Review.
The principal aetiologies of PA include bilateral idiopathic hypertrophy (BIH) and aldosterone-producing adenomas (APAs), while the less frequent causes include unilateral hyperplasia, familial hyperaldosteronism (FH) types I-IV, aldosterone-producing carcinoma, and …
The principal aetiologies of PA include bilateral idiopathic hypertrophy (BIH) and aldosterone-producing adenomas (APAs), while the less fre …
Old and new genes in primary aldosteronism.
Boulkroun S, Fernandes-Rosa FL, Zennaro MC. Boulkroun S, et al. Best Pract Res Clin Endocrinol Metab. 2020 Mar;34(2):101375. doi: 10.1016/j.beem.2020.101375. Epub 2020 Jan 22. Best Pract Res Clin Endocrinol Metab. 2020. PMID: 32007424 Review.
70 results