Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1969 1
1978 1
1981 1
1982 1
1989 1
1992 1
1994 1
1995 8
1996 8
1997 12
1998 9
1999 15
2000 10
2001 9
2002 12
2003 15
2004 6
2005 6
2006 9
2007 4
2008 6
2009 5
2010 9
2011 6
2012 4
2013 1
2014 3
2015 4
2016 3
2017 4
2018 4
2019 5
2020 2
2021 3
2022 4
2023 8
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

192 results

Results by year

Filters applied: . Clear all
Page 1
Liddle Syndrome: Review of the Literature and Description of a New Case.
Tetti M, Monticone S, Burrello J, Matarazzo P, Veglio F, Pasini B, Jeunemaitre X, Mulatero P. Tetti M, et al. Int J Mol Sci. 2018 Mar 11;19(3):812. doi: 10.3390/ijms19030812. Int J Mol Sci. 2018. PMID: 29534496 Free PMC article. Review.
Liddle syndrome is an inherited form of low-renin hypertension, transmitted with an autosomal dominant pattern. The molecular basis of Liddle syndrome resides in germline mutations of the SCNN1A, SCNN1B and SCNN1G genes, encoding the alpha, beta, and g
Liddle syndrome is an inherited form of low-renin hypertension, transmitted with an autosomal dominant pattern. The molecular
Low-Renin Hypertension.
Athimulam S, Lazik N, Bancos I. Athimulam S, et al. Endocrinol Metab Clin North Am. 2019 Dec;48(4):701-715. doi: 10.1016/j.ecl.2019.08.003. Epub 2019 Sep 25. Endocrinol Metab Clin North Am. 2019. PMID: 31655771 Review.
Resistant Hypertension.
Valsan D, Burhan U, Teehan G. Valsan D, et al. Adv Exp Med Biol. 2017;956:181-189. doi: 10.1007/5584_2016_38. Adv Exp Med Biol. 2017. PMID: 27864800 Review.
Mechanosensing Piezo channels in gastrointestinal disorders.
Swain SM, Liddle RA. Swain SM, et al. J Clin Invest. 2023 Oct 2;133(19):e171955. doi: 10.1172/JCI171955. J Clin Invest. 2023. PMID: 37781915 Free PMC article. Review.
Here, we discuss our current understanding of mechanically activated Piezo channels in the pathogenesis of pancreatic and GI diseases, including pancreatitis, diabetes mellitus, irritable bowel syndrome, GI tumors, and inflammatory bowel disease. We also describe how Piezo …
Here, we discuss our current understanding of mechanically activated Piezo channels in the pathogenesis of pancreatic and GI diseases, inclu …
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.
Genetic hypertensive hypokalemia is rare. It includes familial hyperaldosteronism, Liddle syndrome, apparent mineralocorticoid excess,11beta hydroxylase deficiency and Geller syndrome. ...Due to the severity of hypokalemic metabolic alkalosis, this disease ca …
Genetic hypertensive hypokalemia is rare. It includes familial hyperaldosteronism, Liddle syndrome, apparent mineralocorticoid …
Liddle syndrome in a Serbian family and literature review of underlying mutations.
Bogdanović R, Kuburović V, Stajić N, Mughal SS, Hilger A, Ninić S, Prijić S, Ludwig M. Bogdanović R, et al. Eur J Pediatr. 2012 Mar;171(3):471-8. doi: 10.1007/s00431-011-1581-8. Epub 2011 Sep 29. Eur J Pediatr. 2012. PMID: 21956615 Review.
Severe and reproducible low-renin hypertension responsive to salt restriction and amiloride-thiazide therapy in a 13-year-old otherwise asymptomatic boy suggested Liddle syndrome. This assumption was strengthened by a positive family history of hypertension poorly r …
Severe and reproducible low-renin hypertension responsive to salt restriction and amiloride-thiazide therapy in a 13-year-old otherwise asym …
Proteomics and tubulopathies.
Vilasi A, Capasso G. Vilasi A, et al. J Nephrol. 2010 Nov-Dec;23 Suppl 16:S221-7. J Nephrol. 2010. PMID: 21170884 Review.
Some renal stone disorders, such as cystinuria and Dent's disease, have been found to be due to mutations in genes SLC3A1 (type I) (See the section "Molecular biology and genotype-phenotype correlation in tubular dysfunction") and SLC7A9 (type II and type III), (See the section " …
Some renal stone disorders, such as cystinuria and Dent's disease, have been found to be due to mutations in genes SLC3A1 (type I) (See the …
Monogenic Forms of Hypertension.
Ceccato F, Mantero F. Ceccato F, et al. Endocrinol Metab Clin North Am. 2019 Dec;48(4):795-810. doi: 10.1016/j.ecl.2019.08.009. Epub 2019 Sep 19. Endocrinol Metab Clin North Am. 2019. PMID: 31655777 Review.
Monogenic Etiology of Hypertension.
Singh V, Van Why SK. Singh V, et al. Med Clin North Am. 2024 Jan;108(1):157-172. doi: 10.1016/j.mcna.2023.06.005. Epub 2023 Jul 27. Med Clin North Am. 2024. PMID: 37951648 Review.
Endocrine Hypertension: A Practical Approach.
Pappachan JM, Buch HN. Pappachan JM, et al. Adv Exp Med Biol. 2017;956:215-237. doi: 10.1007/5584_2016_26. Adv Exp Med Biol. 2017. PMID: 27864805 Review.
Other conditions that can cause endocrine hypertension are: congenital adrenal hyperplasia, Liddle syndrome, pheochromocytomas, Cushing's syndrome, acromegaly, thyroid diseases, primary hyperparathyroidism and iatrogenic hormone manipulation. ...
Other conditions that can cause endocrine hypertension are: congenital adrenal hyperplasia, Liddle syndrome, pheochromocytomas …
192 results