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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

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192 results

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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 …
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 …
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.
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.
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.
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 …
Diagnostic approach to low-renin hypertension.
Monticone S, Losano I, Tetti M, Buffolo F, Veglio F, Mulatero P. Monticone S, et al. Clin Endocrinol (Oxf). 2018 Oct;89(4):385-396. doi: 10.1111/cen.13741. Epub 2018 Jun 6. Clin Endocrinol (Oxf). 2018. PMID: 29758100 Review.
Resistant Hypertension: A Clinical Perspective.
Hannah-Shmouni F, Gubbi S, Spence JD, Stratakis CA, Koch CA. Hannah-Shmouni F, et al. Endocrinol Metab Clin North Am. 2019 Dec;48(4):811-828. doi: 10.1016/j.ecl.2019.08.010. Endocrinol Metab Clin North Am. 2019. PMID: 31655778 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.
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 …
192 results