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Year Number of Results
2018 3
2019 9
2020 2
2021 5
2022 7
2023 9
2024 9
2025 5
2026 0

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42 results

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Page 1
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.
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.
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.
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.
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.
It includes familial hyperaldosteronism, Liddle syndrome, apparent mineralocorticoid excess,11beta hydroxylase deficiency and Geller syndrome. ...
It includes familial hyperaldosteronism, Liddle syndrome, apparent mineralocorticoid excess,11beta hydroxylase deficiency and …
Reverse Phenotypes of Patients with Genetically Confirmed Liddle Syndrome.
Granhøj J, Nøhr TK, Hinrichs GR, Rasmussen M, Svenningsen P. Granhøj J, et al. Clin J Am Soc Nephrol. 2024 May 1;19(5):610-619. doi: 10.2215/CJN.0000000000000430. Epub 2024 Jan 24. Clin J Am Soc Nephrol. 2024. PMID: 38265765 Free PMC article.
In this study, we used a reverse phenotyping approach to investigate the Liddle syndrome phenotypic spectrum and genotype-phenotype correlations. METHODS: Pubmed, Embase, Scopus, and the Human Gene Mutation Database were searched for articles reporting Liddle …
In this study, we used a reverse phenotyping approach to investigate the Liddle syndrome phenotypic spectrum and genotype-phen …
Liddle Syndrome with a SCNN1A Mutation: A Case Report and Literature Review.
Tian J, Xiang F, Wang L, Wu X, Shao L, Ma L, Fang C. Tian J, et al. Kidney Blood Press Res. 2024;49(1):831-838. doi: 10.1159/000540522. Epub 2024 Sep 5. Kidney Blood Press Res. 2024. PMID: 39236685 Free article. Review.
The aetiology of Liddle syndrome is missense or frameshift mutations in the SCNN1A, SCNN1B, or SCNN1G genes, which encode for the epithelial sodium channel subunits. ...CONCLUSION: A middle-aged patient with Liddle syndrome was diagnosed. A new point m …
The aetiology of Liddle syndrome is missense or frameshift mutations in the SCNN1A, SCNN1B, or SCNN1G genes, which encode for …
42 results