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

Year Number of Results
1998 1
2004 1
2005 1
2006 1
2007 1
2008 1
2010 1
2011 3
2012 1
2013 1
2015 1
2016 7
2017 2
2018 1
2019 1
2021 1
2022 3
2023 1
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23 results

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Page 1
Metabolic Alkalosis Pathogenesis, Diagnosis, and Treatment: Core Curriculum 2022.
Do C, Vasquez PC, Soleimani M. Do C, et al. Am J Kidney Dis. 2022 Oct;80(4):536-551. doi: 10.1053/j.ajkd.2021.12.016. Epub 2022 May 5. Am J Kidney Dis. 2022. PMID: 35525634 Free PMC article. Review.
Major clinical states are associated with metabolic alkalosis, including vomiting, aldosterone or cortisol excess, licorice ingestion, chloruretic diuretics, excess calcium alkali ingestion, and genetic diseases such as Bartter syndrome, Gitelman syndrome, an …
Major clinical states are associated with metabolic alkalosis, including vomiting, aldosterone or cortisol excess, licorice ingestion, chlor …
Diagnosis of hypokalemia: a problem-solving approach to clinical cases.
Assadi F. Assadi F. Iran J Kidney Dis. 2008 Jul;2(3):115-22. Iran J Kidney Dis. 2008. PMID: 19377223 Free article.
Metabolic alkalosis with a higher K/C ratio and a normal blood pressure suggests diuretic use, Bartter syndrome, or Gitelman syndrome. Metabolic alkalosis with a high urine K/C ratio and hypertension suggests primary hyperaldosteronism, Cushing syndrome …
Metabolic alkalosis with a higher K/C ratio and a normal blood pressure suggests diuretic use, Bartter syndrome, or Gitelman …
Genetic diagnosis and treatment of hereditary renal tubular disease with hypokalemia and alkalosis.
Guo W, Ji P, Xie Y. Guo W, et al. J Nephrol. 2023 Mar;36(2):575-591. doi: 10.1007/s40620-022-01428-4. Epub 2022 Aug 22. J Nephrol. 2023. PMID: 35994232 Review.
Meanwhile, understanding these diseases also improves our understanding of the pathogenesis of hypokalemia, alkalosis and other related diseases and ultimately promotes accurate diagnostics and effective disease treatment. The present review summarizes the most common here …
Meanwhile, understanding these diseases also improves our understanding of the pathogenesis of hypokalemia, alkalosis and other relat …
The Dietary Approach to the Treatment of the Rare Genetic Tubulopathies Gitelman's and Bartter's Syndromes.
Francini F, Gobbi L, Ravarotto V, Toniazzo S, Nalesso F, Spinella P, Calò LA. Francini F, et al. Nutrients. 2021 Aug 26;13(9):2960. doi: 10.3390/nu13092960. Nutrients. 2021. PMID: 34578838 Free PMC article. Review.
Gitelman's (GS) and Bartter's (BS) syndromes are rare, inherited autosomal recessive tubulopathies characterized by hypokalemia, metabolic alkalosis, renal sodium, chloride, and potassium and magnesium-wasting. ...The dietary approach to GS and BS may be very import …
Gitelman's (GS) and Bartter's (BS) syndromes are rare, inherited autosomal recessive tubulopathies characterized by hypokalemia …
Gitelman's syndrome: towards genotype-phenotype correlations?
Riveira-Munoz E, Chang Q, Bindels RJ, Devuyst O. Riveira-Munoz E, et al. Pediatr Nephrol. 2007 Mar;22(3):326-32. doi: 10.1007/s00467-006-0321-1. Epub 2006 Oct 24. Pediatr Nephrol. 2007. PMID: 17061123 Review.
Gitelman's syndrome (GS) is a salt-losing tubulopathy characterized by hypokalemic alkalosis with hypomagnesemia and hypocalciuria. ...In this review, we discuss the potential explanations for the failure to identify mutant alleles in SLC12A3, as well as the …
Gitelman's syndrome (GS) is a salt-losing tubulopathy characterized by hypokalemic alkalosis with hypomagnesemia and hy …
Difficulties in the management of hypokalemia in a pregnant patient with Gitelman syndrome.
Sienicka A, Pisula A, Kacperczyk-Bartnik J, Dobrowolska-Redo A, Romejko-Wolniewicz E. Sienicka A, et al. Ginekol Pol. 2022;93(10):856-857. doi: 10.5603/GP.a2022.0111. Ginekol Pol. 2022. PMID: 36748177 Free article.
Gitelman syndrome (GS) is a rare renal disorder, and little is known about its impact on pregnancy. ...
Gitelman syndrome (GS) is a rare renal disorder, and little is known about its impact on pregnancy. ...
RenalTube: a network tool for clinical and genetic diagnosis of primary tubulopathies.
Mejía N, Santos F, Claverie-Martín F, García-Nieto V, Ariceta G, Castaño L; RenalTube group. Mejía N, et al. Eur J Pediatr. 2013 Jun;172(6):775-80. doi: 10.1007/s00431-013-1934-6. Epub 2013 Feb 7. Eur J Pediatr. 2013. PMID: 23389821
The most common tubulopathies are distal renal tubular acidosis (22.5 %) and classical Bartter syndrome (19.3 %) followed by familial hypomagnesemia with hypercalciuria and nephrocalcinosis (15.7 %) and Gitelman syndrome (15 %). ...A web-based a …
The most common tubulopathies are distal renal tubular acidosis (22.5 %) and classical Bartter syndrome (19.3 %) followed by famil …
Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics.
Matsunoshita N, Nozu K, Shono A, Nozu Y, Fu XJ, Morisada N, Kamiyoshi N, Ohtsubo H, Ninchoji T, Minamikawa S, Yamamura T, Nakanishi K, Yoshikawa N, Shima Y, Kaito H, Iijima K. Matsunoshita N, et al. Genet Med. 2016 Feb;18(2):180-8. doi: 10.1038/gim.2015.56. Epub 2015 Apr 16. Genet Med. 2016. PMID: 25880437 Free article.
PURPOSE: Phenotypic overlap exists among type III Bartter syndrome (BS), Gitelman syndrome (GS), and pseudo-BS/GS (p-BS/GS), which are clinically difficult to distinguish. ...Patients with p-BS/GS included a significantly higher percentage of women and had a …
PURPOSE: Phenotypic overlap exists among type III Bartter syndrome (BS), Gitelman syndrome (GS), and pseudo-BS/GS (p-BS …
Genetic screening for Bartter syndrome and Gitelman syndrome pathogenic genes among individuals with hypertension and hypokalemia.
Bao M, Cai J, Yang X, Ma W. Bao M, et al. Clin Exp Hypertens. 2019;41(4):381-388. doi: 10.1080/10641963.2018.1489547. Epub 2018 Jun 28. Clin Exp Hypertens. 2019. PMID: 29953267
PURPOSE: Bartter syndrome (BS) and Gitelman syndrome (GS) are hereditary diseases characterized by hypokalemia with decreased or normal blood pressure (BP). ...CONCLUSIONS: This is the first study performing combined genetic screening for BS and GS pat …
PURPOSE: Bartter syndrome (BS) and Gitelman syndrome (GS) are hereditary diseases characterized by hypokalemia w …
23 results