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 Custom Filters

Results by year

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

Year Number of Results
1956 1
1964 3
1965 2
1966 7
1967 2
1968 9
1969 4
1970 4
1971 3
1972 1
1973 3
1974 2
1975 8
1976 6
1977 6
1978 7
1979 4
1980 11
1981 5
1982 3
1983 6
1984 4
1985 5
1986 8
1987 3
1988 2
1989 10
1990 5
1991 4
1992 13
1993 10
1994 9
1995 17
1996 22
1997 31
1998 34
1999 33
2000 31
2001 31
2002 39
2003 46
2004 48
2005 44
2006 56
2007 37
2008 48
2009 49
2010 78
2011 70
2012 64
2013 72
2014 66
2015 79
2016 65
2017 62
2018 50
2019 77
2020 92
2021 84
2022 74
2023 88
2024 64
2025 49

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

1,710 results

Results by year

Filters applied: . Clear all
Page 1
Bartter's and Gitelman's syndrome.
Seyberth HW, Weber S, Kömhoff M. Seyberth HW, et al. Curr Opin Pediatr. 2017 Apr;29(2):179-186. doi: 10.1097/MOP.0000000000000447. Curr Opin Pediatr. 2017. PMID: 27906863 Review.
PURPOSE OF REVIEW: The clinical presentations of Bartter's syndrome and Gitelman's syndrome will be reviewed including two most recently described hypokalemic salt-losing tubulopathies. ...Thus, when dealing with Bartter's syndrome and Gitelman's syndr …
PURPOSE OF REVIEW: The clinical presentations of Bartter's syndrome and Gitelman's syndrome will be reviewed including two mos …
Gitelman's and Bartter's Syndromes: From Genetics to the Molecular Basis of Hypertension and More.
Ravarotto V, Bertoldi G, Stefanelli LF, Nalesso F, Calò LA. Ravarotto V, et al. Kidney Blood Press Res. 2022;47(9):556-564. doi: 10.1159/000526070. Epub 2022 Jul 20. Kidney Blood Press Res. 2022. PMID: 35858584 Free PMC article. Review.
BACKGROUND: Gitelman's and Bartter's syndromes (GS/BS) are rare genetic tubulopathies characterized by electrolyte imbalance and activation of the renin-angiotensin-aldosterone system (RAAS). ...
BACKGROUND: Gitelman's and Bartter's syndromes (GS/BS) are rare genetic tubulopathies characterized by electrolyte imbalance a …
Spectrum of mutations in Gitelman syndrome.
Vargas-Poussou R, Dahan K, Kahila D, Venisse A, Riveira-Munoz E, Debaix H, Grisart B, Bridoux F, Unwin R, Moulin B, Haymann JP, Vantyghem MC, Rigothier C, Dussol B, Godin M, Nivet H, Dubourg L, Tack I, Gimenez-Roqueplo AP, Houillier P, Blanchard A, Devuyst O, Jeunemaitre X. Vargas-Poussou R, et al. J Am Soc Nephrol. 2011 Apr;22(4):693-703. doi: 10.1681/ASN.2010090907. Epub 2011 Mar 17. J Am Soc Nephrol. 2011. PMID: 21415153 Free PMC article.
Gitelman's syndrome (GS) is a rare, autosomal recessive, salt-losing tubulopathy caused by mutations in the SLC12A3 gene, which encodes the thiazide-sensitive NaCl cotransporter (NCC). ...In summary, missense mutations account for approximately 59% of the mutations …
Gitelman's syndrome (GS) is a rare, autosomal recessive, salt-losing tubulopathy caused by mutations in the SLC12A3 gene, whic …
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. ...
Gitelman's syndrome (GS) is a salt-losing tubulopathy characterized by hypokalemic alkalosis with hypomagnesemia and hypocalci …
Bartter Syndrome and Gitelman Syndrome.
Fulchiero R, Seo-Mayer P. Fulchiero R, et al. Pediatr Clin North Am. 2019 Feb;66(1):121-134. doi: 10.1016/j.pcl.2018.08.010. Pediatr Clin North Am. 2019. PMID: 30454738 Review.
Bartter and Gitelman syndromes are conditions characterized by renal salt-wasting. Clinical presentations range from severe antenatal disease to asymptomatic with incidental diagnosis. ...Bartter variants may be associated with polyuria and weakness. Gitelman syndro …
Bartter and Gitelman syndromes are conditions characterized by renal salt-wasting. Clinical presentations range from severe antenatal …
Molecular pathophysiology of Bartter's and Gitelman's syndromes.
Koulouridis E, Koulouridis I. Koulouridis E, et al. World J Pediatr. 2015 May;11(2):113-25. doi: 10.1007/s12519-015-0016-4. Epub 2015 Mar 9. World J Pediatr. 2015. PMID: 25754753 Review.
Hypercalciuria characterizes the majority of Bartter's syndrome, and hypomagnesemia with hypocalciuria characterizes Gitelman's syndrome. Low blood pressure is a common feature among patients who suffered from these tubulopathies. ...CONCLUSIONS: Recent advances in …
Hypercalciuria characterizes the majority of Bartter's syndrome, and hypomagnesemia with hypocalciuria characterizes Gitelman's …
Bartter's and Gitelman's syndromes: from gene to clinic.
Naesens M, Steels P, Verberckmoes R, Vanrenterghem Y, Kuypers D. Naesens M, et al. Nephron Physiol. 2004;96(3):p65-78. doi: 10.1159/000076752. Nephron Physiol. 2004. PMID: 15056980 Review.
Bartter's and Gitelman's syndromes are characterized by hypokalemia, normal to low blood pressure and hypochloremic metabolic alkalosis. Recently, investigators have been able to demonstrate mutations of six genes encoding several renal tubular transporters and ion …
Bartter's and Gitelman's syndromes are characterized by hypokalemia, normal to low blood pressure and hypochloremic metabolic …
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. ...
Gitelman's (GS) and Bartter's (BS) syndromes are rare, inherited autosomal recessive tubulopathies characterized by hypokalemi …
Gitelman's not-so-benign syndrome.
Pachulski RT, Lopez F, Sharaf R. Pachulski RT, et al. N Engl J Med. 2005 Aug 25;353(8):850-1. doi: 10.1056/NEJMc051040. N Engl J Med. 2005. PMID: 16120871 No abstract available.
1,710 results