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

Year Number of Results
1998 1
2002 2
2003 1
2004 2
2005 1
2006 1
2007 4
2008 3
2009 3
2010 6
2011 8
2012 7
2013 11
2014 11
2015 12
2016 16
2017 15
2018 12
2019 17
2020 13
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Similar Articles for PMID: 31285285

123 results
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Resistance to Insulin in Patients with Gitelman Syndrome and a Subtle Intermediate Phenotype in Heterozygous Carriers: A Cross-Sectional Study.
Blanchard A, Vallet M, Dubourg L, Hureaux M, Allard J, Haymann JP, de la Faille R, Arnoux A, Dinut A, Bergerot D, Becker PH, Courand PY, Baron S, Houillier P, Tack I, Devuyst O, Jeunemaitre X, Azizi M, Vargas-Poussou R. Blanchard A, et al. J Am Soc Nephrol. 2019 Aug;30(8):1534-1545. doi: 10.1681/ASN.2019010031. Epub 2019 Jul 8. J Am Soc Nephrol. 2019. PMID: 31285285 Free PMC article.
A NOVEL COMPOUND HETEROZYGOUS VARIANT OF SLC12A3 GENE IN A PEDIGREE WITH GITELMAN SYNDROME CO-EXISTENT WITH THYROID DYSFUNCTION.
Liu S, Ke J, Zhang B, Yu C, Feng Y, Zhao D. Liu S, et al. Endocr Pract. 2018 Oct 2;24(10):889-893. doi: 10.4158/EP-2018-0218. Epub 2018 Aug 7. Endocr Pract. 2018. PMID: 30084681
A novel SLC12A3 homozygous c2039delG mutation in Gitelman syndrome with hypocalcemia.
Yang W, Zhao S, Xie Y, Mo Z. Yang W, et al. BMC Nephrol. 2018 Dec 17;19(1):362. doi: 10.1186/s12882-018-1163-3. BMC Nephrol. 2018. PMID: 30558554 Free PMC article. Review.
Characteristics and Follow-Up of 13 pedigrees with Gitelman syndrome.
Zhong F, Ying H, Jia W, Zhou X, Zhang H, Guan Q, Xu J, Fang L, Zhao J, Xu C. Zhong F, et al. J Endocrinol Invest. 2019 Jun;42(6):653-665. doi: 10.1007/s40618-018-0966-1. Epub 2018 Nov 10. J Endocrinol Invest. 2019. PMID: 30413979 Free PMC article.
Type 2 diabetes mellitus caused by Gitelman syndrome-related hypokalemia: A case report.
He G, Gang X, Sun Z, Wang P, Wang G, Guo W. He G, et al. Medicine (Baltimore). 2020 Jul 17;99(29):e21123. doi: 10.1097/MD.0000000000021123. Medicine (Baltimore). 2020. PMID: 32702863 Free PMC article.
Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome.
Lee JW, Lee J, Heo NJ, Cheong HI, Han JS. Lee JW, et al. J Korean Med Sci. 2016 Jan;31(1):47-54. doi: 10.3346/jkms.2016.31.1.47. Epub 2015 Dec 24. J Korean Med Sci. 2016. PMID: 26770037 Free PMC article.
A case of hypokalemia and proteinuria with a new mutation in the SLC12A3 Gene.
Chen Q, Wu Y, Zhao J, Jia Y, Wang W. Chen Q, et al. BMC Nephrol. 2018 Oct 19;19(1):275. doi: 10.1186/s12882-018-1083-2. BMC Nephrol. 2018. PMID: 30340552 Free PMC article.
Gitelman syndrome in a South African family presenting with hypokalaemia and unusual food cravings.
van der Merwe PD, Rensburg MA, Haylett WL, Bardien S, Davids MR. van der Merwe PD, et al. BMC Nephrol. 2017 Jan 26;18(1):38. doi: 10.1186/s12882-017-0455-3. BMC Nephrol. 2017. PMID: 28125972 Free PMC article.
A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome pedigree.
Chen Y, Zhang Z, Lin X, Pan Q, Zheng F, Li H. Chen Y, et al. BMC Med Genet. 2018 Jan 29;19(1):17. doi: 10.1186/s12881-018-0527-7. BMC Med Genet. 2018. PMID: 29378538 Free PMC article.
Digenetic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome.
Kong Y, Xu K, Yuan K, Zhu J, Gu W, Liang L, Wang C. Kong Y, et al. BMC Pediatr. 2019 Apr 18;19(1):114. doi: 10.1186/s12887-019-1498-3. BMC Pediatr. 2019. PMID: 30999883 Free PMC article.
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