Similar articles for PMID: 31285285

Year	Number of Results
1948	1
1998	1
2002	2
2003	1
2004	1
2005	1
2006	1
2007	4
2008	2
2009	3
2010	5
2011	8
2012	5
2013	11
2014	11
2015	11
2016	15
2017	17
2018	12
2019	20
2020	20
2021	23
2022	21
2023	5
2024	0

1

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.

2

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

3

Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations.

Zhang JH, Ruan DD, Hu YN, Ruan XL, Zhu YB, Yang X, Wu JB, Lin XF, Luo JW, Tang FQ. Zhang JH, et al. Biomed Res Int. 2021 May 10;2021:9973161. doi: 10.1155/2021/9973161. eCollection 2021. Biomed Res Int. 2021. PMID: 34046503 Free PMC article.

4

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.

5

A novel compound heterozygous mutation of SLC12A3 gene in a pedigree with Gitelman syndrome and literature review.

Yang M, Dong Y, Tian J, Yan L, Chen Y, Qiu H, Liu W, Hu Y. Yang M, et al. Genes Genomics. 2020 Sep;42(9):1035-1040. doi: 10.1007/s13258-020-00960-6. Epub 2020 Jul 25. Genes Genomics. 2020. PMID: 32712837 Review.

6

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.

7

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.

8

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.

9

Identification of compound mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome exhibiting Bartter syndrome-liked phenotypes.

Dong B, Chen Y, Liu X, Wang Y, Wang F, Zhao Y, Sun X, Zhao W. Dong B, et al. BMC Nephrol. 2020 Aug 5;21(1):328. doi: 10.1186/s12882-020-01996-2. BMC Nephrol. 2020. PMID: 32758178 Free PMC article.

10

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.

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