PubMed for id: 343428

Year	Number of Results
1995	1
1996	1
1997	3
1998	8
1999	5
2000	3
2001	4
2002	8
2003	8
2004	5
2005	4
2006	4
2007	3
2008	14
2009	10
2010	9
2011	11
2012	7
2013	7
2014	7
2015	6
2016	7
2017	11
2018	2
2019	7
2020	10
2021	7
2022	13
2023	8
2024	1

1

Late-Onset Bartter Syndrome Type II Due to a Novel Compound Heterozygous Mutation in KCNJ1 Gene: A Case Report and Literature Review.

Tian M, Peng H, Bi X, Wang YQ, Zhang YZ, Wu Y, Zhang BR. Tian M, et al. Front Med (Lausanne). 2022 Apr 7;9:862514. doi: 10.3389/fmed.2022.862514. eCollection 2022. Front Med (Lausanne). 2022. PMID: 35463019 Free PMC article.

2

Clinical exome sequencing uncovers an unsuspected diagnosis of Bartter syndrome type 2 in a child with incidentally detected nephrocalcinosis.

Saha A, Pande P, Vala K, Kapadia S, Patel H. Saha A, et al. CEN Case Rep. 2022 Nov;11(4):417-421. doi: 10.1007/s13730-022-00694-2. Epub 2022 Feb 23. CEN Case Rep. 2022. PMID: 35195872 Free PMC article.

3

Eight novel KCNJ1 variants and parathyroid hormone overaction or resistance in 5 probands with Bartter syndrome type 2.

Zuo J, Guo W, Wang S, Lang Y, Wang S, Shi X, Zhang R, Zhao X, Han Y, Shao L. Zuo J, et al. Clin Chim Acta. 2020 Dec;511:248-254. doi: 10.1016/j.cca.2020.10.002. Epub 2020 Oct 12. Clin Chim Acta. 2020. PMID: 33058840

4

Late-Onset Bartter Syndrome Type II Due to a Homozygous Mutation in KCNJ1 Gene: A Case Report and Literature Review.

Elfert KA, Geller DS, Nelson-Williams C, Lifton RP, Al-Malki H, Nauman A. Elfert KA, et al. Am J Case Rep. 2020 Sep 30;21:e924527. doi: 10.12659/AJCR.924527. Am J Case Rep. 2020. PMID: 32997650 Free PMC article. Review.

5

Transient hyponatremia of prematurity caused by mild Bartter syndrome type II: a case report.

Verma S, Chanchlani R, Siu VM, Filler G. Verma S, et al. BMC Pediatr. 2020 Jun 26;20(1):311. doi: 10.1186/s12887-020-02214-6. BMC Pediatr. 2020. PMID: 32590952 Free PMC article.

6

Late-onset Bartter syndrome type II.

Gollasch B, Anistan YM, Canaan-Kühl S, Gollasch M. Gollasch B, et al. Clin Kidney J. 2017 Oct;10(5):594-599. doi: 10.1093/ckj/sfx033. Epub 2017 May 8. Clin Kidney J. 2017. PMID: 28979772 Free PMC article.

7

Nephrocalcinosis as adult presentation of Bartter syndrome type II.

Huang L, Luiken GP, van Riemsdijk IC, Petrij F, Zandbergen AA, Dees A. Huang L, et al. Neth J Med. 2014 Feb;72(2):91-3. Neth J Med. 2014. PMID: 24659592 Free article.

8

Expanding the spectrum of genetic mutations in antenatal Bartter syndrome type II.

Fretzayas A, Gole E, Attilakos A, Daskalaki A, Nicolaidou P, Papadopoulou A. Fretzayas A, et al. Pediatr Int. 2013 Jun;55(3):371-3. doi: 10.1111/j.1442-200X.2012.03716.x. Pediatr Int. 2013. PMID: 23782368

9

Late onset Bartter syndrome: Bartter syndrome type 2 presenting with isolated nephrocalcinosis and high parathyroid hormone levels mimicking primary hyperparathyroidism.

Yıldız G, Torun Bayram M, Çinleti T, Koç A, Soylu A, Kavukçu S. Yıldız G, et al. J Pediatr Endocrinol Metab. 2022 Aug 12;35(10):1298-1301. doi: 10.1515/jpem-2022-0154. Print 2022 Oct 26. J Pediatr Endocrinol Metab. 2022. PMID: 35952717

10

Antenatal Bartter syndrome: a new compound heterozygous mutation in exon 2 of KCNJ1 gene.

Mani S, Nair J, Handa D. Mani S, et al. BMJ Case Rep. 2021 Oct 18;14(10):e244685. doi: 10.1136/bcr-2021-244685. BMJ Case Rep. 2021. PMID: 34663630 Free PMC article.

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