Review
Published on 03 Jun 2022
Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance
in Pediatric Nephrology
Frontiers in Pediatrics
doi 10.3389/fped.2022.908655
- 13,868 views
- 15 citations
18 articles related to "Bartter Syndrome"
Articles
Case Report
Published on 30 May 2018
Bartter Syndrome Type 3: Phenotype-Genotype Correlation and Favorable Response to Ibuprofen
in Pediatric Nephrology
Frontiers in Pediatrics
doi 10.3389/fped.2018.00153
- 9,699 views
- 10 citations
Case Report
Published on 17 Apr 2023
A mosaic mutation in the CLCNKB gene causing Bartter syndrome: A case report
in Genetics of Common and Rare Diseases
Frontiers in Pediatrics
doi 10.3389/fped.2023.1034923
- 3,147 views
- 4 citations
Case Report
Published on 30 Mar 2023
Bartter syndrome type III with glomerular dysplasia and chronic kidney disease: A case report
in Genetics of Common and Rare Diseases
Frontiers in Pediatrics
doi 10.3389/fped.2023.1169486
- 4,097 views
- 3 citations
Original Research
Published on 15 May 2017
Reduced Membrane Insertion of CLC-K by V33L Barttin Results in Loss of Hearing, but Leaves Kidney Function Intact
in Membrane Physiology and Membrane Biophysics
Frontiers in Physiology
doi 10.3389/fphys.2017.00269
- 4,134 views
- 13 citations
Case Report
Published on 07 Apr 2022
Late-Onset Bartter Syndrome Type II Due to a Novel Compound Heterozygous Mutation in KCNJ1 Gene: A Case Report and Literature Review
in Nephrology
Frontiers in Medicine
doi 10.3389/fmed.2022.862514
- 4,806 views
- 11 citations
Original Research
Published on 21 Feb 2020
Splicing Characterization of CLCNKB Variants in Four Patients With Type III Bartter Syndrome
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2020.00081
- 5,937 views
- 21 citations
Case Report
Accepted on 03 Feb 2026
A newborn with type 1 Bartter syndrome: challenges in the treatment and development during 30 months follow-up – a case report
in Neonatology
Frontiers in Pediatrics
- 137 views
Case Report
Published on 02 Feb 2023
Case Report: Transient antenatal bartter syndrome in an extremely preterm infant with a novel MAGED2 variant
in Genetics of Common and Rare Diseases
Frontiers in Pediatrics
doi 10.3389/fped.2022.1093268
- 3,038 views
- 6 citations
Case Report
Published on 29 Jun 2022
Balancing Benefits and Risks of Indomethacin in the Management of Antenatal Bartter Syndrome: A Case Report
in Obstetrics and Gynecology
Frontiers in Medicine
doi 10.3389/fmed.2022.870503
- 13,452 views
- 3 citations
Correction
Published on 31 May 2023
Corrigendum: Long-term outcome of Bartter syndrome in 54 patients: a multicenter study in Korea
in Nephrology
Frontiers in Medicine
doi 10.3389/fmed.2023.1225353
- 1,740 views
- 1 citation
Original Research
Published on 13 Mar 2023
Long-term outcome of Bartter syndrome in 54 patients: A multicenter study in Korea
in Nephrology
Frontiers in Medicine
doi 10.3389/fmed.2023.1099840
- 6,977 views
- 9 citations
Case Report
Published on 28 Nov 2025
Type 1 Bartter syndrome presenting as primary diabetes insipidus: a rare Case Report with 8-year follow-up
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1672214
- 1,482 views
Review
Published on 07 Oct 2014
CLC channel function and dysfunction in health and disease
in Membrane Physiology and Membrane Biophysics
Frontiers in Physiology
doi 10.3389/fphys.2014.00378
- 23,161 views
- 103 citations
Original Research
Published on 25 Aug 2022
Twelve exonic variants in the SLC12A1 and CLCNKB genes alter RNA splicing in a minigene assay
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.961384
- 4,273 views
- 11 citations
Original Research
Published on 23 Oct 2018
Barttin Regulates the Subcellular Localization and Posttranslational Modification of Human Cl-/H+ Antiporter ClC-5
in Membrane Physiology and Membrane Biophysics
Frontiers in Physiology
doi 10.3389/fphys.2018.01490
- 5,097 views
- 10 citations