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Items: 1 to 20 of 229

1.
Bartter Syndrome: A Systematic Review of Case Reports and Case Series
Rakhtan K. Qasba, Anna Carolina Flumignan Bucharles, Maria Victoria Ferreira Piccoli, Pranjal Sharma, Akshat Banga, Balakrishnan Kamaraj, Faisal A. Nawaz, Harshadayani Jagadish Kumar, Mahika Afrin Happy, Ruman K. Qasba, Gowthami Sai Kogilathota Jagirdhar, Mohammad Yasir Essar, Piyush Garg, Shiva Teja Reddy, Kaanthi Rama, Salim Surani, Rahul Kashyap
Medicina (Kaunas) 2023 Sep; 59(9): 1638. Published online 2023 Sep 11. doi: 10.3390/medicina59091638
PMCID:
PMC10537044
ArticlePubReaderPDF–1.7MCite
2.
Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3
Alejandro García-Castaño, Sara Gómez-Conde, Leire Gondra, María Herrero, Mireia Aguirre, Ana-Belén de la Hoz, Luis Castaño, Renaltube group, Leire Madariaga
Sci Rep. 2023; 13: 12587. Published online 2023 Aug 3. doi: 10.1038/s41598-023-38179-6
PMCID:
PMC10400606
ArticlePubReaderPDF–997KCite
3.
Pseudo-Bartter syndrome in an infant without obvious underlying conditions: A case report
Junya Toyoda, Masanori Adachi, Ayako Ochi, Yuki Okada, Aiko Honda, Katsumi Mizuno, Kandai Nozu
Clin Pediatr Endocrinol. 2023; 32(3): 155–160. Published online 2023 Mar 19. doi: 10.1297/cpe.2022-0069
PMCID:
PMC10288294
ArticlePubReaderPDF–901KCite
4.
Corrigendum: Long-term outcome of Bartter syndrome in 54 patients: a multicenter study in Korea
Naye Choi, Seong Heon Kim, Eun Hui Bae, Eun Mi Yang, Keum Hwa Lee, Sang-Ho Lee, Joo Hoon Lee, Yo Han Ahn, Hae Il Cheong, Hee Gyung Kang, Hye Sun Hyun, Ji Hyun Kim
Front Med (Lausanne) 2023; 10: 1225353. Published online 2023 May 31. doi: 10.3389/fmed.2023.1225353
Corrects:
Front Med (Lausanne). 2023; 10: 1099840.
PMCID:
PMC10266263
CorrectionPDF–64KCite
5.
A mosaic mutation in the CLCNKB gene causing Bartter syndrome: A case report
Lan Zhou, Xiaohui Chen, Jiaojiao Xiong, Ling Lei
Front Pediatr. 2023; 11: 1034923. Published online 2023 Apr 17. doi: 10.3389/fped.2023.1034923
PMCID:
PMC10149701
ArticlePubReaderPDF–5.7MCite
6.
A Rare Presentation of Adult-Onset Bartter Syndrome: A Case Report
Deekshitha Alla, Meghana Krishna Kesineni, Roopeessh Vempati, Hinal Patel, Shenelle Menezes, Sai Santhosha Mrudula Alla, Devkumar Patel, Srajan Gupta, Krish Patel, Anju Pradeep
Cureus. 2023 Mar; 15(3): e36120. Published online 2023 Mar 14. doi: 10.7759/cureus.36120
PMCID:
PMC10099506
ArticlePubReaderPDF–87KCite
7.
Bartter syndrome type III with glomerular dysplasia and chronic kidney disease: A case report
Jingqi Liu, Yudi Zhang, Xiaochuan Wu, Yongzhen Li
Front Pediatr. 2023; 11: 1169486. Published online 2023 Mar 30. doi: 10.3389/fped.2023.1169486
PMCID:
PMC10098006
ArticlePubReaderPDF–9.7MCite
8.
Long-term outcome of Bartter syndrome in 54 patients: A multicenter study in Korea
Naye Choi, Seong Heon Kim, Eun Hui Bae, Eun Mi Yang, Keum Hwa Lee, Sang-Ho Lee, Joo Hoon Lee, Yo Han Ahn, Hae Il Cheong, Hee Gyung Kang, Hye Sun Hyun, Ji Hyun Kim
Front Med (Lausanne) 2023; 10: 1099840. Published online 2023 Mar 13. doi: 10.3389/fmed.2023.1099840
Correction in:
Front Med (Lausanne). 2023; 10: 1225353.
PMCID:
PMC10040751
ArticlePubReaderPDF–979KCite
9.
Case Report: Transient antenatal bartter syndrome in an extremely preterm infant with a novel MAGED2 variant
Hongyuan Yang, Zhiyong Liu, Yaying Wu, Jinglin Xu, Ying He, Ruiquan Wang, Weifeng Zhang, Dongmei Chen
Front Pediatr. 2022; 10: 1093268. Published online 2023 Feb 2. doi: 10.3389/fped.2022.1093268
PMCID:
PMC9932885
ArticlePubReaderPDF–827KCite
10.
Bartter Syndrome: Perspectives of a Pediatric Nephrologist
Naye Choi, Hee Gyung Kang
Electrolyte Blood Press. 2022 Dec; 20(2): 49–56. Published online 2022 Dec 30. doi: 10.5049/EBP.2022.20.2.49
PMCID:
PMC9827044
ArticlePubReaderPDF–841KCite
11.
Genetic diagnosis of Bartter syndrome in Iranian patients and detection of a novel homozygous CLCNKB mutation
Somayeh Takrim Nojehdeh, Marzieh Mojbafan, Nakysa Hooman, Rozita Hoseini, Hasan Otukesh
Clin Case Rep. 2022 Dec; 10(12): e6698. Published online 2022 Dec 9. doi: 10.1002/ccr3.6698
PMCID:
PMC9734084
ArticlePubReaderPDF–471KCite
12.
Clinical exome sequencing uncovers an unsuspected diagnosis of Bartter syndrome type 2 in a child with incidentally detected nephrocalcinosis
Anshuman Saha, Priyadarshini Pande, Kinnari Vala, Shahenaz Kapadia, Himanshu Patel
CEN Case Rep. 2022 Nov; 11(4): 417–421. Published online 2022 Feb 23. doi: 10.1007/s13730-022-00694-2
PMCID:
PMC9626722
ArticlePubReaderPDF–731KCite
13.
A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis
Qianying Zhao, Qinqin Xiang, Yu Tan, Xiao Xiao, Hanbing Xie, He Wang, Mei Yang, Shanling Liu
Mol Genet Genomic Med. 2022 Oct; 10(10): e2027. Published online 2022 Aug 1. doi: 10.1002/mgg3.2027
PMCID:
PMC9544217
ArticlePubReaderPDF–1.0MCite
14.
Neonatal Bartter syndrome diagnosed by rapid genomics following low risk pre‐conception carrier screening
Thomas A Forbes, Jane Wallace, Smitha Kumble, Martin B Delatycki, Zornitza Stark
J Paediatr Child Health. 2022 May; 58(5): 758–761. Published online 2022 Mar 29. doi: 10.1111/jpc.15955
Correction in:
J Paediatr Child Health. 2022 Sep; 58(9): 1710.
PMCID:
PMC9313891
ArticlePubReaderPDF–721KCite
15.
Balancing Benefits and Risks of Indomethacin in the Management of Antenatal Bartter Syndrome: A Case Report
Omar Ala' Alajjuri, Mayar Essam Samaha, Ulrich Honemeyer, Ghada Mohammed, Noha A. Mousa
Front Med (Lausanne) 2022; 9: 870503. Published online 2022 Jun 29. doi: 10.3389/fmed.2022.870503
PMCID:
PMC9276994
ArticlePubReaderPDF–3.5MCite
16.
Diagnostic Challenge of Congenital Chloride Diarrhea and Ulcerative Colitis Overlap in an Adult Misdiagnosed with Bartter Syndrome: Case Report and Literature Review
Laila Fahad Sadagah, Ahmad Zaid Makeen, Eman Talal Kotbi
Am J Case Rep. 2022; 23: e936715-1–e936715-7. Published online 2022 Jul 5. doi: 10.12659/AJCR.936715
PMCID:
PMC9272577
ArticlePubReaderPDF–488KCite
17.
Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance
Laura Florea, Lavinia Caba, Eusebiu Vlad Gorduza
Front Pediatr. 2022; 10: 908655. Published online 2022 Jun 3. doi: 10.3389/fped.2022.908655
PMCID:
PMC9203713
ArticlePubReaderPDF–1.2MCite
18.
Late-Onset Bartter Syndrome Type II Due to a Novel Compound Heterozygous Mutation in KCNJ1 Gene: A Case Report and Literature Review
Mi Tian, Hui Peng, Xin Bi, Yan-Qiu Wang, Yong-Zhe Zhang, Yan Wu, Bei-Ru Zhang
Front Med (Lausanne) 2022; 9: 862514. Published online 2022 Apr 7. doi: 10.3389/fmed.2022.862514
PMCID:
PMC9021870
ArticlePubReaderPDF–1.2MCite
19.
Different roles of the RAAS affect bone metabolism in patients with primary aldosteronism, Gitelman syndrome and Bartter syndrome
Wangna Tang, Yun Chai, Hongwei Jia, Baoping Wang, Tong Liu, Hao Wang, Chenlin Dai
BMC Endocr Disord. 2022; 22: 38. Published online 2022 Feb 11. doi: 10.1186/s12902-022-00955-2
PMCID:
PMC8840772
ArticlePubReaderPDF–772KCite
20.
Antenatal Bartter syndrome: a new compound heterozygous mutation in exon 2 of KCNJ1 gene
Srinivasan Mani, Jayasree Nair, Deepali Handa
BMJ Case Rep. 2021; 14(10): e244685. Published online 2021 Oct 18. doi: 10.1136/bcr-2021-244685
PMCID:
PMC8524263
ArticlePubReaderPDF–184KCite

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