| For: | Shibli AA, Narchi H. Bartter and Gitelman syndromes: Spectrum of clinical manifestations caused by different mutations. World J Methodol 2015; 5(2): 55-61 [PMID: 26140272 DOI: 10.5662/wjm.v5.i2.55] |
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| URL: | https://www.wjgnet.com/2222-0682/full/v5/i2/55.htm |
| Number | Citing Articles |
| 1 |
Naif Hindosh, Rand Hindosh, Bolanle Dada, Swomya Bal. Geller Syndrome: A Rare Cause of Persistent Hypokalemia During Pregnancy. Cureus 2022; doi: 10.7759/cureus.26272
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| 2 |
Samika Jhawar, Rukmini Mysore Srikantiah, Swayam Adappa, Gayathri Renganathan, Kamalakshi G Bhat. Rare confluence: clinically diagnosed Bartter syndrome with sensorineural hearing loss in a young endosulfan-exposed patient. BMJ Case Reports 2026; 19(7) doi: 10.1136/bcr-2025-271920
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| 3 |
Arati Singh, Tarakeswari Surapaneni, Hemamalini Vadlamani. Renal tubular acidosis (RTA) complicated pregnancies: A tertiary centre experience. Obstetric Medicine 2026; doi: 10.1177/1753495X261456364
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| 4 |
Zhenlin Tan, Chen Liu, Zheng Feng, Zhimei Luo, Xiaofen Lian, Donghui Lu. Gitelman syndrome with hypercalcemia and normomagnesemia: A case report. Medicine 2025; 104(22) doi: 10.1097/MD.0000000000042610
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| 5 |
Chunli Wang, Yuan Han, Jiaran Zhou, Bixia Zheng, Wei Zhou, Huaying Bao, Zhanjun Jia, Aihua Zhang, Songming Huang, Guixia Ding, Fei Zhao. Splicing Characterization of CLCNKB Variants in Four Patients With Type III Bartter Syndrome. Frontiers in Genetics 2020; 11 doi: 10.3389/fgene.2020.00081
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| 6 |
Yeji Ham, Heather Mack, Deb Colville, Philip Harraka, Judy Savige. Gitelman syndrome and ectopic calcification in the retina and joints. Clinical Kidney Journal 2021; 14(9) doi: 10.1093/ckj/sfab034
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| 7 |
Georgia Martin, Ibrahim Fahal, Shameer Mehta. Home Parenteral Support in Severe Gitelman Syndrome: A Case Report. Clinical Case Reports 2026; 14(7) doi: 10.1002/ccr3.73210
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| 8 |
Ri-Zhen Yu, Mao-Sheng Chen. Gitelman syndrome caused by a rare homozygous mutation in the <i>SLC12A3</i> gene: A case report. World Journal of Clinical Cases 2020; 8(18): 4252-4258 doi: 10.12998/wjcc.v8.i18.4252
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| 9 |
Megha Priyadarshi, Saurav Sekhar Paul, Sunit Sikdar, Naveet Wig, Manish Soneja. Antibiotic-induced Bartter-like syndrome: a systematic review. Journal of Antimicrobial Chemotherapy 2025; 80(7) doi: 10.1093/jac/dkaf154
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| 10 |
Maryam Najafi, Dor Mohammad Kordi-Tamandani, Farkhondeh Behjati, Simin Sadeghi-Bojd, Zeineb Bakey, Ehsan Ghayoor Karimiani, Isabel Schüle, Anoush Azarfar, Miriam Schmidts. Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis. Orphanet Journal of Rare Diseases 2019; 14(1) doi: 10.1186/s13023-018-0981-5
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| 11 |
Poonam Thakore, Margot Anderson, Ihor V. Yosypiv. Classic Bartter Syndrome: A Cause of Severe Hypokalemic Metabolic Alkalosis. Clinical Pediatrics 2019; 58(14) doi: 10.1177/0009922819857535
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| 12 |
Caesar Ayudi, Nunuk Mardiana. Medical Perioperative Management In Patient with Acute Kidney Disease. Current Internal Medicine Research and Practice Surabaya Journal 2020; 1(2) doi: 10.20473/cimrj.v1i2.21459
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| 13 |
Nandin Sagar, Sham Lohiya. A Comprehensive Review of Chloride Management in Critically Ill Patients. Cureus 2024; doi: 10.7759/cureus.55625
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| 14 |
Christina Schnoz, Monique Carrel, Johannes Loffing. Loss of sodium chloride co-transporter impairs the outgrowth of the renal distal convoluted tubule during renal development. Nephrology Dialysis Transplantation 2020; 35(3) doi: 10.1093/ndt/gfz172
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| 15 |
Chun-Yen Wu, Ming-Hsein Tsai, Chia-Chun Chen, Chuan-Hong Kao. Early diagnosis of Gitelman syndrome in a young child: A case report . World Journal of Clinical Cases 2022; 10(9): 2844-2850 doi: 10.12998/wjcc.v10.i9.2844
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| 16 |
Silas A Culver, Nawar Suleman, Varun Kavuru, Helmy M Siragy. Renal Hypokalemia: An Endocrine Perspective. The Journal of Clinical Endocrinology & Metabolism 2024; 109(7) doi: 10.1210/clinem/dgae201
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| 17 |
Andrea Bezzeccheri, Gianluca Di Giovanni, Martina Belli, Rocco Mollace, Lucy Barone, Massimiliano Macrini, Alessio Di Landro, Saverio Muscoli. The Impact of Gitelman Syndrome on Cardiovascular Disease: From Physiopathology to Clinical Management. Reviews in Cardiovascular Medicine 2022; 23(8) doi: 10.31083/j.rcm2308289
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| 18 |
Pritha Dutta, Anita T. Layton. Modeling calcium and magnesium balance: effects of diuretics. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 2025; 329(2) doi: 10.1152/ajpregu.00031.2025
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| 19 |
Hajar Jamal Teir, Nour AlQaderi, Khadiga Yasser Abdelmonem, Ahmed Elbagir Ibrahim, Abdallah Alzoubi. Gitelman syndrome presenting with lower limb paralysis: a case report. Journal of Medical Case Reports 2025; 19(1) doi: 10.1186/s13256-025-05106-4
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| 20 |
Deekshita Valiveti, Olivia Lahey, Karim Nooruddin, Brandi Addison. Refractory Hypokalemia of Pregnancy: A Rare Case of Non-Aldosterone Mediated Hypokalemia. Cureus 2025; doi: 10.7759/cureus.79242
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| 21 |
Nery Sablón-González, Yanet Parodis-Lopez, Maria Belen Alonso-Ortiz, Angélica Laurin, Emmanuel Andres, Noel Lorenzo Villalba. Recurrent Episodes of Hypokalaemia during Treatment with Inhaled Beta-2 Agonist Revealing Gitelman Syndrome, an Uncommon Clinical Entity. European Journal of Case Reports in Internal Medicine 2022; 9(10) doi: 10.12890/2022_003605
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| 22 |
Gijs A. C. Franken, Anastasia Adella, René J. M. Bindels, Jeroen H. F. de Baaij. Mechanisms coupling sodium and magnesium reabsorption in the distal convoluted tubule of the kidney. Acta Physiologica 2021; 231(2) doi: 10.1111/apha.13528
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| 23 |
Rusdi Zakki Aminy, Nunuk Mardiana. Bartter-like Syndrome In a Patient Receiving Capreomycin For The Treatment Of Multidrug-Resistant Tuberculosis. Current Internal Medicine Research and Practice Surabaya Journal 2020; 1(2) doi: 10.20473/cimrj.v1i2.21555
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| 24 |
Rosanna Fulchiero, Patricia Seo-Mayer. Bartter Syndrome and Gitelman Syndrome. Pediatric Clinics of North America 2019; 66(1) doi: 10.1016/j.pcl.2018.08.010
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| 25 |
Selma KARAAHMETOĞLU, Mehmet Veysel COŞKUN. A Case of Gitelman Syndrome; Incidentally Diagnosed in Elderly. Bezmialem Science 2022; 10(1) doi: 10.14235/bas.galenos.2020.4465
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| 26 |
Alexander G. Marneros. AP-2β/KCTD1 Control Distal Nephron Differentiation and Protect against Renal Fibrosis. Developmental Cell 2020; 54(3) doi: 10.1016/j.devcel.2020.05.026
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| 27 |
Karolina Nocuń-Wasilewska, Anna Biel, Dorota Polak-Jonkisz, Renata Bednorz. Cerebellar-extrapyramidal syndrome as unusual manifestation of Gitelman syndrome in siblings. MedCaseReports 2017; doi: 10.67417/medcasereports.94
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| 28 |
Marie Lim, David Gannon. Diagnosis and outpatient management of Gitelman syndrome from the first trimester of pregnancy. BMJ Case Reports 2021; 14(5) doi: 10.1136/bcr-2021-241756
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| 29 |
Konstantinos Zacharis, Chalent Alexakis, Vasiliki K Tsapadikou, Ismini Anagnostaki, Theodoros Charitos. First Diagnosis of Gitelman Syndrome During Pregnancy in an Adolescent Female: A Case Report. Cureus 2024; doi: 10.7759/cureus.59644
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| 30 |
Maria Helena Vaisbich, Ana Carola Hebbia Lobo Messa, Andréia Cristiane Rangel-Santos, Juliana Caires de Oliveira Achili Ferreira, Fernanda Andrade M. da F. Nunes, Andreia Watanabe. Bartter Syndrome-Related Variants Distribution: Brazilian Data and Its Comparison with Worldwide Cohorts. Nephron 2023; 147(8) doi: 10.1159/000528557
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| 31 |
A Janchevska, V Tasic, O Jordanova, Z Gucev, L Jenkins, N Jovanovska, D Plaseska-Karanfilska, E Ashton, D Bockenhauer. Two Brothers from Macedonia with Gitelman Syndrome. Balkan Journal of Medical Genetics 2023; 26(1) doi: 10.2478/bjmg-2023-0009
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| 32 |
Akshai R, Sakshi Upendra Bhatia, Kishore Narayan, Syed Mohammed, Pallavi Yelkur. An Unusual Presentation of Failure to Thrive in a Toddler: Bartter Syndrome. Cureus 2024; doi: 10.7759/cureus.67289
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| 33 |
Vishrutha Sujith Poojari, Ira Shah, Naman S. Shetty, Akanksha Jaiswal. Transient Bartter-like syndrome in a child with extensively drug-resistant tuberculosis: Answers. Pediatric Nephrology 2021; 36(7) doi: 10.1007/s00467-020-04822-x
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| 34 |
Omar Ala' Alajjuri, Mayar Essam Samaha, Ulrich Honemeyer, Ghada Mohammed, Noha A. Mousa. Balancing Benefits and Risks of Indomethacin in the Management of Antenatal Bartter Syndrome: A Case Report. Frontiers in Medicine 2022; 9 doi: 10.3389/fmed.2022.870503
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| 35 |
Yogita Sharma, Robin Lo, Viktor N. Tomilin, Kotdaji Ha, Holly Deremo, Aishwarya V. Pareek, Wuxing Dong, Xiaohui Liao, Svetlana Lebedeva, Vivek Charu, Neeraja Kambham, Kerim Mutig, Oleh Pochynyuk, Vivek Bhalla. ClC-Kb pore mutation disrupts glycosylation and triggers distal tubular remodeling. JCI Insight 2024; 9(22) doi: 10.1172/jci.insight.175998
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| 36 |
Rachel E. Bridwell, Michael D. April. Adrenal Emergencies. Emergency Medicine Clinics of North America 2023; 41(4) doi: 10.1016/j.emc.2023.06.006
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| 37 |
Xuejun Yang, Gaofu Zhang, Mo Wang, Haiping Yang, Qiu Li. Bartter Syndrome Type 3: Phenotype-Genotype Correlation and Favorable Response to Ibuprofen. Frontiers in Pediatrics 2018; 6 doi: 10.3389/fped.2018.00153
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| 38 |
Viviana Palazzo, Valentina Raglianti, Samuela Landini, Luigi Cirillo, Carmela Errichiello, Elisa Buti, Rosangela Artuso, Lucia Tiberi, Debora Vergani, Elia Dirupo, Paola Romagnani, Benedetta Mazzinghi, Francesca Becherucci. Clinical and Genetic Characterization of Patients with Bartter and Gitelman Syndrome. International Journal of Molecular Sciences 2022; 23(10) doi: 10.3390/ijms23105641
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| 39 |
Hayne Cho Park. From Ion Channels to Blood Pressure: Genetic Disorders of Renal Tubular Transport. Electrolytes & Blood Pressure 2026; 24(2) doi: 10.5049/EBP.2026.24.e5
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| 40 |
Rachel E. Bridwell, Michael D. April. Adrenal Emergencies. Endocrinology and Metabolism Clinics of North America 2026; 55(1) doi: 10.1016/j.ecl.2025.02.006
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| 41 |
Demet Tosun, Sebahat Tülpar, Rümeysa Yasemin Çiçek. A Rare Diagnosis in A Pediatric Case Without Metabolic Alkalosis; Bartter Syndrome. Bagcilar Medical Bulletin 2023; 9(1) doi: 10.4274/BMB.galenos.2023.2023-10-093
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| 42 |
Wei-Fang Wu, Mian Pan. The outcome of two pregnancies in a patient with Gitelman syndrome: case report and review of the literature. The Journal of Maternal-Fetal & Neonatal Medicine 2020; 33(24) doi: 10.1080/14767058.2019.1598359
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| 43 |
Faheemuddin Ahmed, Abdul Mohammed. Magnesium: The Forgotten Electrolyte—A Review on Hypomagnesemia. Medical Sciences 2019; 7(4) doi: 10.3390/medsci7040056
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| 44 |
Shaik Khadeer Ahamed, Shravani Vanga, Sreeteja Panjala, Chandraprakash Gollapelli, Rama Rao Tadikonda. Classic Bartter Syndrome with Refractory Hypokalemia: A Pediatric Case Report. International Journal of Innovative Science and Research Technology 2025; doi: 10.38124/ijisrt/25jun1094
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| 45 |
Amit Singhal, Vishal Vishnu Tewari. Case 1: A Preterm Neonate with Polyhydramnios, Polyuria, and Hearing Loss. NeoReviews 2021; 22(3) doi: 10.1542/neo.22-3-e189
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| 46 |
Seval Yilmaz Ergani, Gokcen Orgul, Harun Egemen Tolunay, Mustafa Arici, Aykan Yucel, Dilek Uygur. Gitelman Syndrome in Pregnancy: A Clinical Challenge. Zeitschrift für Geburtshilfe und Neonatologie 2021; 225(06) doi: 10.1055/a-1498-2940
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| 47 |
Noreen Nasir, Deepali Mohanty, Arun Kumar Pande, Dhanita Khanna, Kavita Vishvakarma, Latika Gupta. Acquired autoimmune Bartter syndrome in a patient with primary hypothyroidism. Rheumatology International 2021; 43(3) doi: 10.1007/s00296-021-05042-8
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| 48 |
Qianying Zhao, Qinqin Xiang, Yu Tan, Xiao Xiao, Hanbing Xie, He Wang, Mei Yang, Shanling Liu. A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis. Molecular Genetics & Genomic Medicine 2022; 10(10) doi: 10.1002/mgg3.2027
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| 49 |
Verdiana Ravarotto, Johannes Loffing, Dominique Loffing-Cueni, Michèle Heidemeyer, Elisa Pagnin, Lorenzo A. Calò, Gian Paolo Rossi. Gitelman’s Syndrome: characterization of a novel c.1181G>A point mutation and functional classification of the known mutations. Hypertension Research 2018; 41(8) doi: 10.1038/s41440-018-0061-1
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| 50 |
Chun-Yen Wu, Ming-Hsein Tsai, Chia-Chun Chen, Chuan-Hong Kao. Early diagnosis of Gitelman syndrome in a young child: A case report . World Journal of Clinical Cases 2022; 10(9) doi: 10.12998/wjcc.v10.i9.2842
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| 51 |
Chen-Han Wilfred Wu, Yu-Ren Mike Huang, Hachem Ziadeh, Bor-En Jong, Prapti Dalal, Hsin-Ti Cindy Lin, Amar Majmundar, Yao-Chou Tsai, Adonis Hijaz, Marshall L. Stoller, Michael Romero, Friedhelm Hildebrandt. Genetic Insights Into Nephrolithiasis and Renal Cancer Predisposition: Precision Medicine in Genes, Diagnosis, and Therapy. Seminars in Nephrology 2025; 45(4) doi: 10.1016/j.semnephrol.2025.151655
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| 52 |
Xiaoyan Peng, Lanping Jiang, Chen Chen, Yan Qin, Tao Yuan, Ou Wang, Xiaoping Xing, Xuemei Li, Min Nie, Limeng Chen, Zhanjun Jia. Increased urinary prostaglandin E2 metabolite: A potential therapeutic target of Gitelman syndrome. PLOS ONE 2017; 12(7) doi: 10.1371/journal.pone.0180811
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| 53 |
Khalid Alhasan, Cynthia D'Alessandri-Silva, Anil Mongia, Rezan Topaloglu, Velibor Tasic, Guido Filler. Young Adults With Hereditary Tubular Diseases: Practical Aspects for Adult-Focused Colleagues. Advances in Chronic Kidney Disease 2022; 29(3) doi: 10.1053/j.ackd.2021.11.004
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| 54 |
Milad Darrat, Hannah Likinyo, Shin-Howe Ryan Winata, Sarah Morgan, Aisling E Courtney, John Lindsay. Successful living kidney donation from a patient with a Gitelman’s syndrome. BMJ Case Reports 2022; 15(2) doi: 10.1136/bcr-2021-246162
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| 55 |
Arki Das, Rohini R, Somnath Panda. Bartter Syndrome With Recurrent Hypokalemic Periodic Paralysis: A Case Report. Cureus 2024; doi: 10.7759/cureus.72406
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| 56 |
Konstantinos Parperis, Argyris Constantinou. Calcium Pyrophosphate Crystal Deposition: Insights to Risks Factors and Associated Conditions. Current Rheumatology Reports 2024; 26(11) doi: 10.1007/s11926-024-01158-5
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| 57 |
Giulio Rivetti, Francesco Emma, Faidra Veligratli, Pierluigi Marzuillo, Detlef Böckenhauer. Failure to thrive in children with tubulopathies. Pediatric Nephrology 2026; 41(8) doi: 10.1007/s00467-025-07047-y
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