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Jun 26, 2015 (publication date) through Nov 28, 2024
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Publication Name
World Journal of Methodology
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2222-0682
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| 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 |
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): 69 doi: 10.2478/bjmg-2023-0009
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| 3 |
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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| 4 |
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): 1975 doi: 10.1007/s00467-020-04822-x
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| 5 |
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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| 6 |
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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| 7 |
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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| 8 |
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): 2023 doi: 10.1093/ckj/sfab034
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| 9 |
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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| 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 |
Rachel E. Bridwell, Michael D. April. Adrenal Emergencies. Emergency Medicine Clinics of North America 2023; 41(4): 795 doi: 10.1016/j.emc.2023.06.006
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| 12 |
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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| 13 |
Poonam Thakore, Margot Anderson, Ihor V. Yosypiv. Classic Bartter Syndrome: A Cause of Severe Hypokalemic Metabolic Alkalosis. Clinical Pediatrics 2019; 58(14): 1557 doi: 10.1177/0009922819857535
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| 14 |
Caesar Ayudi, Nunuk Mardiana. Medical Perioperative Management In Patient with Acute Kidney Disease. Current Internal Medicine Research and Practice Surabaya Journal 2020; 1(2): 38 doi: 10.20473/cimrj.v1i2.21459
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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): 5641 doi: 10.3390/ijms23105641
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| 16 |
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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| 17 |
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): 411 doi: 10.1093/ndt/gfz172
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| 18 |
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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| 19 |
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): 71 doi: 10.4274/BMB.galenos.2023.2023-10-093
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| 20 |
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): 4171 doi: 10.1080/14767058.2019.1598359
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| 21 |
Faheemuddin Ahmed, Abdul Mohammed. Magnesium: The Forgotten Electrolyte—A Review on Hypomagnesemia. Medical Sciences 2019; 7(4): 56 doi: 10.3390/medsci7040056
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| 22 |
Silas A Culver, Nawar Suleman, Varun Kavuru, Helmy M Siragy. Renal Hypokalemia: An Endocrine Perspective. The Journal of Clinical Endocrinology & Metabolism 2024; 109(7): 1694 doi: 10.1210/clinem/dgae201
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| 23 |
Amit Singhal, Vishal Vishnu Tewari. Case 1: A Preterm Neonate with Polyhydramnios, Polyuria, and Hearing Loss. NeoReviews 2021; 22(3): e189 doi: 10.1542/neo.22-3-e189
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| 24 |
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): 526 doi: 10.1055/a-1498-2940
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| 25 |
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): 567 doi: 10.1007/s00296-021-05042-8
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| 26 |
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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| 27 |
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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| 28 |
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): 578 doi: 10.1038/s41440-018-0061-1
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| 29 |
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): 2842 doi: 10.12998/wjcc.v10.i9.2842
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| 30 |
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): e0180811 doi: 10.1371/journal.pone.0180811
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| 31 |
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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| 32 |
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): 44 doi: 10.20473/cimrj.v1i2.21555
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| 33 |
Rosanna Fulchiero, Patricia Seo-Mayer. Bartter Syndrome and Gitelman Syndrome. Pediatric Clinics of North America 2019; 66(1): 121 doi: 10.1016/j.pcl.2018.08.010
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| 34 |
Selma KARAAHMETOĞLU, Mehmet Veysel COŞKUN. A Case of Gitelman Syndrome; Incidentally Diagnosed in Elderly. Bezmialem Science 2022; 10(1): 111 doi: 10.14235/bas.galenos.2020.4465
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| 35 |
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): 292 doi: 10.1053/j.ackd.2021.11.004
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| 36 |
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): e246162 doi: 10.1136/bcr-2021-246162
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| 37 |
Alexander G. Marneros. AP-2β/KCTD1 Control Distal Nephron Differentiation and Protect against Renal Fibrosis. Developmental Cell 2020; 54(3): 348 doi: 10.1016/j.devcel.2020.05.026
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| 38 |
Marie Lim, David Gannon. Diagnosis and outpatient management of Gitelman syndrome from the first trimester of pregnancy. BMJ Case Reports 2021; 14(5): e241756 doi: 10.1136/bcr-2021-241756
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| 39 |
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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| 40 |
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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| 41 |
Konstantinos Parperis, Argyris Constantinou. Calcium Pyrophosphate Crystal Deposition: Insights to Risks Factors and Associated Conditions. Current Rheumatology Reports 2024; 26(11): 375 doi: 10.1007/s11926-024-01158-5
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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): 478 doi: 10.1159/000528557
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