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For: Blanchard A, Bockenhauer D, Bolignano D, Calò LA, Cosyns E, Devuyst O, Ellison DH, Karet Frankl FE, Knoers NV, Konrad M, Lin SH, Vargas-Poussou R. Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int. 2017;91:24-33. [PMID: 28003083 DOI: 10.1016/j.kint.2016.09.046] [Cited by in Crossref: 112] [Cited by in F6Publishing: 84] [Article Influence: 22.4] [Reference Citation Analysis]
Number Citing Articles
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2 Gianesello L, Del Prete D, Ceol M, Priante G, Calò LA, Anglani F. From protein uptake to Dent disease: An overview of the CLCN5 gene. Gene 2020;747:144662. [PMID: 32289351 DOI: 10.1016/j.gene.2020.144662] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
3 Zhang L, Huang K, Wang S, Fu H, Wang J, Shen H, Lu Z, Chen J, Bao Y, Feng C, Dong G, Mao J. Clinical and Genetic Features in 31 Serial Chinese Children With Gitelman Syndrome. Front Pediatr 2021;9:544925. [PMID: 33996672 DOI: 10.3389/fped.2021.544925] [Reference Citation Analysis]
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5 Chen SY, Jie N. Gitelman syndrome: A case report. World J Clin Cases 2022; 10(17): 5893-5898 [DOI: 10.12998/wjcc.v10.i17.5893] [Reference Citation Analysis]
6 Claverie-Martin F, Perdomo-Ramirez A, Garcia-Nieto V. Hereditary kidney diseases associated with hypomagnesemia. Kidney Res Clin Pract 2021. [PMID: 34784661 DOI: 10.23876/j.krcp.21.112] [Reference Citation Analysis]
7 Schlingmann KP, de Baaij JH. The genetic spectrum of Gitelman(-like) syndromes. Current Opinion in Nephrology & Hypertension 2022;31:508-15. [DOI: 10.1097/mnh.0000000000000818] [Reference Citation Analysis]
8 Correia AL, Marques MG, Alves R. Gitelman syndrome - A new mutation in the SLC12A3 gene. Nefrologia 2021:S0211-6995(21)00085-0. [PMID: 34034904 DOI: 10.1016/j.nefro.2021.01.005] [Reference Citation Analysis]
9 Francini F, Gobbi L, Ravarotto V, Toniazzo S, Nalesso F, Spinella P, Calò LA. The Dietary Approach to the Treatment of the Rare Genetic Tubulopathies Gitelman's and Bartter's Syndromes. Nutrients 2021;13:2960. [PMID: 34578838 DOI: 10.3390/nu13092960] [Reference Citation Analysis]
10 Abe Y, Yamamoto T, Izumita Y, Tsukano S. Gitelman syndrome caused by a novel hemiallelic missense mutation in SLC12A3 revealed by 16q12.2q21 microdeletion. Hum Genome Var 2020;7:17. [PMID: 32528714 DOI: 10.1038/s41439-020-0104-4] [Reference Citation Analysis]
11 Bao M, Cai J, Yang X, Ma W. Genetic screening for Bartter syndrome and Gitelman syndrome pathogenic genes among individuals with hypertension and hypokalemia. Clin Exp Hypertens 2019;41:381-8. [PMID: 29953267 DOI: 10.1080/10641963.2018.1489547] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
12 Wu C, Tsai M, Chen C, Kao C. Early diagnosis of Gitelman syndrome in a young child: A case report. WJCC 2022;10:2844-50. [DOI: 10.12998/wjcc.v10.i9.2844] [Reference Citation Analysis]
13 Iancu D, Ashton E. Inherited Renal Tubulopathies-Challenges and Controversies. Genes (Basel) 2020;11:E277. [PMID: 32150856 DOI: 10.3390/genes11030277] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
14 Hureaux M, Ashton E, Dahan K, Houillier P, Blanchard A, Cormier C, Koumakis E, Iancu D, Belge H, Hilbert P, Rotthier A, Del Favero J, Schaefer F, Kleta R, Bockenhauer D, Jeunemaitre X, Devuyst O, Walsh SB, Vargas-Poussou R. High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults. Kidney Int 2019;96:1408-16. [PMID: 31672324 DOI: 10.1016/j.kint.2019.08.027] [Cited by in Crossref: 15] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
15 Bakir M, Ibrahim HAG. A Challenging Case of Persisting Hypokalemia Secondary to Gitelman Syndrome. Cureus 2021;13:e18636. [PMID: 34765380 DOI: 10.7759/cureus.18636] [Reference Citation Analysis]
16 Al-Saud B, Alajlan H, Sabar H, Anwar S, Alruwaili H, Al-Hussain T, Alamri N, Alazami AM. STK4 Deficiency in a Patient with Immune Complex Glomerulonephritis, Salt-Losing Tubulopathy, and Castleman's-Like Disease. J Clin Immunol 2019;39:823-6. [PMID: 31444685 DOI: 10.1007/s10875-019-00682-9] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
17 Louca P, Menni C, Padmanabhan S. Genomic Determinants of Hypertension With a Focus on Metabolomics and the Gut Microbiome. Am J Hypertens 2020;33:473-81. [PMID: 32060494 DOI: 10.1093/ajh/hpaa022] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
18 Courand PY, Marques P, Vargas-Poussou R, Azizi M, Blanchard A; GITAB study investigators. QT Interval in Adult with Chronic Hypokalemia due to Gitelman Syndrome: Not so Frequently Prolonged. Clin J Am Soc Nephrol 2020;15:1640-2. [PMID: 32792351 DOI: 10.2215/CJN.07540520] [Reference Citation Analysis]
19 Konrad M, Nijenhuis T, Ariceta G, Bertholet-Thomas A, Calo LA, Capasso G, Emma F, Schlingmann KP, Singh M, Trepiccione F, Walsh SB, Whitton K, Vargas-Poussou R, Bockenhauer D. Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders. Kidney Int 2021;99:324-35. [PMID: 33509356 DOI: 10.1016/j.kint.2020.10.035] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
20 Gómez CJB, Gil-Peña H, Álvarez FAO, Rodríguez FS. Outcome of primary tubular tubulopathies diagnosed in pediatric age. Nefrologia 2021;41:182-90. [PMID: 34167771 DOI: 10.1016/j.nefroe.2020.07.001] [Reference Citation Analysis]
21 Stefanelli LF, Di Vico V, Davis PA, Calò LA. Magnesium is crucial in renal-cardiovascular fibrosis but the Gitelman's syndrome paradox still awaits resolution. Int Urol Nephrol 2022. [PMID: 35925487 DOI: 10.1007/s11255-022-03333-y] [Reference Citation Analysis]
22 Riaño Ondiviela A, Meseguer González D, Ruiz Arroyo JR. Malignant ventricular arrhythmias in a patient with Gitelman syndrome. Med Clin (Barc) 2021:S0025-7753(21)00070-1. [PMID: 33743984 DOI: 10.1016/j.medcli.2020.12.024] [Reference Citation Analysis]
23 Yang M, Dong Y, Tian J, Yan L, Chen Y, Qiu H, Liu W, Hu Y. A novel compound heterozygous mutation of SLC12A3 gene in a pedigree with Gitelman syndrome and literature review. Genes Genomics 2020;42:1035-40. [PMID: 32712837 DOI: 10.1007/s13258-020-00960-6] [Reference Citation Analysis]
24 Mayan H, Farfel Z, Karlish SJD. Renal Mg handling, FXYD2 and the central role of the Na,K-ATPase. Physiol Rep 2018;6:e13843. [PMID: 30175537 DOI: 10.14814/phy2.13843] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 2.3] [Reference Citation Analysis]
25 Zhang JH, Ruan DD, Hu YN, Ruan XL, Zhu YB, Yang X, Wu JB, Lin XF, Luo JW, Tang FQ. Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations. Biomed Res Int 2021;2021:9973161. [PMID: 34046503 DOI: 10.1155/2021/9973161] [Reference Citation Analysis]
26 Urwin S, Willows J, Sayer JA. The challenges of diagnosis and management of Gitelman syndrome. Clin Endocrinol 2020;92:3-10. [DOI: 10.1111/cen.14104] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
27 Zhong M, Zhai Z, Zhou X, Sun J, Chen H, Lu W. Three Novel Homozygous Mutations of the SLC12A3 Gene in a Gitelman Syndrome Patient. Int J Gen Med 2021;14:1999-2002. [PMID: 34079339 DOI: 10.2147/IJGM.S308246] [Reference Citation Analysis]
28 Gianesello L, Del Prete D, Anglani F, Calò LA. Genetics and phenotypic heterogeneity of Dent disease: the dark side of the moon. Hum Genet 2021;140:401-21. [PMID: 32860533 DOI: 10.1007/s00439-020-02219-2] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
29 Celmina M, Micule I, Inashkina I, Audere M, Kuske S, Pereca J, Stavusis J, Pelnena D, Strautmanis J. EAST/SeSAME syndrome: Review of the literature and introduction of four new Latvian patients. Clin Genet 2019;95:63-78. [PMID: 29722015 DOI: 10.1111/cge.13374] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 2.5] [Reference Citation Analysis]
30 Flisiński M, Skalska E, Mączyńska B, Butt-Hussaim N, Sobczyńska-Tomaszewska A, Haus O, Manitius J. Gitelman syndrome with normocalciuria - a case report. BMC Nephrol 2022;23:170. [PMID: 35509038 DOI: 10.1186/s12882-022-02782-y] [Reference Citation Analysis]
31 Zhao L, Yang K, Fan P, Gong D, Zhang L, Lu Y, Meng X, Zhou X. RET c.1901G>A and Novel SLC12A3 Mutations in Familial Pheochromocytomas. Genes 2022;13:864. [DOI: 10.3390/genes13050864] [Reference Citation Analysis]
32 Besouw MTP, Kleta R, Bockenhauer D. Bartter and Gitelman syndromes: Questions of class. Pediatr Nephrol 2020;35:1815-24. [PMID: 31664557 DOI: 10.1007/s00467-019-04371-y] [Cited by in Crossref: 10] [Cited by in F6Publishing: 5] [Article Influence: 3.3] [Reference Citation Analysis]
33 Peng X, Jiang L, Chen C, Qin Y, Yuan T, Wang O, Xing X, Li X, Nie M, Chen L. Increased urinary prostaglandin E2 metabolite: A potential therapeutic target of Gitelman syndrome. PLoS One. 2017;12:e0180811. [PMID: 28700713 DOI: 10.1371/journal.pone.0180811] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 1.4] [Reference Citation Analysis]
34 Rombach S, Benner A, Schick MA. [Sectio Caesarea under Gitelman Syndrome]. Anasthesiol Intensivmed Notfallmed Schmerzther 2021;56:289-95. [PMID: 33890260 DOI: 10.1055/a-1299-0579] [Reference Citation Analysis]
35 Wu CY, Tsai MH, Chen CC, Kao CH. Early diagnosis of Gitelman syndrome in a young child: A case report . World J Clin Cases 2022; 10(9): 2842-2848 [DOI: 10.12998/wjcc.v10.i9.2842] [Reference Citation Analysis]
36 Van Laecke S. Hypomagnesemia and hypermagnesemia. Acta Clin Belg 2019;74:41-7. [PMID: 30220246 DOI: 10.1080/17843286.2018.1516173] [Cited by in Crossref: 35] [Cited by in F6Publishing: 26] [Article Influence: 11.7] [Reference Citation Analysis]
37 Aymé S, Bockenhauer D, Day S, Devuyst O, Guay-Woodford LM, Ingelfinger JR, Klein JB, Knoers NVAM, Perrone RD, Roberts J, Schaefer F, Torres VE, Cheung M, Wheeler DC, Winkelmayer WC; Conference Participants. Common Elements in Rare Kidney Diseases: Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int 2017;92:796-808. [PMID: 28938953 DOI: 10.1016/j.kint.2017.06.018] [Cited by in Crossref: 21] [Cited by in F6Publishing: 16] [Article Influence: 5.3] [Reference Citation Analysis]
38 Blanchard A, Vallet M, Dubourg L, Hureaux M, Allard J, Haymann JP, de la Faille R, Arnoux A, Dinut A, Bergerot D, Becker PH, Courand PY, Baron S, Houillier P, Tack I, Devuyst O, Jeunemaitre X, Azizi M, Vargas-Poussou R. Resistance to Insulin in Patients with Gitelman Syndrome and a Subtle Intermediate Phenotype in Heterozygous Carriers: A Cross-Sectional Study. J Am Soc Nephrol 2019;30:1534-45. [PMID: 31285285 DOI: 10.1681/ASN.2019010031] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 3.3] [Reference Citation Analysis]
39 Li N, Gu HF. Genetic and Biological Effects of SLC12A3, a Sodium-Chloride Cotransporter, in Gitelman Syndrome and Diabetic Kidney Disease. Front Genet 2022;13:799224. [DOI: 10.3389/fgene.2022.799224] [Reference Citation Analysis]
40 Kumar R, Srimathy V, Annigeri R. Concurrent gitelman syndrome-like tubulopathy and grave's disease. Indian J Nephrol 2022;32:275. [DOI: 10.4103/ijn.ijn_532_20] [Reference Citation Analysis]
41 Meurer M, Höcherl K. Deregulated renal magnesium transport during lipopolysaccharide-induced acute kidney injury in mice. Pflugers Arch 2019;471:619-31. [PMID: 30726531 DOI: 10.1007/s00424-019-02261-8] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
42 Ellison DH, Lin SH. Enemy Action in the Distal Convoluted Tubule. J Am Soc Nephrol 2019;30:1345-8. [PMID: 31366695 DOI: 10.1681/ASN.2019050475] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
43 Zhou H, Ren Y, Lu C, Li Y, Tian H, Chen T, Piccinni G. Thyroid Function in 35 Patients with Gitelman Syndrome. BioMed Research International 2020;2020:1-6. [DOI: 10.1155/2020/7963898] [Reference Citation Analysis]
44 Chen Q, Wang X, Min J, Wang L, Mou L. Kidney stones and moderate proteinuria as the rare manifestations of Gitelman syndrome. BMC Nephrol 2021;22:12. [PMID: 33413160 DOI: 10.1186/s12882-020-02211-y] [Reference Citation Analysis]
45 O'Meara D, Sheward L, Hartman-Munick S, Addison J, Abu-El-Haija A. Craving Answers. N Engl J Med 2022;386:880-6. [PMID: 35235730 DOI: 10.1056/NEJMcps2113517] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
46 Kamel KS, Halperin ML. Use of Urine Electrolytes and Urine Osmolality in the Clinical Diagnosis of Fluid, Electrolytes, and Acid-Base Disorders. Kidney Int Rep 2021;6:1211-24. [PMID: 34013099 DOI: 10.1016/j.ekir.2021.02.003] [Reference Citation Analysis]
47 Clase CM, Carrero J, Ellison DH, Grams ME, Hemmelgarn BR, Jardine MJ, Kovesdy CP, Kline GA, Lindner G, Obrador GT, Palmer BF, Cheung M, Wheeler DC, Winkelmayer WC, Pecoits-filho R, Ashuntantang GE, Bakker SJ, Bakris GL, Bhandari S, Burdmann EA, Campbell KL, Charytan DM, Clegg DJ, Cuppari L, Goldsmith D, Hallan SI, He J, Herzog CA, Hoenig MP, Hoorn EJ, Leipziger JG, Leonberg-yoo AK, Lerma EV, Lopez-almaraz JE, Małyszko J, Mann JF, Marklund M, Mcdonough AA, Nagahama M, Navaneethan SD, Pitt B, Pochynyuk OM, Proença de Moraes T, Rafique Z, Robinson BM, Roger SD, Rossignol P, Singer AJ, Smyth A, Sood MM, Walsh M, Weir MR, Wingo CS. Potassium homeostasis and management of dyskalemia in kidney diseases: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney International 2020;97:42-61. [DOI: 10.1016/j.kint.2019.09.018] [Cited by in Crossref: 67] [Cited by in F6Publishing: 47] [Article Influence: 33.5] [Reference Citation Analysis]
48 Kermond R, Mallett A, McCarthy H. A clinical approach to tubulopathies in children and young adults. Pediatr Nephrol 2022. [PMID: 35585366 DOI: 10.1007/s00467-022-05606-1] [Reference Citation Analysis]
49 Ranaweerage R, Perera S, Gunapala A. Hypokalaemic paralysis and metabolic alkalosis in a patient with Sjögren syndrome: a case report and literature review. BMC Nephrol 2021;22:159. [PMID: 33931020 DOI: 10.1186/s12882-021-02371-5] [Reference Citation Analysis]
50 Veríssimo R, Leite de Sousa L, Carvalho TJ, Fidalgo P. Novel SLC12A3 mutation in Gitelman syndrome. BMJ Case Rep 2021;14:e238097. [PMID: 33462018 DOI: 10.1136/bcr-2020-238097] [Reference Citation Analysis]
51 Barathidasan GS, Krishnamurthy S, Karunakar P, Rajendran R, Ramya K, Dhandapany G, Ramamoorthy JG, Ganesh RN. Systemic lupus erythematosus complicated by a Gitelman-like syndrome in an 8-year-old girl. CEN Case Rep 2020;9:129-32. [PMID: 31853802 DOI: 10.1007/s13730-019-00440-1] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
52 Terker AS, Castañeda-Bueno M, Ferdaus MZ, Cornelius RJ, Erspamer KJ, Su XT, Miller LN, McCormick JA, Wang WH, Gamba G, Yang CL, Ellison DH. With no lysine kinase 4 modulates sodium potassium 2 chloride cotransporter activity in vivo. Am J Physiol Renal Physiol 2018;315:F781-90. [PMID: 29412704 DOI: 10.1152/ajprenal.00485.2017] [Cited by in Crossref: 22] [Cited by in F6Publishing: 19] [Article Influence: 5.5] [Reference Citation Analysis]
53 Qin YZ, Liu YM, Wang Y, You C, Li LN, Zhou XY, Lv WM, Hong SH, Xiao LX. Novel compound heterozygous mutation of SLC12A3 in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review. World J Clin Cases 2022; 10(21): 7483-7494 [DOI: 10.12998/wjcc.v10.i21.7483] [Reference Citation Analysis]
54 Setiawati D, Nuhriawangsa A, Wasita B. Hubungan Magnesium Serum Dengan Kadar Glukosa Darah Pada Dewasa Overweight Dan Obesitas. AMNT 2019;3:239. [DOI: 10.20473/amnt.v3i4.2019.239-246] [Reference Citation Analysis]
55 Gopinath B, Chauhan N, Achappa B. Hypocalcaemia and hyponatraemia masquerading the diagnosis of Gitelman syndrome. BMJ Case Rep 2019;12:bcr-2018-227886. [PMID: 30696651 DOI: 10.1136/bcr-2018-227886] [Reference Citation Analysis]
56 Rapoport RM, Soleimani M. Mechanism of Thiazide Diuretic Arterial Pressure Reduction: The Search Continues. Front Pharmacol 2019;10:815. [PMID: 31543812 DOI: 10.3389/fphar.2019.00815] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 1.3] [Reference Citation Analysis]
57 Ravarotto V, Simioni F, Sabbadin C, Pagnin E, Maiolino G, Armanini D, Calò LA. Proinflammatory/profibrotic effects of aldosterone in Gitelman's syndrome, a human model opposite to hypertension. J Endocrinol Invest 2019;42:521-6. [PMID: 30136149 DOI: 10.1007/s40618-018-0942-9] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
58 Evans RDR, Antonelou M, Sathiananthamoorthy S, Rega M, Henderson S, Ceron-Gutierrez L, Barcenas-Morales G, Müller CA, Doffinger R, Walsh SB, Salama AD. Inherited salt-losing tubulopathies are associated with immunodeficiency due to impaired IL-17 responses. Nat Commun 2020;11:4368. [PMID: 32868758 DOI: 10.1038/s41467-020-18184-3] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
59 Calò LA, Palazzo V, Salviati L, Anglani F. Two unusual cases of Gitelman's syndrome with a complex inheritance: how the phenotype can help interpret the genotype: lesson for the clinical nephrologist. J Nephrol 2021;34:1327-30. [PMID: 32926342 DOI: 10.1007/s40620-020-00861-7] [Reference Citation Analysis]
60 Rossi GM, Regolisti G, Peyronel F, Fiaccadori E. Recent insights into sodium and potassium handling by the aldosterone-sensitive distal nephron: implications on pathophysiology and drug discovery. J Nephrol 2020;33:447-66. [DOI: 10.1007/s40620-020-00700-9] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
61 Su XT, Yang CL, Ellison DH. Kidney Is Essential for Blood Pressure Modulation by Dietary Potassium. Curr Cardiol Rep 2020;22:124. [PMID: 32789612 DOI: 10.1007/s11886-020-01359-1] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
62 Rossanti R, Horinouchi T, Sakakibara N, Yamamura T, Nagano C, Ishiko S, Aoto Y, Kondo A, Nagai S, Awano H, Nagase H, Matsuo M, Iijima K, Nozu K. Detecting pathogenic deep intronic variants in Gitelman syndrome. Am J Med Genet A 2022. [PMID: 35785516 DOI: 10.1002/ajmg.a.62885] [Reference Citation Analysis]
63 Nuñez-Gonzalez L, Carrera N, Garcia-Gonzalez MA. Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Bartter and Gitelman Syndromes: A Primer for Clinicians. Int J Mol Sci 2021;22:11414. [PMID: 34768847 DOI: 10.3390/ijms222111414] [Reference Citation Analysis]
64 Kiss EE, Chandran N, Alex G, Olomu P. Anesthetic Challenges of an Adolescent Patient with Epidermolysis Bullosa and Gitelman's Syndrome Undergoing Posterior Spinal Fusion Surgery. J Pediatr Genet 2021;10:152-5. [PMID: 33996187 DOI: 10.1055/s-0040-1710329] [Reference Citation Analysis]
65 Yan MT, Yang SS, Tseng MH, Cheng CJ, Tsai JD, Sung CC, Hsu YJ, Lin SH. Allele-specific RT-PCR for the rapid detection of recurrent SLC12A3 mutations for Gitelman syndrome. NPJ Genom Med 2021;6:68. [PMID: 34389731 DOI: 10.1038/s41525-021-00230-8] [Reference Citation Analysis]
66 Walsh PR, Tse Y, Ashton E, Iancu D, Jenkins L, Bienias M, Kleta R, Van't Hoff W, Bockenhauer D. Clinical and diagnostic features of Bartter and Gitelman syndromes. Clin Kidney J 2018;11:302-9. [PMID: 29942493 DOI: 10.1093/ckj/sfx118] [Cited by in Crossref: 24] [Cited by in F6Publishing: 20] [Article Influence: 4.8] [Reference Citation Analysis]
67 Sado M, Takano K, Kurata K, Kitahara M. Gitelman syndrome with transient renal tubular damage in early childhood. Pediatr Int 2021;63:1256-8. [PMID: 34268835 DOI: 10.1111/ped.14589] [Reference Citation Analysis]
68 Florea L, Caba L, Gorduza EV. Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance. Front Pediatr 2022;10:908655. [DOI: 10.3389/fped.2022.908655] [Reference Citation Analysis]
69 Jalalzadeh M, Garcia Goncalves de Brito D, Chaudhari S, Poor AD, Baumstein D. Gitelman Syndrome Provisionally Diagnosed During the First Presentation of Diabetic Ketoacidosis. Cureus 2021;13:e14253. [PMID: 33954067 DOI: 10.7759/cureus.14253] [Reference Citation Analysis]
70 Downie ML, Lopez Garcia SC, Kleta R, Bockenhauer D. Inherited Tubulopathies of the Kidney: Insights from Genetics. Clin J Am Soc Nephrol 2021;16:620-30. [PMID: 32238367 DOI: 10.2215/CJN.14481119] [Cited by in Crossref: 11] [Cited by in F6Publishing: 4] [Article Influence: 5.5] [Reference Citation Analysis]
71 Roumeliotou S, Theohari A, Tsamoulis D, Vafeidou K, Siountri I, Siomou E. Persistent mild hypokalemia in an otherwise healthy 6-year-old girl: Answers. Pediatr Nephrol 2022. [PMID: 35118535 DOI: 10.1007/s00467-022-05458-9] [Reference Citation Analysis]
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