{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,27]],"date-time":"2026-10-27T00:21:50Z","timestamp":1793060510688,"version":"4.5.0"},"reference-count":71,"publisher":"JLE","issue":"4","license":[{"start":{"date-parts":[[2020,7,1]],"date-time":"2020-07-01T00:00:00Z","timestamp":1593561600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2021,7,27]],"date-time":"2021-07-27T00:00:00Z","timestamp":1627344000000},"content-version":"am","delay-in-days":391,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.fr","em-consulte.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["N\u00e9phrologie & Th\u00e9rapeutique"],"published-print":{"date-parts":[[2020,7]]},"DOI":"10.1016\/j.nephro.2020.06.001","type":"journal-article","created":{"date-parts":[[2020,7,1]],"date-time":"2020-07-01T22:12:11Z","timestamp":1593641531000},"page":"233-243","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":6,"title":["Syndromes de Bartter\u2013Gitelman"],"prefix":"10.1684","volume":"16","author":[{"given":"Anne","family":"Blanchard","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pierre-Yves","family":"Courand","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marine","family":"Livrozet","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rosa","family":"Vargas-Poussou","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"18929","reference":[{"key":"10.1016\/j.nephro.2020.06.001_bib0370","doi-asserted-by":"crossref","first-page":"811","DOI":"10.1016\/0002-9343(62)90214-0","article-title":"Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome","volume":"33","author":"Bartter","year":"1962","journal-title":"Am J Med"},{"key":"10.1016\/j.nephro.2020.06.001_bib0375","first-page":"43","article-title":"Bartter's syndrome: evidence suggesting a distal tubular defect in a hypocalciuric variant of the syndrome","volume":"18","author":"Sutton","year":"1992","journal-title":"Miner Electrolyte Metab"},{"key":"10.1016\/j.nephro.2020.06.001_bib0380","doi-asserted-by":"crossref","first-page":"760","DOI":"10.1152\/physrev.1985.65.3.760","article-title":"Ion transport mechanisms in thick ascending limb of Henle's loop of mammalian nephron","volume":"65","author":"Greger","year":"1985","journal-title":"Physiol Rev"},{"key":"10.1016\/j.nephro.2020.06.001_bib0385","doi-asserted-by":"crossref","first-page":"15","DOI":"10.1681\/ASN.2004070523","article-title":"Epithelial Ca2+ and Mg2+ channels in health and disease","volume":"16","author":"Hoenderop","year":"2005","journal-title":"J Am Soc Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0390","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1007\/s12519-012-0333-9","article-title":"Understanding Bartter syndrome and Gitelman syndrome","volume":"8","author":"Fremont","year":"2012","journal-title":"World J Pediatr"},{"key":"10.1016\/j.nephro.2020.06.001_bib0395","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1007\/s12519-015-0016-4","article-title":"Molecular pathophysiology of Bartter's and Gitelman's syndromes","volume":"11","author":"Koulouridis","year":"2015","journal-title":"World J Pediatr"},{"key":"10.1016\/j.nephro.2020.06.001_bib0400","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1038\/ng0696-183","article-title":"Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2","volume":"13","author":"Simon","year":"1996","journal-title":"Nat Genet"},{"key":"10.1016\/j.nephro.2020.06.001_bib0405","doi-asserted-by":"crossref","first-page":"152","DOI":"10.1038\/ng1096-152","article-title":"Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK","volume":"14","author":"Simon","year":"1996","journal-title":"Nat Genet"},{"key":"10.1016\/j.nephro.2020.06.001_bib0410","doi-asserted-by":"crossref","first-page":"310","DOI":"10.1038\/ng752","article-title":"Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure","volume":"29","author":"Birkenhager","year":"2001","journal-title":"Nat Genet"},{"key":"10.1016\/j.nephro.2020.06.001_bib0415","doi-asserted-by":"crossref","first-page":"1314","DOI":"10.1056\/NEJMoa032843","article-title":"Salt wasting and deafness resulting from mutations in two chloride channels","volume":"350","author":"Schlingmann","year":"2004","journal-title":"N Engl J Med"},{"key":"10.1016\/j.nephro.2020.06.001_bib0420","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1038\/ng1097-171","article-title":"Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III","volume":"17","author":"Simon","year":"1997","journal-title":"Nat Genet"},{"key":"10.1016\/j.nephro.2020.06.001_bib0425","doi-asserted-by":"crossref","first-page":"2136","DOI":"10.1681\/ASN.2005101071","article-title":"Late-onset manifestation of antenatal Bartter syndrome as a result of residual function of the mutated renal Na\u00b1K\u00b12Cl- co-transporter","volume":"17","author":"Pressler","year":"2006","journal-title":"J Am Soc Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0430","doi-asserted-by":"crossref","first-page":"2259","DOI":"10.1097\/01.ASN.0000025781.16723.68","article-title":"Functional characterization of a calcium-sensing receptor mutation in severe autosomal dominant hypocalcemia with a Bartter-like syndrome","volume":"13","author":"Vargas-Poussou","year":"2002","journal-title":"J Am Soc Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0435","doi-asserted-by":"crossref","first-page":"692","DOI":"10.1016\/S0140-6736(02)09842-2","article-title":"Association between activating mutations of calcium-sensing receptor and Bartter's syndrome","volume":"360","author":"Watanabe","year":"2002","journal-title":"Lancet"},{"key":"10.1016\/j.nephro.2020.06.001_bib0440","doi-asserted-by":"crossref","first-page":"1853","DOI":"10.1056\/NEJMoa1507629","article-title":"Polyhydramnios, transient antenatal Bartter's syndrome, and MAGED2\u00a0mutations","volume":"374","author":"Laghmani","year":"2016","journal-title":"N Engl J Med"},{"key":"10.1016\/j.nephro.2020.06.001_bib0445","doi-asserted-by":"crossref","first-page":"24","DOI":"10.1038\/ng0196-24","article-title":"Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter","volume":"12","author":"Simon","year":"1996","journal-title":"Nat Genet"},{"key":"10.1016\/j.nephro.2020.06.001_bib0450","doi-asserted-by":"crossref","first-page":"1651","DOI":"10.1172\/JCI24134","article-title":"Enhanced passive Ca2+ reabsorption and reduced Mg2+ channel abundance explains thiazide-induced hypocalciuria and hypomagnesemia","volume":"115","author":"Nijenhuis","year":"2005","journal-title":"J Clin Invest"},{"key":"10.1016\/j.nephro.2020.06.001_bib0455","doi-asserted-by":"crossref","first-page":"693","DOI":"10.1681\/ASN.2010090907","article-title":"Spectrum of mutations in Gitelman syndrome","volume":"22","author":"Vargas-Poussou","year":"2011","journal-title":"J Am Soc Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0460","doi-asserted-by":"crossref","first-page":"24","DOI":"10.1046\/j.1523-1755.2003.00730.x","article-title":"A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes","volume":"63","author":"Zelikovic","year":"2003","journal-title":"Kidney Int"},{"issue":"Suppl. 3","key":"10.1016\/j.nephro.2020.06.001_bib0465","first-page":"22S","article-title":"Fetal polyuria and hydramnios associated with Bartter's syndrome","volume":"63","author":"Sieck","year":"1984","journal-title":"Obstet Gynecol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0470","doi-asserted-by":"crossref","first-page":"576","DOI":"10.1038\/nrneph.2015.89","article-title":"Pathophysiology, diagnosis and management of nephrogenic diabetes insipidus","volume":"11","author":"Bockenhauer","year":"2015","journal-title":"Nat Rev Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0475","doi-asserted-by":"crossref","first-page":"669","DOI":"10.1007\/s004310050688","article-title":"Bartter syndrome and its neonatal variant","volume":"156","author":"Proesmans","year":"1997","journal-title":"Eur J Pediatr"},{"key":"10.1016\/j.nephro.2020.06.001_bib0480","doi-asserted-by":"crossref","first-page":"249","DOI":"10.1097\/01.ASN.0000049161.60740.CE","article-title":"Recent advances in molecular genetics of hereditary magnesium-losing disorders","volume":"14","author":"Konrad","year":"2003","journal-title":"J Am Soc Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0485","doi-asserted-by":"crossref","first-page":"1617","DOI":"10.1093\/ndt\/13.7.1617","article-title":"Gitelman syndrome comes of age","volume":"13","author":"Monnens","year":"1998","journal-title":"Nephrol Dial Transplant"},{"key":"10.1016\/j.nephro.2020.06.001_bib0490","doi-asserted-by":"crossref","first-page":"1533","DOI":"10.1093\/ndt\/gfs600","article-title":"Unexpected clinical sequelae of Gitelman syndrome: hypertension in adulthood is common and females have higher potassium requirements","volume":"28","author":"Berry","year":"2013","journal-title":"Nephrol Dial Transplant"},{"key":"10.1016\/j.nephro.2020.06.001_bib0495","first-page":"234","article-title":"New clinical approach to evaluate disorders of potassium excretion","volume":"12","author":"West","year":"1986","journal-title":"Miner Electrolyte Metab"},{"key":"10.1016\/j.nephro.2020.06.001_bib0500","first-page":"120","article-title":"Transtubular potassium concentration gradient (TTKG) and urine ammonium in differential diagnosis of hypokalemia","volume":"13","author":"Joo","year":"2000","journal-title":"J Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0505","doi-asserted-by":"crossref","first-page":"24","DOI":"10.1016\/j.kint.2016.09.046","article-title":"Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) controversies conference","volume":"91","author":"Blanchard","year":"2017","journal-title":"Kidney Int"},{"key":"10.1016\/j.nephro.2020.06.001_bib0510","doi-asserted-by":"crossref","first-page":"454","DOI":"10.2215\/CJN.02950906","article-title":"A thiazide test for the diagnosis of renal tubular hypokalemic disorders","volume":"2","author":"Colussi","year":"2007","journal-title":"Clin J Am Soc Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0515","doi-asserted-by":"crossref","first-page":"1408","DOI":"10.1016\/j.kint.2019.08.027","article-title":"High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults","volume":"96","author":"Hureaux","year":"2019","journal-title":"Kidney Int"},{"key":"10.1016\/j.nephro.2020.06.001_bib0520","doi-asserted-by":"crossref","first-page":"5","DOI":"10.5049\/EBP.2009.7.1.5","article-title":"Acquired gitelman syndrome","volume":"7","author":"Kim","year":"2009","journal-title":"Electrolyte Blood Press"},{"key":"10.1016\/j.nephro.2020.06.001_bib0525","first-page":"822","article-title":"Congenital chloride diarrhea misdiagnosed as pseudo-Bartter syndrome","volume":"18","author":"Saneian","year":"2013","journal-title":"J Res Med Sci"},{"key":"10.1016\/j.nephro.2020.06.001_bib0530","doi-asserted-by":"crossref","first-page":"264","DOI":"10.1016\/j.tem.2004.06.003","article-title":"Mineralocorticoid resistance","volume":"15","author":"Zennaro","year":"2004","journal-title":"Trends Endocrinol Metab"},{"key":"10.1016\/j.nephro.2020.06.001_bib0535","doi-asserted-by":"crossref","first-page":"401","DOI":"10.1007\/s00431-011-1578-3","article-title":"A patient with Dent disease and features of Bartter syndrome caused by a novel mutation of CLCN5","volume":"171","author":"Okamoto","year":"2012","journal-title":"Eur J Pediatr"},{"issue":"Suppl. 4","key":"10.1016\/j.nephro.2020.06.001_bib0540","article-title":"Inherited disorders of renal hypomagnesaemia","volume":"29","author":"Konrad","year":"2014","journal-title":"Nephrol Dial Transplant"},{"key":"10.1016\/j.nephro.2020.06.001_bib0545","doi-asserted-by":"crossref","first-page":"707","DOI":"10.1007\/s00467-015-3142-2","article-title":"HNF1B-associated clinical phenotypes: the kidney and beyond","volume":"31","author":"Bockenhauer","year":"2016","journal-title":"Pediatr Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0550","doi-asserted-by":"crossref","first-page":"1123","DOI":"10.1681\/ASN.2008060633","article-title":"HNF1B mutations associate with hypomagnesemia and renal magnesium wasting","volume":"20","author":"Adalat","year":"2009","journal-title":"J Am Soc Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0555","doi-asserted-by":"crossref","first-page":"2081","DOI":"10.1007\/s00467-012-2219-4","article-title":"SeSAME\/EAST syndrome-phenotypic variability and delayed activity of the distal convoluted tubule","volume":"27","author":"Scholl","year":"2012","journal-title":"Pediatr Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0560","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1186\/1471-2369-7-10","article-title":"Gitelman-like syndrome after cisplatin therapy: a case report and literature review","volume":"7","author":"Panichpisal","year":"2006","journal-title":"BMC Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0565","first-page":"117","article-title":"Mitochondrial cytopathy presenting with features of Gitelman's syndrome","volume":"11","author":"Kari","year":"2006","journal-title":"Neurosciences"},{"key":"10.1016\/j.nephro.2020.06.001_bib0570","doi-asserted-by":"crossref","first-page":"239","DOI":"10.1007\/s00508-006-0559-4","article-title":"A woman with red eyes and hypokalemia: a case of acquired Gitelman syndrome","volume":"118","author":"Schwarz","year":"2006","journal-title":"Wien Klin Wochenschr"},{"key":"10.1016\/j.nephro.2020.06.001_bib0575","first-page":"e3923","article-title":"Acquired Gitelman syndrome associated with systemic sclerosis","volume":"11","author":"Masab","year":"2019","journal-title":"Cureus"},{"key":"10.1016\/j.nephro.2020.06.001_bib0580","first-page":"95","article-title":"Antenatal form of Bartter's syndrome","volume":"40","author":"Deschenes","year":"1993","journal-title":"Ann Pediatr"},{"key":"10.1016\/j.nephro.2020.06.001_bib0585","doi-asserted-by":"crossref","first-page":"580","DOI":"10.1046\/j.1523-1755.2002.00467.x","article-title":"Electrocardiogram with prolonged QT interval in Gitelman disease","volume":"62","author":"Bettinelli","year":"2002","journal-title":"Kidney Int"},{"key":"10.1016\/j.nephro.2020.06.001_bib0590","doi-asserted-by":"crossref","first-page":"274","DOI":"10.1136\/hrt.61.3.274","article-title":"Electrocardiographic findings and frequency of arrhythmias in Bartter's syndrome","volume":"61","author":"Blomstrom-Lundqvist","year":"1989","journal-title":"Br Heart J"},{"key":"10.1016\/j.nephro.2020.06.001_bib0595","doi-asserted-by":"crossref","first-page":"407","DOI":"10.3109\/08860221003632873","article-title":"An unusual presentation of primary renal hypokalemia-hypomagnesemia (Gitelman's syndrome)","volume":"32","author":"Bansal","year":"2010","journal-title":"Ren Fail"},{"key":"10.1016\/j.nephro.2020.06.001_bib0600","doi-asserted-by":"crossref","first-page":"193","DOI":"10.5414\/CNP67193","article-title":"Aborted sudden cardiac death in two patients with Bartter's\/Gitelman's syndromes","volume":"67","author":"Scognamiglio","year":"2007","journal-title":"Clin Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0605","doi-asserted-by":"crossref","first-page":"982","DOI":"10.1016\/j.jacc.2008.12.014","volume":"53","author":"Rautaharju","year":"2009","journal-title":"J Am Coll Cardiol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0610","doi-asserted-by":"crossref","first-page":"797","DOI":"10.1016\/0002-9149(92)90562-D","article-title":"An improved method for adjusting the QT interval for heart rate (the Framingham Heart Study)","volume":"70","author":"Sagie","year":"1992","journal-title":"Am J Cardiol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0615","doi-asserted-by":"crossref","first-page":"1398","DOI":"10.1093\/ndt\/gfh204","article-title":"Cardiac work up in primary renal hypokalaemia-hypomagnesaemia (Gitelman syndrome)","volume":"19","author":"Foglia","year":"2004","journal-title":"Nephrol Dial Transplant"},{"key":"10.1016\/j.nephro.2020.06.001_bib0620","doi-asserted-by":"crossref","first-page":"E47","DOI":"10.1111\/echo.12034","article-title":"The effects of serum potassium and magnesium levels in a patient with Gitelman's syndrome on the timing of ventricular wall motion and the pattern of ventricular strain and torsion","volume":"30","author":"Yildiz","year":"2013","journal-title":"Echocardiography"},{"key":"10.1016\/j.nephro.2020.06.001_bib0625","doi-asserted-by":"crossref","first-page":"888","DOI":"10.1111\/j.1365-2362.2008.02034.x","article-title":"Myocardial perfusion defects in Bartter and Gitelman syndromes","volume":"38","author":"Scognamiglio","year":"2008","journal-title":"Eur J Clin Invest"},{"key":"10.1016\/j.nephro.2020.06.001_bib0630","first-page":"882","article-title":"Abnormalities of Gq-mediated cell signaling in Bartter and Gitelman syndromes","volume":"60","author":"Calo","year":"2001","journal-title":"Kidney Int"},{"key":"10.1016\/j.nephro.2020.06.001_bib0635","doi-asserted-by":"crossref","first-page":"2540","DOI":"10.1681\/ASN.2016101057","article-title":"Clinical and genetic spectrum of bartter syndrome Type 3","volume":"28","author":"Seys","year":"2017","journal-title":"J Am Soc Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0640","doi-asserted-by":"crossref","first-page":"1455","DOI":"10.1093\/ndt\/gfn689","article-title":"Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome","volume":"24","author":"Brochard","year":"2009","journal-title":"Nephrol Dial Transplant"},{"key":"10.1016\/j.nephro.2020.06.001_bib0645","doi-asserted-by":"crossref","first-page":"939","DOI":"10.1093\/qjmed\/hcr095","article-title":"Does hypokalaemia cause nephropathy? An observational study of renal function in patients with Bartter or Gitelman syndrome","volume":"104","author":"Walsh","year":"2011","journal-title":"QJM"},{"key":"10.1016\/j.nephro.2020.06.001_bib0650","doi-asserted-by":"crossref","first-page":"799","DOI":"10.1359\/JBMR.041238","article-title":"Inactivation of the Na-Cl co-transporter (NCC) gene is associated with high BMD through both renal and bone mechanisms: analysis of patients with Gitelman syndrome and Ncc null mice","volume":"20","author":"Nicolet-Barousse","year":"2005","journal-title":"J Bone Miner Res"},{"key":"10.1016\/j.nephro.2020.06.001_bib0655","first-page":"1840","article-title":"Chondrocalcinosis secondary to hypomagnesemia in Gitelman's syndrome","volume":"32","author":"Ea","year":"2005","journal-title":"J Rheumatol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0660","doi-asserted-by":"crossref","first-page":"1506","DOI":"10.1093\/rheumatology\/kem184","article-title":"Familiar association of Gitelman's syndrome and calcium pyrophosphate dihydrate crystal deposition disease\u00a0\u2013\u00a0a case report","volume":"46","author":"Volpe","year":"2007","journal-title":"Rheumatol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0665","doi-asserted-by":"crossref","first-page":"1496","DOI":"10.1002\/art.23106","article-title":"Hypomagnesemia associated with chondrocalcinosis: a cross-sectional study","volume":"57","author":"Richette","year":"2007","journal-title":"Arthritis Rheum"},{"key":"10.1016\/j.nephro.2020.06.001_bib0670","doi-asserted-by":"crossref","first-page":"53","DOI":"10.4081\/reumatismo.2016.884","article-title":"Gitelman syndrome disclosed by calcium pyrophosphate deposition disease: early diagnosis by ultrasonographic study","volume":"68","author":"Della Siega","year":"2016","journal-title":"Reumatismo"},{"key":"10.1016\/j.nephro.2020.06.001_bib0675","doi-asserted-by":"crossref","first-page":"767","DOI":"10.1016\/S0002-9394(99)00277-9","article-title":"Sclerochoroidal calcification associated with Gitelman syndrome","volume":"128","author":"Bourcier","year":"1999","journal-title":"Am J Ophthalmol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0680","doi-asserted-by":"crossref","first-page":"103","DOI":"10.1227\/01.NEU.0000068861.47199.A8","article-title":"Tumoral calcium pyrophosphate dihydrate deposition disease of the ligamentum flavum","volume":"53","author":"Muthukumar","year":"2003","journal-title":"Neurosurgery"},{"key":"10.1016\/j.nephro.2020.06.001_bib0685","doi-asserted-by":"crossref","first-page":"158","DOI":"10.1016\/S1297-319X(00)00246-3","article-title":"Six cases of cervical ligamentum flavum calcification in Blacks in the French West Indies","volume":"68","author":"Cabre","year":"2001","journal-title":"Joint Bone Spine"},{"key":"10.1016\/j.nephro.2020.06.001_bib0690","doi-asserted-by":"crossref","first-page":"1534","DOI":"10.1681\/ASN.2019010031","article-title":"Resistance to insulin in patients with Gitelman syndrome and a subtle intermediate phenotype in heterozygous carriers: a cross-sectional study","volume":"30","author":"Blanchard","year":"2019","journal-title":"J Am Soc Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0695","doi-asserted-by":"crossref","first-page":"1251","DOI":"10.2214\/ajr.152.6.1251","article-title":"Hypercalciuric Bartter syndrome: resolution of nephrocalcinosis with indomethacin","volume":"152","author":"Matsumoto","year":"1989","journal-title":"Am J Roentgenol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0700","doi-asserted-by":"crossref","first-page":"468","DOI":"10.1681\/ASN.2014030293","article-title":"Indomethacin, amiloride or eplerenone for treating hypokalemia in Gitelman syndrome","volume":"26","author":"Blanchard","year":"2015","journal-title":"J Am Soc Nephrol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0705","doi-asserted-by":"crossref","first-page":"508","DOI":"10.1136\/adc.81.6.508","article-title":"Dose related growth response to indometacin in Gitelman syndrome","volume":"81","author":"Liaw","year":"1999","journal-title":"Arch Dis Child"},{"key":"10.1016\/j.nephro.2020.06.001_bib0710","doi-asserted-by":"crossref","first-page":"512","DOI":"10.1097\/AOG.0b013e3182075317","article-title":"Pregnancy in inherited hypokalemic salt-losing renal tubular disorder","volume":"117","author":"Mascetti","year":"2011","journal-title":"Obstet Gynecol"},{"key":"10.1016\/j.nephro.2020.06.001_bib0715","doi-asserted-by":"crossref","first-page":"710","DOI":"10.1046\/j.1523-1755.2001.059002710.x","article-title":"Gitelman's syndrome revisited: an evaluation of symptoms and health-related quality of life","volume":"59","author":"Cruz","year":"2001","journal-title":"Kidney Int"},{"key":"10.1016\/j.nephro.2020.06.001_bib0720","doi-asserted-by":"crossref","first-page":"3196","DOI":"10.1093\/ndt\/gfs017","article-title":"Living with Gitelman disease: an insight into patients\u2019 daily experiences","volume":"27","author":"Caiata-Zufferey","year":"2012","journal-title":"Nephrol Dial Transplant"}],"container-title":["N\u00e9phrologie & Th\u00e9rapeutique"],"original-title":[],"language":"fr","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1769725520300973?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1769725520300973?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.jle.com\/10.1016\/j.nephro.2020.06.001","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,3,5]],"date-time":"2025-03-05T15:56:08Z","timestamp":1741190168000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1769725520300973"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,7]]},"references-count":71,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2020,7]]}},"alternative-id":["S1769725520300973"],"URL":"https:\/\/doi.org\/10.1016\/j.nephro.2020.06.001","relation":{},"ISSN":["1769-7255"],"issn-type":[{"value":"1769-7255","type":"print"}],"subject":[],"published":{"date-parts":[[2020,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Syndromes de Bartter\u2013Gitelman","name":"articletitle","label":"Article Title"},{"value":"N\u00e9phrologie & Th\u00e9rapeutique","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.nephro.2020.06.001","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 Soci\u00e9t\u00e9 francophone de n\u00e9phrologie, dialyse et transplantation. Published by Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}