{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,24]],"date-time":"2026-10-24T02:26:14Z","timestamp":1792808774504,"version":"4.5.0"},"reference-count":102,"publisher":"Springer Science and Business Media LLC","issue":"8","license":[{"start":{"date-parts":[[2025,11,20]],"date-time":"2025-11-20T00:00:00Z","timestamp":1763596800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"},{"start":{"date-parts":[[2025,11,20]],"date-time":"2025-11-20T00:00:00Z","timestamp":1763596800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Pediatr Nephrol"],"published-print":{"date-parts":[[2026,8]]},"DOI":"10.1007\/s00467-025-07047-y","type":"journal-article","created":{"date-parts":[[2025,11,20]],"date-time":"2025-11-20T08:38:49Z","timestamp":1763627929000},"page":"2381-2392","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Failure to thrive in children with tubulopathies"],"prefix":"10.1007","volume":"41","author":[{"given":"Giulio","family":"Rivetti","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Francesco","family":"Emma","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Faidra","family":"Veligratli","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4682-0170","authenticated-orcid":false,"given":"Pierluigi","family":"Marzuillo","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Detlef","family":"B\u00f6ckenhauer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2025,11,20]]},"reference":[{"key":"7047_CR1","volume-title":"Paediatric Nephrology","author":"L Rees","year":"2012","unstructured":"Rees L, Brogan PA, Bockenhauer D, Webb NJA (2012) Paediatric Nephrology. Oxford University Press, Oxford"},{"key":"7047_CR2","doi-asserted-by":"publisher","first-page":"362","DOI":"10.4103\/0971-4065.133002","volume":"24","author":"B Vijay Kiran","year":"2014","unstructured":"Vijay Kiran B, Barman H, Iyengar A (2014) Clinical profile and outcome of renal tubular disorders in children: a single center experience. Indian J Nephrol 24:362\u2013366. https:\/\/doi.org\/10.4103\/0971-4065.133002","journal-title":"Indian J Nephrol"},{"key":"7047_CR3","volume-title":"Nelson\u2019s textbook of pediatrics","author":"R Kliegman","year":"2015","unstructured":"Kliegman R, Stanton B, St. Geme J, Schor N (2015) Nelson\u2019s textbook of pediatrics, 20th edn. Elsevier, Philadelphia","edition":"20"},{"key":"7047_CR4","doi-asserted-by":"publisher","first-page":"127","DOI":"10.1038\/s41366-023-01386-2","volume":"48","author":"C La Scola","year":"2024","unstructured":"La Scola C, Rivetti G, Bertulli C et al (2024) Failure to thrive in children with tubulopathies increases the risk of overweight later in life. Int J Obes 48:127\u2013129. https:\/\/doi.org\/10.1038\/s41366-023-01386-2","journal-title":"Int J Obes"},{"key":"7047_CR5","doi-asserted-by":"publisher","DOI":"10.1007\/978-3-030-52719-8","volume-title":"Pediatric nephrology: eighth edition","author":"F Emma","year":"2022","unstructured":"Emma F, Goldstein SL, Bagga A et al (2022) Pediatric nephrology: eighth edition. Springer, Princeton, NJ"},{"key":"7047_CR6","doi-asserted-by":"publisher","first-page":"55","DOI":"10.5662\/wjm.v5.I2.55","volume":"5","author":"S Amar Al","year":"2015","unstructured":"Amar Al S, Narchi H (2015) Bartter and Gitelman syndromes: spectrum of clinical manifestations caused by different mutations. World J Methodol 5:55. https:\/\/doi.org\/10.5662\/wjm.v5.I2.55","journal-title":"World J Methodol"},{"key":"7047_CR7","doi-asserted-by":"publisher","first-page":"2073","DOI":"10.1007\/s40620-021-01032-y","volume":"34","author":"S Giglio","year":"2021","unstructured":"Giglio S, Montini G, Trepiccione F et al (2021) Distal renal tubular acidosis: a systematic approach from diagnosis to treatment. J Nephrol 34:2073\u20132083. https:\/\/doi.org\/10.1007\/s40620-021-01032-y","journal-title":"J Nephrol"},{"key":"7047_CR8","doi-asserted-by":"publisher","first-page":"2120","DOI":"10.1093\/ndt\/gfaa243","volume":"38","author":"SC Lopez-Garcia","year":"2020","unstructured":"Lopez-Garcia SC, Downie ML, Kim JS et al (2020) Treatment and long-term outcome in primary nephrogenic diabetes insipidus. Nephrol Dial Transplant 38:2120\u20132130. https:\/\/doi.org\/10.1093\/ndt\/gfaa243","journal-title":"Nephrol Dial Transplant"},{"key":"7047_CR9","doi-asserted-by":"publisher","first-page":"712","DOI":"10.1038\/NRNEPH.2013.235","volume":"9","author":"Q Al-Awqati","year":"2013","unstructured":"Al-Awqati Q (2013) Basic research: salt wasting in distal renal tubular acidosis-new look, old problem. Nat Rev Nephrol 9:712\u2013713. https:\/\/doi.org\/10.1038\/NRNEPH.2013.235","journal-title":"Nat Rev Nephrol"},{"key":"7047_CR10","doi-asserted-by":"publisher","first-page":"430","DOI":"10.1016\/j.kint.2016.04.022","volume":"90","author":"A Blanchard","year":"2016","unstructured":"Blanchard A, Curis E, Guyon-Roger T et al (2016) Observations of a large Dent disease cohort. Kidney Int 90:430\u2013439. https:\/\/doi.org\/10.1016\/j.kint.2016.04.022","journal-title":"Kidney Int"},{"key":"7047_CR11","doi-asserted-by":"publisher","DOI":"10.1186\/s13023-016-0426-y","volume":"11","author":"MA Elmonem","year":"2016","unstructured":"Elmonem MA, Veys KR, Soliman NA et al (2016) Cystinosis: a review. Orphanet J Rare Dis 11:47. https:\/\/doi.org\/10.1186\/s13023-016-0426-y","journal-title":"Orphanet J Rare Dis"},{"key":"7047_CR12","doi-asserted-by":"publisher","first-page":"727","DOI":"10.1681\/asn.2017060600","volume":"29","author":"R Kleta","year":"2018","unstructured":"Kleta R, Bockenhauer D (2018) Salt-losing tubulopathies in children: what\u2019s new, what\u2019s controversial? J Am Soc Nephrol 29:727\u2013739. https:\/\/doi.org\/10.1681\/asn.2017060600","journal-title":"J Am Soc Nephrol"},{"key":"7047_CR13","doi-asserted-by":"publisher","first-page":"279","DOI":"10.1038\/966","volume":"19","author":"DS Geller","year":"1998","unstructured":"Geller DS, Rodriguez-Soriano J, Vallo Boado A et al (1998) Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I. Nat Genet 19:279\u2013281. https:\/\/doi.org\/10.1038\/966","journal-title":"Nat Genet"},{"key":"7047_CR14","doi-asserted-by":"publisher","DOI":"10.7759\/cureus.52594","volume":"16","author":"F Manas","year":"2024","unstructured":"Manas F, Singh S (2024) Pseudohypoaldosteronism type II or Gordon syndrome: a rare syndrome of hyperkalemia and hypertension with normal renal function. Cureus 16:e52594. https:\/\/doi.org\/10.7759\/cureus.52594","journal-title":"Cureus"},{"key":"7047_CR15","volume-title":"Hormone resistance and hypersensitivity: from genetics to clinical management","author":"M Maghnie","year":"2012","unstructured":"Maghnie M, Loche S, Cappa M et al (2012) Hormone resistance and hypersensitivity: from genetics to clinical management. Karger, Basel"},{"key":"7047_CR16","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1038\/nrdp.2017.88","volume":"3","author":"P Romagnani","year":"2017","unstructured":"Romagnani P, Remuzzi G, Glassock R et al (2017) (2017) Chronic kidney disease. Nat Rev Dis Primers 3:1\u201324. https:\/\/doi.org\/10.1038\/nrdp.2017.88","journal-title":"Nat Rev Dis Primers"},{"key":"7047_CR17","doi-asserted-by":"publisher","first-page":"769","DOI":"10.1016\/0026-0495(91)90001-d","volume":"40","author":"A Flyvbjerg","year":"1991","unstructured":"Flyvbjerg A, D\u00f8rup I, Everts ME, \u00d8rskov H (1991) Evidence that potassium deficiency induces growth retardation through reduced circulating levels of growth hormone and insulin-like growth factor I. Metabolism 40:769\u2013775. https:\/\/doi.org\/10.1016\/0026-0495(91)90001-d","journal-title":"Metabolism"},{"key":"7047_CR18","doi-asserted-by":"publisher","first-page":"216","DOI":"10.1038\/KI.1997.26","volume":"51","author":"M Br\u00fcngger","year":"1997","unstructured":"Br\u00fcngger M, Hulter HN, Krapf R (1997) Effect of chronic metabolic acidosis on the growth hormone\/IGF-1 endocrine axis: new cause of growth hormone insensitivity in humans. Kidney Int 51:216\u2013221. https:\/\/doi.org\/10.1038\/KI.1997.26","journal-title":"Kidney Int"},{"key":"7047_CR19","doi-asserted-by":"publisher","DOI":"10.6065\/APEM.2013.18.3.152","volume":"18","author":"J-H Lee","year":"2013","unstructured":"Lee J-H, Park JH, Ha T-S, Han H-S (2013) Refractory rickets caused by mild distal renal tubular acidosis. Ann Pediatr Endocrinol Metab 18:152. https:\/\/doi.org\/10.6065\/APEM.2013.18.3.152","journal-title":"Ann Pediatr Endocrinol Metab"},{"key":"7047_CR20","doi-asserted-by":"publisher","first-page":"171","DOI":"10.1016\/8756-3282(86)90014-1","volume":"7","author":"KR Phelps","year":"1986","unstructured":"Phelps KR, Einhorn TA, Vigorita VJ et al (1986) Acidosis-induced osteomalacia: metabolic studies and skeletal histomorphometry. Bone 7:171\u2013179. https:\/\/doi.org\/10.1016\/8756-3282(86)90014-1","journal-title":"Bone"},{"key":"7047_CR21","doi-asserted-by":"publisher","first-page":"1189","DOI":"10.1007\/s00467-007-0472-8","volume":"22","author":"M Boehm","year":"2007","unstructured":"Boehm M, Riesenhuber A, Winkelmayer WC et al (2007) Early erythropoietin therapy is associated with improved growth in children with chronic kidney disease. Pediatr Nephrol 22:1189\u20131193. https:\/\/doi.org\/10.1007\/s00467-007-0472-8","journal-title":"Pediatr Nephrol"},{"issue":"7","key":"7047_CR22","doi-asserted-by":"publisher","first-page":"1","DOI":"10.4103\/2230-8210.145038","volume":"18","author":"A Soliman","year":"2014","unstructured":"Soliman A, De Sanctis V, Kalra S (2014) Anemia and growth. Indian J Endocrinol Metab 18:1. https:\/\/doi.org\/10.4103\/2230-8210.145038","journal-title":"Indian J Endocrinol Metab"},{"key":"7047_CR23","doi-asserted-by":"publisher","first-page":"457","DOI":"10.1053\/J.ajkd.2022.09.019","volume":"81","author":"O Akchurin","year":"2022","unstructured":"Akchurin O, Molino AR, Schneider MF et al (2022) Longitudinal relationship between anemia and statural growth impairment in children and adolescents with nonglomerular CKD: findings from the chronic kidney disease in children (CKiD) study. Am J Kidney Dis 81:457. https:\/\/doi.org\/10.1053\/J.ajkd.2022.09.019","journal-title":"Am J Kidney Dis"},{"key":"7047_CR24","doi-asserted-by":"publisher","DOI":"10.1093\/med\/9780199592548.001.0001","volume-title":"Oxford Textbook of Clinical Nephrology","author":"NN Turner","year":"2015","unstructured":"Turner NN, Lameire N, Goldsmith David J (2015) Oxford Textbook of Clinical Nephrology. Oxford, Oxford UK"},{"key":"7047_CR25","doi-asserted-by":"publisher","first-page":"11","DOI":"10.3339\/ckd.23.001","volume":"27","author":"J Joung","year":"2023","unstructured":"Joung J, Cho H (2023) Tubulopathy: the clinical and genetic approach in diagnosis. Child Kidney Dis 27:11\u201318. https:\/\/doi.org\/10.3339\/ckd.23.001","journal-title":"Child Kidney Dis"},{"key":"7047_CR26","doi-asserted-by":"publisher","first-page":"73","DOI":"10.1159\/000094001","volume":"104","author":"R Kleta","year":"2006","unstructured":"Kleta R, Bockenhauer D (2006) Bartter syndromes and other salt-losing tubulopathies physiology of renal salt handling. Nephron Physiol 104:73\u201380. https:\/\/doi.org\/10.1159\/000094001","journal-title":"Nephron Physiol"},{"key":"7047_CR27","doi-asserted-by":"publisher","first-page":"2201","DOI":"10.1007\/s00467-016-3343-3\/figures\/3","volume":"31","author":"A B\u00f6kenkamp","year":"2016","unstructured":"B\u00f6kenkamp A, Ludwig M (2016) The oculocerebrorenal syndrome of Lowe: an update. Pediatr Nephrol 31:2201\u20132212. https:\/\/doi.org\/10.1007\/s00467-016-3343-3\/figures\/3","journal-title":"Pediatr Nephrol"},{"key":"7047_CR28","doi-asserted-by":"publisher","first-page":"121","DOI":"10.1016\/j.pcl.2018.08.010","volume":"66","author":"R Fulchiero","year":"2019","unstructured":"Fulchiero R, Seo-Mayer P (2019) Bartter syndrome and Gitelman syndrome. Pediatr Clin North Am 66:121\u2013134. https:\/\/doi.org\/10.1016\/j.pcl.2018.08.010","journal-title":"Pediatr Clin North Am"},{"key":"7047_CR29","doi-asserted-by":"publisher","first-page":"829","DOI":"10.1038\/345829a0","volume":"345","author":"A McCormick","year":"1990","unstructured":"McCormick A, Brady H, Theill LE, Karin M (1990) Regulation of the pituitary-specific homeobox gene GHF1 by cell-autonomous and environmental cues. Nature 345:829\u2013832. https:\/\/doi.org\/10.1038\/345829a0","journal-title":"Nature"},{"key":"7047_CR30","doi-asserted-by":"publisher","first-page":"670","DOI":"10.1210\/edrv-14-6-670","volume":"14","author":"LE Theill","year":"1993","unstructured":"Theill LE, Karin M (1993) Transcriptional control of GH expression and anterior pituitary development. Endocr Rev 14:670\u2013689. https:\/\/doi.org\/10.1210\/edrv-14-6-670","journal-title":"Endocr Rev"},{"key":"7047_CR31","doi-asserted-by":"publisher","first-page":"221","DOI":"10.1007\/s00467-018-4142-9","volume":"35","author":"S Iacobelli","year":"2019","unstructured":"Iacobelli S, Guignard J-P (2019) Renal aspects of metabolic acid-base disorders in neonates. Pediatr Nephrol 35:221\u2013228. https:\/\/doi.org\/10.1007\/s00467-018-4142-9","journal-title":"Pediatr Nephrol"},{"key":"7047_CR32","volume-title":"Genetics of bone biology and skeletal disease","author":"R Thakker","year":"2013","unstructured":"Thakker R, Whyte M, Eisman J, Igarashi T (2013) Genetics of bone biology and skeletal disease. Elsevier, London"},{"key":"7047_CR33","doi-asserted-by":"publisher","first-page":"2047","DOI":"10.2337\/diabetes.50.9.2047","volume":"50","author":"C Bingham","year":"2001","unstructured":"Bingham C, Ellard S, Nicholls AJ et al (2001) The generalized aminoaciduria seen in patients with hepatocyte nuclear factor-1alpha mutations is a feature of all patients with diabetes and is associated with glucosuria. Diabetes 50:2047\u20132052. https:\/\/doi.org\/10.2337\/diabetes.50.9.2047","journal-title":"Diabetes"},{"key":"7047_CR34","doi-asserted-by":"publisher","first-page":"1456","DOI":"10.1093\/NDT\/GFU377","volume":"30","author":"ED Klootwijk","year":"2015","unstructured":"Klootwijk ED, Reichold M, Unwin RJ et al (2015) Renal Fanconi syndrome: taking a proximal look at the nephron. Nephrol Dial Transplant 30:1456\u20131460. https:\/\/doi.org\/10.1093\/NDT\/GFU377","journal-title":"Nephrol Dial Transplant"},{"key":"7047_CR35","doi-asserted-by":"publisher","first-page":"2485","DOI":"10.2215\/cjn.02000311","volume":"6","author":"KJ van Stralen","year":"2011","unstructured":"van Stralen KJ, Emma F, Jager KJ et al (2011) Improvement in the renal prognosis in nephropathic cystinosis. Clin J Am Soc Nephrol 6:2485\u20132491. https:\/\/doi.org\/10.2215\/cjn.02000311","journal-title":"Clin J Am Soc Nephrol"},{"key":"7047_CR36","unstructured":"Matarneh AS, Matarneh B, Rout P et al (2025) Fanconi syndrome. In: StatPearls, StatPearls Publishing, Treasure Island, FL"},{"key":"7047_CR37","doi-asserted-by":"publisher","first-page":"527","DOI":"10.1111\/j.1651-2227.1981.tb05735.x","volume":"70","author":"A Aperia","year":"1981","unstructured":"Aperia A, Bergqvist G, Linn\u00e8 T, Zetterstr\u00f6m R (1981) Familial Fanconi syndrome with malabsorption and galactose intolerance, normal kinase and transferase activity. A report on two siblings. Acta Paediatr Scand 70:527\u2013533. https:\/\/doi.org\/10.1111\/j.1651-2227.1981.tb05735.x","journal-title":"Acta Paediatr Scand"},{"key":"7047_CR38","doi-asserted-by":"publisher","first-page":"338","DOI":"10.1016\/j.arcped.2021.03.002","volume":"28","author":"S Brito dos Santos","year":"2021","unstructured":"Brito dos Santos S, Bertholet-Thomas A, Butin M et al (2021) Tyrosinemia type 1 in pediatric nephrology: not always straightforward. Arch Pediatr 28:338\u2013341. https:\/\/doi.org\/10.1016\/j.arcped.2021.03.002","journal-title":"Arch Pediatr"},{"key":"7047_CR39","doi-asserted-by":"publisher","first-page":"849","DOI":"10.1038\/s10038-019-0620-6","volume":"64","author":"A Noguchi","year":"2019","unstructured":"Noguchi A, Takahashi T (2019) Overview of symptoms and treatment for lysinuric protein intolerance. J Hum Genet 64:849\u2013858. https:\/\/doi.org\/10.1038\/s10038-019-0620-6","journal-title":"J Hum Genet"},{"key":"7047_CR40","doi-asserted-by":"publisher","first-page":"971","DOI":"10.1056\/nejm198704163161602","volume":"316","author":"WA Gahl","year":"1987","unstructured":"Gahl WA, Reed GF, Thoene JG et al (1987) Cysteamine therapy for children with nephropathic cystinosis. N Engl J Med 316:971\u2013977. https:\/\/doi.org\/10.1056\/nejm198704163161602","journal-title":"N Engl J Med"},{"key":"7047_CR41","doi-asserted-by":"publisher","first-page":"365","DOI":"10.1007\/S004670050467","volume":"12","author":"E Elenberg","year":"1998","unstructured":"Elenberg E, Norling LL, Kleinman RE, Ingelfinger JR (1998) Feeding problems in cystinosis. Pediatr Nephrol 12:365\u2013370. https:\/\/doi.org\/10.1007\/S004670050467","journal-title":"Pediatr Nephrol"},{"key":"7047_CR42","doi-asserted-by":"publisher","first-page":"2184","DOI":"10.1681\/asn.2019111172","volume":"31","author":"P Florenzano","year":"2020","unstructured":"Florenzano P, Jimenez M, Ferreira CR et al (2020) Nephropathic cystinosis: a distinct form of CKD-mineral and bone disorder that provides novel insights into the regulation of FGF23. J Am Soc Nephrol 31:2184\u20132192. https:\/\/doi.org\/10.1681\/asn.2019111172","journal-title":"J Am Soc Nephrol"},{"key":"7047_CR43","doi-asserted-by":"publisher","first-page":"dgaa267","DOI":"10.1210\/cllnem\/DGAA267","volume":"105","author":"A Ewert","year":"2020","unstructured":"Ewert A, Leifheit-Nestler M, Hohenfellner K et al (2020) Bone and mineral metabolism in children with nephropathic cystinosis compared with other CKD entities. J Clin Endocrinol Metab 105:dgaa267. https:\/\/doi.org\/10.1210\/cllnem\/DGAA267","journal-title":"J Clin Endocrinol Metab"},{"key":"7047_CR44","doi-asserted-by":"publisher","DOI":"10.3390\/ijms21093109","volume":"21","author":"I Machuca-Gayet","year":"2020","unstructured":"Machuca-Gayet I, Quinaux T, Bertholet-Thomas A et al (2020) Bone disease in nephropathic cystinosis: beyond renal osteodystrophy. Int J Mol Sci 21:3109. https:\/\/doi.org\/10.3390\/ijms21093109","journal-title":"Int J Mol Sci"},{"key":"7047_CR45","doi-asserted-by":"publisher","DOI":"10.1186\/1750-1172-1-16","volume":"1","author":"M Loi","year":"2006","unstructured":"Loi M (2006) Lowe syndrome. Orphanet J Rare Dis 1:16. https:\/\/doi.org\/10.1186\/1750-1172-1-16","journal-title":"Orphanet J Rare Dis"},{"key":"7047_CR46","doi-asserted-by":"publisher","first-page":"94","DOI":"10.1016\/j.jpeds.2009.01.049","volume":"155","author":"A B\u00f6kenkamp","year":"2009","unstructured":"B\u00f6kenkamp A, B\u00f6ckenhauer D, Cheong HI et al (2009) Dent-2 disease: a mild variant of Lowe syndrome. J Pediatr 155:94\u201399. https:\/\/doi.org\/10.1016\/j.jpeds.2009.01.049","journal-title":"J Pediatr"},{"key":"7047_CR47","unstructured":"Murdock N, Chou E (2025) Oculocerebrorenal Syndrome. In: StatPearls, StatPearls Publishing, Treasure Island, FL"},{"key":"7047_CR48","doi-asserted-by":"publisher","first-page":"31","DOI":"10.1007\/S12519-020-00370-4","volume":"17","author":"FCC Mrad","year":"2021","unstructured":"Mrad FCC, Soares SBM, de Menezes Silva LAW et al (2021) Bartter\u2019s syndrome: clinical findings, genetic causes and therapeutic approach. World J Pediatr 17:31\u201339. https:\/\/doi.org\/10.1007\/S12519-020-00370-4","journal-title":"World J Pediatr"},{"key":"7047_CR49","unstructured":"Bokhari SRA, Zulfiqar H, Mansur A (2025) Bartter Syndrome. In: StatPearls, StatPearls Publishing, Treasure Island, FL"},{"key":"7047_CR50","doi-asserted-by":"publisher","first-page":"253","DOI":"10.1046\/j.1523-1755.2002.00435.x","volume":"62","author":"SC Reinalter","year":"2002","unstructured":"Reinalter SC, Jeck N, Brochhausen C et al (2002) Role of cyclooxygenase-2 in hyperprostaglandin E syndrome\/antenatal Bartter syndrome. Kidney Int 62:253\u2013260. https:\/\/doi.org\/10.1046\/j.1523-1755.2002.00435.x","journal-title":"Kidney Int"},{"key":"7047_CR51","doi-asserted-by":"publisher","DOI":"10.1155\/2012\/857136","volume":"2012","author":"YR Bhat","year":"2012","unstructured":"Bhat YR, Vinayaka G, Sreelakshmi K (2012) Antenatal bartter syndrome: a review. Int J Pediatr 2012:857136. https:\/\/doi.org\/10.1155\/2012\/857136","journal-title":"Int J Pediatr"},{"key":"7047_CR52","doi-asserted-by":"publisher","first-page":"2474","DOI":"10.1093\/ndt\/gfac029","volume":"37","author":"MFA Verploegen","year":"2022","unstructured":"Verploegen MFA, Vargas-Poussou R, Walsh SB et al (2022) Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study. Nephrol Dial Transplant 37:2474\u20132486. https:\/\/doi.org\/10.1093\/ndt\/gfac029","journal-title":"Nephrol Dial Transplant"},{"key":"7047_CR53","doi-asserted-by":"publisher","first-page":"1269","DOI":"10.1002\/humu.22361","volume":"34","author":"M Keck","year":"2013","unstructured":"Keck M, Andrini O, Lahuna O et al (2013) Novel CLCNKB mutations causing Bartter syndrome affect channel surface expression. Hum Mutat 34:1269\u20131278. https:\/\/doi.org\/10.1002\/humu.22361","journal-title":"Hum Mutat"},{"key":"7047_CR54","doi-asserted-by":"publisher","first-page":"183","DOI":"10.1016\/s0002-9343(01)01086-5","volume":"112","author":"M Peters","year":"2002","unstructured":"Peters M, Jeck N, Reinalter S et al (2002) Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies. Am J Med 112:183\u2013190. https:\/\/doi.org\/10.1016\/s0002-9343(01)01086-5","journal-title":"Am J Med"},{"key":"7047_CR55","doi-asserted-by":"publisher","first-page":"754","DOI":"10.1203\/00006450-200012000-00009","volume":"48","author":"N Jeck","year":"2000","unstructured":"Jeck N, Konrad M, Peters M et al (2000) Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype. Pediatr Res 48:754\u2013758. https:\/\/doi.org\/10.1203\/00006450-200012000-00009","journal-title":"Pediatr Res"},{"key":"7047_CR56","doi-asserted-by":"publisher","first-page":"148","DOI":"10.1053\/j.ackd.2006.01.014","volume":"13","author":"NVAM Knoers","year":"2006","unstructured":"Knoers NVAM (2006) Gitelman syndrome. Adv Chronic Kidney Dis 13:148\u2013154. https:\/\/doi.org\/10.1053\/j.ackd.2006.01.014","journal-title":"Adv Chronic Kidney Dis"},{"key":"7047_CR57","doi-asserted-by":"publisher","first-page":"2553","DOI":"10.1007\/s00467-021-05098-5","volume":"36","author":"D Bockenhauer","year":"2021","unstructured":"Bockenhauer D, Kleta R (2021) Tubulopathy meets Sherlock Holmes: biochemical fingerprinting of disorders of altered kidney tubular salt handling. Pediatr Nephrol 36:2553\u20132561. https:\/\/doi.org\/10.1007\/s00467-021-05098-5","journal-title":"Pediatr Nephrol"},{"key":"7047_CR58","doi-asserted-by":"publisher","first-page":"739","DOI":"10.1016\/s0022-3476(99)70094-6","volume":"135","author":"C Schaedel","year":"1999","unstructured":"Schaedel C, Marthinsen L, Kristoffersson AC et al (1999) Lung symptoms in pseudohypoaldosteronism type 1 are associated with deficiency of the \u03b1-subunit of the epithelial sodium channel. J Pediatr 135:739\u2013745. https:\/\/doi.org\/10.1016\/s0022-3476(99)70094-6","journal-title":"J Pediatr"},{"key":"7047_CR59","doi-asserted-by":"publisher","first-page":"52","DOI":"10.1016\/j.prrv.2024.09.001","volume":"54","author":"AP Chantzaras","year":"2025","unstructured":"Chantzaras AP, Panagiotou P, Koltsida G et al (2025) Pulmonary manifestations of pseudohypoaldosteronism type 1b: a systematic review of the literature. Paediatr Respir Rev 54:52\u201361. https:\/\/doi.org\/10.1016\/j.prrv.2024.09.001","journal-title":"Paediatr Respir Rev"},{"key":"7047_CR60","doi-asserted-by":"publisher","first-page":"4552","DOI":"10.1210\/jc.2006-1161","volume":"91","author":"FG Riepe","year":"2006","unstructured":"Riepe FG, Finkeldei J, De Sanctis L et al (2006) Elucidating the underlying molecular pathogenesis of NR3C2 mutants causing autosomal dominant pseudohypoaldosteronism type 1. J Clin Endocrinol Metab 91:4552\u20134561. https:\/\/doi.org\/10.1210\/jc.2006-1161","journal-title":"J Clin Endocrinol Metab"},{"key":"7047_CR61","doi-asserted-by":"publisher","first-page":"289","DOI":"10.1159\/000167177","volume":"6","author":"F Santos","year":"1986","unstructured":"Santos F, Chan JCM (1986) Renal tubular acidosis in children. Diagnosis, treatment and prognosis. Am J Nephrol 6:289\u2013295. https:\/\/doi.org\/10.1159\/000167177","journal-title":"Am J Nephrol"},{"key":"7047_CR62","doi-asserted-by":"publisher","first-page":"236","DOI":"10.1046\/j.1523-1755.2000.00158.x","volume":"58","author":"Y Boirie","year":"2000","unstructured":"Boirie Y, Broyer M, Gagnadoux MF et al (2000) Alterations of protein metabolism by metabolic acidosis in children with chronic renal failure. Kidney Int 58:236\u2013241. https:\/\/doi.org\/10.1046\/j.1523-1755.2000.00158.x","journal-title":"Kidney Int"},{"key":"7047_CR63","doi-asserted-by":"publisher","DOI":"10.1155\/2013\/970946","volume":"2013","author":"P Salas","year":"2013","unstructured":"Salas P, Pinto V, Rodriguez J et al (2013) Growth retardation in children with kidney disease. Int J Endocrinol 2013:970946. https:\/\/doi.org\/10.1155\/2013\/970946","journal-title":"Int J Endocrinol"},{"key":"7047_CR64","doi-asserted-by":"publisher","first-page":"17","DOI":"10.46439\/nephrology.1.004","volume":"1","author":"C Agrawal","year":"2020","unstructured":"Agrawal C, Chakraborty PP (2020) Rickets in renal tubular acidosis: a clinical appraisal. J Exp Nephrol 1:17\u201324. https:\/\/doi.org\/10.46439\/nephrology.1.004","journal-title":"J Exp Nephrol"},{"key":"7047_CR65","doi-asserted-by":"publisher","first-page":"1585","DOI":"10.1093\/ndt\/gfab171","volume":"36","author":"F Trepiccione","year":"2021","unstructured":"Trepiccione F, Walsh SB, Ariceta G et al (2021) Distal renal tubular acidosis: ERKNet\/ESPN clinical practice points. Nephrol Dial Transplant 36:1585\u20131596. https:\/\/doi.org\/10.1093\/ndt\/gfab171","journal-title":"Nephrol Dial Transplant"},{"key":"7047_CR66","unstructured":"Alexander RT, Gil-Pe\u00f1a H, Greenbaum LA, Santos F (2019) Hereditary distal renal tubular acidosis. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A (eds). GeneReviews\u00ae, University of Washington, Seattle, (WA)"},{"key":"7047_CR67","doi-asserted-by":"publisher","first-page":"511","DOI":"10.1007\/s40620-017-0447-1","volume":"31","author":"N Mohebbi","year":"2018","unstructured":"Mohebbi N, Wagner CA (2018) Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis. J Nephrol 31:511\u2013522. https:\/\/doi.org\/10.1007\/s40620-017-0447-1","journal-title":"J Nephrol"},{"key":"7047_CR68","doi-asserted-by":"publisher","first-page":"2879","DOI":"10.1093\/ndt\/gfm307","volume":"22","author":"AP Sharma","year":"2007","unstructured":"Sharma AP, Sharma RK, Kapoor R et al (2007) Incomplete distal renal tubular acidosis affects growth in children. Nephrol Dial Transplant 22:2879\u20132885. https:\/\/doi.org\/10.1093\/ndt\/gfm307","journal-title":"Nephrol Dial Transplant"},{"key":"7047_CR69","first-page":"334","volume":"43","author":"CY Chang","year":"2002","unstructured":"Chang CY, Lin CY (2002) Failure to thrive in children with primary distal type renal tubular acidosis. Acta Paediatr Taiwan 43:334\u2013339","journal-title":"Acta Paediatr Taiwan"},{"key":"7047_CR70","doi-asserted-by":"publisher","first-page":"981","DOI":"10.1093\/ndt\/gfy409","volume":"34","author":"SC Lopez-Garcia","year":"2019","unstructured":"Lopez-Garcia SC, Emma F, Walsh SB et al (2019) Treatment and long-term outcome in primary distal renal tubular acidosis. Nephrol Dial Transplant 34:981\u2013991. https:\/\/doi.org\/10.1093\/ndt\/gfy409","journal-title":"Nephrol Dial Transplant"},{"key":"7047_CR71","doi-asserted-by":"publisher","first-page":"1243","DOI":"10.1016\/J.KINT.2016.12.017","volume":"91","author":"V Palazzo","year":"2017","unstructured":"Palazzo V, Provenzano A, Becherucci F et al (2017) The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis. Kidney Int 91:1243\u20131255. https:\/\/doi.org\/10.1016\/J.KINT.2016.12.017","journal-title":"Kidney Int"},{"key":"7047_CR72","doi-asserted-by":"publisher","first-page":"987","DOI":"10.1007\/s00467-016-3573-4","volume":"32","author":"MTP Besouw","year":"2017","unstructured":"Besouw MTP, Bienias M, Walsh P et al (2017) Clinical and molecular aspects of distal renal tubular acidosis in children. Pediatr Nephrol 32:987\u2013996. https:\/\/doi.org\/10.1007\/s00467-016-3573-4","journal-title":"Pediatr Nephrol"},{"key":"7047_CR73","doi-asserted-by":"publisher","first-page":"F650","DOI":"10.1152\/ajprenal.1998.274.4.f650","volume":"274","author":"A Sicuro","year":"1998","unstructured":"Sicuro A, Mahlbacher K, Hulter HN, Krapf R (1998) Effect of growth hormone on renal and systemic acid-base homeostasis in humans. Am J Physiol Renal Physiol 274:F650\u2013F657. https:\/\/doi.org\/10.1152\/ajprenal.1998.274.4.f650","journal-title":"Am J Physiol Renal Physiol"},{"key":"7047_CR74","doi-asserted-by":"publisher","first-page":"2258","DOI":"10.1046\/j.1523-1755.2000.00086.x","volume":"57","author":"J Green","year":"2000","unstructured":"Green J, Maor G (2000) Effect of metabolic acidosis on the growth hormone\/IGF-I endocrine axis in skeletal growth centers. Kidney Int 57:2258\u20132267. https:\/\/doi.org\/10.1046\/j.1523-1755.2000.00086.x","journal-title":"Kidney Int"},{"issue":"3","key":"7047_CR75","doi-asserted-by":"publisher","first-page":"190","DOI":"10.4103\/0971-4065.202404","volume":"27","author":"AD Sajgure","year":"2017","unstructured":"Sajgure AD, Dighe TA, Korpe JS et al (2017) The relationship between metabolic acidosis and nutritional parameters in patients on hemodialysis. Indian J Nephrol 27:190. https:\/\/doi.org\/10.4103\/0971-4065.202404","journal-title":"Indian J Nephrol"},{"key":"7047_CR76","doi-asserted-by":"publisher","first-page":"4273","DOI":"10.1093\/ndt\/gfs493","volume":"27","author":"SK Haque","year":"2012","unstructured":"Haque SK, Ariceta G, Batlle D (2012) Proximal renal tubular acidosis: a not so rare disorder of multiple etiologies. Nephrol Dial Transplant 27:4273\u20134287. https:\/\/doi.org\/10.1093\/ndt\/gfs493","journal-title":"Nephrol Dial Transplant"},{"key":"7047_CR77","doi-asserted-by":"publisher","first-page":"1211","DOI":"10.1093\/ndt\/gfm583","volume":"23","author":"Z Katzir","year":"2008","unstructured":"Katzir Z, Dinour D, Reznik-Wolf H et al (2008) Familial pure proximal renal tubular acidosis\u2014a clinical and genetic study. Nephrol Dial Transplant 23:1211\u20131215. https:\/\/doi.org\/10.1093\/ndt\/gfm583","journal-title":"Nephrol Dial Transplant"},{"key":"7047_CR78","doi-asserted-by":"publisher","DOI":"10.1097\/md.0000000000017244","volume":"98","author":"K Huang","year":"2019","unstructured":"Huang K, Dai YL, Zhang JW et al (2019) Gitelman syndrome combined with growth hormone deficiency: three cases report. Medicine (Baltimore) 98:e17244. https:\/\/doi.org\/10.1097\/md.0000000000017244","journal-title":"Medicine (Baltimore)"},{"key":"7047_CR79","doi-asserted-by":"publisher","DOI":"10.1186\/s12967-022-03698-9","volume":"20","author":"Y-T Lu","year":"2022","unstructured":"Lu Y-T, Zhang D, Zhang Q-Y et al (2022) Apparent mineralocorticoid excess: comprehensive overview of molecular genetics. J Transl Med 20:500. https:\/\/doi.org\/10.1186\/s12967-022-03698-9","journal-title":"J Transl Med"},{"key":"7047_CR80","doi-asserted-by":"publisher","first-page":"13","DOI":"10.2147\/ibpc.s188869","volume":"12","author":"BT Enslow","year":"2019","unstructured":"Enslow BT, Stockand JD, Berman JM (2019) Liddle\u2019s syndrome mechanisms, diagnosis and management. Integr Blood Press Control 12:13\u201322. https:\/\/doi.org\/10.2147\/ibpc.s188869","journal-title":"Integr Blood Press Control"},{"key":"7047_CR81","doi-asserted-by":"publisher","first-page":"333","DOI":"10.1093\/ajh\/hpaf005","volume":"38","author":"FR Gallegos","year":"2025","unstructured":"Gallegos FR, Delahunty MP, Hu J et al (2025) Decoding monogenic hypertension: a review of rare hypertension disorders. Am J Hypertens 38:333\u2013351. https:\/\/doi.org\/10.1093\/ajh\/hpaf005","journal-title":"Am J Hypertens"},{"key":"7047_CR82","doi-asserted-by":"publisher","DOI":"10.1038\/s41581-024-00897-z","author":"E Levtchenko","year":"2024","unstructured":"Levtchenko E, Ariceta G, Arguedas Flores O et al (2024) International expert consensus statement on the diagnosis and management of congenital nephrogenic diabetes insipidus (arginine vasopressin resistance). Nat Rev Nephrol. https:\/\/doi.org\/10.1038\/s41581-024-00897-z","journal-title":"Nat Rev Nephrol"},{"key":"7047_CR83","doi-asserted-by":"publisher","first-page":"55","DOI":"10.1385\/endo:24:1:055","volume":"24","author":"H Mizuno","year":"2004","unstructured":"Mizuno H, Sugiyama Y, Ohro Y et al (2004) Clinical characteristics of eight patients with congenital nephrogenic diabetes insipidus. Endocrine 24:55\u201359. https:\/\/doi.org\/10.1385\/endo:24:1:055","journal-title":"Endocrine"},{"key":"7047_CR84","doi-asserted-by":"publisher","first-page":"618","DOI":"10.1038\/ki.1990.251","volume":"38","author":"MD Breyer","year":"1990","unstructured":"Breyer MD, Jacobson HR, Hebert RL (1990) Cellular mechanisms of prostaglandin E2 and vasopressin interactions in the collecting duct. Kidney Int 38:618\u2013624. https:\/\/doi.org\/10.1038\/ki.1990.251","journal-title":"Kidney Int"},{"key":"7047_CR85","doi-asserted-by":"publisher","first-page":"757","DOI":"10.1016\/j.neuron.2017.06.014","volume":"95","author":"ML Andermann","year":"2017","unstructured":"Andermann ML, Lowell BB (2017) Toward a wiring diagram understanding of appetite control. Neuron 95:757\u2013778. https:\/\/doi.org\/10.1016\/j.neuron.2017.06.014","journal-title":"Neuron"},{"key":"7047_CR86","doi-asserted-by":"publisher","first-page":"1144","DOI":"10.1016\/s0016-5085(75)80228-9","volume":"68","author":"JC Meeroff","year":"1975","unstructured":"Meeroff JC, Go VLW, Phillips SF (1975) Control of gastric emptying by osmolality of duodenal contents in man. Gastroenterology 68:1144\u20131151. https:\/\/doi.org\/10.1016\/s0016-5085(75)80228-9","journal-title":"Gastroenterology"},{"key":"7047_CR87","doi-asserted-by":"publisher","DOI":"10.1016\/J.neubiorev.2022.104603","volume":"136","author":"S Althubeati","year":"2022","unstructured":"Althubeati S, Avery A, Tench CR et al (2022) Mapping brain activity of gut-brain signaling to appetite and satiety in healthy adults: a systematic review and functional neuroimaging meta-analysis. Neurosci Biobehav Rev 136:104603. https:\/\/doi.org\/10.1016\/J.neubiorev.2022.104603","journal-title":"Neurosci Biobehav Rev"},{"key":"7047_CR88","doi-asserted-by":"publisher","first-page":"403","DOI":"10.1152\/ajgpi.00308.2003","volume":"286","author":"M Danzer","year":"2004","unstructured":"Danzer M, Jocic M, Samberger C et al (2004) Stomach-brain communication by vagal afferents in response to luminal acid backdiffusion, gastrin, and gastric acid secretion. Am J Physiol Gastrointest Liver Physiol 286:403\u2013411. https:\/\/doi.org\/10.1152\/ajgpi.00308.2003","journal-title":"Am J Physiol Gastrointest Liver Physiol"},{"key":"7047_CR89","doi-asserted-by":"publisher","DOI":"10.1016\/j.metabol.2019.03.009","volume":"103","author":"A Rothenbuhler","year":"2020","unstructured":"Rothenbuhler A, Schnabel D, H\u00f6gler W, Linglart A (2020) Diagnosis, treatment-monitoring and follow-up of children and adolescents with X-linked hypophosphatemia (XLH). Metabolism 103:153892. https:\/\/doi.org\/10.1016\/j.metabol.2019.03.009","journal-title":"Metabolism"},{"key":"7047_CR90","doi-asserted-by":"publisher","first-page":"731","DOI":"10.1016\/j.jbspin.2019.01.012","volume":"86","author":"AS Lambert","year":"2019","unstructured":"Lambert AS, Zhukouskaya V, Rothenbuhler A, Linglart A (2019) X-linked hypophosphatemia: management and treatment prospects. Joint Bone Spine 86:731\u2013738. https:\/\/doi.org\/10.1016\/j.jbspin.2019.01.012","journal-title":"Joint Bone Spine"},{"key":"7047_CR91","doi-asserted-by":"publisher","first-page":"128","DOI":"10.3390\/endocrines4010012","volume":"4","author":"Y Hasegawa","year":"2023","unstructured":"Hasegawa Y, Faienza F, Ikegawa K, Hasegawa Y (2023) Presentation and diagnosis of pediatric X-linked hypophosphatemia. Endocrines 4:128\u2013137. https:\/\/doi.org\/10.3390\/endocrines4010012","journal-title":"Endocrines"},{"key":"7047_CR92","doi-asserted-by":"publisher","unstructured":"Baroncelli GI, Barale M, Brandi ML et al (2025) Experts\u2019 consensus on the management and treatment of individuals with X-linked hypophosphatemia across lifespan. J Endocrinol Invest 1\u201330. https:\/\/doi.org\/10.1007\/s40618-025-02611-7\/figures\/2","DOI":"10.1007\/s40618-025-02611-7\/figures\/2"},{"key":"7047_CR93","doi-asserted-by":"publisher","first-page":"435","DOI":"10.1038\/s41581-019-0152-5","volume":"15","author":"D Haffner","year":"2017","unstructured":"Haffner D, Emma F, Eastwood DM et al (2017) Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia. Nat Rev Nephrol 15:435\u2013455. https:\/\/doi.org\/10.1038\/s41581-019-0152-5","journal-title":"Nat Rev Nephrol"},{"key":"7047_CR94","doi-asserted-by":"publisher","DOI":"10.1002\/9781119467205","volume-title":"Clinical Paediatric Dietetics","author":"V Shaw","year":"2020","unstructured":"Shaw V (2020) Clinical Paediatric Dietetics, 5th edn. Wiley, London","edition":"5"},{"key":"7047_CR95","doi-asserted-by":"publisher","first-page":"945","DOI":"10.1007\/s004670050736","volume":"13","author":"D Joly","year":"1999","unstructured":"Joly D, Rieu P, M\u00e9jean A et al (1999) Treatment of cystinuria. Pediatr Nephrol 13:945\u2013950. https:\/\/doi.org\/10.1007\/s004670050736","journal-title":"Pediatr Nephrol"},{"key":"7047_CR96","doi-asserted-by":"publisher","first-page":"236","DOI":"10.1053\/j.ajkd.2025.03.023","volume":"86","author":"MA Baum","year":"2025","unstructured":"Baum MA, Mandel M, Somers MJG (2025) Understanding rare kidney stone diseases: a review. Am J Kidney Dis 86:236\u2013244. https:\/\/doi.org\/10.1053\/j.ajkd.2025.03.023","journal-title":"Am J Kidney Dis"},{"key":"7047_CR97","doi-asserted-by":"publisher","first-page":"2081","DOI":"10.1007\/s00467-012-2219-4","volume":"27","author":"UI Scholl","year":"2012","unstructured":"Scholl UI, Dave HB, Lu M et al (2012) SeSAME\/EAST syndromephenotypic variability and delayed activity of the distal convoluted tubule. Pediatr Nephrol 27:2081\u20132090. https:\/\/doi.org\/10.1007\/s00467-012-2219-4","journal-title":"Pediatr Nephrol"},{"key":"7047_CR98","doi-asserted-by":"publisher","first-page":"1304","DOI":"10.1016\/j.ekir.2019.05.019","volume":"4","author":"S Adalat","year":"2019","unstructured":"Adalat S, Hayes WN, Bryant WA et al (2019) HNF1B mutations are associated with a Gitelman-like tubulopathy that develops during childhood. Kidney Int Rep 4:1304\u20131311. https:\/\/doi.org\/10.1016\/j.ekir.2019.05.019","journal-title":"Kidney Int Rep"},{"key":"7047_CR99","doi-asserted-by":"publisher","first-page":"134","DOI":"10.1016\/S0377-1237(10)80125-x","volume":"66","author":"KS Rana","year":"2011","unstructured":"Rana KS, Puri P, Badwal S (2011) Prevalence of celiac disease in children with unexplained failure to thrive. Med J Armed Forces India 66:134. https:\/\/doi.org\/10.1016\/S0377-1237(10)80125-x","journal-title":"Med J Armed Forces India"},{"key":"7047_CR100","doi-asserted-by":"publisher","DOI":"10.21037\/tp.2018.12.04","volume":"8","author":"T Ishige","year":"2019","unstructured":"Ishige T (2019) Growth failure in pediatric onset inflammatory bowel disease: mechanisms, epidemiology, and management. Transl Pediatr 8:16. https:\/\/doi.org\/10.21037\/tp.2018.12.04","journal-title":"Transl Pediatr"},{"key":"7047_CR101","doi-asserted-by":"publisher","first-page":"379","DOI":"10.1146\/annurev-phusiol-042222-025000","volume":"86","author":"CA Hoogstraten","year":"2024","unstructured":"Hoogstraten CA, Hoenderop JG, de Baaij JHF (2024) Mitochondrial dysfunction in kidney tubulopathies. Annu Rev Physiol 86:379\u2013403. https:\/\/doi.org\/10.1146\/annurev-phusiol-042222-025000","journal-title":"Annu Rev Physiol"},{"key":"7047_CR102","doi-asserted-by":"publisher","first-page":"1680","DOI":"10.1359\/jbmr.1999.14.10.1680","volume":"14","author":"BD Kuizon","year":"1999","unstructured":"Kuizon BD, Salusky IB (1999) Growth retardation in children with chronic renal failure. J Bone Miner Res 14:1680\u20131690. https:\/\/doi.org\/10.1359\/jbmr.1999.14.10.1680","journal-title":"J Bone Miner Res"}],"container-title":["Pediatric Nephrology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/s00467-025-07047-y.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/article\/10.1007\/s00467-025-07047-y","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/s00467-025-07047-y.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,7,6]],"date-time":"2026-07-06T08:13:38Z","timestamp":1783325618000},"score":1,"resource":{"primary":{"URL":"https:\/\/link.springer.com\/10.1007\/s00467-025-07047-y"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,11,20]]},"references-count":102,"journal-issue":{"issue":"8","published-print":{"date-parts":[[2026,8]]}},"alternative-id":["7047"],"URL":"https:\/\/doi.org\/10.1007\/s00467-025-07047-y","relation":{},"ISSN":["0931-041X","1432-198X"],"issn-type":[{"value":"0931-041X","type":"print"},{"value":"1432-198X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2025,11,20]]},"assertion":[{"value":"31 August 2025","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"7 October 2025","order":2,"name":"revised","label":"Revised","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"20 October 2025","order":3,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"20 November 2025","order":4,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}},{"order":1,"name":"Ethics","group":{"name":"EthicsHeading","label":"Declarations"}},{"value":"Not applicable.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethics approval"}},{"value":"None.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Conflict of interest"}}]}}