{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,31]],"date-time":"2025-12-31T01:22:41Z","timestamp":1767144161928,"version":"build-2238731810"},"reference-count":17,"publisher":"Elsevier BV","issue":"5","license":[{"start":{"date-parts":[[2016,9,1]],"date-time":"2016-09-01T00:00:00Z","timestamp":1472688000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2016,9,6]],"date-time":"2016-09-06T00:00:00Z","timestamp":1473120000000},"content-version":"vor","delay-in-days":5,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["elsevier.es","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Bolet\u00edn M\u00e9dico del Hospital Infantil de M\u00e9xico"],"published-print":{"date-parts":[[2016,9]]},"DOI":"10.1016\/j.bmhimx.2016.04.004","type":"journal-article","created":{"date-parts":[[2016,9,18]],"date-time":"2016-09-18T15:16:21Z","timestamp":1474211781000},"page":"331-334","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":2,"title":["S\u00edndrome de pseudo-Bartter como presentaci\u00f3n de fibrosis qu\u00edstica con mutaci\u00f3n DF508"],"prefix":"10.1016","volume":"73","author":[{"given":"Mar\u00eda de Jes\u00fas","family":"Galaviz-Ballesteros","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Carlos Patricio","family":"Acosta-Rodr\u00edguez-Bueno","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alejandra","family":"Consuelo-S\u00e1nchez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Isidro","family":"Franco-\u00c1lvarez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Odilo Iv\u00e1n","family":"Olalla-Mora","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rodrigo","family":"V\u00e1zquez-Frias","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.bmhimx.2016.04.004_bib0090","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1007\/s00431-007-0413-3","article-title":"An epidemic of pseudo-Bartter syndrome in cystic fibrosis patients","volume":"167","author":"Kose","year":"2008","journal-title":"Eur J Pediatr."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0095","first-page":"38","article-title":"Elevated sweat potassium, hyperaldosteronism and pseudo Bartter's syndrome: a spectrum of disorders associated with cystic fibrosis","volume":"82","author":"Devlin","year":"1989","journal-title":"J R Soc Med."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0100","series-title":"Pediatric gastrointestinal disease.","first-page":"1606","article-title":"Exocrine Pancreatic Dysfunction, Cystic Fibrosis","author":"Gaskin","year":"2004"},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0105","first-page":"19","article-title":"Episodic seasonal pseudo-Bartter syndrome in cystic fibrosis","volume":"15S","author":"Kintu","year":"2014","journal-title":"Paediatr Respir Rev."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0110","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.bmhimx.2016.04.004_bib0115","doi-asserted-by":"crossref","first-page":"119","DOI":"10.1179\/146532805X45719","article-title":"Clinical features and treatment approaches in cystic fibrosis with pseudo-Bartter syndrome","volume":"25","author":"Yal\u00e7in","year":"2005","journal-title":"Ann Trop Paediatr."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0120","doi-asserted-by":"crossref","first-page":"292","DOI":"10.4103\/1319-2442.109579","article-title":"Pseudo-Bartter syndrome, pattern and correlation with other cystic fibrosis features","volume":"24","author":"Dahabren","year":"2013","journal-title":"Saudi J Kidney Dis Transpl."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0125","doi-asserted-by":"crossref","first-page":"367","DOI":"10.2298\/VSP1204367S","article-title":"Atypical presentation of cystic fibrosis-obese adolescent with hypertension and pseudo-Bartter's syndrome","volume":"69","author":"Sovti\u0107","year":"2012","journal-title":"Vojnosanit Pregl."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0130","first-page":"694","article-title":"Rare F311L CFTR gene mutation in a child presented with recurrent electrolyte abnormalities and metabolic alkalosis: case report","volume":"92","author":"Lumpaopong","year":"2009","journal-title":"J Med Assoc Thai."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0135","doi-asserted-by":"crossref","first-page":"485","DOI":"10.1002\/(SICI)1098-1004(200005)15:5<485::AID-HUMU22>3.0.CO;2-3","article-title":"A novel missense mutation (D110E) in exon 4 of CFTER (ABCC7) in a CF infant presenting with hypochloremic metabolic alkalosis","volume":"15","author":"Padoan","year":"2000","journal-title":"Hum Mutat."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0140","doi-asserted-by":"crossref","first-page":"41","DOI":"10.1055\/s-2000-9650","article-title":"Turkish infant with hypoelectrolytemia and metabolic alkalosis as the sole manifestations of a mild form of cystic fibrosis (mutation D110H)","volume":"212","author":"Weller","year":"2000","journal-title":"Klin Padiatr."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0145","doi-asserted-by":"crossref","first-page":"281","DOI":"10.1016\/S0022-3476(95)70310-1","article-title":"A specific cystic fibrosis mutation (T3381) associated with the phenotype of isolated hypotonic dehydration","volume":"127","author":"Leoni","year":"1995","journal-title":"J Pediatr."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0150","doi-asserted-by":"crossref","first-page":"242","DOI":"10.1093\/tropej\/50.4.242","article-title":"Pseudo-Bartter's syndrome in an Egyptian infant with cystic fibrosis mutation N1303K","volume":"50","author":"Wahab","year":"2004","journal-title":"J Trop Pediatr."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0155","doi-asserted-by":"crossref","first-page":"325","DOI":"10.1556\/OH.2008.28239","article-title":"Pseudo-Bartter syndrome in a case of cystic fibrosis caused by C1529G and G3978A compound heterozygosity","volume":"149","author":"Horvatovich","year":"2008","journal-title":"Orv Hetil."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0160","first-page":"337","article-title":"Identification of a novel mutation (S13F) in the CFTR gene in a CF patient of Sardinian origin","volume":"11","author":"Leoni","year":"1998","journal-title":"Hum Mutat."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0165","first-page":"443","article-title":"Deshidrataci\u00f3n con alcalosis hipoclor\u00e9mica: presentaci\u00f3n inusual de fibrosis qu\u00edstica en un lactante","volume":"106","author":"Aranzamendi","year":"2008","journal-title":"Arch Argent Pediatr."},{"key":"10.1016\/j.bmhimx.2016.04.004_bib0170","first-page":"80","article-title":"Fibrosis qu\u00edstica que simula un s\u00edndrome de Bartter","author":"Campa\u00f1\u00e1-Cobas","year":"2008","journal-title":"Rev Cubana Pediatr."}],"updated-by":[{"DOI":"10.1016\/j.bmhimx.2017.01.001","type":"erratum","label":"Erratum","source":"publisher","updated":{"date-parts":[[2017,1,1]],"date-time":"2017-01-01T00:00:00Z","timestamp":1483228800000}}],"container-title":["Bolet\u00edn M\u00e9dico del Hospital Infantil de M\u00e9xico"],"original-title":[],"language":"es","link":[{"URL":"http:\/\/api.elsevier.com\/content\/article\/PII:S1665114616301034?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/api.elsevier.com\/content\/article\/PII:S1665114616301034?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,9,13]],"date-time":"2019-09-13T14:11:12Z","timestamp":1568383872000},"score":1,"resource":{"primary":{"URL":"http:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1665114616301034"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,9]]},"references-count":17,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2016,9]]}},"alternative-id":["S1665114616301034"],"URL":"https:\/\/doi.org\/10.1016\/j.bmhimx.2016.04.004","relation":{},"ISSN":["1665-1146"],"issn-type":[{"value":"1665-1146","type":"print"}],"subject":[],"published":{"date-parts":[[2016,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"S\u00edndrome de pseudo-Bartter como presentaci\u00f3n de fibrosis qu\u00edstica con mutaci\u00f3n DF508","name":"articletitle","label":"Article Title"},{"value":"Bolet\u00edn M\u00e9dico del Hospital Infantil de M\u00e9xico","name":"journaltitle","label":"Journal Title"},{"value":"http:\/\/dx.doi.org\/10.1016\/j.bmhimx.2016.04.004","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2016 Hospital Infantil de M\u00e9xico Federico G\u00f3mez. Published by Masson Doyma M\u00e9xico S.A.","name":"copyright","label":"Copyright"}]}}