{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,23]],"date-time":"2026-08-23T16:48:39Z","timestamp":1787503719303,"version":"build-2736575974"},"reference-count":20,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2017,4,1]],"date-time":"2017-04-01T00:00:00Z","timestamp":1491004800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.com","clinicalkey.es","clinicalkey.com.au","clinicalkey.fr","jpeds.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["The Journal of Pediatrics"],"published-print":{"date-parts":[[2017,4]]},"DOI":"10.1016\/j.jpeds.2016.12.070","type":"journal-article","created":{"date-parts":[[2017,1,18]],"date-time":"2017-01-18T02:17:42Z","timestamp":1484705862000},"page":"196-198","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":12,"special_numbering":"C","title":["Barth Syndrome with Late-Onset Cardiomyopathy: A Missed Opportunity for Diagnosis"],"prefix":"10.1016","volume":"183","author":[{"given":"Leanne","family":"Woiewodski","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2114-3866","authenticated-orcid":false,"given":"David","family":"Ezon","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"James","family":"Cooper","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Brian","family":"Feingold","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jpeds.2016.12.070_bib0010","doi-asserted-by":"crossref","first-page":"1365","DOI":"10.1007\/s00431-011-1575-6","article-title":"Eponym: Barth syndrome","volume":"170","author":"Takeda","year":"2011","journal-title":"Eur J Pediatr"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0015","doi-asserted-by":"crossref","first-page":"2726","DOI":"10.1002\/ajmg.a.35609","article-title":"The Barth Syndrome Registry: distinguishing disease characteristics and growth data from a longitudinal study","volume":"158A","author":"Roberts","year":"2012","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0020","doi-asserted-by":"crossref","first-page":"23","DOI":"10.1186\/1750-1172-8-23","article-title":"Barth syndrome","volume":"8","author":"Clarke","year":"2013","journal-title":"Orphanet J Rare Dis"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0025","doi-asserted-by":"crossref","first-page":"1502","DOI":"10.1016\/0002-8703(91)90158-E","article-title":"Natural history of dilated cardiomyopathy in children","volume":"121","author":"Akagi","year":"1991","journal-title":"Am Heart J"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0030","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1016\/0735-1097(88)90179-9","article-title":"Dilated cardiomyopathy in infants and children","volume":"11","author":"Griffin","year":"1988","journal-title":"J Am Coll Cardiol"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0035","doi-asserted-by":"crossref","first-page":"334","DOI":"10.1007\/s00246-012-0451-0","article-title":"Clinically significant thrombosis in pediatric heart transplant recipients during their waiting period","volume":"34","author":"Law","year":"2013","journal-title":"Pediatr Cardiol"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0040","doi-asserted-by":"crossref","first-page":"70","DOI":"10.1186\/1750-1172-8-70","article-title":"Natural history of Barth syndrome: a national cohort study of 22 patients","volume":"8","author":"Rigaud","year":"2013","journal-title":"Orphanet J Rare Dis"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0045","author":"Ferreira"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0050","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1016\/j.cardfail.2009.01.006","article-title":"Genetic evaluation of cardiomyopathy \u2014 a Heart Failure Society of America practice guideline","volume":"15","author":"Hershberger","year":"2009","journal-title":"J Card Fail"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0055","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1016\/j.ymgme.2014.03.007","article-title":"Clinical laboratory studies in Barth Syndrome","volume":"112","author":"Vernon","year":"2014","journal-title":"Mol Genet Metab"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0060","doi-asserted-by":"crossref","first-page":"443","DOI":"10.1111\/j.1747-0803.2008.00226.x","article-title":"Cardiomyopathy of unknown etiology: Barth syndrome unrecognized","volume":"3","author":"Sweeney","year":"2008","journal-title":"Congenit Heart Dis"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0065","doi-asserted-by":"crossref","DOI":"10.1038\/gim.2015.204","article-title":"New targets for monitoring and therapy in Barth syndrome","author":"Thompson","year":"2016","journal-title":"Genet Med"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0070","doi-asserted-by":"crossref","first-page":"616","DOI":"10.1038\/nm.3545","article-title":"Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies","volume":"20","author":"Wang","year":"2014","journal-title":"Nat Med"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0075","doi-asserted-by":"crossref","first-page":"157","DOI":"10.1007\/BF01799418","article-title":"X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts","volume":"19","author":"Barth","year":"1996","journal-title":"J Inherit Metab Dis"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0080","doi-asserted-by":"crossref","first-page":"273","DOI":"10.1016\/S0022-3476(99)70118-6","article-title":"X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)-MIM 302060","volume":"135","author":"Barth","year":"1999","journal-title":"J Pediatr"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0085","doi-asserted-by":"crossref","first-page":"C33","DOI":"10.1152\/ajpcell.00243.2006","article-title":"Role of cardiolipin alterations in mitochondrial dysfunction and disease","volume":"292","author":"Chicco","year":"2007","journal-title":"Am J Physiol Cell Physiol"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0090","doi-asserted-by":"crossref","first-page":"349","DOI":"10.1002\/ajmg.a.20660","article-title":"X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update","volume":"126A","author":"Barth","year":"2004","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0095","doi-asserted-by":"crossref","first-page":"14","DOI":"10.1097\/MOH.0b013e32831c83f3","article-title":"Mitochondrial defects lie at the basis of neutropenia in Barth syndrome","volume":"16","author":"Van Raam","year":"2009","journal-title":"Curr Opin Hematol"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0100","doi-asserted-by":"crossref","first-page":"345","DOI":"10.2147\/JMDH.S54802","article-title":"Successful management of Barth syndrome: a systematic review highlighting the importance of a flexible and multidisciplinary approach","volume":"8","author":"Reynolds","year":"2015","journal-title":"J Multidiscip Healthc"},{"key":"10.1016\/j.jpeds.2016.12.070_bib0105","doi-asserted-by":"crossref","first-page":"337","DOI":"10.1542\/peds.2005-2667","article-title":"Cardiac and clinical phenotype in Barth syndrome","volume":"118","author":"Spencer","year":"2006","journal-title":"Pediatrics"}],"container-title":["The Journal of Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022347616315657?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022347616315657?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,9,4]],"date-time":"2018-09-04T21:50:37Z","timestamp":1536097837000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0022347616315657"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,4]]},"references-count":20,"alternative-id":["S0022347616315657"],"URL":"https:\/\/doi.org\/10.1016\/j.jpeds.2016.12.070","relation":{},"ISSN":["0022-3476"],"issn-type":[{"value":"0022-3476","type":"print"}],"subject":[],"published":{"date-parts":[[2017,4]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Barth Syndrome with Late-Onset Cardiomyopathy: A Missed Opportunity for Diagnosis","name":"articletitle","label":"Article Title"},{"value":"The Journal of Pediatrics","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jpeds.2016.12.070","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2016 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}