{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,22]],"date-time":"2025-10-22T03:06:01Z","timestamp":1761102361068,"version":"build-2065373602"},"reference-count":13,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2019,10,1]],"date-time":"2019-10-01T00:00:00Z","timestamp":1569888000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,10,1]],"date-time":"2019-10-01T00:00:00Z","timestamp":1569888000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","jaad.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of the American Academy of Dermatology"],"published-print":{"date-parts":[[2019,10]]},"DOI":"10.1016\/j.jaad.2018.11.014","type":"journal-article","created":{"date-parts":[[2019,2,25]],"date-time":"2019-02-25T08:13:14Z","timestamp":1551082394000},"page":"950-955","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":19,"title":["Localization and age distribution of telangiectases in children and adolescents with hereditary hemorrhagic telangiectasia: A retrospective cohort study"],"prefix":"10.1016","volume":"81","author":[{"given":"Cristian D.","family":"Gonzalez","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sarah D.","family":"Cipriano","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Christina A.","family":"Topham","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"David A.","family":"Stevenson","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kevin J.","family":"Whitehead","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sheryll","family":"Vanderhooft","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Angela P.","family":"Presson","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jamie","family":"McDonald","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"7","key":"10.1016\/j.jaad.2018.11.014_bib1","doi-asserted-by":"crossref","first-page":"607","DOI":"10.1097\/GIM.0b013e3182136d32","article-title":"Hereditary hemorrhagic telangiectasia: an overview of diagnosis, management, and pathogenesis","volume":"13","author":"McDonald","year":"2011","journal-title":"Genet Med"},{"issue":"1","key":"10.1016\/j.jaad.2018.11.014_bib2","doi-asserted-by":"crossref","first-page":"66","DOI":"10.1002\/(SICI)1096-8628(20000306)91:1<66::AID-AJMG12>3.0.CO;2-P","article-title":"Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)","volume":"91","author":"Shovlin","year":"2000","journal-title":"Am J Med Genet"},{"issue":"2","key":"10.1016\/j.jaad.2018.11.014_bib3","doi-asserted-by":"crossref","first-page":"73","DOI":"10.1136\/jmg.2009.069013","article-title":"International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia","volume":"48","author":"Faughnan","year":"2011","journal-title":"J Med Genet"},{"issue":"21","key":"10.1016\/j.jaad.2018.11.014_bib4","doi-asserted-by":"crossref","first-page":"2733","DOI":"10.1002\/ajmg.a.32243","article-title":"Genotype-phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia","volume":"146A","author":"Letteboer","year":"2008","journal-title":"Am J Med Genet A"},{"issue":"3","key":"10.1016\/j.jaad.2018.11.014_bib5","doi-asserted-by":"crossref","first-page":"291","DOI":"10.1002\/ajmg.1320320302","article-title":"Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population","volume":"32","author":"Plauchu","year":"1989","journal-title":"Am J Med Genet"},{"issue":"8","key":"10.1016\/j.jaad.2018.11.014_bib6","doi-asserted-by":"crossref","first-page":"585","DOI":"10.1136\/jmg.40.8.585","article-title":"Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations","volume":"40","author":"Berg","year":"2003","journal-title":"J Med Genet"},{"issue":"6","key":"10.1016\/j.jaad.2018.11.014_bib7","first-page":"407","article-title":"Mucocutaneous telangiectases of the head and neck in individuals with hereditary hemorrhagic telangiectasia \u2013 analysis of distribution and symptoms","volume":"14","author":"Folz","year":"2004","journal-title":"Eur J Dermatol"},{"issue":"1","key":"10.1016\/j.jaad.2018.11.014_bib8","doi-asserted-by":"crossref","first-page":"179","DOI":"10.1016\/j.jpeds.2013.02.009","article-title":"Hereditary hemorrhagic telangiectasia: arteriovenous malformations in children","volume":"163","author":"Giordano","year":"2013","journal-title":"J Pediatr"},{"issue":"6","key":"10.1016\/j.jaad.2018.11.014_bib9","doi-asserted-by":"crossref","first-page":"596","DOI":"10.1001\/archpedi.160.6.596","article-title":"Symptomatic children with hereditary hemorrhagic telangiectasia: a pediatric center experience","volume":"160","author":"Mei-Zahav","year":"2006","journal-title":"Arch Pediatr Adolesc Med"},{"issue":"6","key":"10.1016\/j.jaad.2018.11.014_bib10","doi-asserted-by":"crossref","first-page":"e1615","DOI":"10.1542\/peds.2010-2366","article-title":"Symptomatic liver involvement in neonatal hereditary hemorrhagic telangiectasia","volume":"127","author":"Al-Saleh","year":"2011","journal-title":"Pediatrics"},{"issue":"1","key":"10.1016\/j.jaad.2018.11.014_bib11","doi-asserted-by":"crossref","first-page":"E12","DOI":"10.1542\/peds.109.1.e12","article-title":"Intracranial hemorrhage in infants and children with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome)","volume":"109","author":"Morgan","year":"2002","journal-title":"Pediatrics"},{"issue":"4","key":"10.1016\/j.jaad.2018.11.014_bib12","first-page":"163","article-title":"Hereditary hemorrhagic telangiectasia: children need screening too","volume":"37","author":"Sekarski","year":"2011","journal-title":"Pediatr Nurs"},{"issue":"1","key":"10.1016\/j.jaad.2018.11.014_bib13","doi-asserted-by":"crossref","first-page":"289","DOI":"10.1111\/j.2517-6161.1995.tb02031.x","article-title":"Controlling the false discovery rate: a practical and powerful approach to multiple testing","volume":"57","author":"Benjamini","year":"1995","journal-title":"J Royal Stat Soc Ser B"}],"container-title":["Journal of the American Academy of Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0190962218329037?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0190962218329037?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,30]],"date-time":"2025-09-30T22:50:19Z","timestamp":1759272619000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0190962218329037"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,10]]},"references-count":13,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2019,10]]}},"alternative-id":["S0190962218329037"],"URL":"https:\/\/doi.org\/10.1016\/j.jaad.2018.11.014","relation":{},"ISSN":["0190-9622"],"issn-type":[{"type":"print","value":"0190-9622"}],"subject":[],"published":{"date-parts":[[2019,10]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Localization and age distribution of telangiectases in children and adolescents with hereditary hemorrhagic telangiectasia: A retrospective cohort study","name":"articletitle","label":"Article Title"},{"value":"Journal of the American Academy of Dermatology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jaad.2018.11.014","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 by the American Academy of Dermatology, Inc.","name":"copyright","label":"Copyright"}]}}