{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T07:05:58Z","timestamp":1791356758523,"version":"4.3.1"},"reference-count":17,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2015,5,1]],"date-time":"2015-05-01T00:00:00Z","timestamp":1430438400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["cidjournal.com","theclinics.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Clinics in Dermatology"],"published-print":{"date-parts":[[2015,5]]},"DOI":"10.1016\/j.clindermatol.2014.12.014","type":"journal-article","created":{"date-parts":[[2014,12,8]],"date-time":"2014-12-08T18:21:19Z","timestamp":1418062879000},"page":"362-367","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":5,"title":["Systemic conditions in children associated with pigmentary changes"],"prefix":"10.1016","volume":"33","author":[{"given":"Patricia A.","family":"Treadwell","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.clindermatol.2014.12.014_bb0010","doi-asserted-by":"crossref","first-page":"885","DOI":"10.1016\/j.jaad.2013.03.002","article-title":"What\u2019s new in pediatric dermatology?","volume":"68","author":"Pride","year":"2013","journal-title":"J Am Acad Dermatol"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0015","doi-asserted-by":"crossref","first-page":"442","DOI":"10.1097\/MOP.0b013e32834881dd","article-title":"Clinical manifestations of mutations in RAS and related intracellular signal transduction factors","volume":"23","author":"Zenker","year":"2011","journal-title":"Curr Opin Pediatr"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0020","doi-asserted-by":"crossref","first-page":"481","DOI":"10.1007\/s10689-011-9446-x","article-title":"The differential diagnosis of familial lentiginosis syndromes","volume":"10","author":"Lodish","year":"2011","journal-title":"Fam Cancer"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0025","doi-asserted-by":"crossref","first-page":"531","DOI":"10.1016\/j.clindermatol.2010.09.021","article-title":"Skin signs of systemic diseases","volume":"29","author":"Rigopoulos","year":"2011","journal-title":"Clin Dermatol"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0030","doi-asserted-by":"crossref","first-page":"444","DOI":"10.1111\/j.1525-1470.2008.00734.x","article-title":"LEOPARD syndrome: what are caf\u00e9 noir spots?","volume":"25","author":"Rodriquez-Bujaldon","year":"2008","journal-title":"Pediatr Dermatol"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0035","first-page":"146","article-title":"Skin findings associated with obesity","volume":"22","author":"Mathur","year":"2011","journal-title":"Adolesc Med"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0040","doi-asserted-by":"crossref","first-page":"487","DOI":"10.1097\/MOP.0b013e328355a31b","article-title":"Dermatologic manifestations of endocrine disorders","volume":"24","author":"Quatrano","year":"2012","journal-title":"Curr Opin Pediatr"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0045","first-page":"493","article-title":"Photoclinic","volume":"16","author":"Behrangi","year":"2013","journal-title":"Arch Iran Med"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0050","doi-asserted-by":"crossref","first-page":"323","DOI":"10.1016\/j.ejmg.2012.04.007","article-title":"Neurological findings in incontinentia pigmenti: a review","volume":"55","author":"Meuwissen","year":"2012","journal-title":"Eur J Med Genet"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0055","doi-asserted-by":"crossref","first-page":"55","DOI":"10.1002\/ajmg.c.31349","article-title":"47, XXY Klinefelter syndrome: clinical characteristics and age-specific recommendations for medical management","volume":"163C","author":"Aksglaede","year":"2013","journal-title":"Am J Med Genet C Semin Med Genet"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0060","doi-asserted-by":"crossref","first-page":"250","DOI":"10.1111\/j.1525-1470.2012.01729.x","article-title":"A novel X-chromosomal microdeletion encompassing congenital hemidysplasia with ichthyosiform erythroderma and limb defects","volume":"30","author":"Raychaudhury","year":"2013","journal-title":"Pediatr Dermatol"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0065","doi-asserted-by":"crossref","first-page":"46","DOI":"10.1111\/j.1529-8019.2012.01528.x","article-title":"Pathogenesis-based therapies in ichthyosis","volume":"26","author":"Lai-Cheong","year":"2013","journal-title":"Dermatol Ther"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0070","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1186\/1750-1172-8-25","article-title":"Systematic review of central nervous system anomalies in incontinentia pigmenti","volume":"8","author":"Minic","year":"2013","journal-title":"Orphanet J Rare Dis"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0075","first-page":"665","article-title":"Piebaldism","volume":"48","author":"More","year":"2011","journal-title":"Indian Pediatr"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0080","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1097\/MCD.0b013e32835e8ce5","article-title":"Homozygosity for piebaldism with a proven KIT mutation resulting in depigmentation of the skin and hair, deafness, developmental delay and autism spectrum","volume":"22","author":"Kilsby","year":"2013","journal-title":"Clin Dysmorphol"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0085","doi-asserted-by":"crossref","first-page":"13","DOI":"10.5070\/D30546V775","article-title":"Piebaldism in a 2-year-old girl","volume":"17","author":"Lopez","year":"2011","journal-title":"Dermatol Online J"},{"key":"10.1016\/j.clindermatol.2014.12.014_bb0090","doi-asserted-by":"crossref","first-page":"17","DOI":"10.5070\/D39HM4N1KG","article-title":"Piebaldism and neurofibromatosis: state of knowledge","volume":"19","author":"Duarte","year":"2013","journal-title":"Dermatol Online J"}],"container-title":["Clinics in Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0738081X14003137?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0738081X14003137?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2022,4,24]],"date-time":"2022-04-24T01:48:28Z","timestamp":1650764908000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0738081X14003137"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,5]]},"references-count":17,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2015,5]]}},"alternative-id":["S0738081X14003137"],"URL":"https:\/\/doi.org\/10.1016\/j.clindermatol.2014.12.014","relation":{},"ISSN":["0738-081X"],"issn-type":[{"value":"0738-081X","type":"print"}],"subject":[],"published":{"date-parts":[[2015,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Systemic conditions in children associated with pigmentary changes","name":"articletitle","label":"Article Title"},{"value":"Clinics in Dermatology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.clindermatol.2014.12.014","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2015 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}