{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,9]],"date-time":"2025-10-09T21:02:29Z","timestamp":1760043749978,"version":"build-2065373602"},"reference-count":25,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2007,9,1]],"date-time":"2007-09-01T00:00:00Z","timestamp":1188604800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2007,9,1]],"date-time":"2007-09-01T00:00:00Z","timestamp":1188604800000},"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":[[2007,9]]},"DOI":"10.1016\/j.jaad.2007.02.023","type":"journal-article","created":{"date-parts":[[2007,8,16]],"date-time":"2007-08-16T12:53:08Z","timestamp":1187268788000},"page":"463-466","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":16,"title":["Dyskeratosis as a histologic feature in epidermolysis bullosa simplex-Dowling Meara"],"prefix":"10.1016","volume":"57","author":[{"given":"Reuven","family":"Bergman","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Avikam","family":"Harel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eli","family":"Sprecher","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.jaad.2007.02.023_bib1","doi-asserted-by":"crossref","first-page":"1051","DOI":"10.1067\/mjd.2000.106369","article-title":"Revised classification system for\u00a0inherited epidermolysis bullosa: report of the second international consensus meeting on diagnosis and classification of epidermolysis bullosa","volume":"42","author":"Fine","year":"2000","journal-title":"J Am Acad Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib2","doi-asserted-by":"crossref","first-page":"493","DOI":"10.1046\/j.1523-1747.2000.00086.x","article-title":"Herlitz junctional epidermolysis bullosa: novel and recurrent mutations in the LAMB3 gene and the population carrier frequency","volume":"115","author":"Nakano","year":"2000","journal-title":"J Invest Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib3","doi-asserted-by":"crossref","first-page":"33","DOI":"10.1016\/j.clindermatol.2004.09.015","article-title":"Progress in epidermolysis bullosa: from eponyms to molecular genetic classification","volume":"23","author":"Uitto","year":"2005","journal-title":"Clin Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib4","doi-asserted-by":"crossref","first-page":"133","DOI":"10.1046\/j.1469-7580.2003.00141.x","article-title":"Genetic disorders of palm skin and nail","volume":"202","author":"McLean","year":"2003","journal-title":"J Anat"},{"key":"10.1016\/j.jaad.2007.02.023_bib5","series-title":"Epidermolysis bullosa","first-page":"101","article-title":"The molecular biology of epidermolysis bullosa simplex","author":"Fuchs","year":"1999"},{"key":"10.1016\/j.jaad.2007.02.023_bib6","doi-asserted-by":"crossref","first-page":"6","DOI":"10.1016\/j.clindermatol.2004.09.014","article-title":"Inherited defects in keratins","volume":"23","author":"Irvine","year":"2005","journal-title":"Clin Dermatol"},{"issue":"Suppl","key":"10.1016\/j.jaad.2007.02.023_bib7","doi-asserted-by":"crossref","first-page":"6S","DOI":"10.1038\/jid.1994.3","article-title":"Ultrastructural identification of basic abnormalities as clues to genetic disorders of the epidermis","volume":"103","author":"Anton-lamprecht","year":"1994","journal-title":"J Invest Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib8","doi-asserted-by":"crossref","first-page":"561","DOI":"10.1111\/j.1365-2133.1970.tb06096.x","article-title":"An electron microscope study on the acantholytic and dyskeratotic processes in Darier's disease","volume":"82","author":"Mann","year":"1970","journal-title":"Br\u00a0J Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib9","doi-asserted-by":"crossref","first-page":"225","DOI":"10.1001\/archderm.1973.01620170037011","article-title":"Darier's disease","volume":"107","author":"Gottlieb","year":"1973","journal-title":"Arch Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib10","doi-asserted-by":"crossref","first-page":"429","DOI":"10.1111\/j.1600-0560.1997.tb00818.x","article-title":"Delayed postburn blisters: an immunohistochemical and ultrastructural study","volume":"24","author":"Bergman","year":"1997","journal-title":"J Cutan Pathol"},{"key":"10.1016\/j.jaad.2007.02.023_bib11","doi-asserted-by":"crossref","first-page":"498","DOI":"10.1001\/archderm.139.4.498","article-title":"Epidermolysis bullosa simplex in Israel: clinical and genetic features","volume":"139","author":"Ciubotaru","year":"2003","journal-title":"Arch Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib12","doi-asserted-by":"crossref","first-page":"777","DOI":"10.1038\/sj.jid.5700163","article-title":"Molecular epidemiology of hereditary epidermolysis bullosa in a Middle Eastern population","volume":"26","author":"Abu Sa'd","year":"2006","journal-title":"J Invest Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib13","doi-asserted-by":"crossref","first-page":"1654","DOI":"10.1038\/sj.jid.5700296","article-title":"Epidermolysis bullosa simplex with mottled pigmentation resulting from a recurrent mutation in KRT14","volume":"126","author":"Harel","year":"2006","journal-title":"J Invest Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib14","doi-asserted-by":"crossref","first-page":"821","DOI":"10.1111\/j.1365-2133.2004.05904.x","article-title":"Calcium pumps and keratinocytes: lessons from Darier's disease and Hailey-Hailey disease","volume":"150","author":"Dhitavat","year":"2004","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib15","doi-asserted-by":"crossref","first-page":"240","DOI":"10.1038\/ng1097-240","article-title":"Mutations in the plakophilin 1 gene result in\u00a0ectodermal dysplasia\/skin fragility syndrome","volume":"17","author":"McGrath","year":"1997","journal-title":"Nat Genet"},{"key":"10.1016\/j.jaad.2007.02.023_bib16","doi-asserted-by":"crossref","first-page":"297","DOI":"10.1046\/j.1365-2133.1999.02667.x","article-title":"Skin fragility and hypohidrotic ectodermal dysplasia resulting from ablation of plakophilin 1","volume":"140","author":"McGrath","year":"1999","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib17","doi-asserted-by":"crossref","first-page":"368","DOI":"10.1046\/j.1523-1747.2000.00082.x","article-title":"Genomic amplification of the human plakophilin 1 gene and detection of a new mutation in ectodermal dysplasia\/skin fragility syndrome","volume":"115","author":"Whittock","year":"2000","journal-title":"J Invest Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib18","doi-asserted-by":"crossref","first-page":"107","DOI":"10.1034\/j.1600-0625.2002.110202.x","article-title":"Genotype-phenotype correlation in skin fragility-ectodermal dysplasia syndrome resulting from mutations in plakophilin 1","volume":"11","author":"Hamada","year":"2002","journal-title":"Exp Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib19","doi-asserted-by":"crossref","first-page":"647","DOI":"10.1111\/j.0022-202X.2004.22335.x","article-title":"Homozygous splice site mutations in PKP1 result in loss of epidermal plakophilin 1 expression and underlie ectodermal dysplasia\/skin fragility syndrome in two consanguineous families","volume":"122","author":"Sprecher","year":"2004","journal-title":"J Invest Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib20","doi-asserted-by":"crossref","first-page":"333","DOI":"10.1097\/01.dad.0000157451.46657.a6","article-title":"The histopathology of ectodermal dysplasia\/skin fragility syndrome","volume":"27","author":"Bergman","year":"2005","journal-title":"Am J Dermatopathol"},{"key":"10.1016\/j.jaad.2007.02.023_bib21","doi-asserted-by":"crossref","first-page":"1872","DOI":"10.1007\/s00018-003-3050-7","article-title":"Structure and function of desmosomal proteins and their role in development and disease","volume":"60","author":"Huber","year":"2003","journal-title":"Cell Mol Life Sci"},{"key":"10.1016\/j.jaad.2007.02.023_bib22","doi-asserted-by":"crossref","first-page":"510","DOI":"10.1086\/500850","article-title":"Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease","volume":"78","author":"Betz","year":"2006","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.jaad.2007.02.023_bib23","doi-asserted-by":"crossref","first-page":"503","DOI":"10.1038\/35074576","article-title":"A \u2018hot-spot\u2019 mutation alters the mechanical properties of keratin filament networks","volume":"3","author":"Ma","year":"2001","journal-title":"Nat Cell Biol"},{"key":"10.1016\/j.jaad.2007.02.023_bib24","doi-asserted-by":"crossref","first-page":"421","DOI":"10.1111\/j.1365-2133.1992.tb11813.x","article-title":"Epidermolysis bullosa simplex (Dowling-Meara): a clinicopathological review","volume":"126","author":"McGrath","year":"1992","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.jaad.2007.02.023_bib25","doi-asserted-by":"crossref","first-page":"55","DOI":"10.1007\/BF02505044","article-title":"Morphology of the keratin filament network in palm and sole skin: evidence for site-dependent features based on stereological analysis","volume":"288","author":"Swensson","year":"1996","journal-title":"Arch Dermatol Res"}],"container-title":["Journal of the American Academy of Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0190962207004343?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0190962207004343?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,30]],"date-time":"2025-09-30T22:07:20Z","timestamp":1759270040000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0190962207004343"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2007,9]]},"references-count":25,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2007,9]]}},"alternative-id":["S0190962207004343"],"URL":"https:\/\/doi.org\/10.1016\/j.jaad.2007.02.023","relation":{},"ISSN":["0190-9622"],"issn-type":[{"type":"print","value":"0190-9622"}],"subject":[],"published":{"date-parts":[[2007,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Dyskeratosis as a histologic feature in epidermolysis bullosa simplex-Dowling Meara","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.2007.02.023","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2007 American Academy of Dermatology, Inc. Published by Mosby, Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}