{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,1,4]],"date-time":"2024-01-04T00:02:06Z","timestamp":1704326526935},"reference-count":33,"publisher":"Oxford University Press (OUP)","issue":"1","license":[{"start":{"date-parts":[[2015,9,1]],"date-time":"2015-09-01T00:00:00Z","timestamp":1441065600000},"content-version":"tdm","delay-in-days":5356,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2001,1]]},"DOI":"10.1046\/j.1365-2133.2001.03968.x","type":"journal-article","created":{"date-parts":[[2003,3,11]],"date-time":"2003-03-11T05:33:41Z","timestamp":1047360821000},"page":"162-168","source":"Crossref","is-referenced-by-count":13,"title":["Useful applications of DNA repair tests for differential diagnosis of atypical dyschromatosis symmetrica hereditaria from xeroderma pigmentosum"],"prefix":"10.1093","volume":"144","author":[{"given":"E.","family":"Ohtoshi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Y.","family":"Matsumura","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Nishigori","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"K-I.","family":"Toda","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Y.","family":"Horiguchi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Ikenaga","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Y.","family":"Miyachi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","reference":[{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB1","first-page":"95","article-title":"Dyschromatosis symmetrica hereditaria (in Japanese)","volume":"29","author":"Toyama","year":"1929","journal-title":"Jpn J Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB2","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1007\/BF01843639","article-title":"Symmetrische Pigmentanomalie der Extremitaten (in German)","volume":"147","author":"Komaya","year":"1924","journal-title":"Arch Dermatol Syphilol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB3","first-page":"33","article-title":"Statistical study of dyschromatosis symmetrica hereditaria (in Japanese)","volume":"23","author":"Kamide","year":"1981","journal-title":"Rinsho Derma"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB4","first-page":"201","article-title":"Pigmentary disorders (in Japanese)","volume":"8","author":"Kitamura","year":"1943","journal-title":"Rinsho Hihu-Hinyo"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB5","first-page":"152","article-title":"Eine besondere Form der Akropigmentation: acropigmentatio reticularis (in German)","volume":"4","author":"Kitamura","year":"1953","journal-title":"Hautarzt"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB6","doi-asserted-by":"crossref","first-page":"437","DOI":"10.1111\/j.1365-2133.1976.tb00848.x","article-title":"Reticulate acropigmentation of Kitamura","volume":"95","author":"Griffiths","year":"1976","journal-title":"Br J Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB7","doi-asserted-by":"crossref","first-page":"439","DOI":"10.1111\/j.1365-2230.1984.tb00838.x","article-title":"Reticulate pigmentary disorder-a review","volume":"9","author":"Griffiths","year":"1984","journal-title":"Clin Exp Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB8","doi-asserted-by":"crossref","first-page":"317","DOI":"10.1111\/j.1346-8138.1980.tb01978.x","article-title":"Clinical and photobiological differences between dyschromatosis symmetrica hereditaria and xeroderma pigmentosum","volume":"7","author":"Satoh","year":"1980","journal-title":"J Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB9","doi-asserted-by":"crossref","first-page":"410","DOI":"10.1111\/j.1525-1470.1986.tb00552.x","article-title":"A case of xeroderma pigmentosum with clinical appearance of dyschromatosis symmetrica hereditaria","volume":"3","author":"Nishigori","year":"1986","journal-title":"Pediatr Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB10","doi-asserted-by":"crossref","first-page":"460","DOI":"10.1111\/1523-1747.ep12284030","article-title":"Somatic mosaicism for DNA repair capacity in fibroblasts derived from a group A xeroderma pigmentosum patient","volume":"93","author":"Chang","year":"1989","journal-title":"J Invest Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB11","doi-asserted-by":"crossref","first-page":"107","DOI":"10.1269\/jrr.37.107","article-title":"Recovery from ultraviolet light-induced depression of ribosomal RNA synthesis in normal human, xeroderma pigmentosum and Cockayne syndrome cells","volume":"37","author":"Ayaki","year":"1996","journal-title":"J Radiat Res"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB12","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1111\/j.1365-2133.1987.tb05796.x","article-title":"Sensitivity to UV radiation of fibroblasts from a Japanese group A xeroderma pigmentosum patient with mild neurological abnormalities","volume":"116","author":"Sato","year":"1987","journal-title":"Br J Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB13","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1046\/j.1365-2133.1998.02039.x","article-title":"Assignment of three Chinese xeroderma pigmentosum patients to complementation group C and one to group E","volume":"138","author":"Han","year":"1998","journal-title":"Br J Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB14","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1016\/S1085-5629(97)80039-9","article-title":"Dyschromatosis","volume":"16","author":"Urabe","year":"1997","journal-title":"Semin Cutan Med Surg"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB15","first-page":"998","volume-title":"Dermatology in General Medicine","author":"Mosher","year":"1999"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB16","doi-asserted-by":"crossref","first-page":"598","DOI":"10.1111\/j.1346-8138.1994.tb01801.x","article-title":"Spectrum of reticulate flexural and acral pigmentary disorder in northern India","volume":"21","author":"Dhar","year":"1994","journal-title":"J Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB17","doi-asserted-by":"crossref","first-page":"350","DOI":"10.1159\/000017913","article-title":"Overlap of reticulate acropigmentation of Kitamura, acropigmentation of Dohi and Dowling-Degos disease in four generations","volume":"196","author":"Thami","year":"1998","journal-title":"Dermatology"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB18","doi-asserted-by":"crossref","first-page":"242","DOI":"10.1046\/j.1525-1470.1998.1998015242.x","article-title":"Acropigmentation of Dohi in a 12-year-old boy","volume":"15","author":"Dhar","year":"1998","journal-title":"Pediatr Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB19","doi-asserted-by":"crossref","first-page":"544","DOI":"10.1111\/j.1346-8138.1999.tb02045.x","article-title":"Dyschromatosis symmetrica hereditaria in an Indian family","volume":"26","author":"Thappa","year":"1999","journal-title":"J Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB20","first-page":"238","article-title":"Dyschromatosis symmetrica hereditaria-a histochemical and ultrastructual study","volume":"84","author":"Sheu","year":"1985","journal-title":"Taiwan I Hsueh Hui Tsa Chih (J Formoson Med Assoc)"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB21","first-page":"585","article-title":"Dyschromatosis symmetrica hereditaria affecting two families (English summary)","volume":"18","author":"Kim","year":"1980","journal-title":"Korean J Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB22","doi-asserted-by":"crossref","first-page":"296","DOI":"10.1111\/j.1525-1470.1997.tb00962.x","article-title":"Neurofibromatosis and reticulate acropigmentation of Dohi: a case report","volume":"14","author":"Tan","year":"1997","journal-title":"Pediatr Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB23","doi-asserted-by":"crossref","first-page":"135","DOI":"10.2340\/0001555574138139","article-title":"Dyschromatosis symmetrica hereditaria associated with idiopathic torsion dystonia. A case report","volume":"74","author":"Patrizi","year":"1994","journal-title":"Acta Derm Venereol (Stockh)"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB24","doi-asserted-by":"crossref","first-page":"884","DOI":"10.1016\/S0190-9622(97)80018-7","article-title":"Familial reticulate acropigmentation of Dohi","volume":"37","author":"Danese","year":"1997","journal-title":"J Am Acad Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB25","doi-asserted-by":"crossref","first-page":"477","DOI":"10.1111\/j.1365-2230.1995.tb01382.x","article-title":"Reticulate acropigmentation of Dohi","volume":"20","author":"Ostlere","year":"1995","journal-title":"Clin Exp Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB26","first-page":"1777","volume-title":"Textbook of Dermatology","author":"Bleehan","year":"1998"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB27","first-page":"44","volume-title":"Clinical Dermatology","author":"Kamide","year":"1985"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB28","first-page":"202","volume-title":"Illustrated Textbook of Skin Diseases","author":"Nagae","year":"1992"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB29","first-page":"380","volume-title":"Textbook Dermatology","author":"Ueno","year":"1996"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB30","first-page":"767","article-title":"Dyschromatosis symmetrica hereditaria (in Japanese)","volume":"22","author":"Kondo","year":"1968","journal-title":"Rinsho Derma"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB31","doi-asserted-by":"crossref","first-page":"491","DOI":"10.1046\/j.1365-2133.1999.02716.x","article-title":"Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases","volume":"140","author":"Oyama","year":"1999","journal-title":"Br J Dermatol"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB32","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1159\/000249382","article-title":"Density of dopa-positive melanocytes in dyschromatosis symmetrica hereditaria","volume":"171","author":"Hata","year":"1985","journal-title":"Dermatologica"},{"key":"10.1046\/j.1365-2133.2001.03968.x-BIB33","first-page":"107","article-title":"A case of systemic sclerosis with dyschromatosis symmetrica hereditaria with unusual clinical appearances (in Japanese)","volume":"39","author":"Yazawa","year":"1997","journal-title":"Rinsho Derma"}],"container-title":["British Journal of Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1046%2Fj.1365-2133.2001.03968.x","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/onlinelibrary.wiley.com\/wol1\/doi\/10.1046\/j.1365-2133.2001.03968.x\/fullpdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,1,3]],"date-time":"2024-01-03T17:53:57Z","timestamp":1704304437000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/bjd\/article\/144\/1\/162\/6691073"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2001,1]]},"references-count":33,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2001,1]]}},"URL":"https:\/\/doi.org\/10.1046\/j.1365-2133.2001.03968.x","relation":{},"ISSN":["0007-0963","1365-2133"],"issn-type":[{"value":"0007-0963","type":"print"},{"value":"1365-2133","type":"electronic"}],"subject":[],"published":{"date-parts":[[2001,1]]}}}