{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:00:15Z","timestamp":1787014815818,"version":"build-2736575974"},"reference-count":5,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2011,10,13]],"date-time":"2011-10-13T00:00:00Z","timestamp":1318464000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatric Dermatology"],"published-print":{"date-parts":[[2012,5]]},"abstract":"<jats:p>\n                    <jats:bold>Abstract:\u2003<\/jats:bold>\n                    A 10\u2010year\u2010old boy with Hunter syndrome and extensive typical skin lesions underwent 9\u2003months of enzyme replacement therapy, after which the skin lesions disappeared. We believe that treatment with idursulfase probably removes the cutaneous storage of glucosaminoglycans in Hunter syndrome.\n                  <\/jats:p>","DOI":"10.1111\/j.1525-1470.2011.01418.x","type":"journal-article","created":{"date-parts":[[2011,10,13]],"date-time":"2011-10-13T08:25:54Z","timestamp":1318494354000},"page":"369-370","source":"Crossref","is-referenced-by-count":5,"title":["Hunter Syndrome: Resolution of Extensive Typical Skin Lesions After 9\u2003Months of Enzyme Replacement Therapy with Idursulfase"],"prefix":"10.1111","volume":"29","author":[{"given":"Laura L.","family":"Mar\u00edn","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Luis G.","family":"Guti\u00e9rrez\u2010Solana","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Antonio T.","family":"Fern\u00e1ndez","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2011,10,13]]},"reference":[{"key":"e_1_2_3_2_2","first-page":"3421","volume-title":"The metabolic and molecular basis of inherited disease","author":"Neufeld EF","year":"2001"},{"key":"e_1_2_3_3_2","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2230.1999.00448.x"},{"key":"e_1_2_3_4_2","doi-asserted-by":"crossref","first-page":"679","DOI":"10.1111\/j.0736-8046.2004.21615.x","article-title":"What syndrome is this?","volume":"21","author":"Lonergan CL","year":"2004","journal-title":"Pediatr Dermatol"},{"key":"e_1_2_3_5_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1525-1470.1998.tb01367.x"},{"key":"e_1_2_3_6_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1651-2227.2007.00212.x"}],"container-title":["Pediatric Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fj.1525-1470.2011.01418.x","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/j.1525-1470.2011.01418.x","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,29]],"date-time":"2023-10-29T20:45:38Z","timestamp":1698612338000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/j.1525-1470.2011.01418.x"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,10,13]]},"references-count":5,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2012,5]]}},"alternative-id":["10.1111\/j.1525-1470.2011.01418.x"],"URL":"https:\/\/doi.org\/10.1111\/j.1525-1470.2011.01418.x","archive":["Portico"],"relation":{},"ISSN":["0736-8046","1525-1470"],"issn-type":[{"value":"0736-8046","type":"print"},{"value":"1525-1470","type":"electronic"}],"subject":[],"published":{"date-parts":[[2011,10,13]]}}}