{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,31]],"date-time":"2026-03-31T23:54:33Z","timestamp":1775001273769,"version":"3.50.1"},"reference-count":3,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2005,9,1]],"date-time":"2005-09-01T00:00:00Z","timestamp":1125532800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Inher Metab Disea"],"published-print":{"date-parts":[[2005,9]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>Fabry disease is an inherited lysosomal storage disease caused by deficiency of \u03b1\u2010galactosidase A. Enzyme replacement therapy for this multisystem progressive disease has been available only since 2001. We here report the first known successful pregnancy of a female patient receiving such therapy.<\/jats:p>","DOI":"10.1007\/s10545-005-0018-9","type":"journal-article","created":{"date-parts":[[2005,9,7]],"date-time":"2005-09-07T19:05:23Z","timestamp":1126119923000},"page":"787-788","source":"Crossref","is-referenced-by-count":32,"title":["Successful pregnancy outcome in a patient with Fabry disease receiving enzyme replacement therapy with agalsidase alfa"],"prefix":"10.1002","volume":"28","author":[{"given":"S.","family":"Wendt","sequence":"first","affiliation":[{"name":"Children's University Hospital Mainz  Mainz"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Whybra","sequence":"additional","affiliation":[{"name":"Children's University Hospital Mainz  Mainz"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Kampmann","sequence":"additional","affiliation":[{"name":"Children's University Hospital Mainz  Mainz"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Teichmann","sequence":"additional","affiliation":[{"name":"Obstetrician  Northeim Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Beck","sequence":"additional","affiliation":[{"name":"Children's University Hospital Mainz  Mainz"},{"name":"Children's University Hospital Mainz  Langenbeckstrasse 1 Mainz 55101 Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,9]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1023\/B:BOLI.0000005658.14563.77"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajog.2003.08.006"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.38.11.769"}],"container-title":["Journal of Inherited Metabolic Disease"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1007\/s10545-005-0018-9","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1007\/s10545-005-0018-9","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,15]],"date-time":"2023-09-15T01:12:36Z","timestamp":1694740356000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1007\/s10545-005-0018-9"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2005,9]]},"references-count":3,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2005,9]]}},"alternative-id":["10.1007\/s10545-005-0018-9"],"URL":"https:\/\/doi.org\/10.1007\/s10545-005-0018-9","archive":["Portico"],"relation":{},"ISSN":["0141-8955","1573-2665"],"issn-type":[{"value":"0141-8955","type":"print"},{"value":"1573-2665","type":"electronic"}],"subject":[],"published":{"date-parts":[[2005,9]]}}}