{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,22]],"date-time":"2025-10-22T02:53:09Z","timestamp":1761101589995},"reference-count":3,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2000,7,1]],"date-time":"2000-07-01T00:00:00Z","timestamp":962409600000},"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":[[2000,7]]},"DOI":"10.1023\/a:1005676600975","type":"journal-article","created":{"date-parts":[[2002,12,21]],"date-time":"2002-12-21T23:07:17Z","timestamp":1040512037000},"page":"518-519","source":"Crossref","is-referenced-by-count":41,"title":["The HELLP syndrome associated with fetal medium\u2010chain acyl\u2010CoA dehydrogenase deficiency"],"prefix":"10.1002","volume":"23","author":[{"given":"J.","family":"Nelson","sequence":"first","affiliation":[{"name":"Department of Genetic Services King Edward Memorial Hospital  374 Bagot Road Perth WA 6008 Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"B.","family":"Lewis","sequence":"additional","affiliation":[{"name":"Department of Genetic Services King Edward Memorial Hospital  374 Bagot Road Perth WA 6008 Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"B.","family":"Walters","sequence":"additional","affiliation":[{"name":"Department of Genetic Services King Edward Memorial Hospital  374 Bagot Road Perth WA 6008 Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2000,7]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/0002-9378(95)91470-6"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1471-0528.1996.tb09827.x"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0002-9378(98)70446-6"}],"container-title":["Journal of Inherited Metabolic Disease"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1023%2FA%3A1005676600975","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1023\/A%3A1005676600975","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,15]],"date-time":"2023-09-15T20:22:40Z","timestamp":1694809360000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1023\/A%3A1005676600975"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2000,7]]},"references-count":3,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2000,7]]}},"alternative-id":["10.1023\/A:1005676600975"],"URL":"https:\/\/doi.org\/10.1023\/a:1005676600975","archive":["Portico"],"relation":{},"ISSN":["0141-8955","1573-2665"],"issn-type":[{"value":"0141-8955","type":"print"},{"value":"1573-2665","type":"electronic"}],"subject":[],"published":{"date-parts":[[2000,7]]}}}