{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,21]],"date-time":"2026-09-21T01:15:31Z","timestamp":1789953331914,"version":"4.0.1"},"reference-count":39,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2003,11,25]],"date-time":"2003-11-25T00:00:00Z","timestamp":1069718400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Funda\u00e7\u00e3o \u00e0 Pesquisa do Estado de S. 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Old ischemic\u2010anoxic foci of gliosis, with necrosis and calcification, dorsally situated, were present from the pons to the medulla, involving some cranial nerve nuclei (especially the IV, VII, and XII) that were partially or completely depopulated of neural cells.<\/jats:p><\/jats:sec><jats:sec><jats:title>CONCLUSIONS<\/jats:title><jats:p>The findings suggest a circulatory mechanism to the M\u00f6bius sequence, with vascular disruption involving the territory of the subclavian artery, occurring in a critical period of embryonic life between six to eight weeks postconception. These cases add further evidence of the role of misoprostol as a teratogen. Birth Defects Research (Part A) 67:000\u2013000, 2003. \u00a9 2003 Wiley\u2010Liss, Inc.<\/jats:p><\/jats:sec>","DOI":"10.1002\/bdra.10144","type":"journal-article","created":{"date-parts":[[2003,12,12]],"date-time":"2003-12-12T11:00:30Z","timestamp":1071226830000},"page":"1002-1007","source":"Crossref","is-referenced-by-count":45,"title":["M\u00f6bius sequence in children exposed in utero to misoprostol: Neuropathological study of three cases"],"prefix":"10.1002","volume":"67","author":[{"given":"Maria Joaquina","family":"Marques\u2010Dias","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Claudette 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