{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,7,9]],"date-time":"2024-07-09T12:43:22Z","timestamp":1720529002551},"reference-count":6,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2009,1,1]],"date-time":"2009-01-01T00:00:00Z","timestamp":1230768000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Clinical Therapeutics"],"published-print":{"date-parts":[[2009,1]]},"DOI":"10.1016\/s0149-2918(09)00237-9","type":"journal-article","created":{"date-parts":[[2009,8,29]],"date-time":"2009-08-29T09:47:42Z","timestamp":1251539262000},"page":"S3-S4","source":"Crossref","is-referenced-by-count":0,"special_numbering":"S1","title":["PORTYSTROKE: Screening genetic conditions in portuguese young stroke patients"],"prefix":"10.1016","volume":"31","author":[{"given":"Miguel","family":"Viana-Baptista","sequence":"first","affiliation":[]},{"given":"Susana","family":"Ferreira","sequence":"additional","affiliation":[]},{"given":"Teresa","family":"Pinho-e-Melo","sequence":"additional","affiliation":[]},{"given":"Marta","family":"Carvalho","sequence":"additional","affiliation":[]},{"given":"V\u00edtor Tedim","family":"Cruz","sequence":"additional","affiliation":[]},{"given":"C\u00e1tia","family":"Carmona","sequence":"additional","affiliation":[]},{"given":"Fernando","family":"Silva","sequence":"additional","affiliation":[]},{"given":"Assun\u00e7\u00e3o","family":"Tuna","sequence":"additional","affiliation":[]},{"given":"Miguel","family":"Rodrigues","sequence":"additional","affiliation":[]},{"given":"Carla","family":"Ferreira","sequence":"additional","affiliation":[]},{"given":"Ana Am\u00e9lia Nogueira","family":"Pinto","sequence":"additional","affiliation":[]},{"given":"Andr\u00e9","family":"Leit\u00e3o","sequence":"additional","affiliation":[]},{"given":"Joao Paulo","family":"Gabriel","sequence":"additional","affiliation":[]},{"given":"Sofia","family":"Calado","sequence":"additional","affiliation":[]},{"given":"J.P.","family":"Oliveira","sequence":"additional","affiliation":[]},{"given":"J.M.","family":"Ferro","sequence":"additional","affiliation":[]}],"member":"78","reference":[{"key":"10.1016\/S0149-2918(09)00237-9_bib1","doi-asserted-by":"crossref","first-page":"114","DOI":"10.1111\/j.1747-4949.2007.00110.x","article-title":"Genetics: What is relevant for the stroke physician?","volume":"2","author":"Markus","year":"2007","journal-title":"Int J Stroke"},{"key":"10.1016\/S0149-2918(09)00237-9_bib2","doi-asserted-by":"crossref","first-page":"203","DOI":"10.1161\/01.STR.0000048162.16852.88","article-title":"Yield of screening for CADASIL mutations in lacunar stroke and leukoaraiosis","volume":"34","author":"Dong","year":"2003","journal-title":"Stroke."},{"key":"10.1016\/S0149-2918(09)00237-9_bib3","doi-asserted-by":"crossref","first-page":"1794","DOI":"10.1016\/S0140-6736(05)67635-0","article-title":"Prevalence of Fabry disease in patients with cryptogenic stroke: A prospective study [published correction appears in Lancet. 2006;368:2210]","volume":"366","author":"Rolfs","year":"2005","journal-title":"Lancet"},{"key":"10.1016\/S0149-2918(09)00237-9_bib4","doi-asserted-by":"crossref","first-page":"479","DOI":"10.1016\/j.clineuro.2007.03.008","article-title":"Middelheim Fabry Study (MiFaS): A retrospective Belgian study on the prevalence of Fabry disease in young patients with cryptogenic stroke","volume":"109","author":"Brouns","year":"2007","journal-title":"Clin Neurol Neurosurgery"},{"key":"10.1016\/S0149-2918(09)00237-9_bib5","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1161\/01.STR.24.1.35","article-title":"Classification of subtype of acute ischemic stroke. Definitions for use in a multi-center clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment","volume":"24","author":"Adams","year":"1993","journal-title":"Stroke"},{"issue":"Suppl 2","key":"10.1016\/S0149-2918(09)00237-9_bib6","first-page":"75","article-title":"The spectrum of NOTCH3 mutations in Portuguese patients with CADASIL: Implications for diagnostic strategies","volume":"23","author":"Viana-Baptista","year":"2007","journal-title":"Cerebrovasc Dis."}],"container-title":["Clinical Therapeutics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0149291809002379?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0149291809002379?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,12,17]],"date-time":"2018-12-17T14:21:04Z","timestamp":1545056464000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0149291809002379"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,1]]},"references-count":6,"alternative-id":["S0149291809002379"],"URL":"https:\/\/doi.org\/10.1016\/s0149-2918(09)00237-9","relation":{},"ISSN":["0149-2918"],"issn-type":[{"value":"0149-2918","type":"print"}],"subject":[],"published":{"date-parts":[[2009,1]]}}}