{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,23]],"date-time":"2026-06-23T03:46:30Z","timestamp":1782186390284,"version":"3.54.5"},"reference-count":15,"publisher":"Wiley","issue":"S5","license":[{"start":{"date-parts":[[2016,7,13]],"date-time":"2016-07-13T00:00:00Z","timestamp":1468368000000},"content-version":"vor","delay-in-days":12,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Haemophilia"],"published-print":{"date-parts":[[2016,7]]},"abstract":"<jats:p>Rare coagulation disorders (<jats:styled-content style=\"fixed-case\">RCD<\/jats:styled-content>s) include the inherited deficiencies of fibrinogen, factor (F) <jats:styled-content style=\"fixed-case\">II<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> FV<\/jats:styled-content>, combined <jats:styled-content style=\"fixed-case\">FV<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">VIII<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> FVII<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> FX<\/jats:styled-content>, combined <jats:styled-content style=\"fixed-case\">FVII<\/jats:styled-content> and X, <jats:styled-content style=\"fixed-case\">FXI<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> FXIII<\/jats:styled-content> and combined congenital deficiency of vitamin K\u2010dependent factors (<jats:styled-content style=\"fixed-case\">VKCFD<\/jats:styled-content>s). Despite their rarity, a deep comprehension of all these disorders is essential to really understand haemostasis. Indeed, even if they share some common features each <jats:styled-content style=\"fixed-case\">RCD<\/jats:styled-content> has some particularity which makes it unique. In this review, we focus on three disorders: fibrinogen, <jats:styled-content style=\"fixed-case\">FVII<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">FXIII<\/jats:styled-content>.<\/jats:p>","DOI":"10.1111\/hae.12965","type":"journal-article","created":{"date-parts":[[2016,7,13]],"date-time":"2016-07-13T09:32:50Z","timestamp":1468402370000},"page":"61-65","source":"Crossref","is-referenced-by-count":39,"title":["Rare coagulation disorders: fibrinogen, factor <scp>VII<\/scp> and factor <scp>XIII<\/scp>"],"prefix":"10.1111","volume":"22","author":[{"given":"P.","family":"de Moerloose","sequence":"first","affiliation":[{"name":"Division of Angiology and Haemostasis University Hospitals and Faculty of Medicine Geneva Switzerland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J.\u2010F.","family":"Schved","sequence":"additional","affiliation":[{"name":"Hemophilia treatment Center Montpellier France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D.","family":"Nugent","sequence":"additional","affiliation":[{"name":"Department of Hematology Children's Hospital of Orange County Orange CA USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2016,7,13]]},"reference":[{"key":"e_1_2_7_2_1","doi-asserted-by":"publisher","DOI":"10.1055\/s-0033-1349222"},{"key":"e_1_2_7_3_1","doi-asserted-by":"publisher","DOI":"10.1182\/blood-2014-08-532820"},{"key":"e_1_2_7_4_1","doi-asserted-by":"publisher","DOI":"10.1111\/bjh.13058"},{"key":"e_1_2_7_5_1","doi-asserted-by":"publisher","DOI":"10.1182\/blood-2014-06-582866"},{"key":"e_1_2_7_6_1","doi-asserted-by":"publisher","DOI":"10.1160\/TH04-10-0650"},{"key":"e_1_2_7_7_1","doi-asserted-by":"publisher","DOI":"10.1038\/sj.ejhg.5200593"},{"key":"e_1_2_7_8_1","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2141.2002.03545.x"},{"key":"e_1_2_7_9_1","doi-asserted-by":"publisher","DOI":"10.1046\/j.1538-7836.2003.00395.x"},{"key":"e_1_2_7_10_1","first-page":"704","article-title":"Analysis of biological phenotypes from 42 patients with inherited factor VII deficiency: can biological tests predict the bleeding risk?","volume":"89","author":"Giansily\u2010Blaizot M","year":"2004","journal-title":"Haematologica"},{"key":"e_1_2_7_11_1","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2141.2002.03408.x"},{"key":"e_1_2_7_12_1","doi-asserted-by":"publisher","DOI":"10.5482\/HAMO-13-08-0046"},{"key":"e_1_2_7_13_1","doi-asserted-by":"publisher","DOI":"10.1002\/mgg3.138"},{"key":"e_1_2_7_14_1","doi-asserted-by":"publisher","DOI":"10.3324\/haematol.2009.017210"},{"key":"e_1_2_7_15_1","doi-asserted-by":"publisher","DOI":"10.1111\/hae.12616"},{"key":"e_1_2_7_16_1","doi-asserted-by":"publisher","DOI":"10.1111\/hae.12505"}],"container-title":["Haemophilia"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fhae.12965","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/hae.12965","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,11]],"date-time":"2023-09-11T21:12:48Z","timestamp":1694466768000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/hae.12965"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,7]]},"references-count":15,"journal-issue":{"issue":"S5","published-print":{"date-parts":[[2016,7]]}},"alternative-id":["10.1111\/hae.12965"],"URL":"https:\/\/doi.org\/10.1111\/hae.12965","archive":["Portico"],"relation":{},"ISSN":["1351-8216","1365-2516"],"issn-type":[{"value":"1351-8216","type":"print"},{"value":"1365-2516","type":"electronic"}],"subject":[],"published":{"date-parts":[[2016,7]]}}}