{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T11:11:59Z","timestamp":1791112319342,"version":"4.1.0"},"reference-count":38,"publisher":"Wiley","issue":"s4","license":[{"start":{"date-parts":[[2014,4,25]],"date-time":"2014-04-25T00:00:00Z","timestamp":1398384000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Haemophilia"],"published-print":{"date-parts":[[2014,5]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>The diagnosis and management of bleeding disorders is made difficult by the complexity and variety of disorders, clinical symptoms and bleeding type and severity. von Willebrand disease (<jats:styled-content style=\"fixed-case\">VWD<\/jats:styled-content>) and platelet disorders are disorders of primary haemostasis and together represent the most common inherited bleeding disorders. In this article, we describe the diagnosis of <jats:styled-content style=\"fixed-case\">VWD<\/jats:styled-content> and platelet disorders and the treatment options for <jats:styled-content style=\"fixed-case\">VWD<\/jats:styled-content>.<\/jats:p>","DOI":"10.1111\/hae.12414","type":"journal-article","created":{"date-parts":[[2014,4,25]],"date-time":"2014-04-25T09:03:49Z","timestamp":1398416629000},"page":"59-64","source":"Crossref","is-referenced-by-count":22,"title":["von Willebrand disease and platelet disorders"],"prefix":"10.1111","volume":"20","author":[{"given":"E. J.","family":"Favaloro","sequence":"first","affiliation":[{"name":"Diagnostic Haemostasis Haematology Department Institute of Clinical Pathology and Medical Research (ICPMR) Pathology West Westmead Hospital Westmead NSW Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"I.","family":"Bod\u00f3","sequence":"additional","affiliation":[{"name":"Department of Hematology and Stem Cell Transplantation St. Istv\u00e1n &amp; St. L\u00e1szl\u00f3 Hospital Budapest Hungary"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S. J.","family":"Israels","sequence":"additional","affiliation":[{"name":"Department of Pediatrics and Child Health University of Manitoba Winnipeg MB Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S. A.","family":"Brown","sequence":"additional","affiliation":[{"name":"Department of Haematology &amp; Haemophilia Centre Royal Children's Hospital Brisbane Qld Australia"},{"name":"Department of Haematology Pathology Queensland Brisbane Qld Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2014,4,25]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1055\/s-0031-1281028"},{"key":"e_1_2_6_3_1","first-page":"17","article-title":"von Willebrand factor: form for Function","volume":"40","author":"Yee A","year":"2014","journal-title":"Semin Thromb 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