{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,12,20]],"date-time":"2023-12-20T00:09:06Z","timestamp":1703030946645},"reference-count":3,"publisher":"Georg Thieme Verlag KG","issue":"04","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Hamostaseologie"],"published-print":{"date-parts":[[2023,8]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Platelets are key drivers of hemostasis. Low platelet counts, dysfunction in platelet adhesion, and aggregation lead to increased bleeding tendency. Inherited platelet disorders (IPDs) form a highly heterogeneous group of rare diseases with variable bleeding tendency. IPDs may be associated with other signs and symptoms often referred to as \u201csyndromic.\u201d The underlying genetic defect may prone patients to develop hematopoietic diseases such as leukemia. Over the last decade, accumulating knowledge in genetics has led to the detection of many \u201cnew\u201d platelet disorders. However, still many patients with a well-described platelet dysfunction remain undetected until severe bleeding occurs.<\/jats:p>","DOI":"10.1055\/a-2031-7790","type":"journal-article","created":{"date-parts":[[2023,8,23]],"date-time":"2023-08-23T22:33:10Z","timestamp":1692829990000},"page":"238-240","source":"Crossref","is-referenced-by-count":0,"title":["Progress in Hemostasis (Part 1): Improved Management of Inherited Platelet Disorders: Reality or Illusion?"],"prefix":"10.1055","volume":"43","author":[{"given":"Werner","family":"Streif","sequence":"additional","affiliation":[{"name":"Department of Pediatrics 1, Medical University of Innsbruck (MUI), Innsbruck, Austria"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"194","published-online":{"date-parts":[[2023,8,23]]},"reference":[{"key":"ref1","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1055\/a-2099-3266","article-title":"State-of-the-Art Targeted High-Throughput Sequencing for Detecting Inherited Platelet Disorders","volume":"43","author":"J Gebetsberger","year":"2023","journal-title":"Hamostaseologie"},{"key":"ref2","first-page":"255","article-title":"Thrombocytopenia Absent Radius Syndrome: From Current Genetics to Patient Self-Empowerment","volume":"43","author":"G Strauss","year":"2023","journal-title":"HHamostaseologie"},{"key":"ref3","first-page":"262","article-title":"Treatment of Inherited Platelet Disorders: Current Status and Future Options","volume":"43","author":"C Bargehr","year":"2023","journal-title":"Hamostaseologie"}],"container-title":["H\u00e4mostaseologie"],"original-title":[],"language":"de","link":[{"URL":"http:\/\/www.thieme-connect.de\/products\/ejournals\/pdf\/10.1055\/a-2031-7790.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,12,19]],"date-time":"2023-12-19T17:13:49Z","timestamp":1703006029000},"score":1,"resource":{"primary":{"URL":"http:\/\/www.thieme-connect.de\/DOI\/DOI?10.1055\/a-2031-7790"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,8]]},"references-count":3,"journal-issue":{"issue":"04","published-online":{"date-parts":[[2023,8,23]]},"published-print":{"date-parts":[[2023,8]]}},"URL":"https:\/\/doi.org\/10.1055\/a-2031-7790","archive":["Portico","CLOCKSS"],"relation":{},"ISSN":["0720-9355","2567-5761"],"issn-type":[{"value":"0720-9355","type":"print"},{"value":"2567-5761","type":"electronic"}],"subject":[],"published":{"date-parts":[[2023,8]]}}}