{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,11]],"date-time":"2025-11-11T13:34:07Z","timestamp":1762868047453,"version":"build-2065373602"},"reference-count":34,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2020,6,1]],"date-time":"2020-06-01T00:00:00Z","timestamp":1590969600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,6,1]],"date-time":"2020-06-01T00:00:00Z","timestamp":1590969600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","trasci.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Transfusion and Apheresis Science"],"published-print":{"date-parts":[[2020,6]]},"DOI":"10.1016\/j.transci.2020.102728","type":"journal-article","created":{"date-parts":[[2020,1,9]],"date-time":"2020-01-09T11:47:33Z","timestamp":1578570453000},"page":"102728","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":10,"title":["Inherited coagulation disorders in Turkish children: A retrospective, single-center cohort study"],"prefix":"10.1016","volume":"59","author":[{"given":"Nergiz","family":"\u00d6ner","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"T\u00fcrkiz","family":"G\u00fcrsel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Z\u00fchre","family":"Kaya","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ebru Y\u0131lmaz","family":"Keskin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"\u00dclker","family":"Ko\u00e7ak","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Meryem","family":"Albayrak","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Idil","family":"Yenicesu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Burcu Belen","family":"Apak","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Melek","family":"I\u015f\u0131k","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.transci.2020.102728_bib0005","doi-asserted-by":"crossref","first-page":"383","DOI":"10.1016\/S0950-3536(11)80025-9","article-title":"Epidemiology of coagulation disorders","volume":"5","author":"Nathwani","year":"1992","journal-title":"Baillieres Clin Haematol"},{"key":"10.1016\/j.transci.2020.102728_bib0010","doi-asserted-by":"crossref","first-page":"1419","DOI":"10.1016\/j.pcl.2013.09.002","article-title":"Inherited abnormalities of coagulation: hemophilia, von Willebrand disease and beyond","volume":"60","author":"Kumar","year":"2013","journal-title":"Pediatr Clin N Am"},{"key":"10.1016\/j.transci.2020.102728_bib0015","doi-asserted-by":"crossref","first-page":"20","DOI":"10.1111\/j.1365-2516.2009.02127.x","article-title":"A study of variations in the reported haemophilia A prevalence around the World","volume":"16","author":"Stonebraker","year":"2010","journal-title":"Haemophilia"},{"key":"10.1016\/j.transci.2020.102728_bib0020","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1111\/j.1365-2516.2011.02588.x","article-title":"A study of variations in the reported haemophilia B prevalence around the World","volume":"18","author":"Stonebraker","year":"2012","journal-title":"Haemophilia"},{"key":"10.1016\/j.transci.2020.102728_bib0025","doi-asserted-by":"crossref","first-page":"2103","DOI":"10.1111\/j.1538-7836.2006.02146.x","article-title":"Working Party on von Willebrand Disease Classification. Update on the pathogenesis and classification of von Willenbrand disease: a report of the Subcommitee on von Willebrand Factor","volume":"4","author":"Sadler","year":"2006","journal-title":"J Thromb Haemost"},{"key":"10.1016\/j.transci.2020.102728_bib0030","doi-asserted-by":"crossref","first-page":"2067","DOI":"10.1056\/NEJMra1601561","article-title":"Von Willebrand\u2019s disease","volume":"375","author":"Leebeek","year":"2016","journal-title":"N Engl J Med"},{"key":"10.1016\/j.transci.2020.102728_bib0035","series-title":"Textbook of hemophilia","first-page":"286","article-title":"Von Willebrand disease: epidemiology","author":"Rodeghiero","year":"2010"},{"key":"10.1016\/j.transci.2020.102728_bib0040","doi-asserted-by":"crossref","first-page":"349","DOI":"10.1055\/s-0029-1225757","article-title":"Introduction. Rare bleeding disorders: general aspects of clinical features, diagnosis, and management","volume":"35","author":"Peyvandi","year":"2009","journal-title":"Semin Thromb Hemost"},{"key":"10.1016\/j.transci.2020.102728_bib0045","doi-asserted-by":"crossref","first-page":"2052","DOI":"10.1182\/blood-2014-08-532820","article-title":"Rare bleeding disorders: diagnosis and treatment","volume":"125","author":"Palla","year":"2015","journal-title":"Blood"},{"key":"10.1016\/j.transci.2020.102728_bib0050","doi-asserted-by":"crossref","first-page":"248","DOI":"10.1111\/j.1538-7836.2003.t01-1-00553.x","article-title":"North American Rare Bleeding Disorder Study Group. Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias","volume":"2","author":"Acharya","year":"2004","journal-title":"J Thromb Haemost"},{"key":"10.1016\/j.transci.2020.102728_bib0055","doi-asserted-by":"crossref","first-page":"2","DOI":"10.1111\/j.1365-2516.2008.01946.x","article-title":"Haemophilia care then, now and in the future","volume":"15","author":"Oldenburg","year":"2009","journal-title":"Haemophilia"},{"key":"10.1016\/j.transci.2020.102728_bib0060","doi-asserted-by":"crossref","first-page":"1935","DOI":"10.1111\/jth.12672","article-title":"The subcommittee on factor v\u0131\u0131\u0131, factor \u0131x and rare coagulation disorders. Definition in hemophilia: communication from the SSC of the ISTH","volume":"12","author":"Blanchette","year":"2014","journal-title":"J Thromb Haemost"},{"key":"10.1016\/j.transci.2020.102728_bib0065","doi-asserted-by":"crossref","first-page":"304","DOI":"10.1111\/bjh.13058","article-title":"BCSH Committee. Guideline for the diagnosis and management of the rare coagulation disorders: a United Kingdom Haemophilia Centre Doctors\u2019 Organization guideline o behalf of the British Committee for Standard in Haematology","volume":"167","author":"Mumford","year":"2014","journal-title":"Br J Haematol"},{"key":"10.1016\/j.transci.2020.102728_bib0070","doi-asserted-by":"crossref","first-page":"264","DOI":"10.1160\/TH13-02-0135","article-title":"Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort","volume":"110","author":"Hampshire","year":"2013","journal-title":"Thromb Haemost"},{"year":"2015","series-title":"Report on the annual global survay","key":"10.1016\/j.transci.2020.102728_bib0075"},{"key":"10.1016\/j.transci.2020.102728_bib0080","doi-asserted-by":"crossref","first-page":"901","DOI":"10.1177\/1076029617731596","article-title":"Congenital factor deficiencies in children: a report of a single-center experience","volume":"24","author":"\u015ealc\u0131o\u011flu","year":"2018","journal-title":"Clin Appl Thromb Hemost"},{"key":"10.1016\/j.transci.2020.102728_bib0085","first-page":"210","article-title":"Inherited bleeding disorders: a 14-year retrospective study","volume":"21","author":"Eid","year":"2008","journal-title":"Clin Lab Sci"},{"key":"10.1016\/j.transci.2020.102728_bib0090","doi-asserted-by":"crossref","first-page":"411","DOI":"10.1097\/MBC.0b013e3283540bf8","article-title":"A longitudinal prospective study of bleeding diathesis in Egyptian pediatric patients: single-center experience","volume":"23","author":"Mokhtar","year":"2012","journal-title":"Blood Coagul Fibrinolysis"},{"key":"10.1016\/j.transci.2020.102728_bib0095","first-page":"233","article-title":"An investigation of the spectrum of common and rare inherited coagulation disorders in north-eastern Iran","volume":"11","author":"Mansouritorghabeh","year":"2013","journal-title":"Blood Transfus"},{"key":"10.1016\/j.transci.2020.102728_bib0100","doi-asserted-by":"crossref","first-page":"642","DOI":"10.1097\/MBC.0b013e32832f4371","article-title":"Spectrum of inherited bleeding disorder in Southern Iran, before and after the establishment of comprehensive coagulation laboratory","volume":"20","author":"Karimi","year":"2009","journal-title":"Blood Coagul Fibrinolysis"},{"key":"10.1016\/j.transci.2020.102728_bib0105","doi-asserted-by":"crossref","first-page":"569","DOI":"10.1055\/s-2005-922229","article-title":"Epidemiology of von Willebrand disease in developing countries","volume":"31","author":"Srivastava","year":"2005","journal-title":"Semin Thromb Hemost"},{"key":"10.1016\/j.transci.2020.102728_bib0110","doi-asserted-by":"crossref","first-page":"48","DOI":"10.5505\/tjh.2012.02418","article-title":"Rare coagulation disorders: a retrospective analysis of 156 patients in Turkey","volume":"29","author":"F\u0131\u015fg\u0131n","year":"2012","journal-title":"Turk J Haematol"},{"key":"10.1016\/j.transci.2020.102728_bib0115","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1097\/MBC.0000000000000185","article-title":"Molecular basis and bleeding manifestations of faxtor XI deficiency in 11 Turkish families","volume":"26","author":"Keskin","year":"2015","journal-title":"Blood Coagul Fibrinolysis"},{"key":"10.1016\/j.transci.2020.102728_bib0120","doi-asserted-by":"crossref","first-page":"548","DOI":"10.1067\/mpd.2002.128115","article-title":"What factors influence the age at diagnosis of hemophilia? Results of the French hemophilia cohort","volume":"141","author":"Chambost","year":"2002","journal-title":"J Pediatr"},{"key":"10.1016\/j.transci.2020.102728_bib0125","doi-asserted-by":"crossref","first-page":"556","DOI":"10.1111\/hae.12938","article-title":"The incidence, risk and functional outcomes of intracranial haemorrhage in children with inherited bleeding disorders at one haemophilia center","volume":"22","author":"Bladen","year":"2016","journal-title":"Haemophilia"},{"key":"10.1016\/j.transci.2020.102728_bib0130","doi-asserted-by":"crossref","first-page":"162","DOI":"10.1007\/PL00014346","article-title":"Prevalence and outcome of intracranial haemorrhage in haemophiliacs--a survey of the paediatric group of the German Society of Thrombosis and Haemostasis (GTH)","volume":"158","author":"Klinge","year":"1999","journal-title":"Eur J Pediatr"},{"key":"10.1016\/j.transci.2020.102728_bib0135","doi-asserted-by":"crossref","first-page":"359","DOI":"10.1111\/hae.12716","article-title":"Low mortality from intracranial haemorrhage in paediatric patients with haemophilia","volume":"21","author":"Witmer","year":"2015","journal-title":"Haemophilia"},{"key":"10.1016\/j.transci.2020.102728_bib0140","doi-asserted-by":"crossref","first-page":"298","DOI":"10.1111\/bjh.14844","article-title":"Intracranial haemorrhage in children and adolescents with severe hemophilia A or B \u2013the impact of prophylactic treatment","volume":"179","author":"Andersson","year":"2017","journal-title":"Br J Haematol"},{"key":"10.1016\/j.transci.2020.102728_bib0145","doi-asserted-by":"crossref","first-page":"23","DOI":"10.1097\/MBC.0b013e32835975d6","article-title":"Diagnosis and treatment of intracranial hemorrhage in children with hemophilia","volume":"24","author":"Nagel","year":"2013","journal-title":"Blood Coagul Fibrinolysis"},{"key":"10.1016\/j.transci.2020.102728_bib0150","doi-asserted-by":"crossref","first-page":"277","DOI":"10.1111\/j.1365-2516.2009.02140.x","article-title":"Upper gastrointestinal bleeding in children with haemophilia: a clinical significance of Helicobacter pylori infection","volume":"16","author":"Choe","year":"2010","journal-title":"Haemophilia"},{"key":"10.1016\/j.transci.2020.102728_bib0155","doi-asserted-by":"crossref","first-page":"854","DOI":"10.1177\/0009922817732150","article-title":"Gastrointestinal bleeding in children with hemophilia-A","volume":"57","author":"Pickles","year":"2018","journal-title":"Clin Pediatr (Phila)"},{"key":"10.1016\/j.transci.2020.102728_bib0160","doi-asserted-by":"crossref","first-page":"114","DOI":"10.1159\/000070186","article-title":"Two episodes of hemoperitoneum from luteal cysts rupture in a patient with congenital factor X deficiency","volume":"55","author":"Dafopoulos","year":"2003","journal-title":"Gynecol Obstet Invest"},{"key":"10.1016\/j.transci.2020.102728_bib0165","doi-asserted-by":"crossref","first-page":"607","DOI":"10.1111\/j.1365-2516.2008.01930.x","article-title":"Von Willebrand disease and recurrent hematoperitoneum due to the rupture of haemorrhagic ovarian cysts","volume":"15","author":"Radakovic","year":"2009","journal-title":"Haemophilia"},{"key":"10.1016\/j.transci.2020.102728_bib0170","doi-asserted-by":"crossref","first-page":"280","DOI":"10.1046\/j.1365-2516.2002.00626.x","article-title":"Inhibitors: resolving diagnostic and therapeutic dilemmas","volume":"8","author":"Dimichele","year":"2002","journal-title":"Haemophilia"}],"container-title":["Transfusion and Apheresis Science"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1473050220300112?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1473050220300112?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,26]],"date-time":"2025-10-26T08:50:49Z","timestamp":1761468649000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1473050220300112"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,6]]},"references-count":34,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2020,6]]}},"alternative-id":["S1473050220300112"],"URL":"https:\/\/doi.org\/10.1016\/j.transci.2020.102728","relation":{},"ISSN":["1473-0502"],"issn-type":[{"type":"print","value":"1473-0502"}],"subject":[],"published":{"date-parts":[[2020,6]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Inherited coagulation disorders in Turkish children: A retrospective, single-center cohort study","name":"articletitle","label":"Article Title"},{"value":"Transfusion and Apheresis Science","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.transci.2020.102728","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}],"article-number":"102728"}}