{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,11]],"date-time":"2025-11-11T15:31:12Z","timestamp":1762875072203},"reference-count":49,"publisher":"Informa UK Limited","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Hematology"],"published-print":{"date-parts":[[2007,2]]},"DOI":"10.1080\/10245330601111573","type":"journal-article","created":{"date-parts":[[2007,3,30]],"date-time":"2007-03-30T11:21:07Z","timestamp":1175253667000},"page":"55-62","source":"Crossref","is-referenced-by-count":28,"title":["Experience with recombinant-activated factor VII in 30 patients with congenital factor VII deficiency"],"prefix":"10.1080","volume":"12","author":[{"given":"Benjamin","family":"Brenner","sequence":"first","affiliation":[{"name":"Thrombosis and Hemostasis UnitDepartment of Hematology and Bone Marrow Transplantation, Rambam Medical Center, Haifa, Israel"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J\u00f8rgen","family":"Wiis","sequence":"additional","affiliation":[{"name":"Intensive Care Unit 4131, National University Hospital, Copenhagen, Denmark"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"301","published-online":{"date-parts":[[2013,9,4]]},"reference":[{"key":"CIT0002","doi-asserted-by":"publisher","DOI":"10.1055\/s-2000-8459"},{"key":"CIT0003","doi-asserted-by":"publisher","DOI":"10.1055\/s-0037-1615947"},{"key":"CIT0004","first-page":"151","volume":"78","author":"Cooper DN","year":"1997","journal-title":"Tuddenham EG. Inherited factor VII deficiency: Molecular genetics and pathophysiology. Thromb Haemost"},{"key":"CIT0005","first-page":"393","volume":"26","author":"Herrmann FH","year":"2000","journal-title":"Molecular biology and clinical manifestation of hereditary factor WI deficiency. Semin Thromb Hemost"},{"key":"CIT0006","first-page":"481","volume":"93","author":"Mariani G","year":"2005","journal-title":"International factor VII deficiency study group. Clinical phenotypes and factor VII genotype in congenital factor VII deficiency. Thromb Haemost"},{"key":"CIT0007","first-page":"593","volume":"10","author":"Bolton-Maggs PH","year":"2004","journal-title":"The rare coagulation disorders\u2014review with guidelines for management from the United Kingdom Haemophilia Centre Doctors\u2019 Organisation. Haemophilia"},{"key":"CIT0008","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2516.1997.00137.x"},{"key":"CIT0009","doi-asserted-by":"publisher","DOI":"10.1055\/s-0037-1614361"},{"key":"CIT0010","unstructured":"Roberts HR, Lefkowitz JB. Inherited disorders of prothrombin conversion. 3rd ed. Philadelphia, USA: Lippincott JB; 1994. p 206\u2013208."},{"key":"CIT0011","first-page":"131","volume":"77","author":"Mariani G","year":"1999","journal-title":"Use of recombinant, activated factor WI in the treatment of congenital factor WI deficiencies. Vox Sanguinis"},{"key":"CIT0012","doi-asserted-by":"publisher","DOI":"10.1002\/ajh.2830100112"},{"key":"CIT0013","first-page":"248","volume":"2","author":"Acharya SS","year":"2004","journal-title":"Dimichele DM. Rare bleeding disorder registry: Deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias. J Thromb Haemost"},{"key":"CIT0014","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2516.1997.00105.x"},{"issue":"1","key":"CIT0015","first-page":"16","volume":"7","author":"Di Paola J","year":"2001","journal-title":"Current therapy for rare factor deficiencies. Haemophilia"},{"key":"CIT0016","first-page":"1243","volume":"104","author":"Mannucci PM","year":"2004","journal-title":"Recessively inherited coagulation disorders. Blood"},{"key":"CIT0017","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2516.1998.440689.x"},{"key":"CIT0018","first-page":"200","volume":"56","author":"Kohler M","year":"1989","journal-title":"Factor VII half-life after transfusion of a steam-treated prothrombin complex concentrate in a patient with homo-zygous factor WI deficiency. Vox Sanguinis"},{"key":"CIT0019","first-page":"203","volume":"2","author":"White GC","year":"1979","journal-title":"Kingdon HS. Prothrombin complex concentrates: Preparation, properties, and clinical uses. Curr Topics Hematol"},{"key":"CIT0021","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2516.2003.00711.x"},{"key":"CIT0022","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2516.1999.00319.x"},{"key":"CIT0023","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2141.2003.04286.x"},{"key":"CIT0024","first-page":"1778","volume":"82","author":"Chuansumrit A","year":"1999","journal-title":"Successful epistaxis control in a patient with Glanzmann thrombasthenia by increased bolus injection dose of recombinant factor VIIa. Thromb Haemost"},{"key":"CIT0025","doi-asserted-by":"crossref","first-page":"3951","DOI":"10.1182\/blood.V94.11.3951","volume":"94","author":"Poon MC","year":"1999","journal-title":"Blood"},{"key":"CIT0026","first-page":"1096","volume":"2","author":"Poon MC","year":"2004","journal-title":"Prophylactic and therapeutic recombinant factor Vila administration to patients with Glanzmann\u2019s thrombasthenia: Results of an international survey. J Thromb Haemost"},{"key":"CIT0027","doi-asserted-by":"crossref","first-page":"981","DOI":"10.1055\/s-0038-1650411","volume":"75","author":"Tengborn L","year":"1996","journal-title":"Thromb Haemost"},{"issue":"1","key":"CIT0028","first-page":"150","volume":"26","author":"Ciavarella N","year":"1996","journal-title":"Use of recombinant factor VIIa (NovoSeven) in the treatment of two patients with type III von Willebrand\u2019s disease and an inhibitor against von Willebrand factor. Haemostasis"},{"key":"CIT0029","doi-asserted-by":"publisher","DOI":"10.1055\/s-0037-1613878"},{"key":"CIT0030","first-page":"211","volume":"12","author":"Meijer K","year":"2001","journal-title":"Recurrent severe bleeding from gastrointestinal angiodysplasia in a patient with von Willebrand\u2019s disease, controlled with recombinant factor VIIa. Blood Coag Fibrinol"},{"key":"CIT0031","doi-asserted-by":"publisher","DOI":"10.1007\/s00277-005-1080-y"},{"key":"CIT0032","doi-asserted-by":"publisher","DOI":"10.1055\/s-0037-1615209"},{"issue":"1","key":"CIT0033","first-page":"S55\u2013S68","volume":"11","author":"Poon MC","year":"2000","journal-title":"Recombinant activated factor VII (NovoSeven) treatment of platelet-related bleeding disorders. International registry on recombinant factor VIIa and congenital platelet disorders group. Blood Coag Fibrinol"},{"key":"CIT0034","first-page":"551","volume":"12","author":"Billon S","year":"2001","journal-title":"The use of recombinant factor VIIa (NovoSeven) in a patient with factor XI deficiency and a circulating antic-oagulant. Blood Coag Fibrinol"},{"key":"CIT0035","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2516.2002.00590.x"},{"key":"CIT0036","doi-asserted-by":"publisher","DOI":"10.1097\/00001721-199706000-00007"},{"issue":"4","key":"CIT0037","first-page":"S1059\u2013S1064","volume":"85","author":"Chuansumrit A","year":"2002","journal-title":"Outcome of intracranial hemorrhage in infants with congenital factor VII deficiency. J Med Assoc Thailand"},{"key":"CIT0038","first-page":"935","volume":"99","author":"Eskandari N","year":"2002","journal-title":"Factor VII deficiency in pregnancy treated with recombinant factor VIIa. Obst Gynecol"},{"key":"CIT0039","first-page":"1562","volume":"44","author":"Huang WY","year":"2004","journal-title":"The use of recombinant activated factor VII in three patients with central nervous system hemorrhages associated with factor VII deficiency. Transfusion"},{"key":"CIT0040","doi-asserted-by":"publisher","DOI":"10.1097\/00043426-200307000-00024"},{"key":"CIT0041","first-page":"494","volume":"125","author":"Mathijssen NC","year":"2004","journal-title":"Prophylactic effect of recombinant factor VIIa in factor VII deficient patients. Br J Haematol"},{"key":"CIT0042","doi-asserted-by":"publisher","DOI":"10.1016\/j.arth.2004.01.015"},{"key":"CIT0043","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2516.2004.00885.x"},{"key":"CIT0044","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2141.1999.01562.x"},{"key":"CIT0045","doi-asserted-by":"publisher","DOI":"10.1097\/00001721-200011020-00006"},{"key":"CIT0046","first-page":"19","volume":"12","author":"Mariani G","year":"2006","journal-title":"Ingerslev J. Congenital factor VII deficiency: Therapy with recombinant activated factor WI\u2014a critical appraisal. Haemophilia"},{"key":"CIT0047","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2141.2004.05171.x"},{"key":"CIT0048","doi-asserted-by":"publisher","DOI":"10.1111\/j.1538-7836.2004.00922.x"},{"key":"CIT0049","first-page":"169","volume":"13","author":"Mariani G","year":"1983","journal-title":"Clinical picture and classification of the variants. Haemostasis"},{"key":"CIT0050","doi-asserted-by":"publisher","DOI":"10.1111\/j.1538-7836.2004.00759.x"},{"key":"CIT0051","doi-asserted-by":"publisher","DOI":"10.1016\/S0037-1963(01)90148-9"}],"container-title":["Hematology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.tandfonline.com\/doi\/pdf\/10.1080\/10245330601111573","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,4,21]],"date-time":"2020-04-21T04:16:21Z","timestamp":1587442581000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.tandfonline.com\/doi\/full\/10.1080\/10245330601111573"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2007,2]]},"references-count":49,"journal-issue":{"issue":"1","published-online":{"date-parts":[[2013,9,4]]},"published-print":{"date-parts":[[2007,2]]}},"alternative-id":["10.1080\/10245330601111573"],"URL":"https:\/\/doi.org\/10.1080\/10245330601111573","relation":{},"ISSN":["1607-8454"],"issn-type":[{"value":"1607-8454","type":"electronic"}],"subject":[],"published":{"date-parts":[[2007,2]]}}}