Solvent/detergent plasma for prevention of bleeding in recessively inherited coagulation disorders : dosing, pharmacokinetics and clinical efficacySANTAGOSTINO, Elena; MANCUSO, Maria Elisa; MORFINI, Massimo et al.Haematologica (Roma). 2006, Vol 91, Num 5, pp 634-639, issn 0390-6078, 6 p.Article

Bleeding tendency and efficacy of anti-haemorrhagic treatments in patients with type 1 von Willebrand disease and increased von Willebrand factor clearanceCASTAMAN, Giancarlo; TOSETTO, Alberto; FEDERICI, Augusto B et al.Thrombosis and haemostasis. 2011, Vol 105, Num 4, pp 647-654, issn 0340-6245, 8 p.Article

Hypofibrinogenaemia associated with a novel heterozygous γ289 Ala→Val substitution (fibrinogen Dorfen)DEAR, Amy; BRENNAN, Stephen O; DEMPFLE, Carl-Erik et al.Thrombosis and haemostasis. 2004, Vol 92, Num 6, pp 1291-1295, issn 0340-6245, 5 p.Article

Benign FGB (148Lys→Asn, and 448Arg→lys), and novel causative _Y211Tyr->His mutation distinguished by time of flight mass spectrometry in a family with hypofibrinogenaemiaBRENNAN, Stephen O; MANGOS, Hilda; FAED, James M et al.Thrombosis and haemostasis. 2014, Vol 111, Num 4, pp 679-684, issn 0340-6245, 6 p.Article

Long term prognosis of patients with myocardial infarction and normal coronary angiography: impact of inherited coagulation disordersDA COSTA, Antoine; TARDY, Brigitte; HAOUCHETTE, Kamel et al.Thrombosis and haemostasis. 2004, Vol 91, Num 2, pp 388-393, issn 0340-6245, 6 p.Article

Characterisation of 96 mutations in 128 unrelated severe haemophilia A patients from France : Description of 62 novel mutationsVINCIGUERRA, Christine; ZAWADZKI, Christophe; DARGAUD, Yesim et al.Thrombosis and haemostasis. 2006, Vol 95, Num 4, pp 593-599, issn 0340-6245, 7 p.Article

2B or not to be - The 45-year saga of the Montreal Platelet SyndromePOON, Man-Chiu; RAND, Margaret L; JACKSON, Shannon C et al.Thrombosis and haemostasis. 2010, Vol 104, Num 5, pp 903-910, issn 0340-6245, 8 p.Conference Paper

Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor XCHAFA, Ouerdia; TAGZIRT, Madjid; TAPON-BRETAUDIERE, Jacqueline et al.Thrombosis research. 2009, Vol 124, Num 1, pp 144-148, issn 0049-3848, 5 p.Article

Obstetric analgesia and anaesthesia in women with inherited bleeding disordersCHI, Claudia; LEE, Christine A; ENGLAND, Adrian et al.Thrombosis and haemostasis. 2009, Vol 101, Num 6, pp 1104-1111, issn 0340-6245, 8 p.Article

Fibrinogen Hershey IV: A novel dysfibrinogen with a γV4III mutation in the integrin α_IIbβ₃ binding siteFLOOD, Veronica H; AL -MONDHIRY, Hamid A; REIN, Chantelle M et al.Thrombosis and haemostasis. 2008, Vol 99, Num 6, pp 1008-1012, issn 0340-6245, 5 p.Article

Prospective study of ABO blood type and the risk of pulmonary embolism in two large cohort studiesWOLPIN, Brian M; KABRHEL, Christopher; VARRASO, Raphaëlle et al.Thrombosis and haemostasis. 2010, Vol 104, Num 5, pp 962-971, issn 0340-6245, 10 p.Article

Population genetics of venous thromboembolism: A narrative reviewMARGAGLIONE, Maurizio; GRANDONE, Elvira.Thrombosis and haemostasis. 2011, Vol 105, Num 2, pp 221-231, issn 0340-6245, 11 p.Article

Alloantibodies against the B subunit of plasma factor XIII developed in its congenital deficiencyWADA, Hideho; SOURI, Masayoshi; MATSUMOTO, Rui et al.Thrombosis and haemostasis. 2013, Vol 109, Num 4, pp 661-668, issn 0340-6245, 8 p.Article

A NOVEL ASSOCIATION BETWEEN A CHRONIC SUBDURAL HEMATOMA AND A FIBRINOLYTIC PATHWAY DEFECT: CASE REPORTRUGHANI, Anand I; HOLMES, Chris E; PENAR, Paul L et al.Neurosurgery. 2009, Vol 64, Num 6, issn 0148-396X, p. 1192Article

Distribution of von Willebrand factor levels in young women with and without bleeding symptoms. Influence ofABO blood group and promoter haplotypesLETHAGEN, Stefan; HILLARP, Andreas; EKHOLM, Caroline et al.Thrombosis and haemostasis. 2008, Vol 99, Num 6, pp 1013-1018, issn 0340-6245, 6 p.Article

Polymorphisms in the endothelial protein C receptor gene and thrombophilia : Thrombophilia and anticoagulant pathwayMEDINA, Pilar; NAVARRO, Silvia; ESTELLES, Amparo et al.Thrombosis and haemostasis. 2007, Vol 98, Num 3, pp 564-569, issn 0340-6245, 6 p.Article

Coagulation disorders and the risk of retinal vein occlusion: A subgroup analysisKUHLI-HATTENBACH, Claudia; SCHARRER, Inge; LÜCHTENBERG, Marc et al.Thrombosis and haemostasis. 2010, Vol 103, Num 2, pp 299-305, issn 0340-6245, 7 p.Article

A novel homozygous missense mutation in the factor VII gene of severe factor VII deficiency in a newborn babvLEE, Jung H; LEE, Hee J; BIN, Joong H et al.Blood coagulation & fibrinolysis. 2009, Vol 20, Num 2, pp 161-164, issn 0957-5235, 4 p.Article