Rare Bleeding Disorder Registry: deficienceies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias
North american rare bleeding disorder study group
Acharya SS, Coughlin A, DiMichele DM, North american rare bleeding disorder study group. Rare Bleeding Disorder Registry: deficienceies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias. J Thromb Haemost 2004; 2: 248-56.
Severe factor V deficiency presenting with intracranial haemorrhage during gestation
Ellestad SC, Zimmerman SA, Thornburg C, Mitchell TE, Swamy GK, James AH. Severe factor V deficiency presenting with intracranial haemorrhage during gestation. Haemophilia 2007; 13: 432-34.
Homozygous F5 deep-intronic splicing mutation resulting in severe factor V deficiency and undetectable thrombin generation in platelet-rich plasma
Castoldi E, Duckers C, Radu C et al. Homozygous F5 deep-intronic splicing mutation resulting in severe factor V deficiency and undetectable thrombin generation in platelet-rich plasma. J Thromb Hemost 2011; 9: 959-68.
The thrombogramm in rare inherited coagulation disorders: its relation to clinical bleeding
Al Dieri R, Peyvandi F, Santagostino E et al. The thrombogramm in rare inherited coagulation disorders: its relation to clinical bleeding. J Thromb Hemost 2004; 88: 576-82.
Management of patients with factor V deficiency: open issues from the challenging history of a woman with anaphylactic tranfusion reactions
Coppola A, Maruotti M, Feola G et al. Management of patients with factor V deficiency: open issues from the challenging history of a woman with anaphylactic tranfusion reactions. Haemophilia 2010; 16: 560-3.
