Rare bleeding disorders in young women.

[1]  G. Mariani,et al.  Coagulation and Clinical Features Associated with the Arg304gln Mutation (Factor VII Padua) in the Irf7 Study Group Response to Letter to the Editor Regarding Factor VII Deficiency (Semin Thromb Hemost 2009;35(4):400-406) , 2010 .

[2]  K. Tziomalos,et al.  Treatment of congenital fibrinogen deficiency: overview and recent findings , 2009, Vascular health and risk management.

[3]  G. Mariani,et al.  Factor VII Deficiency , 2009, Seminars in thrombosis and hemostasis.

[4]  K. Ghosh,et al.  Menorrhagia and reproductive health in rare bleeding disorders: a study from the Indian subcontinent , 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

[5]  P. Bolton-Maggs.  Factor XI deficiency--resolving the enigma? , 2009, Hematology. American Society of Hematology. Education Program.

[6]  F. Peyvandi,et al.  Combined FV and FVIII deficiency , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

[7]  P. Kouides,et al.  Diagnosis and treatment of inherited factor X deficiency , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

[8]  M. Koerper,et al.  Factor V deficiency: a concise review , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

[9]  A. Shapiro,et al.  Plasminogen activator inhibitor type 1 deficiency , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

[10]  S. Acharya,et al.  Rare inherited disorders of fibrinogen , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

[11]  P. Monahan,et al.  Familial deficiency of vitamin K‐dependent clotting factors , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

[12]  S. Meeks,et al.  Abnormalities of prothrombin: a review of the pathophysiology, diagnosis, and treatment , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

[13]  D. Nugent,et al.  Factor XIII deficiency , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

[14]  G. Dolan,et al.  Diagnosis, clinical features and molecular assessment of the dysfibrinogenaemias , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

[15]  E. Seifried,et al.  International Registry on Factor XIII Deficiency: A basis formed mostly on European data , 2007, Thrombosis and Haemostasis.

[16]  P. Mannucci,et al.  Incidence of bleeding symptoms in 100 patients with inherited afibrinogenemia or hypofibrinogenemia , 2006, Journal of thrombosis and haemostasis : JTH.

[17]  M. Reid-Nicholson,et al.  Capillary hemangioma of the endometrium: a case report and review of the literature. , 2005, Archives of pathology & laboratory medicine.

[18]  P. Mannucci,et al.  Recessively inherited coagulation disorders. , 2004, Blood.

[19]  T. Repine,et al.  Menorrhagia Due to a Qualitative Deficiency of Plasminogen Activator Inhibitor-1: Case Report and Literature Review , 2004, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

[20]  D. Dimichele,et al.  Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias , 2004, Journal of Thrombosis and Haemostasis.

[21]  M. Albisetti.  The Fibrinolytic System in Children , 2003, Seminars in thrombosis and hemostasis.

[22]  A. Shapiro,et al.  Human plasminogen activator inhibitor-1 (PAI-1) deficiency: characterization of a large kindred with a null mutation in the PAI-1 gene. , 1997, Blood.

[23]  Berryman Dl,et al.  Endometrial ablation for severe menorrhagia in a patient with hereditary hemorrhagic telangiectasia : A case report , 1996 .

[24]  Shanberge Jn.  Hemangioma of the uterus associated with hereditary hemorrhagic telangiectasia. , 1994 .

[25]  J. Shanberge.  HEMANGIOMA OF THE UTERUS ASSOCIATED WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA , 1994, Obstetrics and gynecology.