Acquired hemophilia A (AHA) is a rare autoimmune disease caused by autoantibodies against coagulation factor VIII and characterized by spontaneous hemorrhage in patients with no previous family or personal history of bleeding. Although data on several AHA cohorts have been collected, limited information is available on the optimal management of AHA.

Knoebl, P., Marco, P., Baudo, F., Collins, P., Huth Kühne, A., Nemes, L., et al. (2012). Demographic and clinical data in acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2). JOURNAL OF THROMBOSIS AND THROMBOLYSIS, 10(4), 622-631 [10.1111/j.1538-7836.2012.04654.x].

Demographic and clinical data in acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)

Falanga A;POGLIANI, ENRICO MARIA;
2012

Abstract

Acquired hemophilia A (AHA) is a rare autoimmune disease caused by autoantibodies against coagulation factor VIII and characterized by spontaneous hemorrhage in patients with no previous family or personal history of bleeding. Although data on several AHA cohorts have been collected, limited information is available on the optimal management of AHA.
Articolo in rivista - Articolo scientifico
Chi-Square Distribution; Humans; Hemophilia A; Aged; Europe; Hemorrhage; Immunosuppressive Agents; Factor VIII; Risk Assessment; Pregnancy; Registries; Kaplan-Meier Estimate; Prospective Studies; Autoantibodies; Aged, 80 and over; Risk Factors; Hemostatic Techniques; Treatment Outcome; Middle Aged; Male; Female
English
2012
10
4
622
631
none
Knoebl, P., Marco, P., Baudo, F., Collins, P., Huth Kühne, A., Nemes, L., et al. (2012). Demographic and clinical data in acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2). JOURNAL OF THROMBOSIS AND THROMBOLYSIS, 10(4), 622-631 [10.1111/j.1538-7836.2012.04654.x].
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/37336
Citazioni
  • Scopus 382
  • ???jsp.display-item.citation.isi??? 372
Social impact