Results 41 to 50 of about 19,249 (228)
A perioperative uncontrollable bleeding in an elderly patient with acquired hemophilia A: a case report [PDF]
, 2013 Acquired hemophilia A should be taken into account in the differential diagnosis of perioperative bleeding in patients without any apparent reason for activated partial thromboplastin time ...
CORTEGIANI, Andrea +6 more
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On demand treatment and home therapy of hereditary angioedema in Germany - the Frankfurt experience [PDF]
, 2010 Background: Manifestation of acute edema in hereditary angioedema (HAE) is characterized by interindividual and intraindividual variability in symptom expression over time. Flexible therapy options are needed.
Aygören-Pürsün, Emel +4 more
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Acquired hemophilia: a case report
Polish Archives of Internal Medicine, 2008 Acquired hemophilia is a severe bleeding diathesis that affects both males and females. It is caused by suddenly appearing autoantibodies that interfere with coagulation factor VIII activity. This disorder is characterized by spontaneous and post-traumatic subcutaneous bleeds and massive mucosal hemorrhages.
Mariusz, Flisiński +5 more
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Acquired hemophilia A presenting post partum [PDF]
Canadian Medical Association Journal, 2007 The case: A 41-year-old woman (gravida 4, para 3) presented in labour after 39 weeks' gestation. Her medical history included myasthenia gravis and thymectomy in 1995 and immunosuppression with azathioprine, which was stopped at 12 weeks' gestation.
Kristine, Mytopher +3 more
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Retrobulbar Hemorrhage Secondary to Acquired Hemophilia A [PDF]
Cureus, 2021 Acquired hemophilia A (AHA) is a different bleeding disorder to that of classic hemophilia A. It is an autoimmune-mediated bleeding disorder due to the presence of autoantibodies (inhibitors) directed against plasma coagulation factor VIII. This can result in fatal hemorrhage; thus, eradication of the antibody is the mainstay of treatment. Nontraumatic
Jayasundara, Hishali D +2 more
openaire +2 more sources
Haemophilia and joint disease: pathophysiology, evaluation and management [PDF]
, 2011 In patients with haemophilia, regular replacement therapy with clotting factor concentrates (prophylaxis) is effective in preventing recurrent bleeding episodes into joints and muscles.
Berntorp, Erik, Knobe, Karin
core +3 more sources
Treatment of acquired hemophilia A [PDF]
Journal of Thrombosis and Haemostasis, 2007 Acquired hemophilia A (AH) is an autoimmune disease that leads to potentially severe bleeding. Management relies on rapid and accurate diagnosis, control of bleeding episodes and eradication of the inhibitor by immunosuppression. There is extensive literature about the disease but only few controlled data are available.
openaire +2 more sources
Hemophilia in the newborn without family history: Pattern of clinical presentation of three patients [PDF]
, 2010 Introduction. Hemophilia is the most frequently diagnosed inborn clotting factor deficiency in the newborn. In about half of the cases diagnosis is made during neonatal period.
Janković Borisav +4 more
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Hematology, 2006 Acquired hemophilia A is a rare but severe autoimmune bleeding disorder, resulting from the presence of autoantibodies directed against clotting factor VIII. The etiology of the disorder remains obscure, although approximately half of all cases are associated with other underlying conditions.
openaire +2 more sources