Results 191 to 200 of about 19,478 (225)
Some of the next articles are maybe not open access.
Journal of the American Medical Association, 1959
A 22-year-old man was hospitalized with complaints of dyspnea and hemoptysis and a history of heart disease and coagulation defects. Repeated study of the clotting mechanism showed the outstanding deficits to be those of thromboplastin generation characteristic of hemophilia B.
openaire +1 more source
A 22-year-old man was hospitalized with complaints of dyspnea and hemoptysis and a history of heart disease and coagulation defects. Repeated study of the clotting mechanism showed the outstanding deficits to be those of thromboplastin generation characteristic of hemophilia B.
openaire +1 more source
[Rinsho ketsueki] The Japanese journal of clinical hematology, 2020
Acquired hemophilia A (AHA) is a bleeding disorder due to the autoantibody (inhibitor) production targeting blood coagulation factor VIII. It is characterized by a sudden onset, and it often causes extensive and severe bleeding in soft tissue. The incidence of AHA is 1.48 cases per 1 million individuals per year and is common among postpartum women and
openaire +1 more source
Acquired hemophilia A (AHA) is a bleeding disorder due to the autoantibody (inhibitor) production targeting blood coagulation factor VIII. It is characterized by a sudden onset, and it often causes extensive and severe bleeding in soft tissue. The incidence of AHA is 1.48 cases per 1 million individuals per year and is common among postpartum women and
openaire +1 more source
[POSTPARTUM ACQUIRED HEMOPHILIA].
Klinicheskaia meditsina, 2016This review deals with etiology, pathogenesis, clinical picture, diagnostic algorithm, and treatment of acquired hemophilia. In addition, a case of successful treatment of a patient with postpartum acquired hemophilia is reported.
P N, Barlamov +6 more
openaire +1 more source
Dealing with acquired hemophilia
Blood, 2004CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS Twenty-three years ago, Green and Lechner[1][1] published the first survey of patients with spontaneous development of factor VIII inhibitors.
openaire +1 more source
Phase 3 Trial of Concizumab in Hemophilia with Inhibitors
New England Journal of Medicine, 2023Tadashi Matsushita
exaly
[Pemphigoid and acquired hemophilia].
Annales de dermatologie et de venereologie, 2002The association of bullous pemphigoid and acquired haemophilia is reported.A 74 year-old man developed a bullous pemphigoid after decreasing corticotherapy, ecchymosis and haematomas revealing a high level of acquired anti-VIII antibodies (110 Bethesda UB units; TCA 98 s). Immunosuppressive treatment (cyclosporine, prednisone, azathioprine and bolus of
E, Lightburn +7 more
openaire +1 more source
Prophylaxis versus Episodic Treatment to Prevent Joint Disease in Boys with Severe Hemophilia
New England Journal of Medicine, 2007Sharon Funk Dpt +2 more
exaly
Acquired post partum hemophilia
2004We examine the international literature concerning acquired hemophilia subsequent to the observation of a 28-year-old woman who was brought to our attention for important metrorrhagia and hematuria which began on the 2nd day post-partum and led to 3 uterine cavity revisions in the following week, without any benefit.
GRIO R +7 more
openaire +1 more source