Results 51 to 60 of about 19,249 (228)

Diagnosis of von Willebrand disease in Argentina: a single institution experience [PDF]

open access: yes, 2017
von Willebrand disease (VWD) is the most common autosomal bleeding disorder, mostlyinherited as dominant trait. VWD is due to deficiency/abnormality of von Willebrand factor (VWF).
Blanco, Alicia Noemi   +5 more
core   +1 more source

Acquired factor VIII deficiency in prostate adenocarcinoma presenting as multiple hematomas and hemarthrosis

open access: yesSAGE Open Medical Case Reports, 2020
Acquired hemophilia A or acquired factor VIII deficiency is a rare bleeding disorder due to the presence of autoantibodies to factor VIII. It has been associated with autoimmune conditions, certain medications, and malignancy. It has a high morbidity and
Akeem Lewis   +4 more
doaj   +1 more source

Liver Transplantation in a Hemophiliac [PDF]

open access: yes, 1985
To the Editor: A cure rather than a treatment has long been the goal of those caring for and those suffering from hemophilia. Encouraging results were obtained some years ago with the transplantation of normal livers into a dog with mild hemophilia1,2 ...
Bontempo, FA   +4 more
core   +1 more source

Acquired Hemophilia-A Case Series and Review. [PDF]

open access: yesJ Clin Med
Background: Acquired hemophilia A (AHA) is a rare, life-threatening autoimmune disorder characterized by inhibitory autoantibodies against factor VIII (FVIII), resulting in spontaneous or trauma-related bleeding. This study reviews a single-center cohort to evaluate patient characteristics, treatments, and outcomes. Methods: We retrospectively reviewed
Waldman Radinsky L   +8 more
europepmc   +3 more sources

Postpartum-acquired hemophilia A: case report.

open access: yesRevista peruana de medicina experimental y salud publica, 2023
Acquired hemophilia A is a rare bleeding disorder worldwide, characterized by the presence of inhibitory autoantibodies directed against a coagulation factor, most often factor VIII. There are several possible causes, and it can occur during the postpartum period. We present the case of a 34-year-old female patient with back pain, hematuria and a right
Contreras-Pizarro, Carlos H.   +3 more
openaire   +2 more sources

New Developments in Diagnosis and Management of Acquired Hemophilia and Acquired von Willebrand Syndrome

open access: yesHemaSphere, 2021
Acquired hemophilia A and acquired von Willebrand syndrome are rare, but life-threatening bleeding disorders that require prompt diagnosis and treatment by hematologists.
Frank W. G. Leebeek
doaj   +1 more source

Disclosure of Maternal HIV Status to Children: To Tell or Not To Tell . . . That Is the Question [PDF]

open access: yes, 2007
HIV-infected mothers face the challenging decision of whether to disclose their serostatus to their children. From the perspective of both mother and child, we explored the process of disclosure, providing descriptive information and examining the ...
A. Shaffer   +46 more
core   +3 more sources

Acquired hemophilia in patient with Systemic lupus erythematosus: Clinical case report

open access: yesНаучно-практическая ревматология
Acquired hemophilia is a rare disease that develops because of the synthesis of antibodies to endogenous VIII blood clotting factor. The most common symptom of acquired hemophilia is spontaneous bleeding.
S. A. Alekseeva   +2 more
doaj   +1 more source

Acquired Hemophilia A: A Rare, Acquired Coagulopathy in the Postpartum Setting

open access: yesAmerican Journal of Perinatology Reports, 2023
Postpartum hemorrhage (PPH) remains a leading cause of maternal morbidity. Pregnancy-associated acquired hemophilia A (AHA) caused by autoantibodies against factor VIII can present with recurrent episodes of postpartum bleeding.
Austin Oberlin   +10 more
doaj   +1 more source

Cyclosporine treatment of acquired hemophilia due to factor VIII antibodies [PDF]

open access: yes, 2000
Acquired hemophilia, caused by autoantibodies against coagulation factor VIII, is usually treated with steroids, cyclophosphamide, intravenous gammaglobulins and sporadically other drugs.
Baele, Gaston   +2 more
core  

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