Results 181 to 190 of about 19,287 (223)

Atypical acquired hemophilia linked with primary biliary cholangitis: a unique case presentation. [PDF]

Future Sci OA
Megdiche F, Siala N, Kallel F, Krichen I, Hachicha H, Frikha I, Charfi M, Kallel N, Medhaffar M, Masmoudi H, Elloumi M, Kallel C.   +11 more
europepmc   +1 more source

Comment on article: Acquired hemophilia A as a disease of the elderly by Lehoczki A. et al. [PDF]

Geroscience
Mameli A, Marongiu F, Barcellona D.
europepmc   +1 more source

Acquired Hemophilia Associated with Rheumatoid Arthritis: A Case Report and Review of the Literature. [PDF]

Int J Mol Sci
Gioia C, Paroli M, Morace V, Nardacci L, Ruffo SM, Rossi E, Pignatelli P, Accapezzato D.   +7 more
europepmc   +1 more source

Anti-CD19 CAR-T cell therapy for acquired hemophilia A. [PDF]

Leukemia
Schultze-Florey CR, Thol FR, Aleksandrova K, Stoyanov K, Gutierrez Jauregui R, Arseniev L, Leise J, Klöß S, Heidel FH, Tiede A.   +9 more
europepmc   +1 more source

Post-Infectious Acquired Hemophilia A: A Case Report and Review of the Literature. [PDF]

J Brown Hosp Med
Nicacio JM, de Araújo Júnior CMM, Barros NS, Cufua PIDF, Fernandes ALM.   +4 more
europepmc   +1 more source

Four-Year Emicizumab Treatment in an Elderly Patient With Acquired Hemophilia A: A Case Report on Perioperative Management Along With a Literature Review. [PDF]

Cureus
Yamaguchi T, Amano K, Chikasawa Y, Bingo M, Kinai E.   +4 more
europepmc   +1 more source

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Acquired Hemophilia A

Seminars in Thrombosis and Hemostasis, 2012
Acquired hemophilia A is a rare, autoimmune disorder that is caused by autoantibodies that act as inhibitors to factor VIII. It is characterized by severe, unexpected bleeding that may be life-threatening. The incidence of acquired hemophilia A is ~ 0.2 to 1.48 cases per 1 million individuals per year.
openaire   +2 more sources

Acquired Hemophilia A: A Case Report

Journal of Pharmacy Practice, 2019
Hemophilia A, also known as factor VIII deficiency, is a rare disorder caused by an insufficient level of factor VIII, an essential clotting protein. Hemophilia A can be inherited or acquired. Inherited hemophilia A is caused by a mutation to the factor VIII gene on the X chromosome, which is commonly passed down from parents to children.
Mark, Shen, Shan, Wang, Julia, Sessa, Adel, Hanna, Alexander, Axelrad, Fahd, Ali   +5 more
openaire   +2 more sources

On Acquired Hemophilia A

Acta Medica Scandinavica, 1980
ABSTRACT. Acquired hemophilia A due to antibodies of factor VIII procoagulant activity is rare. This paper reports 11 such patients followed up for long periods. They exemplify various forms of associated disorders. Four of them have died from hemorrhages, 4 have had complete remission and 3 are still alive with persistent inhibitors.
I M, Nilsson, S, Lamme
openaire   +2 more sources

An extra X does not prevent acquired hemophilia – Pregnancy-associated acquired hemophilia A

Thrombosis Research, 2017
Acquired hemophilia A (AHA) is a severe bleeding disorder caused by autoantibodies against clotting factor VIII (FVIII). With an estimated annual incidence of 1.3 to 1.5 per million, AHA is a rare disease. An extremely rare form of AHA has been described among women in the peripartum period, and may present with peripartum hemorrhage. Notably, although
Assaf A, Barg, Tami, Livnat, Gili, Kenet
openaire   +2 more sources