Results 201 to 210 of about 62,566 (266)

Hemophilia A: An Ideal Disease for Prenatal Therapy

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Hemophilia A (HA) is the most common inherited coagulation defect. Current state‐of‐the‐art treatment consists of frequent administration of prophylactic infusions of coagulation factor VIII (FVIII) protein or bispecific antibodies that replace the cofactor function of FVIIIa to maintain hemostasis. However, these treatments are far from ideal,
Christopher D. Porada   +2 more
wiley   +1 more source

Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia caused by variants in SPTA1, SPTB, and EPB41. These weaken horizontal interactions in the erythrocyte cytoskeleton, causing membrane fragmentation and splenic sequestration. It will readily cause fetal anemia and often hydrops fetalis. Prenatal diagnosis requires first ruling out
Connor Hartzell   +6 more
wiley   +1 more source

Preoperative predictors of blood component transfusion in living donor liver transplantation.

open access: yesAsian J Transfus Sci, 2013
Makroo RN   +4 more
europepmc   +1 more source

How to undertake a blood component transfusion

Nursing Standard, 2018
Blood component transfusion, commonly referred to as 'blood transfusion', is a general term for the transfusion of red blood cells, platelets, fresh frozen plasma, cryoprecipitate or white blood cells directly into a patient's circulation. This is usually undertaken via intravenous administration.
Katy, Cowan, Anwen, Davies
openaire   +2 more sources

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