Results 201 to 210 of about 4,842,335 (379)

A retrospective analysis of haemolytic reactions to intravenous immunoglobulin using data from the Transfusion‐Transmitted Injuries Surveillance System (Ontario) [PDF]

, 2023
Khalid Batarfi, Yang Liu, Joanne Nixon, Kathryn E. Webert, Melanie St John, Meera Karunakaran, Nour Alhomsi, Jane J. Park, Nancy M. Heddle   +8 more
openalex   +1 more source

Delayed haemolytic transfusion reaction in adults with sickle cell disease: a 5‐year experience

British Journal of Haematology, 2015
Jennifer Vidler, K. Gardner, K. Amenyah, A. Mijovic, S. Thein   +4 more
semanticscholar   +1 more source

Prenatal Exome Sequencing Identifies Dual Maternal‐Fetal Diagnosis of HbF Mission Bay, a Novel HBG2 Variant Associated With Methemoglobinemia, Hypoxia and Hemolytic Anemia

Prenatal Diagnosis, EarlyView.
ABSTRACT Prenatal exome sequencing (ES) can establish rare genetic diagnoses in a fetus but may also lead to occult genetic diagnosis in a biological parent. We present a case of dual fetal and maternal diagnosis by prenatal ES, in a fetus with unexplained anemia and in a pregnant patient with sickle cell disease (SCD) and recurrent unexplained hypoxia.
Matthew A. Shear, Billie Lianoglou, Ugur Hodoglugil, W. Patrick Devine, Ashutosh Lal, Juan Gonzalez, Teresa N. Sparks   +6 more
wiley   +1 more source

Hemophilia A: An Ideal Disease for Prenatal Therapy

Prenatal 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, Anthony Atala, Graça Almeida‐Porada   +2 more
wiley   +1 more source

Prevention of non-hemolytic blood transfusion reaction by cleaning blood platelets.

, 1998
NOBUYUKI MOMONA
openalex   +2 more sources

Acute Hemolytic Transfusion Reaction in a Patient with Bombay Phenotype: Implications for ABO Grouping [PDF]

, 2013
Sheetal Malhotra, Hari Krishan Dhawan, Ashish Jain, Suchet Sachdev, Neelam Marwaha   +4 more
openalex   +1 more source

1953

Journal of Hospital Medicine, EarlyView.
Jamila Mammadova
wiley   +1 more source

Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis

Prenatal 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, Samantha Stover, Nora Gibson, Timothy Olson, James Connelly, Matthew Grace, Jennifer Andrews   +6 more
wiley   +1 more source

Delayed hemolytic transfusion reaction associated with anti-Au^a antibody in a young male with beta-thalassemia. [PDF]

Blood Transfus
Luniewski A, Lawrence CE, Luckey CJ, Gorham JD.   +3 more
europepmc   +1 more source

Physiologic impact of circulating RBC microparticles upon blood-vascular interactions [PDF]

, 2018
Doctor, Allan, Rogers, Stephen C, Said, Ahmed S   +2 more
core   +2 more sources