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Atypical Hemolytic-Uremic Syndrome with Positive Direct Coombs Test: Case Study
Background. Atypical hemolytic-uremic syndrome (aHUS) is an orphan chronic systemic disease resulting from uncontrolled activation of alternative complement pathway and development of complement mediated-thrombotic microangiopathy (TMA).
Dmitry S. Kalaev +4 more
doaj +1 more source
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core +3 more sources
Background: Non-Rhesus D antigen non-ABO, minor blood group alloimmunization in pregnant women is being increasingly recognized as a significant contributor to the development of the hemolytic disease of the fetus and newborn (HDFN).
Shrutiprajna Kar +3 more
doaj +1 more source
Object. We present here the case of severe fetal anemia caused by anti-E antibody positive, which showed a favorable course only with fetal intraperitoneal administration of immunoglobulin. Case.
Masashi Yoshida +5 more
doaj +1 more source
ABSTRACT Chief executive officers (CEOs) play a pivotal role in shaping public discourse on climate change through social media, yet how their language use affects the effectiveness of climate‐related posts remains unclear. Drawing on schema‐congruity theory and leader role expectations, we conceptualize certainty in language as congruent and anxiety ...
Ellen Weber +4 more
wiley +1 more source
Anemia with Positive Direct Coombs' Test Induced by Trypan Blue [PDF]
Abstract An anemia with a positive direct and indirect Coombs' test was induced in Wistar strain rats by injection of the dye trypan blue. The anemia was characterized by a shortened red cell survival time, increased osmotic fragility and reticulocytosis. There was an associated leukopenia and thrombocytopenia. The positive Coombs' tests
D V, BROWN, E M, BOEHNI, L M, NORLIND
openaire +2 more sources
Maximizing Neurovascular Outcomes of Facial Transplantation: A Comprehensive Review
ABSTRACT Facial transplantation is a division of reconstructive surgery which aims to improve the function and appearance of a face that has endured severe disfigurement. Currently, the face transplant procedure uses allogenic tissue, harvested from a brain‐dead donor, to replace damaged facial components.
Olivia A. James, Faye Bennett
wiley +1 more source
We report a rare case of concomitant immune thrombotic thrombocytopenic purpura (iTTP) and Evans syndrome, complicated by multiple cerebral infarctions. The patient presented with severe thrombocytopenia and hemolytic anemia, as well as a positive direct
Shinichi Ogawa +2 more
doaj +1 more source
BACKGROUND: Hemolytic disease of the newborn (HDN) was more common due to Rh incompatibility. Its prevalence has decreased due to introduction of Immunoglobulin G (IgG) prophylaxis against RhD antigen.
Pramod Uttamlal Toshniwal +4 more
doaj +1 more source

