Results 171 to 180 of about 414,209 (326)
Coagulation in the Pathophysiology of Hemolytic Anemias
AbstractCoagulation abnormalities are frequently reported in hemolytic anemias (HA). Several pathophysiologic mechanisms are common to different HA. In this review three different hemolytic disorders will be discussed.In sickle cell disease and in β-thalassemia, a thrombophilic status has been well documented as multifactorial involving hemostatic ...
openaire +4 more sources
Novel immunotherapies for immune-mediated haemolytic anaemia in dogs and people [PDF]
Aerts+111 more
core +1 more source
Causes of mortality in koalas autopsied at the University of Melbourne
Objective To determine the causes of mortality in koalas autopsied at the University of Melbourne based on the retrospective analysis of autopsy reports. Methods The autopsy reports of 239 koalas examined at the University of Melbourne from 1970 to 2023 were reviewed to determine which of the comorbidities present was the primary cause to which death ...
L Wilson+8 more
wiley +1 more source
Progressive feline leukaemia virus (FeLV) infection dramatically shortens the lives of infected cats, causing acquired immunodeficiency, aplastic anaemia, lymphoma, leukaemia and other myeloproliferative diseases. The potential impact of regressive FeLV infection on the development of disease remains largely unknown, although there is evidence it ...
ME Westman+6 more
wiley +1 more source
Iron overload in hereditary spherocytosis: Are genetic factors the cause?
Summary Non‐transfusional iron overload (IOL) in hereditary spherocytosis (HS) is poorly documented compared with other red blood cell disorders. We studied 13 HS adults with confirmed IOL to identify potential genetic factors. Using a next‐generation sequencing panel of 46 genes related to HS, anaemia and iron metabolism, we found no association ...
Lucie Donaty+6 more
wiley +1 more source
Follicular lymphoma (FL), marginal zone lymphoma (MZL), chronic lymphocytic leukaemia (CLL) and mantle cell lymphoma (MCL) are characterized by a continuous incidence of relapse and increasing resistance to therapy. Novel immunotherapy approaches are needed.
Rahul Lakhotia+11 more
wiley +1 more source
Summary Paroxysmal nocturnal haemoglobinuria (PNH) is a rare, life‐threatening disorder characterized by complement‐mediated haemolysis, leading to anaemia and thrombosis. HRS‐5965 is a novel, oral, selective complement factor B inhibitor targeting the alternative pathway, potentially reducing both intra‐ and extravascular haemolysis.
Li Zhang+7 more
wiley +1 more source
Fetomaternal haemorrhage (FMH) in RhD‐negative individuals can cause alloimmunization with future antibody‐mediated destruction of fetal red blood cells. Accurate FMH estimation guides Rh immune globulin dosing. The rosette test, the most used qualitative method, may yield false negatives with fetal RhD variants or false positives with maternal ...
Omar I. Hajjaj+5 more
wiley +1 more source
Summary Clinical outcome after chimeric antigen receptor (CAR)‐T‐cell failure in large B‐cell lymphoma (LBCL) is dismal. Allogeneic stem cell transplantation (alloSCT) represents a potentially curative salvage for relapsed/refractory LBCL, although concerns remain regarding its feasibility and safety in patients exposed to CAR‐T and bispecific ...
Angelica Barone+10 more
wiley +1 more source
Systematic Review of Prognostic Factors for Mortality in Dogs with Immune-mediated Hemolytic Anemia [PDF]
Altman+30 more
core +1 more source