Results 131 to 140 of about 246,759 (191)
Warm autoimmune haemolytic anaemia complicated by simultaneous arterial and venous thromboses: a case report. [PDF]
Pan Afr Med J, 2022 Ćurčić E +5 more
europepmc +1 more source
When to consider an inborn error of immunity: clues for physicians
Internal Medicine Journal, Volume 56, Issue 9, Page 1488-1499, September 2026.Abstract The term inborn errors of immunity (IEIs) refers to the rapidly expanding group of genetic disorders causing dysregulation of the immune system. With improved genetic testing in recent years, the number of defined IEIs and their range of phenotypic presentations has grown vastly, with more than 550 IEIs now described.
Meera Thangarajah, Lucinda J. Berglund
wiley +1 more source
How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome [PDF]
, 2014 Thrombotic thrombocytopenic purpura (TTP) and atypical haemolytic uraemic syndrome (aHUS) are acute, rare life-threatening thrombotic microangiopathies that require rapid diagnosis and treatment.
Goodship, T, Scully, M
core
Disease-modifying treatments for primary autoimmune haemolytic anaemia. [PDF]
Cochrane Database Syst Rev, 2021 Liu AP, Cheuk DK.
europepmc +1 more source
BAFF and APRIL Receptors in B Cell Immunity and Autoimmunity
Immunological Reviews, Volume 342, Issue 1, September 2026.ABSTRACT BAFF and APRIL are TNF superfamily proteins that bind to BAFFR, TACI and BCMA, members of the TNF receptor superfamily. These proteins have both unique and overlapping roles in B cell development and survival and are major therapeutic targets for antibody‐ and B‐cell‐driven pathologies.
Daisy H. Luff +2 more
wiley +1 more source
TREATMENT OF AUTOIMMUNE HEMOLYTIC ANAEMIA WITH RITUXIMAB
Zdravniški Vestnik, 2004 Background. Autoimmune haemolytic anaemia (AIHA) is characterised by the presence of autoantibodies directed against autologous erythrocytes. Depending on temperature at which they are active AIHA is classified as AIHA due to warm or cold-reacting ...
Uroš Mlakar
doaj
Autoimmune haemolysis as an unusual cause of anaemia in von Recklinghausen's disease
, 2004 Von Recklinghausen's disease, now classified as neurofibromatosis type 1 (NF-1), is a relatively frequent autosomal dominant disorder and has clinical manifestations, such as cafe-au-lait spots, freckling, generalised cutaneus neurofibroma, Lisch nodules,
Ilter T. +3 more
core
Journal of Clinical Laboratory Analysis, Volume 40, Issue 18, September 2026.
Filippo Russo +6 more
wiley +1 more source
Transfusion, Volume 66, Issue 9, Page 1830-1839, September 2026.Abstract Background The monocyte monolayer assay (MMA) uses monocytes, but it is known that antibody‐mediated hemolysis occurs in macrophages. Whether the use of macrophages would improve the predictive capacity of the MMA is unclear. Also, it is unclear if RBC alloantibodies contribute to hemolysis via antibody‐dependent cellular cytotoxicity (ADCC ...
Yeniley Ruiz Noa +6 more
wiley +1 more source
Complement-mediated autoimmune haemolytic anaemia as an initial presentation of Legionnaires' disease. [PDF]
BMJ Case Rep, 2021 Sabahat U +3 more
europepmc +1 more source