Results 181 to 190 of about 426,014 (383)

Pathogenesis of Hemolytic Anemia in Homozygous Hemoglobin C Disease* [PDF]

open access: bronze, 1967
Samuel Charache   +4 more
openalex   +1 more source

Autoimmune Hemolytic Anemia

open access: yes, 2014
Autoimmune hemolytic anemia (AIHA) is a classic example of type II hypersensitivity, caused by autoantibodies that bind red blood cells (RBC). The autoantibodies can be divided into cold or warm types, depending on the optimum temperature at which they bind, and AIHA can also be classified as either primary or secondary if there is an underlying ...
Robert N. Barker, Mark A. Vickers
openaire   +2 more sources

Iron overload in hereditary spherocytosis: Are genetic factors the cause?

open access: yesBritish Journal of Haematology, EarlyView.
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

The anti‐CD47 antibody magrolimab with obinutuzumab and venetoclax in relapsed or refractory indolent B‐cell lymphomas

open access: yesBritish Journal of Haematology, EarlyView.
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

Hemolytic Anemia Due to Progressive Enlargement of Silastic Ball Component of Aortic Prosthesis [PDF]

open access: bronze, 1968
MARIO C. GARCIA   +4 more
openalex   +1 more source

Efficacy and safety of HRS‐5965 monotherapy in complement inhibitor–naïve patients with paroxysmal nocturnal haemoglobinuria

open access: yesBritish Journal of Haematology, EarlyView.
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

Respiratory Syncytial Virus Vaccine Induced Thrombotic Microangiopathy

open access: yesJournal of Blood Medicine
Robert Seby,1 Benjamin J McCormick,1 Emily Wolf,2 Justin Kuhlman,2 Nikita Jhawar,1 Sven Peter Oman,1 Adam M Kase,2 Chancey Christenson,3 Marwan Shaikh2 1Department of Internal Medicine, Mayo Clinic, Jacksonville, FL, USA; 2Department of Hematology ...
Seby R   +8 more
doaj  

Novel immunotherapies for immune-mediated haemolytic anaemia in dogs and people [PDF]

open access: yes, 2015
Aerts   +111 more
core   +1 more source

THE LIPID AND MINERAL DISTRIBUTION OF THE SERUM AND ERYTHROCYTES IN THE HEMOLYTIC AND HYPOCHROMIC ANEMIAS OF CHILDHOOD

open access: hybrid, 1937
Betty Nims Erickson   +4 more
openalex   +1 more source

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