Results 121 to 130 of about 181,406 (245)
Diagnosis and treatment of acquired aplastic anemia
Acquired severe aplastic anemia can be treated successfully with either immunosuppressive therapy or bone marrow transplantation. Although immunosuppressive therapy can be readily administered to all patients, it is not a curative approach and is ...
Passweg, Jakob, Bacigalupo, Andrea
core +1 more source
Abstract Background Allogeneic hematopoietic stem cell transplantation (HSCT) is a treatment primarily for hematological malignancies. Infections, relapse, and graft versus host disease (GvHD) are some of the most common adverse events following HSCT. We aimed to evaluate whether the lymphocyte function of the stem cell graft was associated with these ...
Anna Söderström +8 more
wiley +1 more source
Aplastic Anemia Dataset Almawi
This study investigates the relationship between HLA Class I and Class II alleles and the risk of developing aplastic anemia in the Kazakhstani ...
Almawi, Wassim
core +1 more source
Nanosensor schematic functionalized with specific bioreceptors that produce electrochemical signals upon Chloramphenicol binding. Resulting voltammetric readouts (differential pulse, square‐wave, and cyclic voltammetry) are analyzed to identify and quantify Chloramphenicol.
Nava Moghadasian Niaki +5 more
wiley +1 more source
Management of aplastic anemia [PDF]
C, Nissen, A, Gratwohl, B, Speck
openaire +2 more sources
ABSTRACT The RACE study (NCT02009747) compared horse antithymocyte globulin (hATG) plus cyclosporine A (CsA) ± eltrombopag as initial immunosuppressive treatment (IST) for severe aplastic anemia. Here we report the final 2‐year analysis of this prospective randomized phase III study.
Antonio M. Risitano +52 more
wiley +1 more source
Cutaneous Finding in Anti Thymocyte Globulin Induced Serum Sickness
Polyclonal anti-thymocyte globulin (ATG) is used as an immunosuppressive agent in the treatment of aplastic anemia (AA). Serum sickness is a recognized side effect of ATG.
Seyed Hesamedin Nabavizadeh +2 more
doaj
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli +11 more
wiley +1 more source
ABSTRACT Third allogeneic hematopoietic stem cell transplantation (HSCT3) is rarely performed in pediatric patients and is associated with high toxicity and mortality. Data on outcomes in this setting remain scarce. We conducted a retrospective multicenter study within the Spanish GETH‐TC Pediatric group including 29 children and adolescents who ...
Luisa Sisinni +17 more
wiley +1 more source
Acquired aplastic anemia in children
Catedra Pediatrie nr.2 USMF „Nicolae Testemiţanu”Aplastic anemia in children is one of the major problems of pediatric haematology with imprevisible evolution and consequences followed by complications due to pancytopenia and immune supresion.
Ţurea, Valentin, Popa, Olga
core +1 more source

