Results 101 to 110 of about 27,928 (247)
Transfusion, EarlyView.Abstract Background Platelet transfusion refractoriness (PTR) is a major challenge in transfusion medicine and may result from both immune and non‐immune mechanisms. Although alloantibodies are well‐established contributors, Fc‐independent pathways such as platelet desialylation have emerged as alternative mechanisms of clearance.
Karen Ziza +11 more
wiley +1 more source
Acute hepatitis as a prequel to very severe aplastic anemia [PDF]
, 2018 Severe aplastic anemia is a rare and potentially life-threatening disease of the bone marrow often requiring allogeneic hematopoietic stem cell transplantation. Pathogenesis of the disease can vary and often remains enigmatic.
Christoph Schramm +8 more
core +1 more source
Journal of Medical Case Reports, 2010 Introduction Hepatitis-associated aplastic anemia is a common syndrome in patients with bone marrow failure. However, hepatitis-associated aplastic anemia is an immune-mediated disease that does not appear to be caused by any of the known hepatitis ...
Ioannou Savvas +3 more
doaj +1 more source
Transfusion, EarlyView.Abstract Background The aim of this study was to investigate a CD34 expression assay as an additional tool for the total nucleated cell (TNC) count assessment in bone marrow harvest (BMH) obtained from healthy donors. Study Design and Methods Samples obtained from bone marrow donors (n = 71) were analyzed for CD34 expression using a digital PCR assay ...
Miguel Waterhouse +13 more
wiley +1 more source
Analytical Science Advances, Volume 7, Issue 2, December 2026.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
Late Cytomegalovirus Infections After Allogeneic Hematopoietic Cell Transplant
American Journal of Hematology, Volume 101, Issue 8, Page 1828-1838, August 2026.ABSTRACT Graft versus host disease (GVHD) prophylaxis with posttransplant cyclophosphamide (ptCY) and cytomegalovirus (CMV) prophylaxis with letermovir have changed the clinical epidemiology of CMV infection. We studied the incidence, risk factors for, and outcomes of CMV infection after Day + 90 of allogeneic hematopoietic cell transplant (alloHCT ...
George L. Chen +15 more
wiley +1 more source
Idiopathic Intracranial Hypertension (IHH) in Aplastic Anemia [PDF]
, 2010 IHH has been described in patients with different types of anemia: ferropenic, pernicious, hemolytic, paroxysmal nocturnal hemoglobinuria and aplastic ...
Bernardo Sánchez-Dalmau; Mercedes Vázquez-Barrero; M. D. Vela-Payan; Alfredo Adan; Víctor LLorens
core
American Journal of Hematology, Volume 101, Issue 8, Page 1856-1865, August 2026.ABSTRACT Diamond–Blackfan Anemia Syndrome (DBAS) is a rare congenital anemia often requiring chronic red blood cell transfusions from infancy. Without appropriate chelation, iron overload develops early and may be severe; however, no data are available on chelation in patients under 3 years of age.
Francesca Torchio +19 more
wiley +1 more source
eJHaem, Volume 7, Issue 4, August 2026.ABSTRACT Introduction Sickle cell disease involves acute and chronic complications requiring timely recognition and multidisciplinary care. General internal medicine (GIM) physicians often manage affected adults with limited exposure and few supports.
Anas Samman +5 more
wiley +1 more source
Congenital Toxoplasmosis with Aplastic Anemia: A Rare Association [PDF]
, 2021 Congenital toxoplasmosis is caused by transmission of an intracellular obligate coccidian protozoan (Toxoplasma gondii) via vertical transmission during pregnancy.
MANASVIN SAREEN +4 more
core +1 more source