N Sun, H Yu, H Wu, X Shen, C Deng - TrAC Trends in Analytical Chemistry, 2021 - Elsevier
The biological compositions including cells, proteins/peptides, nucleic acids, extracellular vesicles (EVs) and metabolites are no doubt closely related to almost all physiological and …
The American Society for Apheresis (ASFA) JCA Special Issue Writing Committee is charged with reviewing, updating and categorizating indications for therapeutic apheresis …
ST Chou, T Jackson, S Vege… - Blood, The Journal …, 2013 - ashpublications.org
Red blood cell (RBC) transfusion is a key treatment of patients with sickle cell disease (SCD) but remains complicated by RBC immunization. In the present study, we evaluated the …
Transfusions can be a life-saving treatment of patients with sickle-cell disease (SCD). However, availability of matched units can be limiting because of distinctive blood group …
TN Williams, SL Thein - Annual review of genomics and human …, 2018 - annualreviews.org
In the 100 years since sickle cell anemia (SCA) was first described in the medical literature, studies of its molecular and pathophysiological basis have been at the vanguard of scientific …
G Daniels - British journal of haematology, 2013 - Wiley Online Library
Anti‐D (‐RH 1) of the Rh blood group system is clinically important as it causes haemolytic transfusion reactions and haemolytic disease of the fetus and newborn. Although most …
VM Pinto, M Balocco, S Quintino, GL Forni - Internal and emergency …, 2019 - Springer
Sickle cell disease (SCD) is the most important hemoglobinopathy worldwide in terms of frequency and social impact, recently recognized as a global public health problem by the …
NH Roubinian, SE Reese, H Qiao, C Plimier, F Fang… - JCI insight, 2022 - ncbi.nlm.nih.gov
BACKGROUND RBC transfusion effectiveness varies due to donor, component, and recipient factors. Prior studies identified characteristics associated with variation in …
C Moriconi, M Dzieciatkowska, M Roy… - British journal of …, 2022 - Wiley Online Library
Sickle cell disease (SCD) is an inherited blood disorder characterized by sickled red blood cells (RBCs), which are more sensitive to haemolysis and can contribute to disease …