P22.01: Preliminary investigation of the utility of
, 2016 Anqi Duan +10 more
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Epilepsia, EarlyView.Abstract Objective In women with epilepsy who are treated with antiseizure medications (ASMs), folate concentrations in maternal serum may not be a good indicator of fetal folate supply, because ASMs can interfere with folate handling by the placenta. We aimed to assess the transplacental folate transfer at birth in persons with epilepsy in comparison ...
Erez Berman +6 more
wiley +1 more source
Cell-free fetal DNA: the new tool in fetal medicine. [PDF]
, 2014 Chitty, LS, Everett, TR
core +1 more source
The FEBS Journal, EarlyView.We investigated the role of the signal regulatory protein alpha (SIRPα)/CD47 axis in phagocytosis by disrupting the SIRPA gene in the THP‐1 cell line. The SIRPα KO THP‐1 cells retained their monocyte and macrophage characteristics similar to their wild‐type (WT) counterparts.
Saitong Muneekaew +5 more
wiley +1 more source
Fetal hemoglobin reactivation and cell engineering in the treatment of sickle cell anemia
, 2011 S Eridani, Mosca
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EP20.02: Diagnostic performance of middle cerebral artery peak systolic velocity for fetal severe anemia in advanced gestational age of monochorionic diamniotic twin pregnancy [PDF]
, 2017 Jeong‐Won Oh +5 more
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Recent Progress in Double Filtration Plasmapheresis
Hemodialysis International, EarlyView.ABSTRACT Double‐filtration plasmapheresis is an advanced extracorporeal blood purification technique that selectively removes pathogenic macromolecules based on molecular weight. Unlike conventional plasma exchange, double‐filtration plasmapheresis uses a two‐step filtration process to retain beneficial plasma components such as albumin, while ...
Dan Li +3 more
wiley +1 more source
The Effect of Iron Deficiency Anemia Early in the Third Trimester on Small for Gestational Age and Birth Weight: A Retrospective Cohort Study on Iron Deficiency Anemia and Fetal Weight [PDF]
, 2019 İlknur Çöl Madendağ +7 more
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Molecular Testing in Sickle Cell Disease: From Newborn Screening to Transfusion Care
International Journal of Laboratory Hematology, EarlyView.ABSTRACT Sickle cell disease (SCD) is one of the most frequent monogenic diseases worldwide and a highly heterogeneous and complex disease. SCD care carries several challenges. This includes early and accurate diagnosis as well as optimal red blood cell transfusion matching in this population carrying a high risk of alloimmunization.
Thomas Pincez, Yves D. Pastore
wiley +1 more source