Results 141 to 150 of about 38,246 (331)
Machine Learning‐Based Detection of HbS and HbC Carriers in the UK General Population
eJHaem, Volume 6, Issue 6, December 2025.ABSTRACT Background Haemoglobin S (HbS) and C (HbC) are the most important sickling variants on the African continent, imposing major health burdens. Early detection of carrier status is crucial but often hindered by resource limitations. Objectives To develop machine learning (ML) models to accurately classify HbS and HbC carriers using readily ...
Frederik Christensen +7 more
wiley +1 more source
Towards a proteomics meta-classification [PDF]
, 2004 that can serve as a foundation for more refined ontologies in the field of proteomics. Standard data sources classify proteins in terms of just one or two specific aspects.
Kumar, Anand, Smith, Barry
core +1 more source
Journal of Laboratory Physicians, 2018 CONTEXT: Hemoglobinopathies constitute the world's most common genetically inherited red blood cell disorder. Screening and accurate identification of hemoglobin (Hb) variants have become increasingly important in antenatal diagnosis and prevention of Hb
Sandeep Warghade +9 more
semanticscholar +1 more source
eJHaem, Volume 6, Issue 6, December 2025.ABSTRACT Introduction Treatment with luspatercept may improve transfusion requirements in transfusion‐dependent thalassemia (TDT), but the improved erythroid maturation in the bone marrow influences body iron distribution. Case Report We report on sequential organ iron measurements in a TDT patient under luspatercept treatment.
Matthias Bleeke +6 more
wiley +1 more source
, 2017 This article answers the question: My patient carries a diagnosis of chronic anemia and has been treated for irondeficiency in the past with minimal to no improvement.
Coberly, Emily, Ringling, Rebecca
core
Pediatric Blood &Cancer, Volume 72, Issue 12, December 2025.ABSTRACT Background Hemorrhagic cystitis (HC) is a frequent and potentially severe complication following hematopoietic stem cell transplantation (HSCT) in children. It significantly affects the quality of life and prolongs hospitalization. Despite its frequency, no standardized management guidelines exist.
Pauline Mazilier +8 more
wiley +1 more source
Table of Contents, Volume Six, 1970 [PDF]
, 1970 Table of contents for MCV/Q, Medical College of Virginia Quarterly, 1970, Volume ...
core +1 more source
Pediatric Blood &Cancer, Volume 72, Issue 12, December 2025.ABSTRACT Background Pediatric patients with inherited or acquired bone marrow failure syndromes (BMFS) often require an allogeneic hematopoietic stem cell transplant (HSCT) to cure the hematological manifestations. Amongst these, those without a matched sibling donor (MSD), are at increased risk for graft failure and are known to tolerate graft‐versus ...
Zahra Hudda +7 more
wiley +1 more source