Results 91 to 100 of about 4,672,487 (214)
ABSTRACT This retrospective, single‐center study aimed to characterize clonal dynamics of GPI‐deficient cells in patients with paroxysmal nocturnal hemoglobinuria (PNH) or PNH/aplastic anemia (AA) syndrome using multiparameter flow cytometry including FLAER.
Sandra M. Frey +6 more
wiley +1 more source
RETICULOCYTE COUNTS AS A BIOMARKER FOR PAIN CRISES IN SICKLE CELL ANEMIA
Sickle cell anemia (SCA) is a hemolytic disorder characterized by reduced red blood cell lifespan due to repeated sickling processes. Patients have complications as a consequence of hemolysis, vaso-occlusion, inflammation, and endothelial dysfunction ...
CC Guarda +9 more
doaj +1 more source
Evaluating RET-Hb vs Hb in Predicting Early Response in Oral Iron Therapy: A Prospective Interventional Study [PDF]
Introduction: Children are more vulnerable to anaemia due to their rapid growth, which requires an expanding erythroid mass and a high tissue iron demand.
Benita Mary Mathew +4 more
doaj +1 more source
Reticulocyte Parameter Analysis in the Automated Haematology Analyzer used in the Laboratories
Background: Reticulocyte count with immature reticulocyte fraction (IRF) used in the laboratories to evaluate the bone marrow erythropoietic activity and have great diagnostic and prognostic importance in the treatment of anemias and other pathological conditions.
AN Nashimuddin Ahmed +4 more
openaire +2 more sources
What Is Your Diagnosis? Abnormal WNR Scattergram From the Sysmex XN‐1000V in a Dog
Veterinary Clinical Pathology, EarlyView.
Javier Martínez‐Caro +3 more
wiley +1 more source
Acute Neurological Events in Children With Hemoglobin SC Disease: A Multicenter Retrospective Study
ABSTRACT Introduction Neurological manifestations in children with hemoglobin SC (HbSC) disease remain insufficiently characterized, particularly regarding acute events. The aim of this study was to describe the spectrum and frequency of acute neurological events in a multicenter cohort of children with HbSC disease.
Célia Paulmin +11 more
wiley +1 more source
Iron deficiency and heterozygous beta-thalassemia are important causes of hypochromic-microcytic anemia. Two laboratory parameters are suggested for the differentiation of such anemia.
Gisélia Aparecida Freire Maia de Lima +1 more
doaj +1 more source
Acute lymphoblastic leukemia (ALL) is the most common childhood malignancy in Bangladesh. ALL is treated with chemotherapy due to high responsiveness. After chemotherapy infection may occur which increases the time of aplasia.
T Sultana +5 more
core +1 more source
ANK1 and EPB41 Variants and The Risk of Glucocorticoid‐Induced Osteonecrosis
Objective Steroid‐induced osteonecrosis of the femoral head (SONFH) is a refractory skeletal disorder influenced by genetic and environmental factors. However, conclusive pathogenic genetic evidence remains elusive due to the limited exploration of rare damaging variants. In this study, we aimed to identify rare variants associated with SONFH.
Shengbao Chen +21 more
wiley +1 more source
ERYTHROCYTE AND RETICULOCYTE INDICES IN PATIENTS WITH INFLAMMATORY DISEASES OF DIVERSE GENESIS
Use of the latest blood analyzers with a capacity of differentiated determination of reticulocyte and erythrocyte blood indices in modern diagnostic service is an important addition to detection of anemia syndrome.
O. B. Gordeeva +2 more
doaj +1 more source

