A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates
RD Christensen, HM Yaish, PG Gallagher - Pediatrics, 2015 - publications.aap.org
Newborn infants who have hereditary spherocytosis (HS) can develop anemia and
hyperbilirubinemia. Bilirubin-induced neurologic dysfunction is less likely in these neonates …
hyperbilirubinemia. Bilirubin-induced neurologic dysfunction is less likely in these neonates …
[HTML][HTML] Old and new insights into the diagnosis of hereditary spherocytosis
O Ciepiela - Annals of translational medicine, 2018 - ncbi.nlm.nih.gov
Hereditary spherocytosis (HS) belongs to the group of congenital hemolytic anemias
resulting from plasma membrane protein deficiency. When diagnosed too late, HS bares the …
resulting from plasma membrane protein deficiency. When diagnosed too late, HS bares the …
Advances in laboratory diagnosis of hereditary spherocytosis
MG Farias - Clinical Chemistry and Laboratory Medicine (CCLM), 2017 - degruyter.com
Among the red cell membrane disorders, hereditary spherocytosis (HS) is one of the most
common causes of inherited hemolytic anemia. HS results from the deficiency or dysfunction …
common causes of inherited hemolytic anemia. HS results from the deficiency or dysfunction …
[HTML][HTML] Clinical and genetic diagnosis of thirteen Japanese patients with hereditary spherocytosis
KS Yamamoto, T Utshigisawa, H Ogura, T Aoki… - Human Genome …, 2022 - nature.com
Hereditary spherocytosis is the most frequent cause of hereditary hemolytic anemia and is
classified into five subtypes (SPH1-5) according to OMIM. Because the clinical and …
classified into five subtypes (SPH1-5) according to OMIM. Because the clinical and …
Comparison study of the eosin-5′-maleimide binding test, flow cytometric osmotic fragility test, and cryohemolysis test in the diagnosis of hereditary spherocytosis
SH Park, CJ Park, BR Lee, YU Cho… - American journal of …, 2014 - academic.oup.com
Objectives: Current guidelines recommend the eosin-5′-maleimide (EMA) binding test and
cryohemolysis test for screening for hereditary spherocytosis (HS), and the flow cytometric …
cryohemolysis test for screening for hereditary spherocytosis (HS), and the flow cytometric …
Hypoxic exercise training causes erythrocyte senescence and rheological dysfunction by depressed Gardos channel activity
TY Mao, LL Fu, JS Wang - Journal of applied physiology, 2011 - journals.physiology.org
Despite enhancing cardiopulmonary and muscular fitness, the effect of hypoxic exercise
training (HE) on hemorheological regulation remains unclear. This study investigates how …
training (HE) on hemorheological regulation remains unclear. This study investigates how …
Flow cytometric osmotic fragility test and eosin‐5'‐maleimide dye‐binding tests are better than conventional osmotic fragility tests for the diagnosis of hereditary …
RD Arora, J Dass, S Maydeo, V Arya… - International Journal …, 2018 - Wiley Online Library
Introduction Hereditary spherocytosis (HS) is the most common inherited hemolytic anemia
with heterogeneous clinico‐laboratory manifestations. We evaluated the flow‐cytometric …
with heterogeneous clinico‐laboratory manifestations. We evaluated the flow‐cytometric …
[HTML][HTML] Clinical diagnosis of red cell membrane disorders: comparison of osmotic gradient Ektacytometry and eosin Maleimide (EMA) fluorescence test for red cell …
AU Zaidi, S Buck, M Gadgeel… - Frontiers in …, 2020 - frontiersin.org
The measurement of band 3 (AE1, SLC4A1, CD233) content of red cells by eosin-5-
maleimide (EMA) staining is swiftly replacing conventional osmotic fragility (OF) test as a tool …
maleimide (EMA) staining is swiftly replacing conventional osmotic fragility (OF) test as a tool …
Flow cytometric osmotic fragility—an effective screening approach for red cell membranopathies
Background: Among the red cell membrane disorders, hereditary spherocytosis (HS) is one
of the most common causes of inherited hemolytic anemia. The aim of this study was to …
of the most common causes of inherited hemolytic anemia. The aim of this study was to …
Toward the harmonization of result presentation for the eosin‐5′‐maleimide binding test in the diagnosis of hereditary spherocytosis
L Hunt, D Greenwood, H Heimpel… - Cytometry Part B …, 2015 - Wiley Online Library
Background The eosin‐5′‐maleimide (EMA) Binding test measures reduced mean
channel fluorescence (MCF) reading of EMA‐labeled red cells (EMA‐RBCs) from patients …
channel fluorescence (MCF) reading of EMA‐labeled red cells (EMA‐RBCs) from patients …