Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte | Orphanet Journal of Rare Diseases | Full Text
Using the eosin‐5‐maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis - King - 2008 - Cytometry Part B: Clinical Cytometry - Wiley Online Library
Hereditary Spherocytosis | Concise Medical Knowledge
Analysis of erythrocyte membrane proteins in patients with hereditary spherocytosis and other types of haemolytic anaemia
Using the eosin‐5‐maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis - King - 2008 - Cytometry Part B: Clinical Cytometry - Wiley Online Library
Frontiers | Clinical Diagnosis of Red Cell Membrane Disorders: Comparison of Osmotic Gradient Ektacytometry and Eosin Maleimide (EMA) Fluorescence Test for Red Cell Band 3 (AE1, SLC4A1) Content for Clinical Diagnosis
Frontiers | Improving the EMA Binding Test by Using Commercially Available Fluorescent Beads
Reliability of EMA Binding Test in the Diagnosis of Hereditary Spherocytosis in Italian Patients | Semantic Scholar
Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants | Journal of Perinatology
Reply to “Flow cytometry test for hereditary spherocytosis”. Haematologica. 2012;97(12):e47 | Haematologica
COMBINED EMA-BINDING TEST AND OSMOTIC GRADIANT EKTACYTOMETRY.... EHA Library. Glenthøj A. Jun 16 2018; 215449
Testing for hereditary spherocytosis: a French experience | Haematologica
تويتر \ Uriel Suárez على تويتر: "Esferocitosis hereditaria / Hereditary Spherocytosis. * EMA binding test: the sensitivity and specificity of the test appear to be in the ranges of 93 to 96
Red Cell Membrane Defects (Chapter 14) - Anemia
Eosin-5'-maleimide test. (A) Red blood cells are gated in gate "RBCs",... | Download Scientific Diagram
Advances in laboratory diagnosis of hereditary spherocytosis
Delay in the measurement of eosin-5′-maleimide (EMA) binding does not affect the test result for the diagnosis of hereditary spherocytosis
KoreaMed
Hematology Reports | Free Full-Text | Detection of Red Blood Cell Membrane Proteins in Myelodysplastic Syndromes Using Eosin-5-Maleimide (EMA) Staining by Flow Cytometry
Dr. Behzad Poopak, DCLS PhD. - ppt download
Flow Cytometric Eosin-5′-Maleimide Test is a Sensitive Screen for Hereditary Spherocytosis | SpringerLink
Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants | Journal of Perinatology
Fluorescence histogram of EMA-labeled RBCs from normal controls and... | Download Scientific Diagram
Premium Photo | Ema binding assay test or a flow cytometric test widely used to detect hereditary spherocytosis
Flow Cytometric Test with Eosin-5-Maleimide for a Diagnosis of Hereditary Spherocytosis in a Newborn
