Red Cell Membrane Defects (Chapter 14) - Anemia
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
Frontiers | Improving the EMA Binding Test by Using Commercially Available Fluorescent Beads
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
Evaluation of eosin-5-maleimide flow cytometry test in the diagnosis of hereditary spherocytosis | The Journal of Medical Laboratory Science and Technology of South Africa
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
Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians | Cell Physiol Biochem
KoreaMed
Frontiers | Improving the EMA Binding Test by Using Commercially Available Fluorescent Beads
Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders
Dr. Behzad Poopak, DCLS PhD. - ppt download
Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants | Journal of Perinatology
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 | Semantic Scholar
PDF) Stability of eosin-5'-maleimide dye used in flow cytometric analysis for red cell membrane disorders | Neetu Tyagi - Academia.edu
Delay in the measurement of eosin-5′-maleimide (EMA) binding does not affect the test result for the diagnosis of hereditary spherocytosis
PDF) Flow Cytometric Test with Eosin-5-Maleimide for a Diagnosis of Hereditary Spherocytosis in a Newborn
Advances in laboratory diagnosis of hereditary spherocytosis
Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants | Journal of Perinatology
Eosin‐5‐maleimide binding to band 3 and Rh‐related proteins forms the basis of a screening test for hereditary spherocytosis - King - 2004 - British Journal of Haematology - Wiley Online Library
Flow Cytometric Test with Eosin-5-Maleimide for a Diagnosis of Hereditary Spherocytosis in a Newborn
Analysis of the causes of the misdiagnosis of hereditary spherocytosis
Fluorescence histogram of EMA-labeled RBCs from normal controls and... | Download Scientific Diagram
Improved harmonization of eosin‐5‐maleimide binding test across different instruments and age groups - Agarwal - 2016 - Cytometry Part B: Clinical Cytometry - Wiley Online Library
Analysis of erythrocyte membrane proteins in patients with hereditary spherocytosis and other types of haemolytic anaemia
