ORIGINAL ARTICLE: Evaluation of mean sphered corpuscular volume for predicting hereditary spherocytosis
Author:
Publisher
Wiley
Subject
Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine
Reference8 articles.
1. A fortuitous finding of a routine screening test for hereditary spherocytosis;Chiron;Hematology and Cell Therapy,1999
2. Prevalence of increased osmotic fragility of erythrocytes in German blood donors: screening using a modified glycerol lysis test;Eber;Annals of Hematology,1992
3. Usefulness of the eosin-5′-maleimide cytometric method as a first-line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein electrophoresis;Girodon;British Journal of Haematology,2008
4. Experience with eosin-5′-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders;Kedar;Clinical and Laboratory Haematology,2003
5. Eosin-5-maleimide binding to band 3 and Rh-related proteins forms the basis of a screening test for hereditary spherocytosis;King;British Journal of Haematology,2004
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1. Hereditary Spherocytosis Caused by a Novel Compound Heterozygous Mutation of SPTA1 and Autoimmune Hepatitis in a Pediatric Patient;Iranian Journal of Pediatrics;2023-02-22
2. Hereditary Spherocytosis Misdiagnosed as Glucose-6-Phosphate Dehydrogenase Deficiency;The Misdiagnosis Casebook in Clinical Medicine;2023
3. Screening for hereditary spherocytosis in daily practice: what is the best algorithm using erythrocyte and reticulocyte parameters?;Annals of Hematology;2022-04-22
4. Influence of diabetes and hypercholesterolemia on laboratory methods for hereditary spherocytosis diagnosis;Journal of Clinical Laboratory Analysis;2022-01-26
5. Disorders of red cells and platelets;Blood Cells;2021-12-31
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