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Literature DB >> 18162119

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.

François Girodon, Loïc Garçon, Emilie Bergoin, Marie Largier, Jean Delaunay, Madeleine Fénéant-Thibault, Marc Maynadié, Gérard Couillaud, Sophie Moreira, Thérèse Cynober.

Abstract

Entities: Chemical Disease

Mesh：

Substances：

Year: 2007 PMID： 18162119 DOI： 10.1111/j.1365-2141.2007.06944.x

Source DB: PubMed Journal: Br J Haematol ISSN： 0007-1048 Impact factor: 6.998

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16 in total

1. A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis.

Authors: Michael R Hughes; Nicole Anderson; Steven Maltby; Justin Wong; Zorana Berberovic; Connie S Birkenmeier; D James Haddon; Kamal Garcha; Ann Flenniken; Lucy R Osborne; S Lee Adamson; Janet Rossant; Luanne L Peters; Mark D Minden; Robert F Paulson; Chen Wang; Dwayne L Barber; Kelly M McNagny; William L Stanford
Journal: Exp Hematol Date: 2010-12-28 Impact factor: 3.084

Review 2. Hereditary red cell membrane defects: diagnostic and clinical aspects.

Authors: Wilma Barcellini; Paola Bianchi; Elisa Fermo; Francesca G Imperiali; Anna P Marcello; Cristina Vercellati; Anna Zaninoni; Alberto Zanella
Journal: Blood Transfus Date: 2011-01-13 Impact factor: 3.443

3. Testing for hereditary spherocytosis: a French experience.

Authors: Caroline Mayeur-Rousse; Mélanie Gentil; Jérémie Botton; Madeleine Fénéant Thibaut; Corinne Guitton; Véronique Picard
Journal: Haematologica Date: 2012-12 Impact factor: 9.941

4. Flow cytometry test for hereditary spherocytosis.

Authors: Géraud Mackiewicz; François Bailly; Bernardine Favre; Julien Guy; Marc Maynadié; François Girodon
Journal: Haematologica Date: 2012-12 Impact factor: 9.941

5. Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics.

Authors: Paola Bianchi; Elisa Fermo; Cristina Vercellati; Anna P Marcello; Laura Porretti; Agostino Cortelezzi; Wilma Barcellini; Alberto Zanella
Journal: Haematologica Date: 2011-11-04 Impact factor: 9.941

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.

1. A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis.

Review 2. Hereditary red cell membrane defects: diagnostic and clinical aspects.

3. Testing for hereditary spherocytosis: a French experience.

4. Flow cytometry test for hereditary spherocytosis.

5. Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics.

6. Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants.

7. Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer.

Review 8. Old and new insights into the diagnosis of hereditary spherocytosis.

9. Stability of eosin-5'-maleimide dye used in flow cytometric analysis for red cell membrane disorders.

10. Characterization of ENU-induced Mutations in Red Blood Cell Structural Proteins.