Literature DB >> 23204481

Testing for hereditary spherocytosis: a French experience.

Caroline Mayeur-Rousse, Mélanie Gentil, Jérémie Botton, Madeleine Fénéant Thibaut, Corinne Guitton, Véronique Picard.   

Abstract

Entities:  

Mesh：

Year:  2012        PMID： 23204481      PMCID： PMC3590076          DOI： 10.3324/haematol.2012.074070

Source DB:  PubMed          Journal:  Haematologica        ISSN： 0390-6078            Impact factor:   9.941


× No keyword cloud information.
  7 in total

1.  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.

Authors:  François Girodon; Loïc Garçon; Emilie Bergoin; Marie Largier; Jean Delaunay; Madeleine Fénéant-Thibault; Marc Maynadié; Gérard Couillaud; Sophie Moreira; Thérèse Cynober
Journal:  Br J Haematol       Date:  2007-12-19       Impact factor: 6.998

2.  Erythrocyte membrane protein destabilization versus clinical outcome in 160 Portuguese Hereditary Spherocytosis patients.

Authors:  Susana Rocha; Elísio Costa; Petronila Rocha-Pereira; Fátima Ferreira; Esmeralda Cleto; José Barbot; Alexandre Quintanilha; Luís Belo; Alice Santos-Silva
Journal:  Br J Haematol       Date:  2010-03-21       Impact factor: 6.998

3.  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

4.  Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update.

Authors:  Paula H B Bolton-Maggs; Jacob C Langer; Achille Iolascon; Paul Tittensor; May-Jean King
Journal:  Br J Haematol       Date:  2011-11-05       Impact factor: 6.998

5.  A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5'-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocytosis families in Argentina.

Authors:  Renée L Crisp; Liliana Solari; Daiana Vota; Eliana García; Gabriela Miguez; Maria E Chamorro; Gabriel A Schvartzman; Graciela Alfonso; Daniel Gammella; Sergio Caldarola; Cecilia Riccheri; Daniela Vittori; Belen Venegas; Alcira Nesse; Hugo Donato
Journal:  Ann Hematol       Date:  2010-11-16       Impact factor: 3.673

6.  Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia.

Authors:  M J King; J Behrens; C Rogers; C Flynn; D Greenwood; K Chambers
Journal:  Br J Haematol       Date:  2000-12       Impact factor: 6.998

7.  Hereditary spherocytosis.

Authors:  Silverio Perrotta; Patrick G Gallagher; Narla Mohandas
Journal:  Lancet       Date:  2008-10-18       Impact factor: 79.321
  7 in total
  2 in total

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

Authors:  Lydie Da Costa; Ludovic Suner; Julie Galimand; Amandine Bonnel; Tiffany Pascreau; Nathalie Couque; Odile Fenneteau; Narla Mohandas
Journal:  Blood Cells Mol Dis       Date:  2015-09-16       Impact factor: 3.039

Review 2.  Old and new insights into the diagnosis of hereditary spherocytosis.

Authors:  Olga Ciepiela
Journal:  Ann Transl Med       Date:  2018-09
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.