Literature DB >> 21251470

Hereditary red cell membrane defects: diagnostic and clinical aspects.

Wilma Barcellini1, Paola Bianchi, Elisa Fermo, Francesca G Imperiali, Anna P Marcello, Cristina Vercellati, Anna Zaninoni, Alberto Zanella.   

Abstract

Mesh：

Year:  2011        PMID： 21251470      PMCID： PMC3136593          DOI： 10.2450/2011.0086-10

Source DB:  PubMed          Journal:  Blood Transfus        ISSN： 1723-2007            Impact factor:   3.443


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  13 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.  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

Review 3.  Red cell membrane: past, present, and future.

Authors:  Narla Mohandas; Patrick G Gallagher
Journal:  Blood       Date:  2008-11-15       Impact factor: 22.113

4.  Splenectomy in hereditary spherocytosis: Review of 1,657 patients and application of the pediatric quality indicators.

Authors:  Fizan Abdullah; Yiyi Zhang; Melissa Camp; Mark I Rossberg; Melinda A Bathurst; Paul M Colombani; James F Casella; Rosemary Nabaweesi; David C Chang
Journal:  Pediatr Blood Cancer       Date:  2009-07       Impact factor: 3.167

5.  Eosin-5-maleimide binding to band 3 and Rh-related proteins forms the basis of a screening test for hereditary spherocytosis.

Authors:  May-Jean King; Jonathan S Smythe; Rosey Mushens
Journal:  Br J Haematol       Date:  2004-01       Impact factor: 6.998

Review 6.  Hereditary stomatocytosis and cation-leaky red cells--recent developments.

Authors:  Lesley J Bruce
Journal:  Blood Cells Mol Dis       Date:  2009-03-03       Impact factor: 3.039

7.  The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein.

Authors:  Lesley J Bruce; Hélène Guizouarn; Nicholas M Burton; Nicole Gabillat; Joyce Poole; Joanna F Flatt; R Leo Brady; Franck Borgese; Jean Delaunay; Gordon W Stewart
Journal:  Blood       Date:  2008-10-17       Impact factor: 22.113

8.  Hereditary spherocytosis.

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

9.  Laparoscopic partial vs total splenectomy in children with hereditary spherocytosis.

Authors:  Julia Morinis; Sanjeev Dutta; Victor Blanchette; Sheila Butchart; Jacob C Langer
Journal:  J Pediatr Surg       Date:  2008-09       Impact factor: 2.545

10.  Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders.

Authors:  P S Kedar; R B Colah; S Kulkarni; K Ghosh; D Mohanty
Journal:  Clin Lab Haematol       Date:  2003-12
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  21 in total

1.  Identification of new mutations in patients with hereditary spherocytosis by next-generation sequencing.

Authors:  Li Qin; Yanbo Nie; Hong Zhang; Long Chen; Donglei Zhang; Yani Lin; Kun Ru
Journal:  J Hum Genet       Date:  2020-01-24       Impact factor: 3.172

Review 2.  The role of the red blood cell in host defence against falciparum malaria: an expanding repertoire of evolutionary alterations.

Authors:  Morgan M Goheen; Susana Campino; Carla Cerami
Journal:  Br J Haematol       Date:  2017-08-23       Impact factor: 6.998

3.  The coincidence of familial mediterranean Fever and hypereosinophilia in a patient with hereditary elliptocytosis.

Authors:  Muzaffer Keklik; Ali Unal; Serdar Sivgin; Olgun Kontas; Eray Eroglu; Semih Yilmaz; Leylagul Kaynar; Bulent Eser; Mustafa Cetin
Journal:  Indian J Hematol Blood Transfus       Date:  2013-08-27       Impact factor: 0.900

4.  Screening for hereditary spherocytosis in daily practice: what is the best algorithm using erythrocyte and reticulocyte parameters?

Authors:  Anne-Sophie Adam; Frédéric Cotton; Brigitte Cantinieaux; Sara Benyaich; Béatrice Gulbis
Journal:  Ann Hematol       Date:  2022-04-22       Impact factor: 3.673

5.  A novel SPTB mutation causes hereditary spherocytosis via loss-of-function of β-spectrin.

Authors:  Shan Li; Ping Guo; Leyuan Mi; Xiaojing Chai; Kewang Xi; Ting Liu; Li Lu; Juan Li
Journal:  Ann Hematol       Date:  2022-01-31       Impact factor: 3.673

Review 6.  Delivery of drugs bound to erythrocytes: new avenues for an old intravascular carrier.

Authors:  Carlos H Villa; Daniel C Pan; Sergei Zaitsev; Douglas B Cines; Donald L Siegel; Vladimir R Muzykantov
Journal:  Ther Deliv       Date:  2015-07

7.  Clinical utility of targeted gene enrichment and sequencing technique in the diagnosis of adult hereditary spherocytosis.

Authors:  Jun Xue; Qing He; Xiaojing Xie; Ailing Su; Shibin Cao
Journal:  Ann Transl Med       Date:  2019-10

8.  Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis.

Authors:  Fei Xie; Lei Lei; Bin Cai; Lu Gan; Yu Gao; Xiaoying Liu; Lin Zhou; Jinjin Jiang
Journal:  Mol Genet Genomic Med       Date:  2021-02-23       Impact factor: 2.183

9.  Mean corpuscular volume of control red blood cells determines the interpretation of eosin-5'-maleimide (EMA) test result in infants aged less than 6 months.

Authors:  Olga Ciepiela; Anna Adamowicz-Salach; Weronika Bystrzycka; Jan Łukasik; Iwona Kotuła
Journal:  Ann Hematol       Date:  2015-04-25       Impact factor: 3.673

Review 10.  Zebrafish erythropoiesis and the utility of fish as models of anemia.

Authors:  Kasem Kulkeaw; Daisuke Sugiyama
Journal:  Stem Cell Res Ther       Date:  2012-12-20       Impact factor: 6.832
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