Literature DB >> 22170767

A de novo band 3 mutation in hereditary spherocytosis.

Hannah H Bogardus, Yelena D Maksimova, Bernard G Forget, Patrick G Gallagher.   

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Year:  2011        PMID： 22170767     DOI： 10.1002/pbc.23400

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN： 1545-5009            Impact factor:   3.167


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  5 in total

Review 1.  A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates.

Authors:  Robert D Christensen; Hassan M Yaish; Patrick G Gallagher
Journal:  Pediatrics       Date:  2015-06       Impact factor: 7.124

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

Authors:  R D Christensen; A M Agarwal; R H Nussenzveig; N Heikal; M A Liew; H M Yaish
Journal:  J Perinatol       Date:  2014-11-06       Impact factor: 2.521

Review 3.  New insights on hereditary erythrocyte membrane defects.

Authors:  Immacolata Andolfo; Roberta Russo; Antonella Gambale; Achille Iolascon
Journal:  Haematologica       Date:  2016-10-18       Impact factor: 9.941

Review 4.  Old and new insights into the diagnosis of hereditary spherocytosis.

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

5.  Effect of primary lesions in cytoskeleton proteins on red cell membrane stability in patients with hereditary spherocytosis.

Authors:  Cristina Vercellati; Anna Paola Marcello; Bruno Fattizzo; Anna Zaninoni; Agostino Seresini; Wilma Barcellini; Paola Bianchi; Elisa Fermo
Journal:  Front Physiol       Date:  2022-08-12       Impact factor: 4.755
  5 in total

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