Literature DB >> 20512576

A new ankyrin mutation (ANK1 EXON E9X) causing severe hereditary spherocytosis in the neonatal period.

Florian Gundel, Stefan Eber, Axel Heep.   

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Year:  2010        PMID： 20512576     DOI： 10.1007/s00277-010-0989-y

Source DB:  PubMed          Journal:  Ann Hematol        ISSN： 0939-5555            Impact factor:   3.673


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  4 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

3.  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

4.  Severe hyperbilirubinemia in a neonate with hereditary spherocytosis due to a de novo ankyrin mutation: A case report.

Authors:  Jun-Fang Wang; Li Ma; Xiao-Hui Gong; Cheng Cai; Jing-Jing Sun
Journal:  World J Clin Cases       Date:  2021-07-06       Impact factor: 1.337
  4 in total

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