Literature DB >> 12452474

Normal growth and development following in utero diagnosis and treatment of homozygous alpha-thalassaemia.

Karen Sohan1, Martin Billington, Derwood Pamphilon, Nicholas Goulden, Phillipa Kyle.   

Abstract

Mesh：

Year:  2002        PMID： 12452474     DOI： 10.1046/j.1471-0528.2002.01051.x

Source DB:  PubMed          Journal:  BJOG        ISSN： 1470-0328            Impact factor:   6.531


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  6 in total

Review 1.  Haemolytic disease of the newborn.

Authors:  Neil A Murray; Irene A G Roberts
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2007-03       Impact factor: 5.747

Review 2.  An international registry of survivors with Hb Bart's hydrops fetalis syndrome.

Authors:  Duantida Songdej; Christian Babbs; Douglas R Higgs
Journal:  Blood       Date:  2017-01-05       Impact factor: 22.113

Review 3.  Hydrops fetalis caused by homozygous alpha-thalassemia and Rh antigen alloimmunization: report of a survivor and literature review.

Authors:  Divya-Devi Joshi; H James Nickerson; Michael J McManus
Journal:  Clin Med Res       Date:  2004-11

Review 4.  Regulation of iron absorption in hemoglobinopathies.

Authors:  Gideon Rechavi; Stefano Rivella
Journal:  Curr Mol Med       Date:  2008-11       Impact factor: 2.222

5.  Gene therapy in thalassemia and hemoglobinopathies.

Authors:  Laura Breda; Roberto Gambari; Stefano Rivella
Journal:  Mediterr J Hematol Infect Dis       Date:  2009-11-13       Impact factor: 2.576

6.  Recent advances in gene therapy for thalassemia.

Authors:  J V Raja; M A Rachchh; R H Gokani
Journal:  J Pharm Bioallied Sci       Date:  2012-07
  6 in total

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