Literature DB >> 9668569

Hemoglobin E/beta thalassemia: the Canadian experience.

M Fouladi1, M L Macmillan, E Nisbet-Brown, N Klein, J Barlas, J S Waye, N F Olivieri.   

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Year:  1998        PMID： 9668569     DOI： 10.1111/j.1749-6632.1998.tb10506.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN： 0077-8923            Impact factor:   5.691


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  2 in total

1.  Does Profile of Hemoglobin Eβ-thalassemia Patients Change After Splenectomy? Experience of a Tertiary Thalassemia Care Centre in Eastern India.

Authors:  Prakas Kumar Mandal; Malay Kumar Ghosh; Maitreyee Bhattacharyya
Journal:  Indian J Hematol Blood Transfus       Date:  2015-01-13       Impact factor: 0.900

2.  Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait.

Authors:  Emma Jones; Sant-Rayn Pasricha; Angela Allen; Patricia Evans; Chris A Fisher; Katherine Wray; Anuja Premawardhena; Dyananda Bandara; Ashok Perera; Craig Webster; Pamela Sturges; Nancy F Olivieri; Timothy St Pierre; Andrew E Armitage; John B Porter; David J Weatherall; Hal Drakesmith
Journal:  Blood       Date:  2014-12-17       Impact factor: 22.113
  2 in total

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