Effects of alpha thalassaemia and haemoglobin F (HbF) level on the clinical severity of sickle-cell anaemia-Reference-Cited by-同舟云学术

Effects of alpha thalassaemia and haemoglobin F (HbF) level on the clinical severity of sickle-cell anaemia

Published:2009-04-24 Issue:1 Volume:52 Page:13-15
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:

Author:

Falusi A. G.,Olatunji P. O.

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1994.tb01278.x/fullpdf

Reference21 articles.

1. Esan GJF. The clinical spectrum of sickle cell anaemia in Nigerian adults Fleming AF La Drepanocytose/Sickle cell anaemia. Les Editions de l'inserum 1975 43 50

2. Clinical Diversity of Sickle Cell anaemia: Genetic and Cellular Modulation of Disease Severity;Steinberg;Am J Haematol,1983

3. Foetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood;Steven;J Paediatr,1981

4. HbF levels. Longevity of Homozygotes and Clinical course of Sickle Cell anaemia in Brazil;Hutz;Am J Med Genet,1983

5. The Relationship between Fetal Hemoglobin and Disease Severity in Children with Sickle Cell Anaemia;Odenheimer;Am J Med Genet,1987

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