Congenital sideroblastic anaemia in two girls.

Author:

Dolan G,Reid M M

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference6 articles.

1. Hereditary sideroblastic anaemia and autosomal inheritance of erythrocyte dimorphism in a Dutch family;van Waveren Hogervorst GD; van Roermund HPC; PJ, Snijders;Eur J Haematol,1987

2. Familial sideroblastic anaemia: problem of X. and X chromosome inactivation;Weatherall, D.J.; Pembrey, M.E.; Hall, E.G.;Lancet,1970

3. Desferrioxamine and systemic yersiniosis;Robins-Browne, R.M.; Prpic, J.K.;Lancet,1983

4. The Thalassemias;Nienhuis, A.W.; Wolfe, L.,1987

5. Multiple enzymatic defects in mitochondria in hematological cells of patients with primary sideroblastic anemia;Aoki, Y.;J Clin Invest,1980

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1. Characteristics of participants with self-reported hemochromatosis or iron overload at HEIRS study initial screening;American Journal of Hematology;2008-02

2. A Case of Hereditary Sideroblastic Anemia;The Korean Journal of Hematology;2005

3. Sideroblastic anaemias;British Journal of Haematology;2002-03

4. Congenital sideroblastic anaemia successfully treated using allogeneic stem cell transplantation;British Journal of Haematology;2001-06

5. Sideroblastic Anemia: A Mitochondrial Disorder;Journal of Pediatric Hematology/Oncology;1997-07

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