4 Pathophysiology of thalassaemia-Reference-Cited by-同舟云学术

4 Pathophysiology of thalassaemia

Published:1998-03 Issue:1 Volume:11 Page:127-146
ISSN:0950-3536
Container-title:Baillière's Clinical Haematology
language:en
Short-container-title:Baillière's Clinical Haematology

Author:

Weatherall D.J.

Publisher

Elsevier BV

Subject

Hematology

Reference83 articles.

1. Characterization and comparison of the red blood cell membrane damage in severe human alpha- and beta-thalassemia;Advani;Blood,1992

2. Abnormal assembly of membrane proteins in erythroid progenitors of patients with beta-thalassemia major;Aljurf;Blood,1996

3. The contribution of hypogonadism to the development of osteoporosis in thalassaemia major: new therapeutic approaches;Anapliotou;Clinical Endocrinology,1995

4. Serum immunoreactive erythropoietin level: a new parameter for monitoring transfusion management of thalassaemia;André;Nouvelle Revue Française d'Hématologie,1991

5. Progressive dysfunction of monocytes associated with iron overload and age in patients with thalassemia major;Ballart;Blood,1986

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