Hereditary Spherocytosis and Related Disorders-Reference-Cited by-同舟云学术

Hereditary Spherocytosis and Related Disorders

Published:1985-02 Issue:1 Volume:14 Page:15-43
ISSN:0308-2261
Container-title:Clinics in Haematology
language:en
Short-container-title:Clinics in Haematology

Author:

Becker Pamela S.,Lux Samuel E.

Publisher

Elsevier BV

Subject

Oncology,Hematology

Reference173 articles.

1. Deficient red-cell spectrin in severe, recessively inherited spherocytosis;Agre;New England Journal of Medicine,1982

2. Spectrin deficiency is common to all forms of hereditary spherocytosis (HS); the degree of deficiency correlates with osmotic fragility;Agre;Blood,1983

3. Kinetics of red cell membrane phosphorylation: altered affinity of HS membrane protein acceptors;Ali;British Journal of Haematology,1979

4. Increased membrane binding of erythrocyte catalase in hereditary spherocytosis and in metabolically stressed normal cells;Allen;Blood,1977

5. Elevated microviscosity in membranes of erythrocytes affected by hereditary spherocytosis;Aloni;British Journal of Haematology,1975

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1. Quantitative assessment of sensing and sequestration of spherocytic erythrocytes by the human spleen;Blood;2012-07-12

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3. Shape and Biomechanical Characteristics of Human Red Blood Cells in Health and Disease;MRS Bulletin;2010-05

4. OUTCOME OF SPLENECTOMY IN RECESSIVELY AND DOMINANTLY INHERITED HEREDITARY SPHEROCYTOSIS: To the Editor:;European Journal of Haematology;2009-04-24

5. Red cell membrane alteration involving protein 4.1 and protein 3 in a case of recessively inherited haemolytic anaemia;European Journal of Haematology;2009-04-24