Haemolysis and abnormal haemorheology in sickle cell anaemia

Author:

Connes Philippe1234,Lamarre Yann13,Waltz Xavier13,Ballas Samir K.5,Lemonne Nathalie67,Etienne-Julan Maryse67,Hue Olivier4,Hardy-Dessources Marie-Dominique13,Romana Marc13

Affiliation:

1. UMR Inserm 1134; Université des Antilles et de la Guyane; Pointe-à-Pitre Guadeloupe France

2. Institut Universitaire de France; Paris France

3. Laboratory of Excellence GR-Ex (The red cell: from genesis to death); PRES Sorbonne Paris Cité; Paris France

4. Laboratoire ACTES (EA 3596); Département de Physiologie; Université des Antilles et de la Guyane; Pointe-à-Pitre Guadeloupe France

5. Cardeza Foundation for Hematologic Research; Department of Medicine; Thomas Jefferson University; Philadelphia PA USA

6. Unité Transversale de la Drépanocytose; Centre Hospitalier et Universitaire de Pointe-à-Pitre; Pointe-à-Pitre Guadeloupe France

7. Centre de référence maladies rares pour la drépanocytose aux Antilles-Guyane; Centre Hospitalier et Universitaire de Pointe-à-Pitre; Pointe-à-Pitre Guadeloupe France

Publisher

Wiley

Subject

Hematology

Reference44 articles.

1. Effect of alpha-globin genotype on the pathophysiology of sickle cell disease;Ballas;Pediatric Pathology & Molecular Medicine,2001

2. Rheologic predictors of the severity of the painful sickle cell crisis;Ballas;Blood,1988

3. Erythrocyte density in sickle cell syndromes is associated with specific clinical manifestations and hemolysis;Bartolucci;Blood,2012

4. Effect of superoxide anions on red blood cell rheologic properties;Baskurt;Free Radical Biology & Medicine,1998

5. Hemorheology and vascular control mechanisms;Baskurt;Clinical Hemorheology and Microcirculation,2004

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