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Transfusion clinique et biologique, ISSN 1246-7820, 05/2019, Volume 26, Issue 2, p. 116
Intravascular hemolysis is a hallmark of a large spectrum of diseases, including the sickle cell disease (SCD), and is characterized by liberation of red blood... 
Sickle cell anemia | Heme | Hemolysis and hemolysins
Journal Article
Transfusion clinique et biologique, ISSN 1246-7820, 05/2019, Volume 26, Issue 2, pp. 116 - 124
Intravascular hemolysis is a hallmark of a large spectrum of diseases, including the sickle cell disease (SCD), and is characterized by liberation of red blood... 
Drépanocytose | Hémolyse post-transfusionnelle | Hémolyse intravasculaire | Complement | Complément | Sickle cell disease | Intravascular hemolysis | Hemolytic transfusion reaction | HEMOGLOBIN | IMMUNOLOGY | MOUSE MODELS | INHIBITOR ECULIZUMAB | MEDIATED DEPOSITION | HEME | PATHWAY | ENDOTHELIAL-CELLS | THERAPEUTIC PLASMA-EXCHANGE | PATIENT | HEMATOLOGY | HYPERHEMOLYSIS SYNDROME
Journal Article
Nephrologie et Thérapeutique, ISSN 1769-7255, 09/2019, Volume 15, Issue 5, pp. 282 - 283
Journal Article
Molecular Immunology, ISSN 0161-5890, 12/2013, Volume 56, Issue 3, pp. 289 - 290
Journal Article
Molecular Immunology, ISSN 0161-5890, 2011, Volume 48, Issue 14, pp. 1706 - 1706
Journal Article
Kidney International. Supplement, ISSN 2157-1724, 2017, Volume 91, pp. 539 - 551
In both atypical hemolytic uremic syndrome (aHUS) and C3 glomerulopathy (C3G) complement plays a primary role in disease pathogenesis. Herein we report the... 
Journal Article
Molecular Immunology, ISSN 0161-5890, 2011, Volume 48, Issue 14, pp. 1674 - 1674
Journal Article
Molecular Immunology, ISSN 0161-5890, 2011, Volume 48, Issue 14, pp. 1722 - 1722
Journal Article
Journal Article
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