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1. Anti‐HI can cause a severe delayed hemolytic transfusion reaction with hyperhemolysis in sickle cell disease patients. Issue 7 (3rd May 2016)

2. Complement activation in sickle cell disease: Dependence on cell density, hemolysis and modulation by hydroxyurea therapy. Issue 5 (19th February 2020)

3. Cytokine changes in sickle-cell disease patients as markers predictive of the onset of delayed hemolytic transfusion reactions. (December 2020)

4. Evidence of benefits from using fresh and cryopreserved blood to transfuse patients with acute sickle cell disease. Issue 7 (17th May 2016)

5. Incidence and predictive score for delayed hemolytic transfusion reaction in adult patients with sickle cell disease. Issue 12 (31st October 2017)

6. Individual red blood cell fetal hemoglobin quantification allows to determine protective thresholds in sickle cell disease. Issue 11 (25th August 2020)

7. New molecular basis associated with CD36‐negative phenotype in the sub‐Saharan African population. Issue 11 (19th September 2020)

8. Predisposing factors for anti‐D immune response in D− patients with chronic liver disease transfused with D+ platelet concentrates. Issue 4 (3rd January 2019)

9. Red blood cell Thomsen‐Friedenreich antigen expression and galectin‐3 plasma concentrations in Streptococcus pneumoniae–associated hemolytic uremic syndrome and hemolytic anemia. Issue 6 (30th December 2014)

10. Red blood cells for transfusion in patients with sepsis: respective roles of unit age and exposure to recipient plasma. Issue 8 (31st May 2017)