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Author/Creator Aloui, Chaker

12. Molecular genetic diagnosis of Tunisian Glanzmann thrombasthenia patients reveals a common nonsense mutation in the ITGA2B gene that seems to be specific for the studied population. Issue 8 (December 2018)

Authors:
Aloui, Chaker; Chakroun, Tahar; Granados, Viviana; Jemni-Yacoub, Saloua; Fagan, Jocelyne; Khelif, Abderrahim; Kahloul, Najoua; Hammami, Sabeur; Chkioua, Latifa; Barlier, Céline; Cognasse, Fabrice; Laradi, Sandrine; Garraud, Olivier
Journal:
Blood coagulation and fibrinolysis
Issue:
Volume 29:Issue 8(2018)
Page Start:
Record Type:
Journal Article
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16. Platelet components associated with adverse reactions: predictive value of mitochondrial DNA relative to biological response modifiers. Issue 2 (7th October 2015)

Authors:
Cognasse, Fabrice; Aloui, Chaker; Anh Nguyen, Kim; Hamzeh‐Cognasse, Hind; Fagan, Jocelyne; Arthaud, Charles‐Antoine; Eyraud, Marie‐Ange; Sebban, Marc; Fromont, Elisa; Pozzetto, Bruno; Laradi, Sandrine; Garraud, Olivier
Journal:
Transfusion
Issue:
Volume 56:Issue 2(2016:Feb.)
Page Start:
497
Record Type:
Journal Article
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20. Soluble CD40L and CD62P levels differ in single‐donor apheresis platelet concentrates and buffy coat–derived pooled platelet concentrates. Issue 1 (6th October 2018)

Authors:
Sut, Caroline; Tariket, Sofiane; Aloui, Chaker; Arthaud, Charles‐Antoine; Eyraud, Marie‐Ange; Fagan, Jocelyne; Chavarin, Patricia; Hamzeh‐Cognasse, Hind; Laradi, Sandrine; Garraud, Olivier; Cognasse, Fabrice
Journal:
Transfusion
Issue:
Volume 59:Issue 1(2019)
Page Start:
16
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗