C. Chenet

发表

The αIIb p.Leu841Met (Cab3a+) polymorphism results in a new human platelet alloantigen involved in neonatal alloimmune thrombocytopenia

Pierre Poulain, V. Jallu, C. Kaplan, 2013, Transfusion.

HPA‐13bw neonatal alloimmune thrombocytopenia and low frequency alloantigens: case report and review of the literature

V. Jallu, C. Kaplan, G. Bertrand, 2007, Transfusion.

A severe case of neonatal thrombocytopenia with a fatal outcome, implicating HPA‐12bw fetomaternal platelet alloimmunization

C. Kaplan, G. Bertrand, F. Bianchi, 2013, Transfusion.

A new efficient tool for non‐invasive diagnosis of fetomaternal platelet antigen incompatibility

W. Vainchenker, D. Drubay, J. Cartron, 2020, British journal of haematology.

Safe fetal platelet genotyping: new developments

C. Kaplan, C. Chenet, Emilie Le Toriellec, 2013, Transfusion.

New mutation in the platelet β3‐integrin gene: implication for the diagnosis of fetomaternal alloimmunization

C. Kaplan, G. Bertrand, F. Bianchi, 2006, Transfusion.

Cab4b, the first human platelet antigen carried by glycoprotein IX discovered in a context of severe neonatal thrombocytopenia

V. Jallu, F. Bianchi, C. Chenet, 2017, Journal of thrombosis and haemostasis : JTH.

New αIIbβ3 variants in 28 Turkish Glanzmann patients; structural hypothesis for complex activation by residues variations in I-EGF domains

A. D. de Brevern, B. Zulfikar, V. Jallu, 2021, Platelets.

HPA‐5 typing discrepancy reveals an Ile503Leu substitution in platelet GPIa (α2 integrin)

V. Jallu, C. Kaplan, G. Bertrand, 2013, Vox sanguinis.