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4. Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC

17. Normal B cells express ZAP70 in chronic lymphocytic leukemia: A link between autoimmunity and lymphoproliferation?

22. A gain-of-function variant in the Wiskott-Aldrich syndrome gene is associated with a MYH9-related disease-like syndrome

26. Chirurgie des hernies ventrales : nouvelles approches minimalement invasives

32. Atypical focal segmental glomerulosclerosis associated with a new PODXL nonsense variant

33. Correction: An essential role for α4A-tubulin in platelet biogenesis

34. The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology

40. Influence of anionic ligands (X) on the nature and magnetic properties of dinuclear LCuGdX (sub)3.nH (sub)2 O complexes (LH (sub)2 standing for tetradentate Schiff base ligands deriving from 2-hydroxy-3-methoxybenzaldehyde and X being Cl, N (sub)3 C (sub)2, and CF (sub)3 COO)

41. Structures and magnetic properties of two novel dinuclear complexes with a mu-phenolato-mu-oximato (Cu,Gd) core

42. Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk disorders. In patients the SPATA-DVT with inherited study platelet

44. High prevalence of the natural Asn89Asp mutation in the GP1BB gene associated with Bernard–Soulier syndrome in French patients from the genetic isolate of Reunion Island

47. Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT Study

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