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1. Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States

3. BAY 81–8973 safety and efficacy for prophylaxis and treatment of bleeds in previously treated children with severe haemophilia A: results of the LEOPOLD Kids Trial

7. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura

13. Clinical and molecular variability in congenital dyserythropoietic anaemia type I

22. Data Coming out of the Human Inhibitor PUP Study (HIPS) Reveal 4 Subgroups of Patients with Distinct Antibody Signatures

24. Longitudinal Antibody Signatures Following FVIII Replacement Therapy in Previously Untreated Patients with Severe Hemophilia Α- New Insights from the Hemophilia Inhibitor PUP Study (HIPS)

25. Appearance of High-Affinity Antibodies Precedes Clinical Diagnosis of FVIII Inhibitors - Preliminary Analysis from the Hemophilia Inhibitor PUP Study (HIPS)

28. Evidence for the transmission of parvovirus B19 in patients with bleeding disorders treated with plasma-derived factor concentrates in the era of nucleic acid test screening

31. Atypical haemolytic uraemic syndrome in a patient with sickle cell disease, successfully treated with eculizumab.

32. Integrin αIIb-Mediated PI3K/Akt Activation in Platelets

33. Continued Transmission of Parvovirus B19 in Plasma-Derived Factor Concentrates After the Implementation of B19 Nucleic Acid Plasma Minipool Screening,

36. Integrated analysis of safety and efficacy of a plasma- and albumin-free recombinant factor VIII (rAHF-PFM) from six clinical studies in patients with hemophilia A

39. A Phase II Open-Label Study Evaluating Hemostatic Activity, Pharmacokinetics and Safety of Recombinant Porcine Factor VIII (OBI-1) in Hemophilia A Patients with Alloantibody Inhibitors Directed Against Human FVIII.

46. Therapeutic choices for patients with hemophilia and high-titer inhibitors

48. Therapeutic choices for patients with hemophilia and high‐titer inhibitors

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