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5. Factor VIII trafficking to CD4+ T cells shapes its immunogenicity and requires several types of antigen-presenting cells

6. Advances in Clinical and Basic Science of Coagulation: Illustrated abstracts of the 9th Chapel Hill Symposium on Hemostasis

9. Enhanced procoagulant activity of select hemophilia B causing factor IX variants with emicizumab

11. Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65-mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial

12. Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: facilitating research through infrastructure, workforce, resources and funding

17. Long-Term Durable FVIII Expression with Improvements in Bleeding Rates Following AAV-Mediated FVIII Gene Transfer for Hemophilia A: Multiyear Follow-up on the Phase I/II Trial of SPK-8011

22. Total Knee Arthroplasty after Gene Therapy for Hemophilia B

23. Hemophilia B Gene Therapy with a High-Specific-Activity Factor IX Variant

26. Design and Benchmarking of a Network-In-the-Loop Simulation for Use in a Hardware-In-the-Loop System

27. Plain language summary for the manuscript: Factor IX assay discrepancies in the setting of liver gene therapy using a hyperfunctional variant factor IX-Padua

29. Multiyear Factor VIII Expression after AAV Gene Transfer for Hemophilia A

30. Follow-up of More Than 5 Years in a Cohort of Patients with Hemophilia B Treated with Fidanacogene Elaparvovec Adeno-Associated Virus Gene Therapy

39. Housing for people with serious mental illness: challenges for system-level community development

41. Current Clinical Applications of In Vivo Gene Therapy with AAVs

45. Core data set on safety, efficacy, and durability of hemophilia gene therapy for a global registry: Communication from the SSC of the ISTH

46. Long-Term Follow-Up of the First in Human Intravascular Delivery of AAV for Gene Transfer: AAV2-hFIX16 for Severe Hemophilia B

49. Efficacy and Safety in 15 Hemophilia B Patients Treated with the AAV Gene Therapy Vector Fidanacogene Elaparvovec and Followed for at Least 1 Year

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