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3. Etranacogene dezaparvovec gene therapy for haemophilia B (HOPE-B): 24-month post-hoc efficacy and safety data from a single-arm, multicentre, phase 3 trial

6. Vascular Anomalies

7. Etranacogene dezaparvovec gene therapy for haemophilia B (HOPE-B): 24-month post-hoc efficacy and safety data from a single-arm, multicentre, phase 3 trial

10. Treatment practices and response in kaposiform hemangioendothelioma: A multicenter cohort study.

11. Vascular Anomalies

13. Hematologic outcomes after total splenectomy and partial splenectomy for congenital hemolytic anemia

14. Gene Therapy with Etranacogene Dezaparvovec for Hemophilia B

15. Gene Therapy with Etranacogene Dezaparvovec for Hemophilia B

19. A case of bruising and joint hypermobility: The need to consider genetic testing for platelet disorders.

24. Clinical outcomes of splenectomy in children: Report of the splenectomy in congenital hemolytic anemia registry

26. Long‐term biological effects in sickle cell disease: insights from a post‐crizanlizumab study

29. A Phase 3 Study of Eltrombopag Vs. Standard First-Line Management for Newly Diagnosed Immune Thrombocytopenia in Children: Trial in Progress Update

43. Second‐line treatments in children with immune thrombocytopenia: Effect on platelet count and patient‐centered outcomes

46. Physician decision making in selection of second-line treatments in immune thrombocytopenia in children

48. Physician Factors Determining Treatment Decisions in Selecting Second Line Agents for Pediatric ITP

49. Comparison of Bleeding Tools in a Cohort of Pediatric Patients with ITP: Data from the Pediatric ITP Consortium of North America ICON1 Study

50. Clinical Characteristics and Quality of Life of Children with ITP Starting Second Line Treatments: Data from the ITP Consortium of North America ICON1 Study

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