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3. Health Equity Requires Working Toward Antiracist Local Public Health Departments.

11. Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities in health services; diversity, equity, and inclusion; and implementation science

12. Applying anti-racist approaches to informatics: a new lens on traditional frames.

23. Respecting Autonomy and Enabling Diversity: The Effect of Eligibility and Enrollment on Research Data Demographics

26. How do you solve a problem like Maria? The politics of disaster response in Puerto Rico, Florida and Texas.

28. A Call to Action: Moving the Scientific Publication Process toward Social Justice

31. Paper-based microchip electrophoresis for point-of-care hemoglobin testing

32. Racism is an ethical issue for healthcare artificial intelligence

35. Racism and the Textures of Visibility.

37. State-based surveillance for selected hemoglobinopathies

40. Sickle Cell Disease

41. Public Health Implications of Sickle Cell Trait

44. Factor VIII and Factor IX Mutation Analysis in 600 U.S. Hemophilia Patients: Correlation of Mutation Type with History of Inhibitor

45. Experience with a Modified Nijmegen-Bethesda Method for Measurement of Inhibitors in Hemophilia Patients: The CDC Inhibitor Surveillance Pilot Project.

50. Sickle Cell Disease: The Need for a Public Health Agenda

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