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4. Discordant pathologic diagnoses of myelodysplastic neoplasms and their implications for registries and therapies

5. Cancer Informatics for Cancer Centers (CI4CC): Building a Community Focused on Sharing Ideas and Best Practices to Improve Cancer Care and Patient Outcomes.

13. Examining disparities in large‐scale patient‐reported data capture using digital tools among cancer patients at clinical intake

14. Oncology Providers' and Professionals' Experiences With Suicide Risk Screening Among Patients With Head and Neck Cancer: A Qualitative Study

17. Health-Related Quality of Life and Vulnerability among People with Myelodysplastic Syndromes: A US National Study

18. Telemedicine Adoption in an NCI-Designated Cancer Center During the COVID-19 Pandemic: A Report on Patient Experience of Care

22. Supplementary Data from Cutaneous Human Papillomaviruses and the Risk of Keratinocyte Carcinomas

26. Advancing Digital Health Innovation in Oncology: Priorities for High-Value Digital Transformation in Cancer Care

30. Demographic disparities in receipt of care at a comprehensive cancer center.

39. Current and Emerging Informatics Initiatives Impactful to Cancer Registries

47. Longitudinal patient-reported outcomes and survival among early-stage non-small cell lung cancer patients receiving stereotactic body radiotherapy

48. Natural History of Incident and Persistent Cutaneous Human Papillomavirus and Human Polyomavirus Infections

50. Enabling Precision Medicine in Cancer Care Through a Molecular Data Warehouse: The Moffitt Experience

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