160 results on '"Lehmann, Lisa Soleymani"'
Search Results
2. Patients should be informed when AI systems are used in clinical trials
3. Could Partnerships with Places of Worship Improve COVID-19 Vaccine Access in the US?
4. The Effects of Public Disclosure of Industry Payments to Physicians on Patient Trust: A Randomized Experiment
5. Implementing Goals-of-Care Conversations: Lessons From High- and Low-Performing Sites From a VA National Initiative
6. Early Changes in Rates of Documented Goals-of-Care Conversations in the Veterans Health Administration During the COVID-19 Pandemic
7. Doctors’ duty to provide abortion information
8. Responding to Patients Who Refuse to Wear Masks During the Covid-19 Pandemic
9. Consumer Perspectives on Access to Direct-to-Consumer Genetic Testing: Role of Demographic Factors and the Testing Experience
10. Implementing a Social Needs Screening and Referral Program Among Veterans: Assessing Circumstances & Offering Resources for Needs (ACORN)
11. Gender Wage Disparities in Medicine: Time to Close the Gap
12. Public Awareness of and Contact With Physicians Who Receive Industry Payments: A National Survey
13. A Randomized Trial of Displaying Paid Price Information on Imaging Study and Procedure Ordering Rates
14. How Primary Care Physicians Integrate Price Information into Clinical Decision-Making
15. Biobank Participants' Preferences for Disclosure of Genetic Research Results: Perspectives From the OurGenes, OurHealth, OurCommunity Project
16. Medical Students’ Views and Knowledge of the Affordable Care Act: A Survey of Eight U.S. Medical Schools
17. Discordant Views of Experts and Laypersons on the Adoption of New Fertility Technology
18. A web-based, patient-centered toolkit to engage patients and caregivers in the acute care setting: a preliminary evaluation
19. Effect of Pharmacogenomic Testing for Drug-Gene Interactions on Medication Selection and Remission of Symptoms in Major Depressive Disorder
20. The Ethics Of Medical Education
21. ‘Someday it will be the norm’: physician perspectives on the utility of genome sequencing for patient care in the MedSeqProject
22. Pragmatic, adaptive clinical trials: Is 2020 the dawning of a new age?
23. Responding to Patients Who Refuse to Wear Masks During the Covid-19 Pandemic
24. Informed consent and the process of cadaver donation
25. Heart Failure Dashboard Design and Validation to Improve Care of Veterans
26. IRB perspectives on obligations to disclose genetic incidental findings to research participants
27. Protecting User Privacy and Rights in Academic Data-Sharing Partnerships: Principles From a Pilot Program at Crisis Text Line
28. Physicians as fundraisers: medical philanthropy and the doctor-patient relationship
29. Consumer Perspectives on Access to Direct‐to‐Consumer Genetic Testing: Role of Demographic Factors and the Testing Experience
30. Navigating the research–clinical interface in genomic medicine: analysis from the CSER Consortium
31. Oncofertility: Fertile Ground for Conflict Between Patient Autonomy and Medical Values
32. A Randomized Trial of Displaying Paid Price Information on Imaging Study and Procedure Ordering Rates
33. How Primary Care Physicians Integrate Price Information into Clinical Decision-Making
34. Institutional review board perspectives on obligations to disclose genetic incidental findings to research participants
35. How can we improve amniocentesis decision-making?
36. Is Editing the Genome for Climate Change Adaptation Ethically Justifiable?
37. The Effects of Public Disclosure of Industry Payments to Physicians on Patient Trust: A Randomized Experiment.
38. A web-based, patient-centered toolkit to engage patients and caregivers in the acute care setting: a preliminary evaluation
39. Precision medicine and the FDA's draft guidance on laboratory-developed tests
40. Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between
41. Religious Perspectives on the Use of Psychopharmaceuticals as an Enhancement Technology
42. Patients' perceived utility of whole-genome sequencing for their healthcare: findings from the MedSeq project.
43. Preceding the procedure: Medical devices and shared decision making
44. Population-based study of attitudes toward posthumous reproduction
45. Navigating a research partnership between academia and industry to assess the impact of personalized genetic testing
46. Public perceptions of providing IVF services to cancer and HIV patients
47. Final exam: a surgeon's reflections on mortality
48. A population-based study of Ashkenazi Jewish women’s attitudes toward genetic discrimination and BRCA1/2 testing
49. The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.
50. Preceding the procedure: Medical devices and shared decision making.
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