82 results on '"Ross, Lainie Friedman"'
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2. Revise the Uniform Determination of Death Act to Align the Law With Practice Through Neurorespiratory Criteria
3. 50 Years Ago in The Journal of Pediatrics: Editorial Comment: Therapeutic Orphans
4. Threading the Needle for the Tiniest Babies
5. 50 Years Ago in The Journal of Pediatrics: Conference on Treatment of Phenylketonuria
6. Gender Differences in the Authorship of Original Research in Pediatric Journals, 2001–2016
7. To tell or not to tell: attitudes of transplant surgeons and transplant nephrologists regarding the disclosure of recipient information to living kidney donors
8. Age and Equity in Liver Transplantation: An Organ Allocation Model
9. Racial disparities in reaching the renal transplant waitlist: is geography as important as race?
10. The OHRP and SUPPORT
11. Outcomes After Kidney Donation
12. Decision making in liver transplantation—Limited application of the liver donor risk index
13. Pediatric Professionalsʼ Attitudes about Secondary Findings in Genomic Sequencing of Children
14. Young Physiciansʼ Recall about Pediatric Training in Ethics and Professionalism and Its Practical Utility
15. Premature guidance about whole-genome sequencing
16. Mandatory Extended Searches in All Genome Sequencing: “Incidental Findings,” Patient Autonomy, and Shared Decision Making
17. Newborns and Other Children: In Defense of Differential Attitudes and Treatment
18. Should Age be a Factor in the Allocation of Deceased Donor Kidneys: Age Should Not Be Considered in the Allocation of Deceased Donor Kidneys
19. Comparison of Serum Phenylalanine Levels with Growth in Guthrieʼs Inhibition Assay in Newborn Infants
20. Identification of Heterozygotes with Phenylketonuria on Basis of Blood Tyrosine Responses
21. Mass Screening for Phenylketonuria
22. Parents: Critical Stakeholders in Expanding Newborn Screening
23. Attitudes of African-American parents about biobank participation and return of results for themselves and their children
24. Newborn screening for lysosomal storage diseases: an ethical and policy analysis
25. Biobank participation and returning research results: Perspectives from a deliberative engagement in South Side Chicago
26. A Re–Examination of the Use of Ethnicity in Prenatal Carrier Testing
27. In further defense of the American Academy of Pediatrics Committee on Bioethics “children as hematopoietic stem cell donors” statement
28. A pilot study to determine whether health care professionals perceive stigma in heterozygote carrier identification and disclosure decisions
29. Are we adequately protecting vulnerable patients in longitudinal observational studies?
30. Risk, Prognosis, and Unintended Consequences in Kidney Allocation
31. In defense of the American Academy of Pediatrics Policy Statement—Children as Hematopoietic Stem Cell Donors
32. A Pilot Study to Evaluate Knowledge and Attitudes of Illinois Pediatricians toward Newborn Screening for Sickle Cell Disease and Cystic Fibrosis
33. Are We Ready to Expand Donation after Cardiac Death to the Newborn Population?
34. An Ethical and Policy Analysis of Elective Transplantation for Metabolic Conditions Diagnosed by Newborn Screening
35. THE PEDIATRIC FORUM
36. CLINICAL AND ETHICAL CONSIDERATIONS IN MANAGING CARRIER DETECTION
37. Hypoplastic Left Heart Syndrome: A Paradigm Case for Examining Conscientious Objection in Pediatric Practice
38. From Genetics to Genomics: Ethics, Policy, and Parental Decision-making
39. Long-Term Consequences of Kidney Donation
40. Fragile X Screening: Attitudes of Genetic Health Professionals
41. Ethical and policy lessons to be learned from a family with inherited bone marrow failure
42. Paediatriciansʼ attitudes and practices towards HPV vaccination
43. Newborn Screening for Cystic Fibrosis A Lesson in Public Health Disparities
44. Ethical and policy issues in pediatric genetics
45. Empirical data about womenʼs attitudes towards a hypothetical pediatric biobank
46. Empirical data about womenʼs attitudes toward a biobank focused on pregnancy outcomes
47. Ethics of Hematopoietic Stem Cell Transplantation in Type 1 Diabetes Mellitus
48. Against Newborn Screening for Type 1 Diabetes
49. The participation of children in nontherapeutic diabetes research in the US
50. Growth Attenuation by Commission and Omission May Be Ethically Justifiable in Children With Profound Disabilities
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