347 results on '"Tarini, Beth A."'
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2. DNA data offers benefits many of us will never realise
3. Clusters of adverse childhood experiences and unmet need for care coordination
4. Emerging challenges in lysosomal newborn screening: A multi-state cohort analyzing the benefits and harms of uncertain prognoses
5. Comparison of Video, App, and Standard Consent Processes on Decision-Making for Biospecimen Research : A Randomized Controlled Trial
6. Pediatric Home Blood Pressure Monitoring: Feasibility and Concordance With Clinic-Based Manual Blood Pressure Measurements
7. Vulnerable Child Syndrome and Newborn Screening Carrier Results for Cystic Fibrosis or Sickle Cell
8. 493: FOOD INSECURITY IN THE PEDIATRIC INTENSIVE CARE UNIT
9. The Krabbe Conundrum Is Really a Newborn Screening Conundrum
10. An Assessment of a Shortened Consent Form for the Storage and Research Use of Residual Newborn Screening Blood Spots
11. An Assessment of Public Preferences for Newborn Screening Using Best–Worst Scaling
12. Misclassification of VLCAD carriers due to variable confirmatory testing after a positive NBS result
13. The american pediatric society and society for pediatric research joint statement against racism and social injustice
14. Correction: The american pediatric society and society for pediatric research joint statement against racism and social injustice
15. Systems Integration: The Next Frontier in Newborn-Screening Timeliness
16. Newborn Screening Collection and Delivery Processes in Michigan Birthing Hospitals: Strategies to Improve Timeliness
17. Measuring high‐risk parents' opinions about direct‐to‐consumer genetic testing for adult‐onset inherited cancer syndromes in their adolescent and young adult children
18. Primary Care Providers' Initial Evaluation of Children with Global Developmental Delay: A Clinical Vignette Study
19. Healthcare team communication training in the United States: A scoping review.
20. Justice, Equity, Diversity, and Inclusion in the Pediatric Faculty Research Workforce: Call to Action.
21. Survey of family history taking and genetic testing in pediatric practice
22. Parent and Public Interest in Whole-Genome Sequencing
23. Screening Practices for Identifying Type 2 Diabetes in Adolescents
24. Biobank participant support of newborn screening for disorders with variable treatment and intervention options
25. Elevated Parental Stress Is Associated With Lower Self-Efficacy in Provider Communication During a Pandemic
26. Parents’ Experiences and Needs Regarding Infant Sickle Cell Trait Results
27. Pediatrician Adherence to Guidelines for Diagnosis and Management of High Blood Pressure
28. Healthcare team communication training in the United States: A scoping review
29. Genomics and Newborn Screening: Perspectives of Public Health Programs
30. 493: FOOD INSECURITY IN THE PEDIATRIC INTENSIVE CARE UNIT
31. The Effect of BabySeq on Pediatric and Genomic Research—More Than Baby Steps
32. Effects of Undergoing Multiplex Genetic Susceptibility Testing on Parent Attitudes towards Testing Their Children
33. Effect of “Pink Eye” Label on Parentsʼ Intent to Use Antibiotics and Perceived Contagiousness
34. Associations between adverse childhood experiences and need and unmet need for care coordination
35. Correction: The american pediatric society and society for pediatric research joint statement against racism and social injustice
36. Primary Care Providersʼ Experiences Notifying Parents of Cystic Fibrosis Newborn Screening Results
37. Anticipating the arrival of low-penetrance genetic testing to primary care medicine
38. The Value of Cognitive Pretesting: Improving Validity and Revealing Blind Spots through the Development of a Newborn Screening Parent Experiences Survey
39. Genetic services and attitudes in primary care pediatrics
40. State newborn screening in the tandem mass spectrometry era: more tests, more false-positive results
41. Effects of Hypothetical Type 2 Diabetes Genetic Testing on Parentsʼ Efforts to Prevent Diabetes in Children
42. Personalized medicine in primary care: the need for relevance
43. Lessons that newborn screening in the USA can teach us about biobanking and large-scale genetic studies
44. Does presentation format at the pediatric academic societies' annual meeting predict subsequent publication?
45. A Policy Impact Analysis of the Mandatory NCAA Sickle Cell Trait Screening Program
46. Communicating With Parents About Newborn Screening: The Skill of Eliciting Unspoken Emotions
47. Response to the Commentary: Children and Predictive Genomic Testing
48. Commentary: Children and Predictive Genomic Testing: Disease Prevention, Research Protection, and Our Future
49. Genetic Screening
50. Genetic Testing and Youth Sports
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