172 results on '"Lin, Allison"'
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2. Top-down attention shifts behavioral and neural event boundaries in narratives with overlapping event scripts
3. A “rotating menu” of medical uncertainty for families affected by telomere biology disorders: A qualitative interview study
4. Early outcomes in heart transplantation using donation after circulatory death donors in patients bridged with durable left ventricular assist devices
5. Living with rare genetic disease during the COVID-19 pandemic: A qualitative study of adolescents and young adults with Li-Fraumeni syndrome
6. Family communication challenges of adolescents and young adults with Li-Fraumeni syndrome: Implications for psychosocial care
7. Shifting and intersecting needs: Parents’ experiences during and following the withdrawal of life sustaining treatments in the paediatric intensive care unit
8. Embodied risk for families with Li-Fraumeni syndrome: Like electricity through my body
9. Periodicity significance testing with null-signal templates: reassessment of PTF's SMBH binary candidates.
10. Benefits and burdens of risk management for young people with inherited cancer: A focus on Li-Fraumeni syndrome
11. “I Didnʼt Want My Baby to Pass, But I Didnʼt Want Him Suffering Either”: Comparing Bereaved Parentsʼ Narratives With Nursing End-of-Life Assessments in the Pediatric Intensive Care Unit
12. Reproductive Beliefs Among Families With Li-Fraumeni Syndrome: Generations of Cancer Risk.
13. Actions and Uncertainty : How Prenatally Diagnosed Variants of Uncertain Significance Become Actionable
14. Waiting and “weighted down”: the challenge of anticipatory loss for individuals and families with Li-Fraumeni Syndrome
15. An Observational Study of Children’s Involvement in Informed Consent for Exome Sequencing Research
16. ADHD Diagnosis in Children of Non-US-Born Parents: A Cross-Sectional Analysis.
17. Talking with Children About Adult-Onset Hereditary Cancer Risk: A Developmental Approach for Parents
18. Family Strategies for Living with Rare Disease : The Experience of Cystinosis
19. Reporting of Sample Size Calculations in Analgesic Clinical Trials: ACTTION Systematic Review
20. Data Interpretation in Analgesic Clinical Trials With Statistically Nonsignificant Primary Analyses: An ACTTION Systematic Review
21. Adverse event reporting in nonpharmacologic, noninterventional pain clinical trials: ACTTION systematic review
22. Disclosure of authorship contributions in analgesic clinical trials and related publications: ACTTION systematic review and recommendations
23. Reporting of primary analyses and multiplicity adjustment in recent analgesic clinical trials: ACTTION systematic review and recommendations
24. Gratitude, protective buffering, and cognitive dissonance: How families respond to pediatric whole exome sequencing in the absence of actionable results
25. Discrepancies between registered and published primary outcome specifications in analgesic trials: ACTTION systematic review and recommendations
26. “Something Extra on Chromosome 5”: Parents’ Understanding of Positive Prenatal Chromosomal Microarray Analysis (CMA) Results
27. Balancing Genetics (Science) and Counseling (Art) in Prenatal Chromosomal Microarray Testing
28. Teaching Future Teachers: A Model Workshop for Doctoral Education
29. Adverse event assessment, analysis, and reporting in recent published analgesic clinical trials: ACTTION systematic review and recommendations
30. A standard database format for clinical trials of pain treatments: An ACTTION–CDISC initiative
31. Along the Cancer Continuum: Integrating Therapeutic Support and Bereavement Groups for Children and Teens of Terminally Ill Cancer Patients
32. 'Cancer doesn't have an age': Genetic testing and cancer risk management in BRCA1/2 mutation-positive women aged 18–24
33. “They Canʼt Find Anything Wrong with Him, Yet”: Mothers’ experiences of parenting an infant with a prenatally diagnosed copy number variant (CNV)
34. Adherence to CONSORT harms-reporting recommendations in publications of recent analgesic clinical trials: An ACTTION systematic review
35. That eagle covering me: transitioning and connected autonomy for emerging adults with cystinosis
36. How do young people with a hereditary cancer predisposition syndrome understand and experience cancer survivorship? "With Li‐Fraumeni syndrome, it's just an intermission".
37. Serotonin stimulation of cAMP-dependent plasticity in Aplysia sensory neurons is mediated by calmodulin-sensitive adenylyl cyclase
38. Building the Cancer Family: Family Planning in the Context of Inherited Breast and Ovarian Cancer Risk
39. Meta-Analysis of Assay Sensitivity and Study Features in Clinical Trials of Pharmacologic Treatments for Osteoarthritis Pain
40. 'My funky genetics': BRCA1/2 mutation carriers' understanding of genetic inheritance and reproductive merger in the context of new reprogenetic technologies
41. There’s No Place Like Home: Preparing Children for Geographical and Relational Attachment Disruptions Following Parental Death to Cancer
42. Family illness narratives of inherited cancer risk: continuity and transformation
43. Edible marijuana products and potential risks for pediatric populations.
44. Defining self-disclosure of personal cancer coping experiences in oncology social workers' helping relationships: When cancer "hits home".
45. Nursing Care at End of Life in Pediatric Intensive Care Unit Patients Requiring Mechanical Ventilation.
46. Danger Zones: Risk Perceptions of Young Women From Families With Hereditary Breast and Ovarian Cancer
47. Incorporating information regarding preimplantation genetic diagnosis into discussions concerning testing and risk management for BRCA1/2 mutations: A qualitative study of patient preferences
48. Reproduction and Genetic Responsibility: An Interpretive Description of Reproductive Decision-Making for Young People With Li-Fraumeni Syndrome.
49. Family Identity and Roles in the Context of Li-Fraumeni Syndrome: "No One's Like Us Mutants".
50. Birth Order and Up-to-Date Vaccination Status.
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