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Ethnicity & Disease
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January 1, 2020
Access and Management: Indigenous Perspectives on Genomic Data Sharing
Nanibaa' A Garrison, Krysta S Barton, Kathryn M Porter, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
May 5, 2022
Ethical Considerations in Balancing Use of Seclusion and Restraint With Risk of COVID-19 Exposure: Recommendations for Youth Inpatient Psychiatry Units
Alysha D Thompson, Emily R Berkman, Shannon W Simmons, et al.
The Journal of Infectious Diseases
|
February 10, 2004
Dihydrofolate reductase mutations in Plasmodium vivax from Indonesia and therapeutic response to sulfadoxine plus pyrimethamine
Michele D Hastings, Kathryn M Porter, Jason D Maguire, et al.
JAMA Network Open
|
August 1, 2020
Assessing Parent Decisions About Child Participation in a Behavioral Health Intervention Study and Utility of Informed Consent Forms
Stephanie A Kraft, Kathryn M Porter, Devan M Duenas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 3, 2024
Genetic research within Indigenous communities: Engagement opportunities and pathways forward
Krysta S Barton, Kathryn M Porter, Thyvu Mai, et al.
Journal of Clinical and Translational Science
|
January 2, 2023
Relationship building in pediatric research recruitment: Insights from qualitative interviews with research staff
Stephanie A Kraft, Kathryn M Porter, Tara R Sullivan, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
November 24, 2023
Experiences and preferences for learning about neonatal research: insights from parent interviews
Elliott Mark Weiss, Kathryn M Porter, Ellie Oslin, et al.
Clinical Trials (London, England)
|
September 15, 2016
A randomized study of multimedia informational aids for research on medical practices: Implications for informed consent
Stephanie A Kraft, Melissa Constantine, David Magnus, et al.
American Journal of Medical Genetics. Part A
|
December 19, 2017
Patient perspectives on the use of categories of conditions for decision making about genomic carrier screening results
Stephanie A Kraft, Carmit K McMullen, Kathryn M Porter, et al.
The Journal of Pediatrics
|
March 16, 2024
Motivations for and against Participation in Neonatal Research: Insights from Interviews of Diverse Parents Approached for Neonatal Research in the United States
Elliott Mark Weiss, Pamela K Donohue, Susan H Wootton, et al.
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of 5
Search research articles
Search
Showing results (11-20 of 41) with videos related to
Sort By:
Page
of 5
Ethnicity & Disease
|
January 1, 2020
Access and Management: Indigenous Perspectives on Genomic Data Sharing
Nanibaa' A Garrison, Krysta S Barton, Kathryn M Porter, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
May 5, 2022
Ethical Considerations in Balancing Use of Seclusion and Restraint With Risk of COVID-19 Exposure: Recommendations for Youth Inpatient Psychiatry Units
Alysha D Thompson, Emily R Berkman, Shannon W Simmons, et al.
The Journal of Infectious Diseases
|
February 10, 2004
Dihydrofolate reductase mutations in Plasmodium vivax from Indonesia and therapeutic response to sulfadoxine plus pyrimethamine
Michele D Hastings, Kathryn M Porter, Jason D Maguire, et al.
JAMA Network Open
|
August 1, 2020
Assessing Parent Decisions About Child Participation in a Behavioral Health Intervention Study and Utility of Informed Consent Forms
Stephanie A Kraft, Kathryn M Porter, Devan M Duenas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 3, 2024
Genetic research within Indigenous communities: Engagement opportunities and pathways forward
Krysta S Barton, Kathryn M Porter, Thyvu Mai, et al.
Journal of Clinical and Translational Science
|
January 2, 2023
Relationship building in pediatric research recruitment: Insights from qualitative interviews with research staff
Stephanie A Kraft, Kathryn M Porter, Tara R Sullivan, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
November 24, 2023
Experiences and preferences for learning about neonatal research: insights from parent interviews
Elliott Mark Weiss, Kathryn M Porter, Ellie Oslin, et al.
Clinical Trials (London, England)
|
September 15, 2016
A randomized study of multimedia informational aids for research on medical practices: Implications for informed consent
Stephanie A Kraft, Melissa Constantine, David Magnus, et al.
American Journal of Medical Genetics. Part A
|
December 19, 2017
Patient perspectives on the use of categories of conditions for decision making about genomic carrier screening results
Stephanie A Kraft, Carmit K McMullen, Kathryn M Porter, et al.
The Journal of Pediatrics
|
March 16, 2024
Motivations for and against Participation in Neonatal Research: Insights from Interviews of Diverse Parents Approached for Neonatal Research in the United States
Elliott Mark Weiss, Pamela K Donohue, Susan H Wootton, et al.
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of 5