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Complementary Therapies in Medicine
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March 10, 2020
Vitamin D supplementation and pain-related emergency department visits in children with sickle cell disease
Anna M Hood, Charles T Quinn, Christopher D King, et al.
Pediatric Blood & Cancer
|
April 2, 2026
Clinical Practice Patterns for Discussing Hydroxyurea Initiation With Families of Children With Sickle Cell Disease
Aimee K Hildenbrand, Amy Lang, Anna M Hood, et al.
Ethnicity & Health
|
September 8, 2020
The influence of perceived racial bias and health-related stigma on quality of life among children with sickle cell disease
Anna M Hood, Lori E Crosby, Eva Hanson, et al.
Neuroimage. Clinical
|
September 8, 2019
White and gray matter brain development in children and young adults with phenylketonuria
Zoë Hawks, Anna M Hood, Dov B Lerman-Sinkoff, et al.
Clinical Trials (London, England)
|
February 16, 2023
Using the consolidated framework for implementation research to identify recruitment barriers and targeted strategies for a shared decision-making randomized clinical trial in pediatric sickle cell disease
Heather Strong, Anna M Hood, Yolanda Johnson, et al.
Clinical Psychology Review
|
March 3, 2026
Building resilience to chronic pain during childhood: The Situate - Experience - Learn - Feel (SELF) Framework
Sarah B Wallwork, Tanja Hechler, Anja C Feneberg, et al.
Pediatric Blood & Cancer
|
July 4, 2019
Higher executive abilities following a blood transfusion in children and young adults with sickle cell disease
Anna M Hood, Allison A King, Melanie E Fields, et al.
Pain Medicine (Malden, Mass.)
|
March 16, 2021
Pain-Related Injustice Appraisals in Youth with Sickle Cell Disease: A Preliminary Investigation
Megan M Miller, Deanna D Rumble, Adam T Hirsh, et al.
Translational Behavioral Medicine
|
May 5, 2021
Mobile health use predicts self-efficacy and self-management in adolescents with sickle cell disease
Anna M Hood, Cara Nwankwo, Ashley Walton, et al.
Journal of Racial and Ethnic Health Disparities
|
December 9, 2024
Pain-Related Injustice Appraisals, Sickle Cell Stigma, and Racialized Discrimination in the Youth with Sickle Cell Disease: A Preliminary Investigation
Megan M Miller, Ama Kissi, Deanna D Rumble, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 40) with videos related to
Sort By:
Page
of 4
Complementary Therapies in Medicine
|
March 10, 2020
Vitamin D supplementation and pain-related emergency department visits in children with sickle cell disease
Anna M Hood, Charles T Quinn, Christopher D King, et al.
Pediatric Blood & Cancer
|
April 2, 2026
Clinical Practice Patterns for Discussing Hydroxyurea Initiation With Families of Children With Sickle Cell Disease
Aimee K Hildenbrand, Amy Lang, Anna M Hood, et al.
Ethnicity & Health
|
September 8, 2020
The influence of perceived racial bias and health-related stigma on quality of life among children with sickle cell disease
Anna M Hood, Lori E Crosby, Eva Hanson, et al.
Neuroimage. Clinical
|
September 8, 2019
White and gray matter brain development in children and young adults with phenylketonuria
Zoë Hawks, Anna M Hood, Dov B Lerman-Sinkoff, et al.
Clinical Trials (London, England)
|
February 16, 2023
Using the consolidated framework for implementation research to identify recruitment barriers and targeted strategies for a shared decision-making randomized clinical trial in pediatric sickle cell disease
Heather Strong, Anna M Hood, Yolanda Johnson, et al.
Clinical Psychology Review
|
March 3, 2026
Building resilience to chronic pain during childhood: The Situate - Experience - Learn - Feel (SELF) Framework
Sarah B Wallwork, Tanja Hechler, Anja C Feneberg, et al.
Pediatric Blood & Cancer
|
July 4, 2019
Higher executive abilities following a blood transfusion in children and young adults with sickle cell disease
Anna M Hood, Allison A King, Melanie E Fields, et al.
Pain Medicine (Malden, Mass.)
|
March 16, 2021
Pain-Related Injustice Appraisals in Youth with Sickle Cell Disease: A Preliminary Investigation
Megan M Miller, Deanna D Rumble, Adam T Hirsh, et al.
Translational Behavioral Medicine
|
May 5, 2021
Mobile health use predicts self-efficacy and self-management in adolescents with sickle cell disease
Anna M Hood, Cara Nwankwo, Ashley Walton, et al.
Journal of Racial and Ethnic Health Disparities
|
December 9, 2024
Pain-Related Injustice Appraisals, Sickle Cell Stigma, and Racialized Discrimination in the Youth with Sickle Cell Disease: A Preliminary Investigation
Megan M Miller, Ama Kissi, Deanna D Rumble, et al.
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of 4