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Neurocognitive and emotional factors predict pain‐related healthcare utilization in children with sickle cell disease
Pediatric blood & cancer, 2023-06, Vol.70 (6), p.e30346-n/a
2023
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Sluggish Cognitive Tempo in Pediatric Sickle Cell Disease
Frontiers in neurology, 2022-07, Vol.13, p.867437-867437
2022
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Posttraumatic Growth in Children and Youth: Clinical Implications of an Emerging Research Literature
American journal of orthopsychiatry, 2014-09, Vol.84 (5), p.506-518
2014
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Integrative holistic approaches for children, adolescents, and young adults with sickle cell disease: A single center experience
Complementary therapies in medicine, 2021-08, Vol.60, p.102680-102680, Article 102680
2021
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Neurocognitive and psychological effects of persistent pain in pediatric sickle cell disease
Pediatric blood & cancer, 2019-09, Vol.66 (9), p.e27823-n/a
2019
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A Randomized Controlled Trial of Working Memory Training in Pediatric Sickle Cell Disease
Journal of pediatric psychology, 2021-09, Vol.46 (8), p.1001-1014
2021
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Social-environmental factors and cognitive and behavioral functioning in pediatric sickle cell disease
Child neuropsychology, 2020-01, Vol.26 (1), p.83-99
2020
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Cognitive Abilities Moderate the Effect of Disease Severity on Health-Related Quality of Life in Pediatric Sickle Cell Disease
Journal of pediatric psychology, 2018-09, Vol.43 (8), p.882-894
2018
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Alteration of grey matter volume is associated with pain and quality of life in children with sickle cell disease
Translational research : the journal of laboratory and clinical medicine, 2022-02, Vol.240, p.17-25
2022
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Acupuncture as an Adjunctive Treatment for Pain in Hospitalized Children With Sickle Cell Disease
Journal of pain and symptom management, 2021-12, Vol.62 (6), p.1239-1244
2021
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Feasibility and preliminary efficacy of the Balance Program to reduce pain‐related disability in pediatric sickle cell disease
Pediatric blood & cancer, 2023-12, Vol.70 (12), p.e30667-e30667
2023
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Clinical Considerations for Behavioral Pain Management in Co-Occurring Acute and Chronic Pain Presentations
Clinical practice in pediatric psychology, 2023-06, Vol.11 (2), p.121-133
2023
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Feasibility of Home-Based Computerized Working Memory Training With Children and Adolescents With Sickle Cell Disease
Pediatric blood & cancer, 2016-09, Vol.63 (9), p.1578-1585
2016
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Commentary on the ASH 2020 guidelines on cognitive screening and intervention in sickle cell disease
Blood advances, 2023-07, Vol.7 (14), p.3680-3682
2023
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Views of parents of children with sickle cell disease on pre‐implantation genetic diagnosis
Pediatric blood & cancer, 2018-08, Vol.65 (8), p.e27102-n/a
2018
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Acupuncture for pain management in children with sickle cell disease
Complementary therapies in medicine, 2020-03, Vol.49, p.102287-102287, Article 102287
2020
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Reliability of Parent Proxy-Report Measures of Quality of Life and Cognitive Functioning in Pediatric Sickle Cell Disease
Blood, 2022-11, Vol.140 (Supplement 1), p.10881-10882
2022
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Disease Burden and Pre-Transplant Health-Related Quality of Life in Pediatric Sickle Cell Disease Patients Receiving Nonmyeloablative HLA-Identical Sibling Donor Transplantation
Blood, 2021-11, Vol.138 (Supplement 1), p.4073-4073
2021
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Implementing ASH Guidelines: Clinical Utility of a Signaling Question for Detecting Cognitive Deficits in Pediatric Sickle Cell Disease
Blood, 2022-11, Vol.140 (Supplement 1), p.10756-10757
2022
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Preliminary Feasibility and Efficacy of the Balance Program to Reduce Pain-Related Disability in Pediatric Sickle Cell Disease
Blood, 2022-11, Vol.140 (Supplement 1), p.2153-2154
2022
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Mental Health Screening in a Pediatric Sickle Cell Disease Clinic: Acceptability and Impact on Mental Health Discussions, Referrals, and Patient Satisfaction
Blood, 2019-11, Vol.134 (Supplement_1), p.4687-4687
2019
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Cognitive and Emotional Factors and Pain-Related Outcomes in Youth with Sickle Cell Disease
Blood, 2020-11, Vol.136 (Supplement 1), p.11-11
2020
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Adoption of a Multidimensional Approach to Assessing the Impact of Socioeconomic Status on Neurocognitive and Behavioral Outcomes in Pediatric Sickle Cell Disease
Blood, 2016-12, Vol.128 (22), p.3589-3589
2016
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Nonmyeloablative HLA-Identical Sibling Donor Transplantation for Children and Young Adults with Sickle Cell Disease: Interim Results of the SUN Multicenter Phase II Trial
Blood, 2021-11, Vol.138 (Supplement 1), p.1799-1799
2021
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A New Phen X Collection: Sickle Cell Disease Psychosocial and Social Determinants of Health Protocols
Blood, 2022-11, Vol.140 (Supplement 1), p.7898-7899
2022
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