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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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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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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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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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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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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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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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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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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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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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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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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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Biomarkers of Disease Severity Predict Neurocognitive Functioning in Pediatric SCD

Blood, 2016-12, Vol.128 (22), p.248-248

2016

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Initial Results of a Randomized Controlled Trial of Computerized Working Memory Training in Pediatric Sickle Cell Disease

Blood, 2016-12, Vol.128 (22), p.247-247

2016

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Psychosocial Care and Education of Children with Sickle Cell Disease Undergoing Hematopoietic Stem Cell Transplant and Their Families

Sickle Cell Disease and Hematopoietic Stem Cell Transplantation, p.221-233

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Use of an Isolated Joint Model to Detect Early Changes Induced by Intra-Articular Injection of Paclitaxel-Impregnated Polymeric Microspheres

Journal of investigative surgery, 2001, Vol.14 (3), p.169-182

Bonnie Bragdon, Alicia L. Bertone, Joanne Hardy, Emily J. Simmons, Steven E. Weisbrode

2001

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Hematology/Oncology and Palliative Care Collaboration

Palliative Care in Hematologic Malignancies and Serious Blood Disorders, p.83-92

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Metabarcoding of benthic eukaryote communities predicts the ecological condition of estuaries

Environmental pollution (1987), 2015-08, Vol.203, p.165-174

2015

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Sluggish Cognitive Tempo in Pediatric Sickle Cell Disease

Integrative holistic approaches for children, adolescents, and young adults with sickle cell disease: A single center experience

Social-environmental factors and cognitive and behavioral functioning in pediatric sickle cell disease

A Randomized Controlled Trial of Working Memory Training in Pediatric Sickle Cell Disease

Cognitive Abilities Moderate the Effect of Disease Severity on Health-Related Quality of Life in Pediatric Sickle Cell Disease

Alteration of grey matter volume is associated with pain and quality of life in children with sickle cell disease

Acupuncture as an Adjunctive Treatment for Pain in Hospitalized Children With Sickle Cell Disease

Clinical Considerations for Behavioral Pain Management in Co-Occurring Acute and Chronic Pain Presentations

Commentary on the ASH 2020 guidelines on cognitive screening and intervention in sickle cell disease

Acupuncture for pain management in children with sickle cell disease

Reliability of Parent Proxy-Report Measures of Quality of Life and Cognitive Functioning in Pediatric Sickle Cell Disease

Disease Burden and Pre-Transplant Health-Related Quality of Life in Pediatric Sickle Cell Disease Patients Receiving Nonmyeloablative HLA-Identical Sibling Donor Transplantation

Mental Health Screening in a Pediatric Sickle Cell Disease Clinic: Acceptability and Impact on Mental Health Discussions, Referrals, and Patient Satisfaction

Preliminary Feasibility and Efficacy of the Balance Program to Reduce Pain-Related Disability in Pediatric Sickle Cell Disease

Implementing ASH Guidelines: Clinical Utility of a Signaling Question for Detecting Cognitive Deficits in Pediatric Sickle Cell Disease

Cognitive and Emotional Factors and Pain-Related Outcomes in Youth with Sickle Cell Disease

Adoption of a Multidimensional Approach to Assessing the Impact of Socioeconomic Status on Neurocognitive and Behavioral Outcomes in Pediatric Sickle Cell Disease

Nonmyeloablative HLA-Identical Sibling Donor Transplantation for Children and Young Adults with Sickle Cell Disease: Interim Results of the SUN Multicenter Phase II Trial

A New Phen X Collection: Sickle Cell Disease Psychosocial and Social Determinants of Health Protocols

Biomarkers of Disease Severity Predict Neurocognitive Functioning in Pediatric SCD

Initial Results of a Randomized Controlled Trial of Computerized Working Memory Training in Pediatric Sickle Cell Disease

Psychosocial Care and Education of Children with Sickle Cell Disease Undergoing Hematopoietic Stem Cell Transplant and Their Families

Use of an Isolated Joint Model to Detect Early Changes Induced by Intra-Articular Injection of Paclitaxel-Impregnated Polymeric Microspheres

Hematology/Oncology and Palliative Care Collaboration

Metabarcoding of benthic eukaryote communities predicts the ecological condition of estuaries

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