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Identifying treatment responders and predictors of improvement after cognitive-behavioral therapy for juvenile fibromyalgia

Pain (Amsterdam), 2014-07, Vol.155 (7), p.1206-1212

2014

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Cross-Sectional Study of Young Adults Diagnosed With Juvenile Fibromyalgia: Social Support and Its Impact on Functioning and Mood

Journal of adolescent health, 2015-11, Vol.57 (5), p.482-487

2015

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Videogame Distraction using Virtual Reality Technology for Children Experiencing Cold Pressor Pain: The Role of Cognitive Processing

Journal of pediatric psychology, 2011-01, Vol.36 (1), p.84-94

2011

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Psychosocial and Functional Outcomes in Youth With Chronic Sickle Cell Pain

The Clinical journal of pain, 2016-06, Vol.32 (6), p.527-533

2016

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Pediatric Pain Screening Identifies Youth at Risk for Chronic Pain in Sickle Cell Disease

Blood, 2017-12, Vol.130, p.3548-3548

2017

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Pediatric pain screening identifies youth at risk of chronic pain in sickle cell disease

Pediatric blood & cancer, 2019-03, Vol.66 (3), p.e27538-n/a

2019

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The distinct longitudinal impact of pain catastrophizing on pain interference among youth living with sickle cell disease and chronic pain

Journal of behavioral medicine, 2022-08, Vol.45 (4), p.622-631

2022

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Identifying Chronic Pain Subgroups in Pediatric Sickle Cell Disease: A Cluster-Analytic Approach

The Clinical journal of pain, 2022-10, Vol.38 (10), p.601-611

2022

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Pediatric Sickle Cell Disease and Parent and Child Catastrophizing

The journal of pain, 2016-09, Vol.17 (9), p.963-971

2016

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Moving Beyond Patient-Level Drivers of Racial/Ethnic Disparities in Childhood Cancer

Cancer epidemiology, biomarkers & prevention, 2022-06, Vol.31 (6), p.1154-1158

2022

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A dyadic analysis of parent and child pain catastrophizing and health-related quality of life in pediatric sickle cell disease

Pain (Amsterdam), 2023-07, Vol.164 (7), p.1537-1544

2023

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An Empirical Classification of Chronic Pain Subgroups in Pediatric Sickle Cell Disease: A Cluster-Analytic Approach

Blood, 2021-11, Vol.138 (Supplement 1), p.491-491

2021

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Changes in Pain and Psychosocial Functioning and Transition to Chronic Pain in Pediatric Sickle Cell Disease: A Cohort Follow-up Study

The Clinical journal of pain, 2020-06, Vol.36 (6), p.463-471

2020

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Stigma and Pain in Adolescents Hospitalized for Sickle Cell Vasoocclusive Pain Episodes

The Clinical journal of pain, 2018-05, Vol.34 (5), p.438-444

2018

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Differential changes in functional disability and pain intensity over the course of psychological treatment for children with chronic pain

Pain (Amsterdam), 2014-10, Vol.155 (10), p.1955-1961

2014

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Building Adaptive Coping and Knowledge to Improve Daily Life (Back2Life): A Pilot Feasibility Trial for Youth with Chronic Sickle Cell Pain

Blood, 2023-11, Vol.142 (Supplement 1), p.3734-3734

2023

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Racial Discrimination and Pain in Adults with Sickle Cell Disease: Depression As a Mediator

Blood, 2023-11, Vol.142 (Supplement 1), p.2371-2371

2023

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Topical Review: State of the Field of Child Self-Report of Acute Pain

Journal of pediatric psychology, 2020-04, Vol.45 (3), p.239-246

2020

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The influence of child pain catastrophizing and parent behavior on health‐related quality of life in pediatric sickle cell disease

Pediatric blood & cancer, 2023-08, Vol.70 (8), p.e30372-n/a

2023

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Parental Psychosocial Distress in Pediatric Sickle Cell Disease and Chronic Pain

Journal of pediatric psychology, 2021-06, Vol.46 (5), p.557-569

2021

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Biopsychosocial Factors Associated with Parenting Stress in Pediatric Sickle Cell Disease

Journal of clinical psychology in medical settings, 2022-06, Vol.29 (2), p.365-374

2022

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Pain and QOL in Pediatric Sickle Cell Disease: Buffering by Resilience Processes

Journal of pediatric psychology, 2021-09, Vol.46 (8), p.1015-1024

2021

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The comfort ability program for adolescents with sickle cell pain: Evaluating feasibility and acceptability of an inpatient group‐based clinical implementation

Pediatric blood & cancer, 2021-06, Vol.68 (6), p.e29013-n/a

2021

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Assessing Psychosocial Readiness for Gene Therapy in Sickle Cell Disease: A Consensus Statement

Blood, 2023-11, Vol.142 (Supplement 1), p.371-371

2023

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Executive Functioning Mediates the Relationship Between Pain Coping and Quality of Life in Youth With Sickle Cell Disease

Journal of pediatric psychology, 2018-11, Vol.43 (10), p.1160-1169

2018

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Identifying treatment responders and predictors of improvement after cognitive-behavioral therapy for juvenile fibromyalgia

Cross-Sectional Study of Young Adults Diagnosed With Juvenile Fibromyalgia: Social Support and Its Impact on Functioning and Mood

Videogame Distraction using Virtual Reality Technology for Children Experiencing Cold Pressor Pain: The Role of Cognitive Processing

Psychosocial and Functional Outcomes in Youth With Chronic Sickle Cell Pain

Pediatric Pain Screening Identifies Youth at Risk for Chronic Pain in Sickle Cell Disease

Pediatric pain screening identifies youth at risk of chronic pain in sickle cell disease

The distinct longitudinal impact of pain catastrophizing on pain interference among youth living with sickle cell disease and chronic pain

Identifying Chronic Pain Subgroups in Pediatric Sickle Cell Disease: A Cluster-Analytic Approach

Pediatric Sickle Cell Disease and Parent and Child Catastrophizing

Moving Beyond Patient-Level Drivers of Racial/Ethnic Disparities in Childhood Cancer

A dyadic analysis of parent and child pain catastrophizing and health-related quality of life in pediatric sickle cell disease

An Empirical Classification of Chronic Pain Subgroups in Pediatric Sickle Cell Disease: A Cluster-Analytic Approach

Changes in Pain and Psychosocial Functioning and Transition to Chronic Pain in Pediatric Sickle Cell Disease: A Cohort Follow-up Study

Stigma and Pain in Adolescents Hospitalized for Sickle Cell Vasoocclusive Pain Episodes

Differential changes in functional disability and pain intensity over the course of psychological treatment for children with chronic pain

Building Adaptive Coping and Knowledge to Improve Daily Life (Back2Life): A Pilot Feasibility Trial for Youth with Chronic Sickle Cell Pain

Racial Discrimination and Pain in Adults with Sickle Cell Disease: Depression As a Mediator

Topical Review: State of the Field of Child Self-Report of Acute Pain

The influence of child pain catastrophizing and parent behavior on health‐related quality of life in pediatric sickle cell disease

Parental Psychosocial Distress in Pediatric Sickle Cell Disease and Chronic Pain

Biopsychosocial Factors Associated with Parenting Stress in Pediatric Sickle Cell Disease

Pain and QOL in Pediatric Sickle Cell Disease: Buffering by Resilience Processes

The comfort ability program for adolescents with sickle cell pain: Evaluating feasibility and acceptability of an inpatient group‐based clinical implementation

Assessing Psychosocial Readiness for Gene Therapy in Sickle Cell Disease: A Consensus Statement

Executive Functioning Mediates the Relationship Between Pain Coping and Quality of Life in Youth With Sickle Cell Disease

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