E. Waters

Theme development in qualitative content analysis and thematic analysis

The PedsQL™* 4.0 as a Pediatric Population Health Measure: Feasibility, Reliability, and Validity

Defining consensus: A systematic review recommends methodologic criteria for reporting of Delphi studies

Qualitative research and content validity: developing best practices based on science and experience

Measuring What Matters in Cerebral Palsy: A Breadth of Important Domains and Outcome Measures

Evidence That School-Age Children Can Self-Report on Their Health

The development of the pediatric cardiac quality of life inventory: a quality of life measure for children and adolescents with heart disease

Childhood Functional Gastrointestinal Disorders: Child/Adolescent

Development and Preliminary Validation of the Questionnaire on Pediatric Gastrointestinal Symptoms to Assess Functional Gastrointestinal Disorders in Children and Adolescents

Are We There Yet? Data Saturation in Qualitative Research

Development and Validation of a Pharmacy‐Based Comorbidity Measure in a Population‐Based Automated Health Care Database

Item Banks for Measuring Emotional Distress From the Patient-Reported Outcomes Measurement Information System (PROMIS®): Depression, Anxiety, and Anger

Parent- Versus Child-Reported Functional Health Status After the Fontan Procedure

The national healthcare system claims databases in France, SNIIRAM and EGB: Powerful tools for pharmacoepidemiology

Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management

The impact of childhood conditions and concurrent morbidities on child health and well‐being

Development of a condition‐specific measure of quality of life for children with cerebral palsy: empirical thematic data reported by parents and children

Agreement between adolescent self‐report and parent reports of health and well‐being: results of an epidemiological study

RELIABILITY AND VALIDITY OF THE CEREBRAL PALSY QUALITY OF LIFE QUESTIONNAIRE FOR CHILDREN (CP QOL- Child)