Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine metabolism
caused by deficiency in the enzyme phenylalanine hydroxylase that converts phenylalanine …

Purpose This review aims to provide a broad overview of the issues and clinical challenges
of nonadherence in adolescents and young adults (AYAs) with cancer. Nonadherence can …

Objective To estimate the effectiveness of adherence-promoting psychological interventions
for pediatric populations with chronic health conditions. Methods A meta-analysis was …

Phenylketonuria (PKU) is caused by deficient activity of the enzyme phenylalanine
hydroxylase, needed to convert the essential amino acid (AA) phenylalanine (phe) to …

Objective: The Girls health Enrichment Multisite Studies (GEMS) Fun, Food, and Fitness
Project (FFFP) was designed to prevent obesity among 8-year-old African-American girls …

The present chapter provides an overview of pediatric adherence and is divided into three
major sections. The first focuses on issues of definition and measurement; the second …

Phenylketonuria (PKU) is an inherited metabolic disorder that requires lifelong adherence to
a low-phenylalanine (Phe) diet to prevent severe neurological complications. However …

Purpose To describe the reported health-related quality of life (HRQOL) in children and
adolescents with inflammatory bowel disease (IBD) after attending an IBD summer camp …

This study explored the experiences of a summer camp for adolescents with serious
illnesses and included interview responses from campers with different types of serious …

Objective This study aimed to identify psychosocial predictors of two-year antiepileptic drug
(AED) adherence trajectories among youth with newly diagnosed epilepsy, controlling for …