期刊： PEDIATRIC INVESTIGATION, 2021; 5 (1)
Obstructive sleep apnea (OSA) is a common sleep-disordered breathing disease that often leads to many comorbidities (e.g., cognitive dysfunction), whi......
期刊： PEDIATRIC INVESTIGATION, 2021; 5 (1)
ImportanceChildhood and adolescence are critical periods for lifelong bone mineral accrual, but few studies have determined the impact of childhood ad......
期刊： PEDIATRIC INVESTIGATION, 2021; 5 (1)
ImportanceThe impact of long-term burden of excessive body weight, beginning in childhood, on inflammatory status in adulthood has been poorly describ......
期刊： PEDIATRIC INVESTIGATION, 2021; 5 (1)
ImportanceSeveral methods have been established in recent decades that allow use of spot urine to estimate dietary sodium intake. However, their accur......
期刊： PEDIATRIC INVESTIGATION, 2021; 5 (1)
ImportanceScimitar syndrome (SS) is a rare type of congenital heart disease characterized by total or partial anomalous venous drainage of the right l......
期刊： PEDIATRIC INVESTIGATION, 2021; 5 (1)
ImportanceExtensive population-based studies have explored the prevalence of primary hypertension (HTN) in children and adolescents. However, there is......
期刊： PEDIATRIC INVESTIGATION, 2021; 5 (1)
IntroductionNasal glial heterotopia is a rare congenital developmental disorder characterized by meningeal epithelium and/or glial components. Case pr......
期刊： PEDIATRIC INVESTIGATION, 2021; 5 (1)
ImportanceThe use of factor VIII (FVIII) concentrates under pharmacokinetic (PK) guidance has become the main approach for treatment of hemophilia. Ho......
期刊： PEDIATRIC INVESTIGATION, 2022; 6 (2)
Importance: Cadherin-11 (CDH11), a cell-to-cell adhesion molecule, is implicated in the fibrotic process of several organs. Biliary atresia (BA) is a ......
期刊： PEDIATRIC INVESTIGATION, 2022; 6 (4)
Importance Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is considered the only effective treatment for chronic active Epstein-Barr v......
期刊： PEDIATRIC INVESTIGATION, 2022; 6 (1)
Importance The phenotypes of ATP1A3 gene mutations are diverse. Relapsing encephalopathy with cerebellar ataxia and fever-induced paroxysmal weakness ......
