期刊： JOURNAL OF CHILD NEUROLOGY, 2021; 36 (6)
Objective: Hydrocephalus is a potentially lethal complication of neonatal purulent meningitis. Early detection of hydrocephalus helps to determine opt......
期刊： JOURNAL OF CHILD NEUROLOGY, 2021; 36 (9)
Intrauterine growth restriction is a condition that prevents normal fetal development, and previous studies have reported that intrauterine growth res......
期刊： JOURNAL OF CHILD NEUROLOGY, 2021; 36 (10)
Ethylmalonic encephalopathy is a rare autosomal recessive mitochondrial disorder caused by pathogenic biallelic variants in the ETHE1 gene. The phenot......
期刊： JOURNAL OF CHILD NEUROLOGY, 2020; 35 (13)
Objective: To evaluate the effect of the COVID-19 pandemic on global access to care and practice patterns for children with epilepsy. Methods: We cond......
期刊： JOURNAL OF CHILD NEUROLOGY, 2020; 35 (13)
Many parents of children do not recall anticipatory guidance on acute seizure management, which can lead to unnecessary emergency department visits. T......
期刊： JOURNAL OF CHILD NEUROLOGY, 2020; 35 (10)
Acute necrotizing encephalopathy (ANE) is a rare disease in childhood. We reviewed the 10-year data from a local pediatric department, reported the cl......
期刊： JOURNAL OF CHILD NEUROLOGY, 2020; 35 (12)
Objective: To develop an orthostatic intolerance symptom scoring system to assess orthostatic intolerance and then to compare the symptom score among ......
期刊： JOURNAL OF CHILD NEUROLOGY, 2019; 34 (1)
Objective: To explore the clinical characteristics of and analyze the risk factors for hydrocephalus in children with bacterial meningitis. Methods: R......
期刊： JOURNAL OF CHILD NEUROLOGY, 2019; 34 (1)
Objective: To assess the efficacy of oral rehydration salts in children with neurally mediated syncope of different hemodynamic types. Methods: Childr......
期刊： JOURNAL OF CHILD NEUROLOGY, 2019; 34 (2)
This study aimed to investigate the treatment-related annual cost of childhood epilepsy and its related factors in mainland China. A total of 244 case......
期刊： JOURNAL OF CHILD NEUROLOGY, 2019; 34 (13)
The ring-finger protein 213 (RNF213) gene is a major susceptibility gene for moyamoya disease. The homozygote of the p.R4810K variant on RNF213 exhibi......
期刊： JOURNAL OF CHILD NEUROLOGY, 2020; 35 (2)
Background: Assessing motor impairment in spastic cerebral palsy is a key factor in the treatment and rehabilitation of patients. We intend to investi......
