期刊： INDIAN PEDIATRICS, 2021; 58 (3)
We report on 16 children with ingestion of magnetic foreign bodies, who were identified by a medical record review of our hospital data for the time p......
期刊： INDIAN PEDIATRICS, 2021; 58 (2)
Objective We conducted a systematic review and network meta-analysis to compare the efficacy and safety of nine non-steroidal antiinflammatory drugs (......
期刊： INDIAN PEDIATRICS, 2020; 57 (11)
Objective To study the clinical characteristics and factors associated with mortality among children with Shigella encephalopathy. Methods The data co......
期刊： INDIAN PEDIATRICS, 2020; 57 (11)
Objectives To investigate the lead exposure levels, and the effect of blood lead level (BLL) on recurrent respiratory infections in children aged 3-7 ......
期刊： INDIAN PEDIATRICS, 2020; 57 (1)
Objective To determine the diagnostic accuracy of pneumococcal antigen detection in diagnosis of pneumococcal meningitis in children. Methods Purulent......
期刊： INDIAN PEDIATRICS, 2020; 57 (2)
Objective To investigate the prevalence and risk factors of congenital heart disease in Yunnan, China which has diverse ethnic groups. Methods This cr......
期刊： INDIAN PEDIATRICS, 2020; 57 (2)
Objective To identify the factors influencing brain injury in infants with congenital heart disease (CHD) after cardiac surgery. Methods This retrospe......
期刊： INDIAN PEDIATRICS, 2020; 57 (5)
Objective: The purpose of this study was to investigate chest computed tomography (CT) findings in children with coronavirus disease-19 (COVID-19) pne......
期刊： INDIAN PEDIATRICS, 2020; 57 (9)
Objective To assess the effects of delayed cord clamping (DCC) on hemoglobin (Hb), mean corpuscular volume (MCV) and ferritin level in infants 2 month......
期刊： INDIAN PEDIATRICS, 2019; 56 (9)
Background Bainbridge-Ropers syndrome is a rare autosomal dominant genetic disorder. Case characteristics A 26-day-old neonate presented with feeding ......
期刊： INDIAN PEDIATRICS, 2019; 56 (9)
Background Prader-Willi syndrome (PWS) is a complex neurobehavioral disorder caused by failure of expression of paternally inherited genes in the PWS ......
