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期刊名:Clinical and experimental pediatrics

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ISSN:N/A

e-ISSN:2713-4148

IF/分区:3.9/Q1

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共收录本刊相关文章索引711条
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Varissara Kaewchaivijit,Pornthep Tanpowpong,Songpon Getsuwan et al. Varissara Kaewchaivijit et al.
Background: Biliary atresia (BA) is a common cause of cirrhosis in children, and serious bacterial infections may worsen clinical outcomes. Purpose: ...
Hanyudh Prichayudh,Kanhatai Chiengthong,Khwaunrat Whaidee et al. Hanyudh Prichayudh et al.
Background: Iron-deficiency anemia is challenging to diagnose in patients with cyanotic congenital heart disease (CCHD) because of the high hemoglobin concentration as a compensatory mechanism for cyanosis. ...
Yoon Gi Chung,Jaeso Cho,Anna Cho et al. Yoon Gi Chung et al.
Background: Automated seizure detection using scalp electroencephalography (EEG) is essential to the efficient monitoring of seizures in patients with epilepsy. However, patient-independent seizure detection remains chall...
Thomas Saliba,Guillaume Fahrni Thomas Saliba
Needle-involving procedures often cause significant pain and anxiety, particularly in the pediatric population. Virtual reality (VR) has emerged as a nonpharmacological tool for alleviating these effects. However, the methodological quality...
Ashraf T Soliman,Fawzia Alyafei,Nada Alaaraj et al. Ashraf T Soliman et al.
Youth-onset type 2 diabetes mellitus (T2DM) is a rapidly growing pediatric metabolic disorder that parallels the global childhood obesity epidemic. Despite multiple population-based registries and a global meta-analysis documenting near-uni...
Amresh Kumar Mishra,Moinak Sen Sarma,Anchal Dubey et al. Amresh Kumar Mishra et al.
Background: Genotype-phenotype correlations in Wilson disease (WD) have so far been inconclusive. Purpose: ATP7B variants with loss of ...