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期刊名:Turkish archives of pediatrics

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ISSN:N/A

e-ISSN:2757-6256

IF/分区:2.3/Q2

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共收录本刊相关文章索引716
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
Kubra Aykac,Zehra Tan Develi,Berivan Onel et al. Kubra Aykac et al.
Objective: Human metapneumovirus (hMPV) is a significant agent of respiratory infections in pediatric populations. Despite its global prevalence, the epidemiological characteristics and clinical burden of hMPV infections ...
Onur Dirican,Ayşe Derya Buluş,Abbas Ali Husseini et al. Onur Dirican et al.
Objective: This study explores whether GSTM1, GSTT1, and TP53 rs1042522 polymorphisms, key regulators of detoxification and oxidative stress responses, influence obesity risk and related metabolic profiles in children. ...
Fatma Sargın,Mehmet Alçı,Büşra Kaygusuz Aydemir et al. Fatma Sargın et al.
Objective: Accessible, high-quality online health information is essential for patient understanding, particularly in specialized fields such as pediatric neurology. However, little is known about the readability and qual...
Semih Ercan Akgun,Derya Guler,Tugba Kontbay et al. Semih Ercan Akgun et al.
Objective: To describe oral health status and its relationship with glycemic control in children with type 1 diabetes mellitus (T1DM) using standardized indices. ...
Mehmet Ali Oktay,Ceyda Karadeniz,Hatice Tuba Atalay et al. Mehmet Ali Oktay et al.
Objective: Improved survival among pediatric oncology patients has increased the burden of late treatment-related complications, including retinal toxicity, a recognized acute and chronic effect of platinum chemotherapy. ...
Salih Türk,Nilay Güneş,Anıl Gök et al. Salih Türk et al.
Objective: Joubert syndrome (JS) is a rare neurodevelopmental ciliopathy defined by the molar tooth sign (MTS) on brain magnetic resonance imaging accompanied by hypotonia, oculomotor apraxia (OMA), developmental delay, a...
Handan Kekec,Tugba Sismanlar Eyuboglu,Ayse Tana Aslan et al. Handan Kekec et al.
Objective: Cystic fibrosis (CF) is a genetic disorder associated with high morbidity and mortality. Elevated immunoreactive trypsinogen (IRT) levels are used for CF newborn screening (NBS). This study aims to identify fac...
Harun Bayrak,Harun Yıldız,Parisa Sharafi et al. Harun Bayrak et al.
The expression of protein-coding genes is regulated by microRNAs (miRNAs), which are small non-coding RNAs typically 18-24 nucleotides in size. miRNAs have been found to play a critical role in regulating biological functions such as prolif...