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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:1.7/Q2

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共收录本刊相关文章索引681
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
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...
Kotb Abbass Metwalley,Hekma Saad Farghaly Kotb Abbass Metwalley
Turner syndrome (TS) is a common, non-heritable genetic condition affecting ~1 in 2000 females and is brought on by complete or partial absence of the second sex chromosome. Neurocognitive impairments and a variety of conditions, including ...