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期刊名:Turkish archives of pediatrics

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e-ISSN:2757-6256

IF/分区:2.3/Q2

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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
Eviç Zeynep Başar,Hafize Emine Sönmez,Selim Öncel et al. Eviç Zeynep Başar et al.
Objective: Multisystem inflammatory syndrome in children (MIS-C) associated with the coronavirus disease 2019 (COVID-19) is a new concern emerging as a severe presentation of COVID-19 in children. We aimed to describe the...
Sinem Gülcan Kersin,Eren Özek Sinem Gülcan Kersin
Each mammal produces milk specific to its newborn that meets all nutritional needs. Breast milk is not only a secretory product but is also a complex liquid containing several components that provide enteral nutrition. The stage of lactatio...
Ela Tarakcı,Eylül Pınar Kısa,Nilay Arman et al. Ela Tarakcı et al.
Childhood rheumatic diseases are a group of diseases that can affect many organs and systems, resulting in pain, joint stiffness, muscle atrophy and weakness. Physical inactivity has been reported in many childhood rheumatic diseases. There...
Osman Yeşilbaş,Irmak Tahaoğlu,Can Yılmaz Yozgat et al. Osman Yeşilbaş et al.
Streptococcus anginosus can be frequently isolated from brain abscesses, but is a rare cause of the liver, lung, and deep tissue abscesses. In this report, we present a patient with subdural empyema, brain abscess, and superior sagittal cer...
Bashar Abuzayed,Khaled Alawneh,Majdi Al Qawasmeh et al. Bashar Abuzayed et al.
A 14-year-old female patient presented with symptoms of chronic mid and low back pain that radiated to both lower limbs for 5 months, with rapidly progressive lower limb weakness and urine retention. Radiologic evaluation revealed an intram...
Gülin Karacan Küçükali,Şenay Savaş Erdeve,Semra Çetinkaya et al. Gülin Karacan Küçükali et al.
Prohormone convertase 1/3, encoded by the proprotein convertase subtilisin/kexin type 1 gene, is essential for processing prohormones; therefore, its deficiency is characterized by a deficiency of variable levels in all hormone systems. Alt...
Mehmet Satar,Ahmet İbrahim Kurtoğlu,Hacer Y Yıldızdaş et al. Mehmet Satar et al.
Molybdenum cofactor deficiency is a rare neurometabolic disease that is usually characterized by seizures, abnormal muscle tonus, developmental delay and poor nutrition, and is seen soon after birth. Pyloric stenosis causes serious vomiting...