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期刊名:Turkish archives of pediatrics

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e-ISSN:2757-6256

IF/分区:1.7/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
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...
Dilara Ceylan,Elvan Bayramoğlu,Emine Polat et al. Dilara Ceylan et al.
Three infants aged between 38 days and 43 days all presented with poor weight gain, hyponatremia, hyperkalemia, and were diagnosed as having urinary tract infections, which were accompanied by urinary tract malformations in our cases. Hydra...
Ulaş Emre Akbulut,Nadide Cemre Randa,İshak Abdurrahman Işık et al. Ulaş Emre Akbulut et al.
Benign recurrent intrahepatic cholestasis is a rare disorder characterized by recurrent episodes of cholestatic jaundice without liver damage. A mutation in the ABCB11 gene encoding bile salt export pump protein causes the disease. A 16-yea...
Miraç Yıldırım,Hatice Koçak Eker,Melih Timuçin Doğan Miraç Yıldırım
Mutations in protein O-mannosyltransferase 2 can cause a wide spectrum of clinical phenotypes from severe congenital muscular dystrophy such as Walker-Warburg syndrome to milder limb-girdle muscular dystrophy 2N. We aimed to describe the cl...
Songül Yılmaz,Meryem Erat Nergiz,Sare Gülfem Özlü Songül Yılmaz
Objective: Enuresis is a major problem affecting both the child and his family. This study aimed to investigate the effect of enuresis on mother acceptance-rejection perceived by children. ...
Gamze Durmazoğlu,Özlem Çiçek,Hülya Okumuş Gamze Durmazoğlu
Objective: To examine the effect of mothers' perceived spousal support on breastfeeding during lactation. Material and methods: This is...