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期刊名:Turk pediatri arsivi-turkish archives of pediatrics

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ISSN:1306-0015

e-ISSN:1308-6278

IF/分区:0.0/N/A

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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
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[This corrects the article DOI: 10.5152/TurkPediatriArs.2016.4119.]. 2018 authors.
Ömer Erdeve,Merih Çetinkaya,Ahmet Yağmur Baş et al. Ömer Erdeve et al.
Achille Marino,Francesco Canonico,Raffaella Maria Pinzani et al. Achille Marino et al.
Rhomboencephalitis is a potentially life-threatening condition due to inflammation of the hindbrain with an unpredictable outcome depending on the wide spectrum of etiologies and the promptness of diagnosis and treatment. A 23-month-old Cau...
Necmiye Öztürk,Köksal Atay,İbrahim Engin Çekin et al. Necmiye Öztürk et al.
Pott's puffy tumor is a rare and serious complication of frontal sinusitis, characterized by the development of osteomyelitis and subperiostal abscess in the frontal bone. Paranasal sinus osteomas are benign osteoblastic tumors, usually see...
Özlem Kalaycık Şengül,Bilge Şahin Akkelle,Burcu Volkan et al. Özlem Kalaycık Şengül et al.
Sarcoidosis is a chronic multisystemic granulomatous disease that predominantly involves the thoracic lymph nodes and lungs and primarily occurs in young adults. Isolated extrapulmonary localization is uncommon in adults, and exceptionally ...
Mirzaman Huseynov Mirzaman Huseynov
Pneumothorax is the most common type of air leak. Although the majority of pneumothoraces resolves spontaneously, some continue several days after the lung injury. Autologous blood patch pleurodesis is the most commonly used technique in th...
Semih Bolu,Recep Eröz,Mustafa Doğan et al. Semih Bolu et al.
Heterozygous inactivating mutations in the glucokinase gene cause the mildest form of maturity-onset diabetes of the adolescents. However, homozygous or compound heterozygous mutations in the glucokinase gene are a rare cause of permanent n...