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期刊名:Turkish journal of pediatrics

缩写:TURKISH J PEDIATR

ISSN:0041-4301

e-ISSN:

IF/分区:0.8/Q4

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共收录本刊相关文章索引2673
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
Zahra Movahedi,Shima Mahmoudi,Setareh Mamishi Zahra Movahedi
Impairment of cellular immunity related to human immunodeficiency virus (HIV) infection predisposes patients to opportunistic infections. In this report, we describe a 16-month-old boy with salmonella meningitis and acquired immunodeficienc...
Hacer Neslihan Bildik,Sahin Takcı,Murat Yurdakök et al. Hacer Neslihan Bildik et al.
We present two cases of Rhodococcus equi bacteremia as a cause of sepsis in premature infants who had increasing respiratory distress with multiple episodes of apnea. When we investigated these infants for apnea etiology, blood cultures wer...
Demet Alaygut,Meral Bayram,Alper Soylu et al. Demet Alaygut et al.
Acute focal bacterial nephritis (AFBN) is a rare cause of interstitial bacterial nephritis. Ultrasound identifies AFBN as a hypoechogenic and hypoperfused parenchymal lesion, which requires its differentiation from renal abscess and tumor. ...
Erdem Topal,Odül Eğritaş,Mustafa Arga et al. Erdem Topal et al.
Food allergies are often seen in infancy and usually show the clinical signs in the form of type I hypersensitivity reaction. However, a combination of food allergies can sometimes be found in the same patient. In this report, we present an...
Maşallah Baran,Kayı Eliaçık,Ismail Kurt et al. Maşallah Baran et al.
Congenital erythropoietic porphyria is a rare autosomal recessive disorder of porphyrin metabolism in which the genetic defect is the deficiency of uroporphyrinogen III cosynthase (UIIIC). Deficiency of this enzyme results in an accumulatio...
Fatma Narter,Nesimi Büyükbabani,Heybet Yararlı et al. Fatma Narter et al.
Bart's syndrome, first described by Bart in 1966, consists of congenital localized absence of skin, congenital epidermolysis bullosa, and associated nail abnormalities. A newborn infant with Bart's syndrome is reported since it is a very ra...
Omer Bektaş,Halil Ozdemir,Arzu Yılmaz et al. Omer Bektaş et al.
Brucellosis is a public health problem in most countries in the Mediterranean. Involvement of the central nervous system is seen in 4-13% of patients with brucellosis. A 13-year-old girl was admitted because of gait disturbance, diplopia, a...