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Toplam kayıt 25, listelenen: 21-25
Unusual presentation: Concurrent IgA deficiency and idiopathic pulmonary hemosiderosis
(Wiley-Blackwell, 2016)
Idiopathic pulmonary hemosiderosis (IPH) is a rare disorder that should be considered in the differential diagnosis of patients with hemoptysis, recurrent alveolar hemorrhage, dyspnea and iron deficiency anemia (IDA). The ...
Severe Cutaneous Adverse Drug Reactions in Pediatric Patients: A Multicenter Study
(Elsevier, 2017)
BACKGROUND: The severe cutaneous adverse drug reactions (SCARs) are rare but could be life-threatening. These include drug reaction with eosinophilia and systemic symptoms (DRESS), Stevens-Johnson syndrome, toxic epidermal ...
The long-term neurodevelopmental outcomes of infants born full-term with low birth weight
(Turkish J Pediatrics, 2017)
In this study, it was aimed to evaluate the neurological developments of preschool or school-aged children together with their school successes, intelligence quotient and symptom severity of attention deficit hyperactivity ...
Allergic and autoimmune disorders in families with selective IgA deficiency
(Tubitak Scientific & Technical Research Council Turkey, 2017)
Background/aim: IgA deficiency is the most common human primary immunodeficiency. The prevalence of allergic disorders and autoimmunity is thought to be increased in selective IgA deficiency (sIgAD). However, it is currently ...
HOMOCYSTEINE, PYRIDOXINE, FOLATE AND VITAMIN B12 LEVELS IN CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER
(Medicinska Naklada, 2018)
Background: In our study, we aimed to evaluate the serum homocysteine levels, pyridoxine, folate and vitamin B12 levels in children with attention deficit hyperactivity disorders (ADHD). Subjects and methods: This study ...