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Toplam kayıt 44, listelenen: 1-10
Kırıkkale Üniversitesi Tıp Fakültesi'ne başvuran çocuklarda demir eksikliği anemisi sıklığı ve beslenme durumu ile ilişkisi
(2005)
Amaç: Daha önce bu konu ile ilgili çalışma yapılmamış Kırıkkale ilinde demir eksikliği anemisinin sıklığı ve beslenme durumu ile ilişkisinin araştırılması. Yöntem: Ocak 2001-Temmuz 2001 tarihleri arasında herhangi bir ...
Yüz yüze eğitim anne davranışını değiştirebilir mi?
(2004)
Amaç: Annelerin anne sütü, bebek beslenmesi, aşılanması, vitamin desteği ve bebek bakımı konularındaki bilgi, tutum ve davranışlarını ölçmek, bebek bakımı ve beslenmesi konularında yanlış uygulamaları ortaya çıkarmak, ...
An Assesment Of Unexpectedly High Hba1c Level In A Case With Type 1 Diabetes
(Nobel Ilac, 2016)
The HbA1c test provides information about blood glucose levels of previous months depending on the erythrocyte lifetime when monitoring diabetic patients. However, various factors such as HbF and other hemoglobin variants ...
Association of CYP3A5 Expression and Vincristine Neurotoxicity in Pediatric Malignancies in Turkish Population
(Lippincott Williams & Wilkins, 2017)
Vincristine is a widely used chemotherapeutic agent in the treatment of childhood malignancies. Neuropathy is the most common adverse effect. CYP3A4 and CYP3A5 enzymes of cytochrome p450 enzyme system are responsible in ...
Identification of three novel mutations in fourteen patients with citrullinemia type 1
(Pergamon-Elsevier Science Ltd, 2017)
Objectives: Citrullinemia type 1 (CTLN1) is an autosomal recessive genetic disorder caused by mutations in the argininosuccinate synthetase 1 (ASST) gene, which encodes for the argininosuccinate synthetase enzyme. Here, ...
Initial Ophthalmic Findings in Turkish Children with Autism Spectrum Disorder
(Springer/Plenum Publishers, 2015)
Children with autism spectrum disorders (ASD) frequently have ophthalmologic disorders. Due to poor cooperation with ophthalmological examination, ocular abnormalities in such children may be overlooked. We retrospectively ...
Association of MTHFR A1298C polymorphism with conotruncal heart disease
(Cambridge Univ Press, 2015)
Congenital heart diseases are common congenital anomalies with 1% prevalence worldwide and are associated with significant childhood morbidity and mortality. Among a wide range of aetiologically heterogeneous conditions, ...
Prognostic Factors and Long-Term Outcome in 52 Turkish Children With Hemophagocytic Lymphohistiocytosis
(Lippincott Williams & Wilkins, 2015)
Objectives: Hemophagocytic lymphohistiocytosis is a syndrome of pathologic immune activation that shares similar clinical and laboratory phenotypes with severe sepsis. Recent studies led to better recognition of hemophagocytic ...
Atypical Hemolytic Uremic Syndrome in Children Aged < 2 Years
(Karger, 2018)
Background: There are limited data on infants with atypical hemolytic uremic syndrome (aHUS). The aim of this study was to determine the clinical and laboratory features, and to evaluate treatment modalities and outcomes ...
Helicobacter pylori resistance to clarithromycin and fluoroquinolones in a pediatric population in Turkey: A cross-sectional study
(Wiley, 2019)
BackgroundHelicobacter pylori antimicrobial resistance is gradually increasing around the world. However, there are a limited number of studies reporting on this issue in the pediatric population. In this study, we aimed ...