Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ece Selma Solak"'
Publikováno v:
Case Reports in Pediatrics, Vol 2013 (2013)
Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a rare but potentially life-threatening syndrome characterized by skin rash, fever, lymph node enlargement, and involvement of internal organs. It is most commonly induced by a
Externí odkaz:
https://doaj.org/article/527f5713bd0545b5bbc3d40be14ae149
Publikováno v:
Anemia, Vol 2013 (2013)
The aim of this study was to investigate the characteristics of our hospitalized patients with the diagnosis of iron deficiency anemia (IDA) and effects of the IDA prevention project of the Turkish Ministry of Health which was started in 2004. The re
Externí odkaz:
https://doaj.org/article/619d8ad586984eff9fbc777ed8fbaf09
Publikováno v:
Dicle Medical Journal, Vol 42, Iss 1, Pp 28-35 (2015)
Volume: 42, Issue: 1 28-35
Dicle Tıp Dergisi
Volume: 42, Issue: 1 28-35
Dicle Tıp Dergisi
Amaç: Bu çalışmada, kliniğimizde Kawasaki hastalığı (KH) tanısıyla takip ettiğimiz vakalarımızın klinik ve laboratuvar özelliklerini sunmayı amaçladık. Yöntemler: Konya Eğitim ve Araştırma Hastanesi Çocuk Sağlığı ve Hastal
Publikováno v:
Child's Nervous System. 30:535-540
Posterior reversible encephalopathy syndrome (PRES) is a condition characterized by varying degrees of headache, nausea, vomiting, visual disturbances, focal neurologic deficit, and seizures due to severe systemic hypertension. The knowledge of secon
Publikováno v:
Anemia
Anemia, Vol 2013 (2013)
Anemia, Vol 2013 (2013)
The aim of this study was to investigate the characteristics of our hospitalized patients with the diagnosis of iron deficiency anemia (IDA) and effects of the IDA prevention project of the Turkish Ministry of Health which was started in 2004. The re
Publikováno v:
Journal of Clinical and Analytical Medicine, Vol 6, Iss 100, Pp 522-524 (2014)
Achondroplasia is one of the common chondrodysplasias with an inheritance is autosomal dominant, but in around 85% the phenotype is the result of a new mutation. Achondroplasia develops as a result of dysplasia of enchondral formation due to the muta
Publikováno v:
Case Reports in Clinical Medicine. :338-340
X-linked agammaglobulinemia also known as Bruton’s disease, is a humoral immunodeficiency disease characterized by recurrent bacterial infections due to low levels or absence of serum immunoglobulins. It has been shown to be caused by mutations in
Publikováno v:
World journal of pediatrics : WJP. 12(2)
The effects of Helicobacter pylori (H. pylori) infection on growth are a controversial issue. We investigated the effects of long-term H. pylori infection on height and weight in children.A total of 200 children of 7-18 years old suffering from dyspe
Publikováno v:
Medicinski glasnik : official publication of the Medical Association of Zenica-Doboj Canton, Bosnia and Herzegovina. 11(1)
To investigate serum creatinine and electrolyte status of children with diarrhea-related hyponatremic or hypernatremic dehydration.Medical history of 83 patients admitted to the Pediatric Intensive Care Unit of the Konya Education and Research Hospit
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2013 (2013)
Case Reports in Pediatrics, Vol 2013 (2013)
Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a rare but potentially life-threatening syndrome characterized by skin rash, fever, lymph node enlargement, and involvement of internal organs. It is most commonly induced by a