Ara
Toplam kayıt 4, listelenen: 1-4
Çocuklarda elektroanatomik haritalama eşliğinde sınırlı floroskopi ile supraventriküler taşikardilerin ablasyonu
(Logos Medical Publishing, 2018)
Amaç: Çocuklarda supraventriküler taşikardi (SVT)’lerin tedavisinde kateter ablasyon başarılı olarak uygulanmakla birlikte, geleneksel yöntemleyapılan ablasyon işlemlerinde X-ışınları kullanılmaktadır. Son dönemlerde, ...
Lethal very long-chain acyl-coa dehydrogenase deficiency with a novel mutation
(Gazi University, 2019)
Very long chain acyl-CoA dehydrogenase deficiency is an autosomal recessive genetic disorder in which the first step in the mitochondrial beta-oxidation of fatty acids for 14-20 carbons is defective. Clinical presentation ...
Investigation of beta globin gene mutations in Syrian refugee patients with thalassemia major
(De Gruyter, 2019)
Objectives: This study, detection of beta globin gene mutations in thalassemia major patients who migrated from Syria to Kahramanmaraş region were planned. Materials and methods: The study included 35 Syrian national beta ...
Clinical features, prognostic factors and outcome of children with ewing sarcoma: A single-center experience
(Galenos Publishing House, 2023)
Introduction: Ewing sarcoma (ES) is a rare, aggressive, malignant tumor. It is the second most common malignant bone tumor in children. A total of 20-25% of patients are metastatic at the time of diagnosis. The survival ...