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Toplam kayıt 18, listelenen: 1-18
Fanconi Anemia: A Single Center Experience Of A Large Cohort
(2019)
Fanconi anemia (FA) is an inherited disease, characterized by congenital malformations, short stature, progressive bone marrow failure and predisposition to leukemia and solid tumors. The aim of this study was to evaluate ...
Number of Erythrocyte Transfusions is more Predictive than Serum Ferritin in Estimation of Cardiac Iron Loading in Pediatric Patients with Acute Lymphoblastic Leukemia.
(Elsevier, 2014)
Background
Transfusions with packed erythrocytes is a common practice in pediatric patients with acute lymphoblastic leukemia (ALL) who are on chemotherapy. Since there is no physiological excretion mechanism for iron, ...
Infant lymphoblastic Leukemia: A Single Centers 10 Year Experience
(2019)
Yaman-Bajin İ, Aytaç S, Kuşkonmaz B, Uçkan-Çetinkaya D, Ünal Ş, Gümrük F, Çetin M. Infant lymphoblastic leukemia: a single centers 10 year experience. Turk J Pediatr 2019; 61: 325-329.
Infant acute lymphoblastic leukemia ...
Fanconi Anemia: A Single Center Experience of a Large Cohort
(Hacettepe Medical Center, 2019)
Diamond–Blackfan Anemia Associated Withb-Thalassemia Trait
(WILEY, 2006)
A 14-month-old boy was referred to our hospital for evaluation of severe anemia. In the bone marrow aspiration smear, normal cellularity with severe erythroblastopenia (3%) was observed. The hemoglobin electrophoresis of ...
The Clinical and Laboratory Evaluation of Familial Hemophagocytic Lymphohistiocytosis and the Importance of Hepatic and Spinal Cord Involvement: A Single Center Experience
(2018)
Familial hemophagocytic lymphohistiocytosis is an autosomal recessive, life-threatening condition characterized by defective immune response. A retrospective analysis was performed on 57 patients diagnosed with familial ...
Hypereosinophilic Syndrome: Hacettepe Experience.
(Lippincott Williams & Wilkins, 2016)
The aim was to evaluate baseline demographic, clinical,
and laboratory characteristics, treatment modalities, and outcome
of children with idiopathic hypereosinophilic syndrome (HES)
followed up in our center. Children ...
Secondary Hemophagocytic Lymphohistiocytosis in Turkish Children
(Lippincott Williams & Wilkins, 2005)
: Between January 1998 and January 2005, a total of 18
children 2 weeks–72 months of age were diagnosed as having
secondary hemophagocytic lymphohistiocytosis. The frequency of
secondary hemophagocytic lymphohistiocytosis ...