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Toplam kayıt 8, listelenen: 1-8
The Rate of Hepatitis B and C Virus Infections and the Importance of HBV Vaccination in Children with Acute lymphoblastic Leukemia
(2007)
Aim: The aim of the study was to evaluate the rate of hepatitis B and C virus infection and emphasize the importance of hepatitis B virus (HBV) vaccination in leukemic children.
Methods: One hundred and sixty children ...
Hepatitis B Immunoglobulin in Combination with Lamivudine for Prevention of Hepatitis B Virus Reactivation in Children Undergoing Bone Marrow Transplantation
(WILEY, 2006)
Abstract: There is little information in literature about the use of hepatitis B immunoglobulin (HBIg) in recipients of bone marrow transplantation (BMT). Here, we report two children who received IV HBIg (Hepatect‐CP) and ...
An Unusual Case of Reactive Lymphocytosis Mimicking Acute Leukemia
(Taylor and Francis, 2007)
The diagnosis of acute leukemia is based on a combination of clinical, hematological, morphological, cytogenetic, and immunophenotypic data. The authors report a case of reactive lymphocytosis with extremely elevated ...
A Prompt Graft-Versus-Thalassemia Effect upon Withdrawal of CyclosporineA in A Child Who Received Allogeneic Peripheral Blood Stem Cell Transplantation
(Nature, 2006)
Stable mixed chimerism is a common event in children with thalassemia major who have undergone bone marrow transplantation (BMT). However, persistence of unstable mixed chimerism in these children is associated with a ...
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 ...
Dysplasia and Disorder of cell Membrane Entirety in Iron-Deficiency Anemia
(Taylor and Francis, 2008)
Peripheral blood smears of 43 patients (26 males, median age 18 months, range: 6-180 months) with nutritional iron-deficiency anemia (IDA) were examined for the presence of trilineage hematological dysplasia. Twelve patients ...
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 ...