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Hematopoietic Stem Cell Transplantation Using Preimplantation Genetic Diagnosis And Human Leukocyte Antigen Typing For Human Leukocyte Antigen-Matched Sibling Donor: A Turkish Multicenter Study
(Elsevier Science Inc, 2017)
Preimplantation genetic diagnosis involves the diagnosis of a genetic disorder in embryos obtained through in vitro fertilization, selection of healthy embryos, and transfer of the embryos to the mother's uterus. Preimplantation ...
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 ...
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 ...
Varicella Zoster-Associated Severe Aplastic Anemia in a Child and Its Successful Treatment with Peripheral Blood Stem Cell Transplantation from HLA-5/6-Identical Donor
(ISI, 2007)
Background: Varicella zoster virus is very rarely associated with aplastic anemia. Bone marrow transplantation from an HLA-identical sibling is the treatment of choice.
Case report: A seven-year-old boy presented with ...
Atypical Skin Graft-vs.-Host Disease Following Bone Marrow Transplantation in an Infant
(Wiley, 2007)
Herein, we describe an unusual presentation of acute graft versus host disease (GVHD) mimicking contact dermatitis in an infant who underwent 5/6 HLA-matched bone marrow transplantation (BMT) from his mother for malignant ...
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 ...
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 ...
Naturally Acquired Hepatitis a Antibodies After Haematopoetic Stem Cell Transplantation
(Cambridge University Press, 2011)
Haematopoietic stem cell transplant (HSCT) recipients lose immune memory of exposure to
infectious agents and vaccines accumulated throughout their lifetime and therefore need to be
revaccinated. We aimed to evaluate the ...
Successful Hematopoietic Stem Cell Transplantation in a Patient with Congenital Dyserythropoietic Anemia Type II.
(WILEY, 2014)
Abstract
CDA are a group of inherited, rare diseases that are characterized by dyserythropoiesis and ineffective erythropoiesis associated with transfusion dependency in approximately 10% of cases. For these latter patients, ...
Fanconi Anemia: A Single Center Experience of a Large Cohort
(Hacettepe Medical Center, 2019)
Transfusion-Transmitted Virus Prevalence in Turkish Patients with Thalassemia
(Taylor & Francis, 2006)
In hematology patients on chronic transfusion regimes, liver diseases are frequent, and mostly related to the agents transmitted by blood products and concominant iron deposition in liver. Besides hepatitis B (HBV) and C ...
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 ...
Cyclosporine Level at the Second Hour in Pediatric Hematopoietic Stem Cell Transplant Patients
(2011)
In this retrospective study, cyclosporine levels at the second hour (C2 levels) were measured during oral cyclosporine intake in 28 pediatric hematopoietic stem cell transplant patients, and the relations between cyclosporine ...
Hyperacute Graft-vs.-Host Disease After Related HLA-Identical Umbilical Cord Blood Transplantation
(Wiley, 2007)
haGVHD has been described following bone marrow and peripheral blood stem cell transplantation and in a single case who received unrelated HLA mismatched CB. An unusual case of haGVHD following HLA 6/6-matched sibling CBT ...
Serological Response to Influenza Vaccine After Hematopoetic Stem Cell Transplantation
(Springer, 2010)
Vaccination is the best strategy to prevent influenza infection that is a potential cause of morbidity and mortality in immunosuppressed patients. Here, we evaluated the factors that may affect serological response to ...
