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Early Detection of Pulmonary Fungal Infection By Ct Scan in Pediatric All Patients Under Chemotherapy or In Post-Transplantation Period With Primary Complaint of Chest Pain
(Aves Yayincilik, 2010)
We describe herein four children with acute lymphoblastic leukemia who were diagnosed as pulmonary fungal infection after presenting with chest pain. The plain radiologic evaluations failed to reveal any positive findings, ...
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 ...
Gray Platelet Syndrome: Natural History Of A Large Patient Cohort And Locus Assignment To Chromosome 3P
(Amer Soc Hematology, 2010)
Gray platelet syndrome (GPS) is an inherited bleeding disorder characterized by macrothrombocytopenia and absence of platelet alpha-granules resulting in typical gray platelets on peripheral smears. GPS is associated with ...
Molecular Diagnosis Of Shwachman-Diamond Syndrome Presenting With Pancytopenia At An Early Age: The First Report From Turkey
(Springer India, 2013)
A three-month-old boy presented with growth failure, skeletal abnormalities, otitis media and pancytopenia. Exocrine pancreatic insufficiency was confirmed by low levels of fecal elastase. He was diagnosed as Shwachman-Diamond ...
Autoimmune Hemolytic Anemia and Giant Cell Hepatitis: Report of Three Infants
(Galenos Yayıncılık, 2010)
Giant cell hepatitis associated with direct Coombs' test-positive hemolytic anemia is a rare condition of childhood and the pathogenesis remains unclear. An autoimmune activation and loss of self-tolerance in these patients ...
The Frequency of A91V in the Perforin Gene and the Effect of Tumor Necrosis Factor-Alpha Promoter Polymorphism on Acquired Hemophagocytic Lympholmstiocytosis
(Galenos Yayıncılık, 2011)
Objective: Numerous acquired etiological factors, such as infections, malignancies, and collagen tissue disorders, are involved in the development of acquired hemophagocytic lymphohistiocytosis (AHLH). Not everyone with ...