Browsing by Author "Cipe, Funda"
Now showing items 1-4 of 4
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Comparison of allogeneic stem cell transplantation results from related or unrelated donors in beta-thalassemia major
Aydoğdu, Selime; Mergen, Azize; Aksoy, Başak; Çokluk, Mila N.; Dikme, Gürcan; Cipe, Funda; Bozkurt, Ceyhun (Nature Publishing Group, 2019)Allogeneic hematopoietic stem cell transplantation (HSCT) is the curative therapy for beta-thalassemias that induces severe life-threatening complications. The human leukocyte antigen (HLA) registries and umbilical cord ... -
Comparison of turkish stem cell coordination center (TURKOK) with Istanbul University bone marrow bank (TRIS); a single center experience in match unrelated donors
Mergen, Azize; Aydoğdu, Selime; Aksoy, Başak; Savcı, Yunus Emre; Dikme, Gürcan; Cipe, Funda; Fışgın, Tunç (Nature Publishing Group, 2019)[No abstract available] -
Donor lymphocyte infusion administrations after allogeneic stem cell transplantations in pediatrics: A single center experience
Aydoğdu, Selime; Mergen, Azize; Aksoy, Başak; Akbay, Hazal S.; Cipe, Funda; Dikme, Gürcan; Bozkurt, Ceyhun; Fışgın, Tunç (Nature Publishing Group, 2019)Allogeneic stem cell transplantation (allo-SCT) is considered the cornerstone in the treatment of several malignant and not malignant hematological diseases. However, relapse of hematological disease after allo-SCT is ... -
Malignancies and lymphoproliferations in children with primary immune deficiency-a single-center experience
Aydogmus, Cigdem; Turkyilmaz Ucar, Ozge; Kaplan Sarikavak, Sibel; Cipe, Funda; Ulas, Selami; Turan, Isilay; Naiboglu, Sezin; Yildirim, Ilke; Kalay, Gulsah; Kapci, Nermin; Al, Serdar; Gokmirza Ozdemir, Pinar; Celiksoy, Mehmet Halil (2024)Primary immune deficiencies (PIDs) are rare genetic disorders characterized by impaired immune function, leading to frequent infections and immune dysregulation. Studies have shown that individuals with PID are at an ...
