Yazar "Guner, Sukru N." için listeleme
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A Case of Ataxia-telangiectasia Presented With Hemophagocytic Syndrome
Celiksoy, Mehmet H.; Cubuk, Pelin Ozyavuz; Guner, Sukru N.; Yildiran, Alisan (Lippincott Williams & Wilkins, 2018)Ataxia-telangiectasia (A-T) is a multisystem disease caused by a genetic defect located on the long arm of chromosome 11 (11p22-23). The gene defect results in the loss of A-T-mutated protein, subsequently leading to ... -
Hemophagocytic Bone Marrow Aplasia With Plasma Cells in a RAG2-deficient SCID Case After a Nonconditioned Transplantation From a Fully Matched Sibling
Yildiran, Alisan; Fisgin, Tunc; Guner, Sukru N.; Kilic, Mehtap; Sancak, Recep; Ozyurek, Emel; Duru, Feride (Lippincott Williams & Wilkins, 2013)We report a RAG2-deficient patient with severe combined immunodeficiency and hemophagocytic bone marrow aplasia with plasma cells after a nonconditioned transplantation from a fully matched sibling. After engraftment, ...