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Toplam kayıt 184, listelenen: 181-184
Jacobsen syndrome: a case report and clinical features of a rare genetic syndrome
(2022)
Objective: Jacobsen syndrome is an infrequent contiguous gene syndrome that involves the deletion of the long arm of chromosome 11. It is mostly accompanied by intellectual disability and other abnormalities. The majority ...
A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome
(2022)
[Abstract Not Available]
The Relationship Between KRAS Mutation and 18F-FDG Uptake Parameters in Colorectal Cancer
(2022)
Objective: Our purpose in this study was to evaluate whether Kirsten rat sarcoma viral oncogene (KRAS) exon-2 mutation affected 18F-fluorodeoxyglucose (FDG) accumulation patterns, total lesion glycolysis and metabolic tumor ...
Immunological Risk Monitoring in Patients with High Immunologic Risk and Its Effects on Clinical Outcomes
(2023)
Objective: In this study, it was aimed to follow up the immunological risk of patients with high immunological risk and to determine the effect of desensitization treatment in these patients. Materials and Methods: Living ...