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73 results on '"Ikinciogullari, Aydan"'

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1. Author Correction: GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway

2. GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway

5. Impaired thymic AIRE expression underlies autoantibodies against type I IFNs in humans with inborn errors of the alternative NF-kB pathway

6. The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity

8. The Determining Factors for Outcome of Pediatric Intensive Care Admitted Children After Stem Cell Transplantation

10. Hematopoietic cell transplantation in severe combined immunodeficiency: The SCETIDE 2006-2014 European cohort

11. Effects of Umbilical Cord Management Strategies on Stem Cell Transfusion, Delivery Room Adaptation, and Cerebral Oxygenation in Term and Late Preterm Infants

12. Newborn Screening for SCID: The very first prospective pilot study from Turkey

14. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

15. Impaired respiratory burst contributes to infections in PKCδ-deficient patients

16. Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child

17. Single-Center Study of 72 Patients with Severe Combined Immunodeficiency: Clinical and Laboratory Features and Outcomes

18. Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations

20. Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency

21. Correction: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

23. Hematopoietic stem cell transplantation for CD40 ligand deficiency: Results from an EBMT/ESID-IEWP-SCETIDE-PIDTC study

24. Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 Deficiency

25. X-linked agammaglobulinemia (XLA): Phenotype, diagnosis, and therapeutic challenges around the world

26. Human IFN-γ immunity to mycobacteria is governed by both IL-12 and IL-23

27. Disruption of an antimycobacterial circuit between dendritic and helper T cells in human SPPL2a deficiency

28. Multiple Presentations of LRBA Deficiency: a Single-Center Experience

31. Primary T-cell immunodeficiency with functional revertant somatic mosaicism in CD247

32. Combined immunodeficiency and Epstein-Barr virus–induced B cell malignancy in humans with inherited CD70 deficiency

33. Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency

36. Natural killer cell hyporesponsiveness and impaired development in a CD247-deficient patient

38. Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasis

41. The seroprevalence of Kaposi′s sarcoma associated herpes virus and human herpes virus-6 in pediatric patients with cancer and healthy children in a Turkish pediatric oncology center

42. Diagnosis of immunodeficiency caused by a purine nucleoside phosphorylase defect by using tandem mass spectrometry on dried blood spots

44. BCG vaccination in patients with severe combined immunodeficiency: Complications, risks, and vaccination policies

49. Selenium in the Prevention of Anthracycline-Induced Cardiac Toxicity in Children with Cancer

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