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1. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency.

2. DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans

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

4. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

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

7. Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome.

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

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

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

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

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

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

18. Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score

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

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

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

22. BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policies.

23. Clinical Features and HSCT Outcome for SCID in Turkey

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

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

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

30. Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies

31. What happens to basophils and tryptase, LXA4 and CysLTs during aspirin desensitization?

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

38. Clinical Features of Candidiasis in Patients With Inherited Interleukin 12 Receptor β1 Deficiency

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

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

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

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

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

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

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