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2. MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort

4. Regulatory T-cell dysfunction and cutaneous exposure to Staphylococcus aureus underlie eczema in DOCK8 deficiency

5. Evaluating the efficacy and safety of pozelimab in patients with CD55 deficiency with hyperactivation of complement, angiopathic thrombosis, and protein-losing enteropathy disease: an open-label phase 2 and 3 study

6. Diagnostic evaluation of paediatric autoimmune lymphoproliferative immunodeficiencies (ALPID): a prospective cohort study

7. Human germline gain-of-function in STAT6: from severe allergic disease to lymphoma and beyond

8. Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiency

9. Outcomes of hematopoietic stem cell gene therapy for Wiskott-Aldrich syndrome

10. Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients

11. Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

12. Biallelic NFATC1 mutations cause an inborn error of immunity with impaired CD8+ T-cell function and perturbed glycolysis

13. Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1

14. Severe allergic dysregulation due to a gain of function mutation in the transcription factor STAT6

15. Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes

16. Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry

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

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

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

23. Diagnostic Modalities Based on Flow Cytometry for Chronic Granulomatous Disease: A Multicenter Study in a Well-Defined Cohort

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

25. Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency

26. Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency

29. Corrigendum to “Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients” [Clinical Immunology 255 (2023) 109757]

31. 25 A phase 2/3 study evaluating the efficacy and safety of pozelimab in patients with CD55 deficiency with hyperactivation of complement, angiopathic thrombosis, and protein-losing enteropathy (CHAPLE disease)

34. TNFRSF13B VARIANTS ACT AS MODIFIERS TO CLINICAL PHENOTYPES IN COMMON VARIABLE IMMUNE DEFICIENCY DISORDERS.

35. Expanding the clinical and immunological phenotypes and natural history of MALT1 deficiency

38. GIMAP5 maintains liver endothelial cell homeostasis and

41. Reference values for T and B lymphocyte subpopulations in Turkish children and adults

44. Multiple Brain Abscesses Due to Actinomyces Odontolyticus: A Rare Infection In a Previously Healthy Child

45. Multiple brain abscesses due to actinomyces odontolyticus: a rare infection in a previously healthy child

46. The Diagnostic Value of Flow Cytometry in DOCK8 Deficiency

47. Lymphocyte Functions in Patients with Chronic Granulomatous Disease and Carrier Individuals

48. Akan Hücre ile CD55 Eksikliği Hastalığı Taraması

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