Search

Your search keyword '"BariŞ, Safa"' showing total 26 results

Search Constraints

Start Over You searched for: Author "BariŞ, Safa" Remove constraint Author: "BariŞ, Safa" Publication Year Range Last 3 years Remove constraint Publication Year Range: Last 3 years
26 results on '"BariŞ, Safa"'

Search Results

1. Extended clinical phenotypes and treatment modalities in 32 JAGN1-deficient patients: a multicenter study by ESID and EBMT IEWP

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

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

6. 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

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

8. Ruxolitinib treatment ameliorates clinical, immunologic, and transcriptomic aberrations in patients with STAT3 gain-of-function disease

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

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

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

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

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

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

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

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

17. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome

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

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

20. Mucus sialylation determines intestinal host-commensal homeostasis

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

22. 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)

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

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

Catalog

Books, media, physical & digital resources