26 results on '"BariŞ, Safa"'
Search Results
2. DOCK8 deficiency due to a deep intronic variant in two kindreds with hyper-IgE syndrome
3. MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort
4. Neurocognitive Impairment in Patients With Ataxia Telangiectasia and Their Unaffected Parents: Is It Similar?
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)
23. A Rare Immunodeficiency As a Cause of Inflammatory Bowel Disease; ARPC1B Deficiency
24. Clinical and immunological outcomes of SARS-CoV-2 infection in patients with inborn errors of immunity receiving different brands and doses of COVID-19 vaccines.
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
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.