130 results on '"BARIŞ, SAFA"'
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2. MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort
3. Neurocognitive Impairment in Patients With Ataxia Telangiectasia and Their Unaffected Parents: Is It Similar?
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
19. A set of clinical and laboratory markers differentiates hyper-IgE syndrome from severe atopic dermatitis
20. Oral Moniliasis and Failure to Thrive
21. Recurrent Respiratory Infections and Chronic Hepatic Disease
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
27. Haploidentical Related Donor Hematopoietic Stem Cell Transplantation for Dedicator-of-Cytokinesis 8 Deficiency Using Post-Transplantation Cyclophosphamide
28. Basophil activation test for inhalant allergens in pediatric patients with allergic rhinitis
29. Corrigendum to “Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients” [Clinical Immunology 255 (2023) 109757]
30. Nebulized fluticasone propionate, a viable alternative to systemic route in the management of childhood moderate asthma attack: A double-blind, double-dummy study
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)
32. A Rare Immunodeficiency As a Cause of Inflammatory Bowel Disease; ARPC1B Deficiency
33. 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.
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
36. DNA repair gene XPD and XRCC1 polymorphisms and the risk of febrile neutropenia and mucositis in children with leukemia and lymphoma
37. Outcome of hypogammaglobulinemia in children: Immunoglobulin levels as predictors
38. GIMAP5 maintains liver endothelial cell homeostasis and
39. DNA repair gene XPD and XRCC1 polymorphisms and the risk of childhood acute lymphoblastic leukemia
40. The evaluation of radiosensitivity in patients with STAT3 deficiency
41. Reference values for T and B lymphocyte subpopulations in Turkish children and adults
42. Autosomal recessive agammaglobulinemic patient with a novel large deletion in IGHM presenting with mild clinical phenotype
43. Lrba ve ctla4eksi̇kli̇kleri̇ni̇n tanısında ve ayırımda akım si̇tometri̇ni̇n yeri̇
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
49. A FLOW-CYTOMETRY BASED SCREENING FOR CD55 DEFICIENCY IS A RAPID
50. Mothers of Autosomal Recessive Chronic Granulomatous Disease Patients Do Not Show Autoimmune Findings in contrast to X-Linked Patients
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