301 results on '"Barbouche, Mohamed Ridha"'
Search Results
2. Increased IL-22 in cerebrospinal fluid of neuro-behçet’s disease patients
3. Regulatory T-cell dysfunction and cutaneous exposure to Staphylococcus aureus underlie eczema in DOCK8 deficiency
4. Development and comparative evaluation of SARS-CoV-2 S-RBD and N based ELISA tests in various African endemic settings
5. Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry
6. Incidence and risk factors of SARS-CoV-2 infection among workers in a public health laboratory in Tunisia
7. The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity
8. A Novel Point-of-Care Rapid Diagnostic Test for Screening Individuals for Antibody Deficiencies
9. A Longitudinal Study in Tunisia to Assess the Anti-RBD IgG and IgA Responses Induced by Three Different COVID-19 Vaccine Platforms
10. The Seven STAT3-Related Hyper-IgE Syndromes
11. Performance of GeneXpert ultra in the diagnosis of Tuberculous Cervical lymphadenitis in formalin fixed paraffin embedded tissues
12. Toward personalization of asthma treatment according to trigger factors
13. HBHA-IGRA and cytotoxic mediators release assays for the diagnosis of cervical tuberculous lymphadenitis
14. Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families
15. Contributors
16. Defects in intrinsic and innate immunity
17. Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels
18. New insights into physiopathology of immunodeficiency-associated vaccine-derived poliovirus infection; systematic review of over 5 decades of data
19. Specific immune responses in mice following subchronic exposure to acetamiprid
20. Comprehensive review of autoantibodies in patients with hyper-IgM syndrome
21. Genetics of Inborn Errors of Immunity in highly consanguineous Middle Eastern and North African populations
22. Correction to: The Seven STAT3‑Related Hyper‑IgE Syndromes
23. Diagnostic challenge in a series of eleven patients with hyper IgE syndromes
24. The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity
25. The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
26. African Society for Immunodeficiency (Asid) Guidelines for Diagnosis and Management of Inborn Errors of Immunity in Africa: Core Concept, Development and Initial Results
27. Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry
28. Consanguinity and Primary Immunodeficiencies
29. A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients
30. Glycoproteomic studies of IgE from a novel hyper IgE syndrome linked to PGM3 mutation
31. X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations
32. Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients
33. Increased T-bet/GATA-3 and ROR-γt /Foxp3 Ratios in Cerebrospinal Fluid as Potential Criteria for Definite Neuro-Behçet’s Disease
34. Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity
35. Long-Term Observational Study of Chronic Granulomatous Disease About 41 Patients From Tunisia and Comparison to Other Long-Term Follow-Up Studies
36. Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988–2012)
37. COVID-19 in Tunisia (North Africa): Seroprevalence of SARS-CoV-2 in the General Population of the Capital City Tunis
38. B Cells Specific CpG Induces High IL-10 and IL-6 Expression In Vitro in Neuro-Behçet’s Disease
39. COVID-19 in Tunisia (North Africa): IgG and IgG subclass antibody responses to SARS-CoV-2 according to disease severity
40. CFP32 as a target to attenuate the heterogeneous antibody response against Mycobacterium tuberculosis antigens in different endemic settings
41. COVID-19 in Tunisia (North Africa): Seroprevalence of SARS-CoV-2 in the general population of the capital city Tunis
42. Editorial: Immune-Related Non-Communicable Diseases in Africa
43. Culture filtrate protein 32 as a potential target to attenuate the heterogeneous antibody response against Mycobacterium tuberculosis Antigens in different endemic settings
44. A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients
45. Diagnostic challenge in a series of eleven patients with hyper IgE syndromes.
46. Homozygous transcription factor 3 gene (TCF3) mutation is associated with severe hypogammaglobulinemia and B-cell acute lymphoblastic leukemia
47. Clinical and Genetic Heterogeneity of Inherited Autosomal Recessive Susceptibility to Disseminated Mycobacterium bovis Bacille Calmette-Guérin Infection
48. A Novel Point-of-Care Rapid Diagnostic Test for Screening Individuals for Antibody Deficiencies
49. Profound differences in IgE and IgG recognition of micro‐arrayed allergens in hyper‐IgE syndromes
50. Two distinct conformational states of Mycobacterium tuberculosis virulent factor early secreted antigenic target 6 kDa are behind the discrepancy around its biological functions
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