315 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. Genetics of Inborn Errors of Immunity in highly consanguineous Middle Eastern and North African populations
5. The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity
6. Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry
7. Incidence and risk factors of SARS-CoV-2 infection among workers in a public health laboratory in Tunisia
8. A Novel Point-of-Care Rapid Diagnostic Test for Screening Individuals for Antibody Deficiencies
9. The Seven STAT3-Related Hyper-IgE Syndromes
10. Performance of GeneXpert ultra in the diagnosis of Tuberculous Cervical lymphadenitis in formalin fixed paraffin embedded tissues
11. Discriminative expression of CD39 and CD73 in Cerebrospinal fluid of patients with Multiple Sclerosis and Neuro-Behçet’s disease
12. Toward personalization of asthma treatment according to trigger factors
13. A Longitudinal Study in Tunisia to Assess the Anti-RBD IgG and IgA Responses Induced by Three Different COVID-19 Vaccine Platforms
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. HBHA-IGRA and cytotoxic mediators release assays for the diagnosis of cervical tuberculous lymphadenitis
19. Impaired TGF-β signaling in patients with active systemic lupus erythematosus is associated with an overexpression of IL-22
20. Cerebrospinal fluid IL-10 as an early stage discriminative marker between multiple sclerosis and neuro-Behçet disease
21. Specific immune responses in mice following subchronic exposure to acetamiprid
22. A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients
23. Comprehensive review of autoantibodies in patients with hyper-IgM syndrome
24. Correction to: The Seven STAT3‑Related Hyper‑IgE Syndromes
25. Activation induced cytidine deaminase mutant (AID-His130Pro) from Hyper IgM 2 patient retained mutagenic activity on SHM artificial substrate
26. Diagnostic challenge in a series of eleven patients with hyper IgE syndromes
27. Development and comparative evaluation of SARS-CoV-2 S-RBD and N based ELISA tests in various African endemic settings
28. The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
29. African Society for Immunodeficiency (Asid) Guidelines for Diagnosis and Management of Inborn Errors of Immunity in Africa: Core Concept, Development and Initial Results
30. Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry
31. Consanguinity and Primary Immunodeficiencies
32. A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients
33. Glycoproteomic studies of IgE from a novel hyper IgE syndrome linked to PGM3 mutation
34. X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations
35. Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients
36. Increased T-bet/GATA-3 and ROR-γt /Foxp3 Ratios in Cerebrospinal Fluid as Potential Criteria for Definite Neuro-Behçet’s Disease
37. 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
38. Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988–2012)
39. Long-Term Observational Study of Chronic Granulomatous Disease About 41 Patients From Tunisia and Comparison to Other Long-Term Follow-Up Studies
40. COVID-19 in Tunisia (North Africa): Seroprevalence of SARS-CoV-2 in the General Population of the Capital City Tunis
41. B Cells Specific CpG Induces High IL-10 and IL-6 Expression In Vitro in Neuro-Behçet’s Disease
42. CFP32 as a target to attenuate the heterogeneous antibody response against Mycobacterium tuberculosis antigens in different endemic settings
43. COVID-19 in Tunisia (North Africa): IgG and IgG subclass antibody responses to SARS-CoV-2 according to disease severity
44. COVID-19 in Tunisia (North Africa): Seroprevalence of SARS-CoV-2 in the general population of the capital city Tunis
45. Editorial: Immune-Related Non-Communicable Diseases in Africa
46. Culture filtrate protein 32 as a potential target to attenuate the heterogeneous antibody response against Mycobacterium tuberculosis Antigens in different endemic settings
47. A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients
48. Diagnostic challenge in a series of eleven patients with hyper IgE syndromes.
49. Homozygous transcription factor 3 gene (TCF3) mutation is associated with severe hypogammaglobulinemia and B-cell acute lymphoblastic leukemia
50. Clinical and Genetic Heterogeneity of Inherited Autosomal Recessive Susceptibility to Disseminated Mycobacterium bovis Bacille Calmette-Guérin Infection
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