25 results on '"Barbouche, Mohamed-Ridha"'
Search Results
2. Regulatory T-cell dysfunction and cutaneous exposure to Staphylococcus aureus underlie eczema in DOCK8 deficiency
3. Genetics of Inborn Errors of Immunity in highly consanguineous Middle Eastern and North African populations
4. The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity
5. Development and comparative evaluation of SARS-CoV-2 S-RBD and N based ELISA tests in various African endemic settings
6. Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry
7. CFP32 as a target to attenuate the heterogeneous antibody response against Mycobacterium tuberculosis antigens in different endemic settings
8. Performance of GeneXpert ultra in the diagnosis of Tuberculous Cervical lymphadenitis in formalin fixed paraffin embedded tissues
9. Discriminative expression of CD39 and CD73 in Cerebrospinal fluid of patients with Multiple Sclerosis and Neuro-Behçet’s disease
10. Toward personalization of asthma treatment according to trigger factors
11. Defective glycosylation leads to defective gp130-dependent STAT3 signaling in PGM3-deficient patients
12. Impaired TGF-β signaling in patients with active systemic lupus erythematosus is associated with an overexpression of IL-22
13. Cerebrospinal fluid IL-10 as an early stage discriminative marker between multiple sclerosis and neuro-Behçet disease
14. New insights into physiopathology of immunodeficiency-associated vaccine-derived poliovirus infection; systematic review of over 5 decades of data
15. Specific immune responses in mice following subchronic exposure to acetamiprid
16. A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients
17. Homozygous transcription factor 3 gene (TCF3) mutation is associated with severe hypogammaglobulinemia and B-cell acute lymphoblastic leukemia
18. Autoimmune lymphoproliferative syndrome caused by homozygous FAS mutations with normal or residual protein expression
19. Adénite granulomateuse révélant un déficit en récepteur de l’IL12
20. Activation induced cytidine deaminase mutant (AID-His130Pro) from Hyper IgM 2 patient retained mutagenic activity on SHM artificial substrate
21. The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
22. Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels
23. IL-17 T Cells’ Defective Differentiation In Vitro Despite Normal Range Ex Vivo in Chronic Mucocutaneous Candidiasis Due to STAT1 Mutation
24. Relationship between toll-like receptor 2 nonsynonymous single nucleotide polymorphisms and the effectiveness of Bacille Calmette-Guérin immunotherapy in preventing recurrence of superficial bladder cancer: A prospective study
25. Promoter and neck region length variation of DC-SIGN is not associated with susceptibility to tuberculosis in Tunisian patients
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