14 results on '"Barbouche, Mohamed-Ridha"'
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2. A Novel Point-of-Care Rapid Diagnostic Test for Screening Individuals for Antibody Deficiencies
3. Correction to: The Seven STAT3‑Related Hyper‑IgE Syndromes
4. The Seven STAT3-Related Hyper-IgE Syndromes
5. Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families
6. Comprehensive review of autoantibodies in patients with hyper-IgM syndrome
7. A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients
8. X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations
9. Glycoproteomic studies of IgE from a novel hyper IgE syndrome linked to PGM3 mutation
10. Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients
11. Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988–2012)
12. A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients
13. Clinical, Immunological and Genetic Findings of a Large Tunisian Series of Major Histocompatibility Complex Class II Deficiency Patients
14. Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome)
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