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Journal of Clinical Immunology|January 15, 2013
Clinical, immunological and genetic findings of a large tunisian series of major histocompatibility complex class II deficiency patientsImen Ben-Mustapha, Khaoula Ben-Farhat, Naouel Guirat-Dhouib, et al.
Cellular & Molecular Immunology|February 6, 2018
Comprehensive review of autoantibodies in patients with hyper-IgM syndromeMohamed-Ridha Barbouche, Qubo Chen, Marco Carbone, et al.
Frontiers in Immunology|October 2, 2025
Immunogenetic investigation of WAS patients revealing impaired IL-6/STAT3 signaling in T cellsFiras Bouzakoura, Najla Mekki, Monia Ben Khaled, et al.
Diagnostics (Basel, Switzerland)|April 23, 2022
COVID-19 in Tunisia (North Africa): Seroprevalence of SARS-CoV-2 in the General Population of the Capital City TunisInes Cherif, Ghassen Kharroubi, Sana Chaabane, et al.
Immunogenetics|November 8, 2015
Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patientsHanen Ouadani, Imen Ben-Mustapha, Meriem Ben-ali, et al.
BMJ Global Health|March 27, 2026
Lessons learnt from the COVID-19 pandemic: Middle East and North Africa regional perspective for future preparednessNoha H Farag, Ahmet Ozen, Alicen B Spaulding, et al.
Microbiology Spectrum|November 1, 2023
HBHA-IGRA and cytotoxic mediators release assays for the diagnosis of cervical tuberculous lymphadenitisSoumaya Bchiri, Asma Bouzekri, Rym Ouni, et al.
Journal of Clinical Immunology|May 26, 2016
A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven PatientsKhaoula Ben-Farhat, Imen Ben-Mustapha, Meriem Ben-Ali, et al.
Journal of Digestive Diseases|May 22, 2019
Autoantibodies in patients with interleukin 12 receptor beta 1 deficiencyVincenzo Ronca, Qu Bo Chen, Vasiliky Lygoura, et al.
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