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Maryam Kallel-Sellami

Showing results (21-30 of 26) with videos related to

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Frontiers in Immunology|July 2, 2021
SFRP5 Enhances Wnt5a Induced-Inflammation in Rheumatoid Arthritis Fibroblast-Like SynoviocytesDorra Elhaj Mahmoud, Wajih Kaabachi, Nadia Sassi, et al.
The Indian Journal of Tuberculosis|April 13, 2021
Interferon-γ (+874 T/A) and interleukin-10 (-1082 G/A) genes polymorphisms are associated with active tuberculosis in the Algerian population of Oran's cityMohamed Ghermi, Sofiane Reguieg, Khadidja Attab, et al.
Nephrology (Carlton, Vic.)|January 3, 2018
Molecular basis of complement factor I deficiency in Tunisian atypical haemolytic and uraemic syndrome patientsHend Jlajla, Fatma Dehman, Manel Jallouli, et al.
Frontiers in Immunology|September 2, 2025
High prevalence of the hotspot complement factor I p.Ile357Met pathogenic variant in Tunisian atypical hemolytic uremic syndrome patients: report of three new cases and review of the literatureAsma Tajouri, Imen Ayadi, Rimeh BenBrahim, et al.
Frontiers in Immunology|August 25, 2025
Urticarial hypocomplementemic vasculitis syndrome and systemic lupus erythematosus: a case report and review of the literatureYasmina Ouerdani, Tayssir Ben Achour, Ahlem Ben Hmid, et al.
Journal of Autoimmunity|June 30, 2015
Marked variability in clinical presentation and outcome of patients with C1q immunodeficiencyRosanne A van Schaarenburg, Lone Schejbel, Lennart Truedsson, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Frontiers in Immunology|July 2, 2021
SFRP5 Enhances Wnt5a Induced-Inflammation in Rheumatoid Arthritis Fibroblast-Like SynoviocytesDorra Elhaj Mahmoud, Wajih Kaabachi, Nadia Sassi, et al.
The Indian Journal of Tuberculosis|April 13, 2021
Interferon-γ (+874 T/A) and interleukin-10 (-1082 G/A) genes polymorphisms are associated with active tuberculosis in the Algerian population of Oran's cityMohamed Ghermi, Sofiane Reguieg, Khadidja Attab, et al.
Nephrology (Carlton, Vic.)|January 3, 2018
Molecular basis of complement factor I deficiency in Tunisian atypical haemolytic and uraemic syndrome patientsHend Jlajla, Fatma Dehman, Manel Jallouli, et al.
Frontiers in Immunology|September 2, 2025
High prevalence of the hotspot complement factor I p.Ile357Met pathogenic variant in Tunisian atypical hemolytic uremic syndrome patients: report of three new cases and review of the literatureAsma Tajouri, Imen Ayadi, Rimeh BenBrahim, et al.
Frontiers in Immunology|August 25, 2025
Urticarial hypocomplementemic vasculitis syndrome and systemic lupus erythematosus: a case report and review of the literatureYasmina Ouerdani, Tayssir Ben Achour, Ahlem Ben Hmid, et al.
Journal of Autoimmunity|June 30, 2015
Marked variability in clinical presentation and outcome of patients with C1q immunodeficiencyRosanne A van Schaarenburg, Lone Schejbel, Lennart Truedsson, et al.
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