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Fatima Ailal

Showing results (31-40 of 68) with videos related to

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The Journal of Allergy and Clinical Immunology|December 23, 2018
IFN-γ and CD25 drive distinct pathologic features during hemophagocytic lymphohistiocytosisStéphanie Humblet-Baron, Dean Franckaert, James Dooley, et al.
Frontiers in Immunology|July 24, 2025
Clinical, immunological, and genetic landscape of common variable immunodeficiency in Morocco: a nationwide multicenter studyAbire Allaoui, Abderrahmane Moundir, Ibtihal Benhsaien, et al.
Annals of the New York Academy of Sciences|December 2, 2011
Primary immunodeficiencies in highly consanguineous North African populationsMohamed-Ridha Barbouche, Nermeen Galal, Imen Ben-Mustapha, et al.
Clinical and Experimental Immunology|February 7, 2025
Application of whole-exome sequencing to predict inborn errors of immunity in pediatric severe infections and sepsisAbderrahmane Moundir, Ouissal Aissaoui, Nassima Akhrichi, et al.
La Tunisie Medicale|January 15, 2025
Prevalence of pathogenic variants of inborn errors of immunity in critically ill children admitted to the pediatric intensive care unit for sepsis: A Moroccan cohort studyOuissal Aissaoui, Abderrahmane Moundir, Asmaa Drissi Boughanbour, et al.
Frontiers in Immunology|December 11, 2025
Case Report: A novel CIITA mutation causing MHC class II deficiency: first reported case in MoroccoAziza Bachir Kattra, Fatima Ailal, Ibtihal Benhsaien, et al.
BMC Medical Genomics|January 8, 2025
Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case reportZakaria Kasmi, Imane Ain El Hayat, Zahra Aadam, et al.
BMC Medical Genomics|February 3, 2025
Correction: Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case reportZakaria Kasmi, Imane Ain El Hayat, Zahra Aadam, et al.
Clinical Immunology (Orlando, Fla.)|March 19, 2010
Primary immunodeficiencies of protective immunity to primary infectionsAziz Bousfiha, Capucine Picard, Stéphanie Boisson-Dupuis, et al.
The Journal of Experimental Medicine|February 25, 2020
Homozygous STAT2 gain-of-function mutation by loss of USP18 activity in a patient with type I interferonopathyConor Gruber, Marta Martin-Fernandez, Fatima Ailal, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 7
The Journal of Allergy and Clinical Immunology|December 23, 2018
IFN-γ and CD25 drive distinct pathologic features during hemophagocytic lymphohistiocytosisStéphanie Humblet-Baron, Dean Franckaert, James Dooley, et al.
Frontiers in Immunology|July 24, 2025
Clinical, immunological, and genetic landscape of common variable immunodeficiency in Morocco: a nationwide multicenter studyAbire Allaoui, Abderrahmane Moundir, Ibtihal Benhsaien, et al.
Annals of the New York Academy of Sciences|December 2, 2011
Primary immunodeficiencies in highly consanguineous North African populationsMohamed-Ridha Barbouche, Nermeen Galal, Imen Ben-Mustapha, et al.
Clinical and Experimental Immunology|February 7, 2025
Application of whole-exome sequencing to predict inborn errors of immunity in pediatric severe infections and sepsisAbderrahmane Moundir, Ouissal Aissaoui, Nassima Akhrichi, et al.
La Tunisie Medicale|January 15, 2025
Prevalence of pathogenic variants of inborn errors of immunity in critically ill children admitted to the pediatric intensive care unit for sepsis: A Moroccan cohort studyOuissal Aissaoui, Abderrahmane Moundir, Asmaa Drissi Boughanbour, et al.
Frontiers in Immunology|December 11, 2025
Case Report: A novel CIITA mutation causing MHC class II deficiency: first reported case in MoroccoAziza Bachir Kattra, Fatima Ailal, Ibtihal Benhsaien, et al.
BMC Medical Genomics|January 8, 2025
Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case reportZakaria Kasmi, Imane Ain El Hayat, Zahra Aadam, et al.
BMC Medical Genomics|February 3, 2025
Correction: Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case reportZakaria Kasmi, Imane Ain El Hayat, Zahra Aadam, et al.
Clinical Immunology (Orlando, Fla.)|March 19, 2010
Primary immunodeficiencies of protective immunity to primary infectionsAziz Bousfiha, Capucine Picard, Stéphanie Boisson-Dupuis, et al.
The Journal of Experimental Medicine|February 25, 2020
Homozygous STAT2 gain-of-function mutation by loss of USP18 activity in a patient with type I interferonopathyConor Gruber, Marta Martin-Fernandez, Fatima Ailal, et al.
Pageof 7