Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Fatima Ailal

Showing results (11-20 of 68) with videos related to

Pageof 7
Sort By:
Annales De Biologie Clinique|October 27, 2021
[Genetic basis of common variable immunodeficiency: from common to variable]Abire Allaoui, Khaoula Mokhantar, Leila Jeddane, et al.
Qatar Medical Journal|May 22, 2025
Clinical manifestations of 42 Moroccan patients with chronic granulomatous diseaseAssma Dably, Ibtihal Benhssaein, Jalila El Bakkouri, et al.
Journal of Clinical Immunology|March 30, 2017
Poikiloderma with Neutropenia in Morocco: a Report of Four CasesAyoub Aglaguel, Houria Abdelghaffar, Fatima Ailal, et al.
Qatar Medical Journal|August 1, 2022
Chronic upper airway inflammation related to high Th2 cytokines in Mendelian susceptibility to mycobacterial disease caseIbtihal Benhsaien, Rui Yang, Fatima Ailal, et al.
The Pan African Medical Journal|December 16, 2022
[Autoimmune lymphoproliferative syndrome: a case report]Houda Ben Youssif, Fatima Ailal, Ibtihal Benhsaien, et al.
Cureus|June 16, 2025
CHARGE Syndrome in a Six-Month-Old Male Infant: A Case ReportKawtar El Ouassifi, Anas Douami, Hind Ouair, et al.
Qatar Medical Journal|November 29, 2023
Classification of common variable immunodeficiency through immunological and clinical phenotyping in Moroccan patientsKhaoula Mokhantar, Abir Allaoui, Fatima Ailal, et al.
Journal of Clinical Immunology|January 6, 2021
Pediatric Demodicosis Associated with Gain-of-Function Variant in STAT1 Presenting as Rosacea-Type RashBouchra Baghad, Fatima Zahra El Fatoiki, Ibtihal Benhsaien, et al.
Pathogens (Basel, Switzerland)|August 26, 2022
HPV-Related Skin Phenotypes in Patients with Inborn Errors of ImmunityAssiya El Kettani, Fatima Ailal, Jalila El Bakkouri, et al.
European Journal of Pediatrics|April 24, 2010
The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan populationHamid Naamane, Ouafaa El Maataoui, Fatima Ailal, et al.
Pageof 7

Showing results (11-20 of 68) with videos related to

Sort By:
Pageof 7
Annales De Biologie Clinique|October 27, 2021
[Genetic basis of common variable immunodeficiency: from common to variable]Abire Allaoui, Khaoula Mokhantar, Leila Jeddane, et al.
Qatar Medical Journal|May 22, 2025
Clinical manifestations of 42 Moroccan patients with chronic granulomatous diseaseAssma Dably, Ibtihal Benhssaein, Jalila El Bakkouri, et al.
Journal of Clinical Immunology|March 30, 2017
Poikiloderma with Neutropenia in Morocco: a Report of Four CasesAyoub Aglaguel, Houria Abdelghaffar, Fatima Ailal, et al.
Qatar Medical Journal|August 1, 2022
Chronic upper airway inflammation related to high Th2 cytokines in Mendelian susceptibility to mycobacterial disease caseIbtihal Benhsaien, Rui Yang, Fatima Ailal, et al.
The Pan African Medical Journal|December 16, 2022
[Autoimmune lymphoproliferative syndrome: a case report]Houda Ben Youssif, Fatima Ailal, Ibtihal Benhsaien, et al.
Cureus|June 16, 2025
CHARGE Syndrome in a Six-Month-Old Male Infant: A Case ReportKawtar El Ouassifi, Anas Douami, Hind Ouair, et al.
Qatar Medical Journal|November 29, 2023
Classification of common variable immunodeficiency through immunological and clinical phenotyping in Moroccan patientsKhaoula Mokhantar, Abir Allaoui, Fatima Ailal, et al.
Journal of Clinical Immunology|January 6, 2021
Pediatric Demodicosis Associated with Gain-of-Function Variant in STAT1 Presenting as Rosacea-Type RashBouchra Baghad, Fatima Zahra El Fatoiki, Ibtihal Benhsaien, et al.
Pathogens (Basel, Switzerland)|August 26, 2022
HPV-Related Skin Phenotypes in Patients with Inborn Errors of ImmunityAssiya El Kettani, Fatima Ailal, Jalila El Bakkouri, et al.
European Journal of Pediatrics|April 24, 2010
The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan populationHamid Naamane, Ouafaa El Maataoui, Fatima Ailal, et al.
Pageof 7