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Aziz Bousfiha

Showing results (51-60 of 152) with videos related to

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La Tunisie Medicale|August 12, 2024
Jean Claude Majambere, Sanae Zaidi, Abderrahmane Errami, 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.
La Tunisie Medicale|March 28, 2024
Mohamed Hbibi, Mounira El Alaoui El Hanafi, Zakaria Kasmi, et al.
Respiratory Medicine Case Reports|July 7, 2018
Alpha1 antitrypsin deficiency due to an homozygous PI* Null Q0Cairo mutation: Early onset of pulmonary manifestations and variability of clinical expressionZineb Jouhadi, Marie Francoise Odou, Farid Zerimech, et al.
Frontiers in Immunology|February 16, 2026
Case Report: IL2RA (CD25) deficiency: first reported cases in MoroccoAhamada Elamine, Ibtihal Benhsaien, Abderrahmane Errami, et al.
Case Reports in Immunology|August 4, 2025
Major Histocompatibility Complex Class II Deficiency Beyond InfancyAziza Bachir Kattra, Ibtihal Benhsaien, Asmaa Drissi Bourhanbour, et al.
BMC Pediatrics|April 6, 2026
Levels of IL-1β and IL-1 receptor antagonist (IL-1Ra) in Moroccan children admitted to the pediatric emergency department for febrile seizuresImane Abbari, Sara Missaoui, Halima Kholaiq, 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.
BMC Infectious Diseases|December 16, 2025
Molecular characterization of extended spectrum beta-lactamase-producing Enterobacterales from urinary tract infections in BurundiArmstrong Ndihokubwayo, Néhémie Nzoyikorera, Joseph Nyandwi, et al.
Global Pediatric Health|November 4, 2024
Multisystem Inflammatory Syndrome in Children (MIS-C) Associated With COVID-19 Infection in MoroccoNaima Amenzoui, Siham Zouiter, Meriem Nassid, et al.
Pageof 16

Showing results (51-60 of 152) with videos related to

Sort By:
Pageof 16
La Tunisie Medicale|August 12, 2024
Jean Claude Majambere, Sanae Zaidi, Abderrahmane Errami, 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.
La Tunisie Medicale|March 28, 2024
Mohamed Hbibi, Mounira El Alaoui El Hanafi, Zakaria Kasmi, et al.
Respiratory Medicine Case Reports|July 7, 2018
Alpha1 antitrypsin deficiency due to an homozygous PI* Null Q0Cairo mutation: Early onset of pulmonary manifestations and variability of clinical expressionZineb Jouhadi, Marie Francoise Odou, Farid Zerimech, et al.
Frontiers in Immunology|February 16, 2026
Case Report: IL2RA (CD25) deficiency: first reported cases in MoroccoAhamada Elamine, Ibtihal Benhsaien, Abderrahmane Errami, et al.
Case Reports in Immunology|August 4, 2025
Major Histocompatibility Complex Class II Deficiency Beyond InfancyAziza Bachir Kattra, Ibtihal Benhsaien, Asmaa Drissi Bourhanbour, et al.
BMC Pediatrics|April 6, 2026
Levels of IL-1β and IL-1 receptor antagonist (IL-1Ra) in Moroccan children admitted to the pediatric emergency department for febrile seizuresImane Abbari, Sara Missaoui, Halima Kholaiq, 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.
BMC Infectious Diseases|December 16, 2025
Molecular characterization of extended spectrum beta-lactamase-producing Enterobacterales from urinary tract infections in BurundiArmstrong Ndihokubwayo, Néhémie Nzoyikorera, Joseph Nyandwi, et al.
Global Pediatric Health|November 4, 2024
Multisystem Inflammatory Syndrome in Children (MIS-C) Associated With COVID-19 Infection in MoroccoNaima Amenzoui, Siham Zouiter, Meriem Nassid, et al.
Pageof 16