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Aziz Bousfiha

Showing results (31-40 of 151) with videos related to

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The Pan African Medical Journal|December 6, 2014
[Neonatal erythroderma: do not ignore an immune deficiency]Aziza El Ouali, Yousra El Boussaadni, Fatima Ailal, et al.
La Tunisie Medicale|November 16, 2019
Bibliometric profil of medical publication at Faculty of Medicine of Casablanca (2008-2017)Sofia Zoukal, Ahmed Ben Abdelaziz, Nadia Tahiri Jouti, et al.
Human Heredity|October 19, 2020
A Homozygous RAG1 Gene Mutation in a Case of Combined Immunodeficiency: Clinical, Molecular, and Computational AnalysisSoukaina Essadssi, Ibtihal Benhsaien, Amina Bakhchane, et al.
La Tunisie Medicale|December 26, 2022
When to suspect an immune deficiency in adults?Abire Allaoui, Khaoula Mokhantar, Leila Jeddane, et al.
European Journal of Case Reports in Internal Medicine|July 10, 2025
Vexas Syndrome in a Moroccan Patient: The Story of a Two-Year Diagnostic LagAbire Allaoui, Lilia Zizi, Halima Hadri, et al.
Journal of Clinical Immunology|August 1, 2012
Primary immunodeficiency diseases worldwide: more common than generally thoughtAhmed Aziz Bousfiha, Leïla Jeddane, Fatima Ailal, et al.
International Journal for Quality in Health Care : Journal of the International Society for Quality in Health Care|January 29, 2026
ISO 9001 in hospitals: a systematic review and implementation framework for clinical services in emerging countriesJihad Boukhaldi, Hind Kechkar, Abderrahmane Errami, et al.
Frontiers in Immunology|March 27, 2026
Autoimmunity and inborn errors of immunity: a complex coexistenceAhamada Elamine, Ibtihal Benhsaien, Fatima Ailal, et al.
Immunobiology|May 8, 2021
Omenn syndrome caused by a novel homozygous mutation in recombination activating gene 1Ibtihal Benhsaien, Soukaina Essadssi, Lamiae Elkhattabi, 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.
Pageof 16

Showing results (31-40 of 151) with videos related to

Sort By:
Pageof 16
The Pan African Medical Journal|December 6, 2014
[Neonatal erythroderma: do not ignore an immune deficiency]Aziza El Ouali, Yousra El Boussaadni, Fatima Ailal, et al.
La Tunisie Medicale|November 16, 2019
Bibliometric profil of medical publication at Faculty of Medicine of Casablanca (2008-2017)Sofia Zoukal, Ahmed Ben Abdelaziz, Nadia Tahiri Jouti, et al.
Human Heredity|October 19, 2020
A Homozygous RAG1 Gene Mutation in a Case of Combined Immunodeficiency: Clinical, Molecular, and Computational AnalysisSoukaina Essadssi, Ibtihal Benhsaien, Amina Bakhchane, et al.
La Tunisie Medicale|December 26, 2022
When to suspect an immune deficiency in adults?Abire Allaoui, Khaoula Mokhantar, Leila Jeddane, et al.
European Journal of Case Reports in Internal Medicine|July 10, 2025
Vexas Syndrome in a Moroccan Patient: The Story of a Two-Year Diagnostic LagAbire Allaoui, Lilia Zizi, Halima Hadri, et al.
Journal of Clinical Immunology|August 1, 2012
Primary immunodeficiency diseases worldwide: more common than generally thoughtAhmed Aziz Bousfiha, Leïla Jeddane, Fatima Ailal, et al.
International Journal for Quality in Health Care : Journal of the International Society for Quality in Health Care|January 29, 2026
ISO 9001 in hospitals: a systematic review and implementation framework for clinical services in emerging countriesJihad Boukhaldi, Hind Kechkar, Abderrahmane Errami, et al.
Frontiers in Immunology|March 27, 2026
Autoimmunity and inborn errors of immunity: a complex coexistenceAhamada Elamine, Ibtihal Benhsaien, Fatima Ailal, et al.
Immunobiology|May 8, 2021
Omenn syndrome caused by a novel homozygous mutation in recombination activating gene 1Ibtihal Benhsaien, Soukaina Essadssi, Lamiae Elkhattabi, 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.
Pageof 16