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Ibtihal Benhsaien

Showing results (1-10 of 47) with videos related to

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Journal of Clinical Immunology|November 27, 2016
Primary Immunodeficiency Classification on SmartphoneLeïla Jeddane, Hind Ouair, Ibtihal Benhsaien, et al.
Case Reports in Immunology|January 28, 2021
Severe Combined Immunodeficiency Disorder due to a Novel Mutation in Recombination Activation Gene 2: About 2 CasesIbtihal Benhsaien, Fatima Ailal, Khadija Elazhary, 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.
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|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.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Journal of Clinical Immunology|November 27, 2016
Primary Immunodeficiency Classification on SmartphoneLeïla Jeddane, Hind Ouair, Ibtihal Benhsaien, et al.
Case Reports in Immunology|January 28, 2021
Severe Combined Immunodeficiency Disorder due to a Novel Mutation in Recombination Activation Gene 2: About 2 CasesIbtihal Benhsaien, Fatima Ailal, Khadija Elazhary, 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.
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|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.
Pageof 5