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Fatima Ailal

Showing results (51-60 of 69) with videos related to

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Journal of Clinical Immunology|November 11, 2022
Genetic Diagnosis of Inborn Errors of Immunity in an Emerging Country: a Retrospective Study of 216 Moroccan PatientsAbderrahmane Moundir, Hind Ouair, Ibtihal Benhsaien, et al.
La Tunisie Medicale|October 23, 2024
Phenotypes of 126 Moroccan HIES patients according to NIH ScoreIlham Fadil, Ibtihal Benhsaien, Jalila El Bakkouri, et al.
Journal of Human Immunity|July 8, 2026
Chronic granulomatous disease: A multicenter study from the MENA regionSalem Al-Tamemi, Najla Mekki, Fatima Ailal, et al.
Journal of Clinical Immunology|May 10, 2013
A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedsideAhmed Aziz Bousfiha, Leïla Jeddane, Fatima Ailal, et al.
Journal of Clinical Immunology|October 9, 2015
The 2015 IUIS Phenotypic Classification for Primary ImmunodeficienciesAziz Bousfiha, Leïla Jeddane, Waleed Al-Herz, et al.
Journal of Clinical Immunology|March 6, 2014
Chronic granulomatous disease in Morocco: genetic, immunological, and clinical features of 12 patients from 10 kindredsLaila Ait Baba, Fatima Ailal, Naima El Hafidi, et al.
Journal of Clinical Immunology|December 12, 2017
The 2017 IUIS Phenotypic Classification for Primary ImmunodeficienciesAziz Bousfiha, Leïla Jeddane, Capucine Picard, et al.
The Journal of Experimental Medicine|March 8, 2022
A partial form of inherited human USP18 deficiency underlies infection and inflammationMarta Martin-Fernandez, Sofija Buta, Tom Le Voyer, et al.
The Journal of Allergy and Clinical Immunology|December 25, 2016
Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variantsReiko Kagawa, Ryoji Fujiki, Miyuki Tsumura, et al.
Journal of Clinical Immunology|March 3, 2016
X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK MutationsZahra Aadam, Nadia Kechout, Abdelhamid Barakat, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
Journal of Clinical Immunology|November 11, 2022
Genetic Diagnosis of Inborn Errors of Immunity in an Emerging Country: a Retrospective Study of 216 Moroccan PatientsAbderrahmane Moundir, Hind Ouair, Ibtihal Benhsaien, et al.
La Tunisie Medicale|October 23, 2024
Phenotypes of 126 Moroccan HIES patients according to NIH ScoreIlham Fadil, Ibtihal Benhsaien, Jalila El Bakkouri, et al.
Journal of Human Immunity|July 8, 2026
Chronic granulomatous disease: A multicenter study from the MENA regionSalem Al-Tamemi, Najla Mekki, Fatima Ailal, et al.
Journal of Clinical Immunology|May 10, 2013
A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedsideAhmed Aziz Bousfiha, Leïla Jeddane, Fatima Ailal, et al.
Journal of Clinical Immunology|October 9, 2015
The 2015 IUIS Phenotypic Classification for Primary ImmunodeficienciesAziz Bousfiha, Leïla Jeddane, Waleed Al-Herz, et al.
Journal of Clinical Immunology|March 6, 2014
Chronic granulomatous disease in Morocco: genetic, immunological, and clinical features of 12 patients from 10 kindredsLaila Ait Baba, Fatima Ailal, Naima El Hafidi, et al.
Journal of Clinical Immunology|December 12, 2017
The 2017 IUIS Phenotypic Classification for Primary ImmunodeficienciesAziz Bousfiha, Leïla Jeddane, Capucine Picard, et al.
The Journal of Experimental Medicine|March 8, 2022
A partial form of inherited human USP18 deficiency underlies infection and inflammationMarta Martin-Fernandez, Sofija Buta, Tom Le Voyer, et al.
The Journal of Allergy and Clinical Immunology|December 25, 2016
Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variantsReiko Kagawa, Ryoji Fujiki, Miyuki Tsumura, et al.
Journal of Clinical Immunology|March 3, 2016
X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK MutationsZahra Aadam, Nadia Kechout, Abdelhamid Barakat, et al.
Pageof 7