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Year Number of Results
2011 1
2014 1
2015 2
2016 1
2017 1
2020 6
2021 2
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2023 3
2024 0

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Page 1
Inherited and acquired immunodeficiencies underlying tuberculosis in childhood.
Boisson-Dupuis S, Bustamante J, El-Baghdadi J, Camcioglu Y, Parvaneh N, El Azbaoui S, Agader A, Hassani A, El Hafidi N, Mrani NA, Jouhadi Z, Ailal F, Najib J, Reisli I, Zamani A, Yosunkaya S, Gulle-Girit S, Yildiran A, Cipe FE, Torun SH, Metin A, Atikan BY, Hatipoglu N, Aydogmus C, Kilic SS, Dogu F, Karaca N, Aksu G, Kutukculer N, Keser-Emiroglu M, Somer A, Tanir G, Aytekin C, Adimi P, Mahdaviani SA, Mamishi S, Bousfiha A, Sanal O, Mansouri D, Casanova JL, Abel L. Boisson-Dupuis S, et al. Among authors: el hafidi n. Immunol Rev. 2015 Mar;264(1):103-20. doi: 10.1111/imr.12272. Immunol Rev. 2015. PMID: 25703555 Free PMC article. Review.
Polymorphic erythema associated with mycoplasma pneumoniae.
Debono L, Hafidi NE. Debono L, et al. Among authors: hafidi ne. Pan Afr Med J. 2020 Jul 28;36:224. doi: 10.11604/pamj.2020.36.224.24439. eCollection 2020. Pan Afr Med J. 2020. PMID: 33708315 Free PMC article. No abstract available.
In Silico Analyses of All STAT3 Missense Variants Leading to Explore Divergent AD-HIES Clinical Phenotypes.
Mansouri M, El Haddoumi G, Bendani H, Boumajdi N, Hakmi M, Abbou H, Bouricha EM, Elgharbaoui B, Kartti S, El Jaoudi R, Belyamani L, Kandoussi I, Ibrahimi A, El Hafidi N. Mansouri M, et al. Among authors: el hafidi n. Evol Bioinform Online. 2023 Apr 24;19:11769343231169374. doi: 10.1177/11769343231169374. eCollection 2023. Evol Bioinform Online. 2023. PMID: 37123531 Free PMC article.
Clinical and Immunological Features of 96 Moroccan Children with SCID Phenotype: Two Decades' Experience.
Benhsaien I, Ailal F, El Bakkouri J, Jeddane L, Ouair H, Admou B, Bouskraoui M, Hbibi M, Hida M, Amenzoui N, Jouhadi Z, El Hafidi N, Rada N, Benajiba N, Abilkassem R, Badou A, Bousfiha AA. Benhsaien I, et al. Among authors: el hafidi n. J Clin Immunol. 2021 Apr;41(3):631-638. doi: 10.1007/s10875-020-00960-x. Epub 2021 Jan 7. J Clin Immunol. 2021. PMID: 33411152
Novel ITGB2 Mutation Is Responsible for a Severe Form of Leucocyte Adhesion Deficiency Type 1.
Bouhouche A, Tabache Y, Askander O, Charoute H, Mesnaoui N, Belayachi L, El Hafidi N, Hardizi H, El Fahime E, Erreimi N, Barakat A, Khattab M, Seghrouchni F, El Hassani A. Bouhouche A, et al. Among authors: el hafidi n. Biomed Res Int. 2022 Mar 3;2022:1141280. doi: 10.1155/2022/1141280. eCollection 2022. Biomed Res Int. 2022. PMID: 35281597 Free PMC article.
Targeting the GRP78-Dependant SARS-CoV-2 Cell Entry by Peptides and Small Molecules.
Allam L, Ghrifi F, Mohammed H, El Hafidi N, El Jaoudi R, El Harti J, Lmimouni B, Belyamani L, Ibrahimi A. Allam L, et al. Among authors: el hafidi n. Bioinform Biol Insights. 2020 Oct 21;14:1177932220965505. doi: 10.1177/1177932220965505. eCollection 2020. Bioinform Biol Insights. 2020. PMID: 33149560 Free PMC article.
Genetic Diagnosis of Inborn Errors of Immunity in an Emerging Country: a Retrospective Study of 216 Moroccan Patients.
Moundir A, Ouair H, Benhsaien I, Jeddane L, Rada N, Amenzoui N, Jouhadi Z, Adnane F, Hafidi NE, Kili A, Bourhanbour Drissi A, Babakhouya A, Benmiloud S, Hbibi M, Benajiba N, Hida M, Bouskraoui M, Mahraoui C, Admou B, Bakkouri JE, Ailal F, Bousfiha AA. Moundir A, et al. Among authors: hafidi ne. J Clin Immunol. 2023 Feb;43(2):485-494. doi: 10.1007/s10875-022-01398-z. Epub 2022 Nov 11. J Clin Immunol. 2023. PMID: 36367635
19 results