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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2011 1
2012 1
2013 1
2014 2
2015 3
2016 2
2017 2
2020 5
2021 2
2022 2
2023 2
2024 0

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24 results

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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.
Molecular defects in Moroccan patients with ataxia-telangiectasia.
Jeddane L, Ailal F, Dubois-d'Enghien C, Abidi O, Benhsaien I, Kili A, Chaouki S, Kriouile Y, El Hafidi N, Fadil H, Abilkassem R, Rada N, Bousfiha AA, Barakat A, Stoppa-Lyonnet D, Bellaoui H. Jeddane L, et al. Among authors: el hafidi n. Neuromolecular Med. 2013 Jun;15(2):288-94. doi: 10.1007/s12017-013-8218-1. Epub 2013 Jan 16. Neuromolecular Med. 2013. PMID: 23322442
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.
Whole-Genome Shotgun Sequences of Three Multidrug-Resistant Mycobacterium tuberculosis Strains Isolated from Morocco.
Lahlou L, El Mrimar N, Laamarti M, Alouane T, Bendahou MA, Bssaibis F, Ben Lahlou Y, Zegmout A, El Hafidi N, ElJaoudi R, Frikh M, Lemnouar A, Elouennass M, Ibrahimi A. Lahlou L, et al. Among authors: el hafidi n. Genome Announc. 2017 Nov 16;5(46):e01275-17. doi: 10.1128/genomeA.01275-17. Genome Announc. 2017. PMID: 29146858 Free PMC article.
[Rubinstein-Taybi syndrome: a familial form ].
El Hafidi N, Ghanimi Z, Gaouzi A, Benhamou B, Alaoui-M'sseffer F. El Hafidi N, et al. Arch Pediatr. 2004 Aug;11(8):978-9. doi: 10.1016/j.arcped.2004.05.014. Arch Pediatr. 2004. PMID: 15288097 French. No abstract available.
24 results