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Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical, Immunological, and Genetic Features of 22 Patients from 15 Moroccan Kindreds.
Errami A, Baghdadi JE, Ailal F, Benhsaien I, Bakkouri JE, Jeddane L, Rada N, Benajiba N, Mokhantar K, Ouazahrou K, Zaidi S, Abel L, Casanova JL, Boisson-Dupuis S, Bustamante J, Bousfiha AA. Errami A, et al. Among authors: benajiba n. J Clin Immunol. 2023 May;43(4):728-740. doi: 10.1007/s10875-022-01419-x. Epub 2023 Jan 11. J Clin Immunol. 2023. PMID: 36630059 Free PMC article.
Chronic granulomatous disease in Morocco: genetic, immunological, and clinical features of 12 patients from 10 kindreds.
Baba LA, Ailal F, El Hafidi N, Hubeau M, Jabot-Hanin F, Benajiba N, Aadam Z, Conti F, Deswarte C, Jeddane L, Aglaguel A, El Maataoui O, Tissent A, Mahraoui C, Najib J, Martinez-Barricarte R, Abel L, Habti N, Saile R, Casanova JL, Bustamante J, Salih Alj H, Bousfiha AA. Baba LA, et al. Among authors: benajiba n. J Clin Immunol. 2014 May;34(4):452-8. doi: 10.1007/s10875-014-9997-3. Epub 2014 Mar 5. J Clin Immunol. 2014. PMID: 24596025
First report on the Moroccan registry of primary immunodeficiencies: 15 years of experience (1998-2012).
Bousfiha AA, Jeddane L, El Hafidi N, Benajiba N, Rada N, El Bakkouri J, Kili A, Benmiloud S, Benhsaien I, Faiz I, Maataoui O, Aadam Z, Aglaguel A, Baba LA, Jouhadi Z, Abilkassem R, Bouskraoui M, Hida M, Najib J, Alj HS, Ailal F; Moroccan Society for Primary Immunodeficiencies (MSPID). Bousfiha AA, et al. Among authors: benajiba n. J Clin Immunol. 2014 May;34(4):459-68. doi: 10.1007/s10875-014-0005-8. Epub 2014 Mar 12. J Clin Immunol. 2014. PMID: 24619622
[Neonatal erythroderma: do not ignore an immune deficiency].
El Ouali A, El Boussaadni Y, Ailal F, Bousfiha AA, Dikhaye S, Benajiba N. El Ouali A, et al. Among authors: benajiba n. Pan Afr Med J. 2014 Aug 21;18:317. doi: 10.11604/pamj.2014.18.317.5182. eCollection 2014. Pan Afr Med J. 2014. PMID: 25478038 Free PMC article. French.
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: benajiba 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
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: benajiba n. 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
Atypical Kawasaki Disease in an Adolescent with Multivisceral Involvement.
El Haddar Z, El Ouali A, Ghanam A, Rkain M, Benajiba N, Babakhouya A. El Haddar Z, et al. Among authors: benajiba n. Case Rep Pediatr. 2021 Jul 27;2021:8941847. doi: 10.1155/2021/8941847. eCollection 2021. Case Rep Pediatr. 2021. PMID: 34367708 Free PMC article.
Molecular heterogeneity of β-thalassemia variants in the Eastern region of Morocco.
Belmokhtar I, Lhousni S, Elidrissi Errahhali M, Ghanam A, Elidrissi Errahhali M, Sidqi Z, Ouarzane M, Charif M, Bellaoui M, Boulouiz R, Benajiba N. Belmokhtar I, et al. Among authors: benajiba n. Mol Genet Genomic Med. 2022 Aug;10(8):e1970. doi: 10.1002/mgg3.1970. Epub 2022 May 26. Mol Genet Genomic Med. 2022. PMID: 35615994 Free PMC article.
76 results