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Page 1
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: benhsaien i. Neuromolecular Med. 2013 Jun;15(2):288-94. doi: 10.1007/s12017-013-8218-1. Epub 2013 Jan 16. Neuromolecular Med. 2013. PMID: 23322442
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: benhsaien i. 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
Primary Immunodeficiency Classification on Smartphone.
Jeddane L, Ouair H, Benhsaien I, Bakkouri JE, Bousfiha AA. Jeddane L, et al. Among authors: benhsaien i. J Clin Immunol. 2017 Jan;37(1):1-2. doi: 10.1007/s10875-016-0354-6. J Clin Immunol. 2017. PMID: 27888368 No abstract available.
33 results