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Page 1
X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations.
Aadam Z, Kechout N, Barakat A, Chan KW, Ben-Ali M, Ben-Mustapha I, Zidi F, Ailal F, Attal N, Doudou F, Abbadi MC, Kaddache C, Smati L, Touri N, Chemli J, Gargah T, Brini I, Bakhchane A, Charoute H, Jeddane L, El Atiqi S, El Hafidi N, Hida M, Saile R, Alj HS, Boukari R, Bejaoui M, Najib J, Barbouche MR, Lau YL, Mellouli F, Bousfiha AA. Aadam Z, et al. Among authors: bejaoui m. J Clin Immunol. 2016 Apr;36(3):187-94. doi: 10.1007/s10875-016-0251-z. Epub 2016 Mar 1. J Clin Immunol. 2016. PMID: 26931785
[Hereditary immune deficiency in Tunisia].
Barbouche MR, Béjaoui M, Larguèche B, Sassi A, Bouguerra A, Lakhoua R, Dellagi K. Barbouche MR, et al. Among authors: bejaoui m. Arch Inst Pasteur Tunis. 1994 Jul-Oct;71(3-4):465-7. Arch Inst Pasteur Tunis. 1994. PMID: 8801844 French. No abstract available.
[Primary immunodeficiency in Tunisia: study of 152 cases].
Bejaoui M, Barbouche MR, Sassi A, Larguche B, Miladi N, Bouguerra A, Dellagi K. Bejaoui M, et al. Arch Pediatr. 1997 Sep;4(9):827-31. doi: 10.1016/s0929-693x(97)88145-6. Arch Pediatr. 1997. PMID: 9345562 French.
[Chronic septic granulomatous disease. 14 cases].
Barbouche MR, Sghiri R, Mellouli F, Boukhdir Y, Dellagi K, Béjaoui M. Barbouche MR, et al. Among authors: bejaoui m. Presse Med. 1999 Nov 27;28(37):2034-6. Presse Med. 1999. PMID: 10605470 French.
[The hyper-IgM syndrome: 13 observations].
Bejaoui M, Mellouli F, Chouanine R, Dellagi K, Barbouche MR. Bejaoui M, et al. Presse Med. 2003 Mar 29;32(12):544-9. Presse Med. 2003. PMID: 12714921 French.
210 results