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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: barbouche mr. 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. Arch Inst Pasteur Tunis. 1994 Jul-Oct;71(3-4):465-7. Arch Inst Pasteur Tunis. 1994. PMID: 8801844 French. No abstract available.
[Chronic septic granulomatous disease. 14 cases].
Barbouche MR, Sghiri R, Mellouli F, Boukhdir Y, Dellagi K, Béjaoui M. Barbouche MR, et al. Presse Med. 1999 Nov 27;28(37):2034-6. Presse Med. 1999. PMID: 10605470 French.
110 results