1. Boushaki S, Tahiat A, Meddour Y, Chan KW, Chaib S, Benhalla N, Smati L, Bensenouci A, Lau YL, Magdinier F, Djidjik R. Prevalence of BTK mutations in male Algerian patterns with agammaglobulinemia and severe B cell lymphopenia.Clin Immunol. 2015 Dec;161(2):286-90.
  2. El Azbaoui S, Alaoui Mrani N, Sabri A, Jouhadi Z, Ailal F, Bousfiha AA, Najib J, El Hafidi N, Deswarte C, Schurr E, Bustamante J, Boisson-Dupuis S, Casanova JL, Abel L, El Baghdadi J.Pott's disease in Moroccan children: clinical features an investigation of the interleukin-12/interferon-γ pathway. Int J Tuberc Lung Dis. 2015 Dec;19(12):1455-62.
  3. Ouadani H, Ben-Mustapha I, Ben-ali M, Ben-khemis L, Larguèche B, Boussoffara R, Maalej S, Fetni I, Hassayoun S, Mahfoudh A, Mellouli F, Yalaoui S, Masmoudi H, Bejaoui M, Barbouche MR. Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients. Immunogenetics. 2016 Jan;68(1):19-28.

  1. Development of Primary Immunodeficiencies in Africa. Bousfiha AA, Jeddane L, Erwa N, Dieye TN, Mellouli F, Reda SM, Esser M, Boukari R. J Clin Immunol. 2015 May; 35(4):329-30.
  2. Bousfiha AA, Jeddane L, Erwa N, Dieye TN,Mellouli F, Reda SM, Esser M, Boukari R. Development of Primary Immunodeficiencies in Africa. J Clin Immunol. 2015 May;35(4):329-30. 
  3. Meshaal S, El Hawary R, Elsharkawy M, Mousa RK, Farid RJ, Abd Elaziz D, Alkady R,Galal N, Massaad MJ, Boutros J, Elmarsafy A.Mutations in Recombination Activating Gene 1 and 2 in patients with severe combined immunodeficiency disorders in Egypt.Clin Immunol. 2015 Jun;158(2):167-73. 
  4. Meshaal S, El Hawary R, Abd Elaziz D, Alkady R,Galal N, Boutros J, Elmarsafy A.Chronic granulomatous disease: Review of a cohort of Egyptian patients.Allergol Immunopathol (Madr). 2015 May-Jun;43(3):279-85.

  1. Engelhardt KR, Gertz ME, Keles S, Schäffer AA, Sigmund EC, Glocker C, Saghafi S, Pourpak Z, Ceja R, Sassi A, Graham LE, Massaad MJ, Mellouli F, Ben-Mustapha I, Khemiri M, Kilic SS, Etzioni A, Freeman AF, Thiel J, Schulze I, Al-Herz W, Metin A, Sanal Ö, Tezcan I, Yeganeh M, Niehues T, Dueckers G, Weinspach S, Patiroglu T, Unal E, Dasouki M, Yilmaz M, Genel F, Aytekin C, Kutukculer N, Somer A, Kilic M, Reisli I, Camcioglu Y, Gennery AR, Cant AJ, Jones A, Gaspar BH, Arkwright PD, Pietrogrande MC, Baz Z, Al-Tamemi S, Lougaris V, Lefranc G, Megarbane A, Boutros J, Galal N, Bejaoui M, Barbouche MR, Geha RS, Chatila TA, Grimbacher B. The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency. J Allergy Clin Immunol. 2015 Feb 25.
  2. Cheikh A, Ziani M, Cheikh Z, Barakat A, El Menzhi O, Braikat M, Benomar A, Cherrah Y, El Hassani A. Measles in morocco: epidemiological profile and impact of vaccination strategy. Adv Ther. 2015 Feb;32(2):172-83.

  1. Driss N, Mellouli F, Ben Yahia A, Touzi H, Barbouche MR, Triki H, Bejaoui M.Sequential asymptomatic enterovirus infections in a patient with major histocompatibility complex class II primary immunodeficiency.J Clin Microbiol. 2014 Sep;52(9):3486-9.
  2. Haoues M, Refai A, Mallavialle A, Barbouche MR, Laabidi N, Deckert M, Essafi M.Forkhead box O3 (FOXO3) transcription factor mediates apoptosis in BCG-infected macrophages.Cell Microbiol. 2014 Sep;16(9):1378-90.
  3. Meddour Y, Chaib S, Bousseloub A, Kaddache N, Kecili L, Gamar L, Nakkemouche M, Djidjik R, Abbadi MC, Charron D, Boucekkine TE, Tamouza R.NOD2/CARD15 and IL23R genetic variability in 204 Algerian Crohn's disease.Clin Res Hepatol Gastroenterol. 2014 Sep;38(4):499-504.
  4. Nassar A, Elgohary G, Elhassan T, Nurgat Z, Mohamed SY, Aljurf M.Methotrexate for the Treatment of Graft-versus-Host Disease after Allogeneic Hematopoietic Stem Cell Transplantation. J Transplant. Oct 2014;2014:980301.

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