• banniere5.jpg

    banniere5.jpg

  • banniere4.jpg

    banniere4.jpg

  • banniere2.jpg

    banniere2.jpg

  • banniere3.jpg

    banniere3.jpg

African PID publications

  1. El-Gamal YM, Hossny EM, El-Sayed ZA, Reda SM. Allergy and immunology in Africa: Challenges and unmet needs. J Allergy ClinImmunol. 2017 Nov;140(5):1240-1243. Nominated for the the Elsevier Atlas Award.

  2. Sullivan KE, Bassiri H, Bousfiha AA, Costa-Carvalho BT, Freeman AF, Hagin D, Lau YL, Lionakis MS, Moreira I, Pinto JA, de Moraes-Pinto MI, Rawat A, Reda SM, Reyes SOL, Seppänen M, Tang MLK. Emerging Infections and Pertinent Infections Related to Travel for Patients with Primary Immunodeficiencies. J ClinImmunol. 2017 Oct;37(7):650-692. doi: 10.1007/s10875-017-0426-2. Epub 2017 Aug 7.

  3. El Hawary RE, Meshaal SS, AbdElaziz DS, Elsharkawy MA, Alkady RS, Lotfy S, El-Sheikhah A, Hassan A, Galal NM, Boutros JA, Elmarsafy AM. Genetic Counseling in Primary Immunodeficiency Disorders: An Emerging Experience in Egypt. MolDiagnTher. 2017 Dec;21(6):677-684.Galal N, Meshaal S, Elhawary R, ElAziz DA, Alkady R, Lotfy S, Eldash A, Boutros J, Elmarsafy A. Patterns of Primary Immunodeficiency Disorders Among a Highly Consanguineous Population: Cairo University Pediatric Hospital's 5-Year Experience. J ClinImmunol. 2016 Oct; 36(7):649-55.

  4. Picard C, Bobby Gaspar H, Al-Herz W, Bousfiha A, Casanova JL, Chatila T, Crow YJ, Cunningham-Rundles C, Etzioni A, Franco JL, Holland SM, Klein C, Morio T, Ochs HD, Oksenhendler E, Puck J, Tang MLK, Tangye SG, Torgerson TR, Sullivan KE. International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity. J ClinImmunol. 2018 Jan;38(1):96-128. doi: 10.1007/s10875-017-0464-9. Epub 2017 Dec 11.

1: El-Gamal YM, Hossny EM, El-Sayed ZA, Reda SM. Allergy and immunology in Africa: Challenges and unmet needs. J Allergy Clin Immunol. 2017 Sep 26. pii: S0091-6749(17)31508-7. doi: 10.1016/j.jaci.2017.09.004. [Epub ahead of print] PubMed PMID: 28962920.

2: Petersen BS, August D, Abt R, Alddafari M, Atarod L, Baris S, Bhavsar H, Brinkert F, Buchta M, Bulashevska A, Chee R, Cordeiro AI, Dara N, Dückers G, Elmarsafy A, Frede N, Galal N, Gerner P, Glocker EO, Goldacker S, Hammermann J, Hasselblatt P, Havlicekova Z, Hübscher K, Jesenak M, Karaca NE, Karakoc-Aydiner E, Kharaghani MM, Kilic SS, Kiykim A, Klein C, Klemann C, Kobbe R, Kotlarz D, Laass MW, Leahy TR, Mesdaghi M, Mitton S, Neves JF, Öztürk B, Pereira LF, Rohr J, Restrepo JLR, Ruzaike G, Saleh N, Seneviratne S, Senol E, Speckmann C, Tegtmeyer D, Thankam P, van der Werff Ten Bosch J, von Bernuth H, Zeissig S, Zeissig Y, Franke A, Grimbacher B. Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea. Inflamm Bowel Dis. 2017 Sep 19.  doi: 10.1097/MIB.0000000000001235. [Epub ahead of print] PubMed PMID: 28930861.

3: El Hawary RE, Meshaal SS, Abd Elaziz DS, Elsharkawy MA, Alkady RS, Lotfy S, El-Sheikhah A, Hassan A, Galal NM, Boutros JA, Elmarsafy AM. Genetic Counseling in Primary Immunodeficiency Disorders: An Emerging Experience in Egypt. Mol Diagn Ther. 2017 Sep 12. doi: 10.1007/s40291-017-0297-5. [Epub ahead of print] PubMed PMID: 28900865.

  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.

  1. Meurs L, Mbow M, Boon N, Vereecken K, Amoah AS, Labuda LA, Dièye TN, Mboup S, Yazdanbakhsh M, Polman K. Cytokine Responses to Schistosoma mansoni and Schistosoma haematobium in Relation to Infection in a Co-endemic Focus in Northern Senegal. PLoS Negl Trop Dis. 2014 Aug 7;8(8).
  2. Sabri A, Grant AV, Cosker K, El Azbaoui S, Abid A, Abderrahmani Rhorfi I, Souhi H, Janah H, Alaoui-Tahiri K, Gharbaoui Y, Benkirane M, Orlova M, Boland A, Deswarte C, Migaud M, Bustamante J, Schurr E, Boisson-Dupuis S, Casanova JL, Abel L, El Baghdadi J. Association Study of Genes Controlling IL-12-dependent IFN-γ Immunity: STAT4 Alleles Increase Risk of Pulmonary Tuberculosis in Morocco.J Infect Dis. 2014 Aug 15;210(4):611-8.
  3. 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. Molecular defects in Moroccan patients with ataxia-telangiectasia. Neuromolecular Med. 2013 Jun;15(2):288-94.
  4. Innes S, Lazarus E, Otwombe K, Liberty A, Germanus R, Van Rensburg AJ, Grobbelaar N, Hurter T, Eley B, Violari A, Cotton MF. Early severe HIV disease precedes early antiretroviral therapy in infants: Are we too late? J Int AIDS Soc. 2014 Jun 11;17:18914.

  1. 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. Chronic granulomatous disease in morocco: genetic, immunological, and clinical features of 12 patients from 10 kindreds. J Clin Immunol. 2014 May;34(4):452-8. doi: 10.1007/s10875-014-9997-3.
  2. Jlajla H, Sellami MK, Sfar I, Laadhar L, Zerzeri Y, Abdelmoula MS, Gorgi Y, Dridi MF, Makni S. New C1q mutation in a Tunisian family. Immunobiology. 2014 Mar;219(3):241-6. doi: 10.1016/j.imbio.2013.10.010.
  3. Mekki N, Ben-Mustapha I, Liu L, Boussofara L, Okada S, Cypowyj S, Ghariani N, Saidi W, Denguezli M, Casanova JL, Puel A, Barbouche MR.IL-17 T cells' defective differentiation in vitro despite normal range ex vivo in chronic mucocutaneous candidiasis due to STAT1 mutation.J Invest Dermatol. 2014 Apr;134(4):1155-7. doi: 10.1038/jid.2013.480.

  1. Benajiba N, Amrani R, Rkain M, Zizi N, Ailal F, Bousfiha AA, Dikhaye S. Serratia marcescens cutaneous gumma and chronic septic granulomatosis. Med Mal Infect. 2014 Jan;44(1):39-41. doi: 10.1016/j.medmal.2013.10.004.

  2. Ouederni M, Sanal O, Ikinciogullari A, Tezcan I, Dogu F, Sologuren I, Pedraza-Sánchez S, Keser M, Tanir G, Nieuwhof C, Colino E, Kumararatne D, Levy J, Kutukculer N, Aytekin C, Herrera-Ramos E, Bhatti M, Karaca N, Barbouche R, Broides A, Goudouris E, Franco JL, Parvaneh N, Reisli I, Strickler A, Shcherbina A, Somer A, Segal A, Angel-Moreno A, Lezana-Fernandez JL, Bejaoui M, Bobadilla-Del Valle M, Kachboura S, Sentongo T, Ben-Mustapha I, Bustamante J, Picard C, Puel A, Boisson-Dupuis S, Abel L, Casanova JL, Rodríguez-Gallego C. Clinical features of Candidiasis in patients with inherited interleukin 12 receptor β1 deficiency. Clin Infect Dis. 2014 Jan;58(2):204-13. doi: 10.1093/cid/cit722.

  3. Ben-Mustapha I, Ben-Ali M, Mekki N, Patin E, Harmant C, Bouguila J, Elloumi-Zghal H, Harbi A, Béjaoui M, Boughammoura L, Chemli J, Barbouche MR. A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients. Immunogenetics. 2014 Jan;66(1):67-71. doi: 10.1007/s00251-013-0739-0.

Login

Partners

 

Site Last Modified

  • Last Modified: Friday 20 June 2025, 23:14:17.

Visitors Counter

955457
TodayToday87
YesterdayYesterday201
This WeekThis Week288
This MonthThis Month7316
All DaysAll Days955457

HONcode

This website is certified by Health On the Net Foundation. Click to verify. This site complies with the HONcode standard for trustworthy health information:
verify here.

Casablanca September A-Project

  Rwanda

  Cameroun

 Zambia

 Gabon

 Sudan

Program

 Benin

Go to top