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Page 1
Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry.
Jamee M, Azizi G, Baris S, Karakoc-Aydiner E, Ozen A, Kiliç SŞ, Kose H, Chavoshzadeh Z, Mahdaviani SA, Momen T, Shamsian BS, Fallahi M, Sharafian S, Gülez N, Aygun A, Karaca NE, Kutukculer N, Al Sukait N, Al Farsi T, Al-Tamemi S, Khalifa N, Shereen R, El-Ghoneimy D, El-Owaidy R, Radwan N, Alzyoud R, Barbouche MR, Ben-Mustapha I, Mekki N, Rais A, Boukari R, Belbouab R, Djenouhat K, Tahiat A, Touri S, Elghazali G, Al-Hammadi S, Shendi HM, Alkuwaiti A, Belaid B, Djidjik R, Artac H, Adeli M, Sobh A, Elnagdy MH, Bahgat SA, Nasrullayeva G, Chou J, Rezaei N, Al-Herz W, Geha RS, Abolhassani H; MENA-I. E. I. Study Group. Jamee M, et al. Among authors: djenouhat k. Clin Immunol. 2022 Nov;244:109131. doi: 10.1016/j.clim.2022.109131. Epub 2022 Sep 27. Clin Immunol. 2022. PMID: 36179983 Free article.
Consensus Middle East and North Africa Registry on Inborn Errors of Immunity.
Aghamohammadi A, Rezaei N, Yazdani R, Delavari S, Kutukculer N, Topyildiz E, Ozen A, Baris S, Karakoc-Aydiner E, Kilic SS, Kose H, Gulez N, Genel F, Reisli I, Djenouhat K, Tahiat A, Boukari R, Ladj S, Belbouab R, Ferhani Y, Belaid B, Djidjik R, Kechout N, Attal N, Saidani K, Barbouche R, Bousfiha A, Sobh A, Rizk R, Elnagdy MH, Al-Ahmed M, Al-Tamemi S, Nasrullayeva G, Adeli M, Al-Nesf M, Hassen A, Mehawej C, Irani C, Megarbane A, Quinn J; MENA-I. E. I. Study Group; Maródi L, Modell V, Modell F, Al-Herz W, Geha RS, Abolhassani H. Aghamohammadi A, et al. Among authors: djenouhat k. J Clin Immunol. 2021 Aug;41(6):1339-1351. doi: 10.1007/s10875-021-01053-z. Epub 2021 May 29. J Clin Immunol. 2021. PMID: 34052995 Free PMC article.
Algerian Registry for Inborn Errors of Immunity in Children: Report of 887 Children (1985-2021).
Yagoubi A, Tahiat A, Touri NS, Ladj MS, Drali O, Belaid B, Mohand-Oussaid A, Dehimi A, Belbouab R, Ferhani Y, Melzi S, Guedouar A, Hakem S, Khemici O, Inouri Y, Meddour Y, Dib S, Mansouri Z, Iddir S, Boufersaoui A, Boudiaf H, Bouhdjila A, Ibsaine O, Maouche H, Dahlouk D, Mekki A, Bioud B, Bouzerar Z, Zeroual Z, Benhassine F, Bekkat-Berkani D, Naamoune S, Salah SS, Chaib S, Attal N, Bensaadi N, Bouchair N, Cherif N, Kedji L, Bendeddouche S, Atif ML, Djenouhat K, Kechout N, Djidjik R, Benhalla KN, Smati L, Boukari R. Yagoubi A, et al. Among authors: djenouhat k. J Clin Immunol. 2022 Nov;42(8):1660-1671. doi: 10.1007/s10875-022-01330-5. Epub 2022 Jul 15. J Clin Immunol. 2022. PMID: 35838820
F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects.
Calzoni E, Platt CD, Keles S, Kuehn HS, Beaussant-Cohen S, Zhang Y, Pazmandi J, Lanzi G, Pala F, Tahiat A, Artac H, Heredia RJ, Dmytrus J, Reisli I, Uygun V, Uygun D, Bingol A, Basaran E, Djenouhat K, Benhalla N, Bendahmane C, Emiroglu M, Kirchhausen T, Pasham M, Jones J, Wallace JG, Zheng L, Boisson B, Porta F, Rosenzweig SD, Su H, Giliani S, Lenardo M, Geha RS, Boztug K, Chou J, Notarangelo LD. Calzoni E, et al. Among authors: djenouhat k. J Allergy Clin Immunol. 2019 Jun;143(6):2317-2321.e12. doi: 10.1016/j.jaci.2019.02.014. Epub 2019 Feb 26. J Allergy Clin Immunol. 2019. PMID: 30822429 Free PMC article.
Diagnostic and Predictive Contribution of Autoantibodies Screening in a Large Series of Patients With Primary Immunodeficiencies.
Tahiat A, Yagoubi A, Ladj MS, Belbouab R, Aggoune S, Atek L, Bouziane D, Melzi S, Boubidi C, Drali W, Bendahmane C, Iguerguesdaoune H, Taguemount S, Soufane A, Oukil A, Ketfi A, Messaoudi H, Boukhenfouf N, Ifri MA, Bencharif Madani T, Belhadj H, Benhala KN, Khiari M, Cherif N, Smati L, Arada Z, Zeroual Z, Bouzerar Z, Ibsaine O, Maouche H, Boukari R, Djenouhat K. Tahiat A, et al. Among authors: djenouhat k. Front Immunol. 2021 Apr 1;12:665322. doi: 10.3389/fimmu.2021.665322. eCollection 2021. Front Immunol. 2021. PMID: 33868317 Free PMC article.
[Association of markers of rheumatoid arthritis in lupus. Is it a rhupus?].
Bouchedoub Y, Djenouhat K, Rachedi N, Babasaci R, Ould Ali L, Salah K, Kherrache R, Kherbeche M, Khlifati A, Guernou FZ, Benzitouni A, Semmana M, Meghlaoui A. Bouchedoub Y, et al. Among authors: djenouhat k. Ann Biol Clin (Paris). 2020 Apr 1;78(2):201-205. doi: 10.1684/abc.2020.1518. Ann Biol Clin (Paris). 2020. PMID: 32319950 Free article. French.
Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema.
Deroux A, Boccon-Gibod I, Fain O, Pralong P, Ollivier Y, Pagnier A, Djenouhat K, Du-Thanh A, Gompel A, Faisant C, Launay D, Bouillet L. Deroux A, et al. Among authors: djenouhat k. Clin Exp Immunol. 2016 Sep;185(3):332-7. doi: 10.1111/cei.12820. Clin Exp Immunol. 2016. PMID: 27271546 Free PMC article.
Enzymatic assays for the diagnosis of bradykinin-dependent angioedema.
Defendi F, Charignon D, Ghannam A, Baroso R, Csopaki F, Allegret-Cadet M, Ponard D, Favier B, Cichon S, Nicolie B, Fain O, Martin L, Drouet C; National Reference Centre for Angioedema CREAK. Defendi F, et al. PLoS One. 2013 Aug 5;8(8):e70140. doi: 10.1371/journal.pone.0070140. Print 2013. PLoS One. 2013. PMID: 23940538 Free PMC article.
Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.
Charignon D, Ghannam A, Defendi F, Ponard D, Monnier N, López Trascasa M, Launay D, Caballero T, Djenouhat K, Fain O, Cichon S, Martin L, Drouet C. Charignon D, et al. Among authors: djenouhat k. Allergy. 2014 Dec;69(12):1659-65. doi: 10.1111/all.12515. Epub 2014 Oct 10. Allergy. 2014. PMID: 25134986
21 results