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Page 1
A juvenile pleomorphic adenoma of the palate.
Hammami B, Achour I, Yousfi G, Walha O, Mnejja M, Chaabouni MA, Charfeddine I. Hammami B, et al. Among authors: charfeddine i. SAGE Open Med Case Rep. 2023 Jun 8;11:2050313X231180374. doi: 10.1177/2050313X231180374. eCollection 2023. SAGE Open Med Case Rep. 2023. PMID: 37325167 Free PMC article.
SLC26A4 variations among Graves' hyper-functioning thyroid gland.
Hadj-Kacem H, Kallel R, Belguith-Maalej S, Mnif M, Charfeddine I, Ghorbel A, Abid M, Ayadi H, Masmoudi S. Hadj-Kacem H, et al. Among authors: charfeddine i. Dis Markers. 2010;29(2):63-9. doi: 10.3233/DMA-2010-0727. Dis Markers. 2010. PMID: 21045265 Free PMC article.
Abstracts of the Communications of the Sixteenth Francophone Allergology Meetings Hammamet, 4-7 October 2017.
Abdelghani A, Abouda M, Adelmoulah K, Aichaouia C, Ajmi N, Akad A, Akrout I, Ammar J, Amouri Z, Aouadi S, Aouina H, Aounallah A, Atitallah S, Ayadi H, Ayadi N, Ayadi S, Azzabi S, Baccar MA, Bahloul N, Bdira B, Bejar D, Beji M, Belajouza C, Belhadj I, Belhaja R, Ben Abdelghaffar H, Ben Amar J, Ben Jemia E, Ben Mahmoud L, Ben Mansour A, Ben Romdhane M, Ben Saad A, Ben Saad H, Ben Saad S, Ben Salah N, Ben Salem N, Ben Tkhayat A, Benzarti M, Berraïes A, Besma H, Bouakkez H, Bouhoula M, Boussetta K, Boussoffara L, Bouzekri H, Brahem A, Brini I, Chaouech N, Charfeddine I, Charfi MR, Charrad R, Chatti S, Cheikh R, Cheikh M'hamed S, Cheikh Rouhou S, Cherif H, Cherif J, Dabboussi S, Daghfous H, Daghfous J, Dahmouni A, Denguezli M, Dhahri B, Djaman Allico J, Douik El Gharbi L, El Gharbi L, El Guedr S, El Kamel A, El Maalel O, Elfekih L, Essalah M, Fahem N, Fessi R, Fki W, Gammoudi R, Garrouch A, Ghariani N, Gharsalli H, Ghedira H, Ghorbel A, Ghozzi H, Ghrairi N, Greb D, Gribaa Y, Guedri S, Gueriani A, Guermazi E, Habouria C, Hadj Hassine S, Hajjej S, Hamdi B, Hamdia B, Hammami A, Hamouda S, Hamzaoui A, Hamzaoui K, Hassen H, Hayouni M, Hedhli A, Houaneb Marghli Y, Jdidi S, Joober S, K… See abstract for full author list ➔ Abdelghani A, et al. Among authors: charfeddine i. Tunis Med. 2017 Aug-Sep;95(8-9):806-836. Tunis Med. 2017. PMID: 29873051 No abstract available.
Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss.
Mkaouar-Rebai E, Tlili A, Masmoudi S, Louhichi N, Charfeddine I, Ben Amor M, Lahmar I, Driss N, Drira M, Ayadi H, Fakhfakh F. Mkaouar-Rebai E, et al. Among authors: charfeddine i. Biochem Biophys Res Commun. 2006 Feb 24;340(4):1251-8. doi: 10.1016/j.bbrc.2005.12.123. Epub 2006 Jan 5. Biochem Biophys Res Commun. 2006. PMID: 16406239 Clinical Trial.
Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.
Khattab A, Haider S, Kumar A, Dhawan S, Alam D, Romero R, Burns J, Li D, Estatico J, Rahi S, Fatima S, Alzahrani A, Hafez M, Musa N, Razzghy Azar M, Khaloul N, Gribaa M, Saad A, Charfeddine IB, Bilharinho de Mendonça B, Belgorosky A, Dumic K, Dumic M, Aisenberg J, Kandemir N, Alikasifoglu A, Ozon A, Gonc N, Cheng T, Kuhnle-Krahl U, Cappa M, Holterhus PM, Nour MA, Pacaud D, Holtzman A, Li S, Zaidi M, Yuen T, New MI. Khattab A, et al. Among authors: charfeddine ib. Proc Natl Acad Sci U S A. 2017 Mar 7;114(10):E1933-E1940. doi: 10.1073/pnas.1621082114. Epub 2017 Feb 22. Proc Natl Acad Sci U S A. 2017. PMID: 28228528 Free PMC article.
Analysis of GJB2 mutation: evidence for a Mediterranean ancestor for the 35delG mutation.
Belguith H, Hajji S, Salem N, Charfeddine I, Lahmar I, Amor MB, Ouldim K, Chouery E, Driss N, Drira M, Mégarbané A, Rebai A, Sefiani A, Masmoudi S, Ayadi H. Belguith H, et al. Among authors: charfeddine i. Clin Genet. 2005 Aug;68(2):188-9. doi: 10.1111/j.1399-0004.2005.00474.x. Clin Genet. 2005. PMID: 15996220 No abstract available.
105 results