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Page 1
Molecular investigation of distal renal tubular acidosis in Tunisia, evidence for founder mutations.
Nagara M, Voskarides K, Nouira S, Ben Halim N, Kefi R, Aloulou H, Romdhane L, Ben Abdallah R, Ben Rhouma F, Aissa K, Boughamoura L, Kammoun T, Azzouz H, Abroug S, Ben Turkia H, Ayadi A, Mrad R, Chabchoub I, Hachicha M, Chemli J, Deltas C, Abdelhak S. Nagara M, et al. Among authors: abroug s. Genet Test Mol Biomarkers. 2014 Nov;18(11):741-8. doi: 10.1089/gtmb.2014.0175. Epub 2014 Oct 6. Genet Test Mol Biomarkers. 2014. PMID: 25285676 Free PMC article. Clinical Trial.
[Henoch-Schonlein purpura and renal tuberculosis].
Chemli J, Abroug S, Harbi A. Chemli J, et al. Among authors: abroug s. Presse Med. 2004 Apr 10;33(7):456-7. doi: 10.1016/s0755-4982(04)98630-7. Presse Med. 2004. PMID: 15105765 French.
[Primary hyperoxaluria in children in central Tunisia].
Chemli J, Abdennabi H, Zorgati M, Abdelhak S, Nabli N, Abroug S, Sfar MT, Ben Dhia N, Amri F, Harbi A. Chemli J, et al. Among authors: abroug s. Tunis Med. 2007 Jun;85(6):513-8. Tunis Med. 2007. PMID: 17644908 French.
Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian Population.
Ben Charfeddine I, Ben Lazreg T, M'sakni A, Amara A, Mlika A, Chaïeb A, Hlel K, Zouari N, Zbidi F, Bouguila J, Soyah N, Ayedi A, Ben Hamouda H, Abroug S, Boughamoura L, Saad A, Gribaa M. Ben Charfeddine I, et al. Among authors: abroug s. Hemoglobin. 2015;39(4):251-5. doi: 10.3109/03630269.2015.1041605. Epub 2015 May 27. Hemoglobin. 2015. PMID: 26016902
Mutational Analysis of Agxt in Tunisian Population with Primary Hyperoxaluria Type 1.
M'dimegh S, Omezzine A, M'barek I, Moussa A, Mabrouk S, Kaarout H, Souche G, Chemli J, Aloui S, Aquaviva-Bourdain C, Achour A, Abroug S, Bouslama A. M'dimegh S, et al. Among authors: abroug s. Ann Hum Genet. 2017 Jan;81(1):1-10. doi: 10.1111/ahg.12178. Epub 2016 Dec 9. Ann Hum Genet. 2017. PMID: 27935012
Clinical and imaging features of malignant infantile osteopetrosis.
Tfifha M, Gaha M, Gamaoun W, Chemli J, Mabrouk S, Hassayoun S, Zouari N, Jemni H, Abroug S. Tfifha M, et al. Among authors: abroug s. Turk J Pediatr. 2017;59(4):452-457. doi: 10.24953/turkjped.2017.04.012. Turk J Pediatr. 2017. PMID: 29624226 Free article.
Tfifha M, Gaha M, Gamaoun W, Chemli J, Mabrouk S, Hassayoun S, Zouari N, Jemni H, Abroug S. Clinical and imaging features of malignant infantile osteopetrosis. ...
Tfifha M, Gaha M, Gamaoun W, Chemli J, Mabrouk S, Hassayoun S, Zouari N, Jemni H, Abroug S. Clinical and imaging …
Preliminary national report on cystic fibrosis epidemiology in Tunisia: the actual state of affairs.
Hamouda S, Fredj SH, Hilioui S, Khalsi F, Ameur SB, Bouguila J, Boussoffara R, Besbes H, Ajmi H, Mattoussi N, Messaoud T, Mehrezi A, Hachicha M, Boughamoura L, Sfar MT, Gueddiche N, Abroug S, Becheur SB, Barsaoui S, Tebib N, Samoud A, Gandoura N, Tinsa F, Boussetta K. Hamouda S, et al. Among authors: abroug s. Afr Health Sci. 2020 Mar;20(1):444-452. doi: 10.4314/ahs.v20i1.51. Afr Health Sci. 2020. PMID: 33402933 Free PMC article.
Turner syndrome: results of the first Tunisian study group on Turner syndrome (TuSGOT).
Essaddam L, Zitouni O, Kraoua L, Trabelsi M, Sassi H, Kmiha S, Charfi F, El Guiche D, Kebaïli R, Jaballah N, Rjeb M, Zouari N, El Aribi Y, Hizem S, Wannes S, Fkih Romdhane I, Sfar MT, Ben Hamouda H, Hadj Salem R, Khlayfia Z, Khmiss T, Monastiri K, Siala N, Chouchane S, Souaa H, Khochtali I, Mahjoub B, Sfar H, Ben Jemâa L, Abroug S, Boughamoura L, Kamoun I, Kamoun T, Mrad R, Ben Becher S. Essaddam L, et al. Among authors: abroug s. J Pediatr Endocrinol Metab. 2023 Apr 21;36(6):577-583. doi: 10.1515/jpem-2022-0360. Print 2023 Jun 27. J Pediatr Endocrinol Metab. 2023. PMID: 37084413
68 results