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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2006 2
2007 1
2008 2
2009 3
2010 2
2012 3
2013 1
2014 4
2015 3
2016 3
2017 4
2018 2
2019 2
2020 2
2023 1
2024 2

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31 results

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Page 1
[Hematologic abnormalities in infantile visceral leishmaniasis].
Chouchene S, Braham N, Bouatay A, Hizem S, Berriri S, Eljemai A, Boughamoura L, Kortas M. Chouchene S, et al. Among authors: boughamoura l. Arch Pediatr. 2015 Nov;22(11):1107-11. doi: 10.1016/j.arcped.2015.08.012. Arch Pediatr. 2015. PMID: 26433577 French.
Primary ciliary dyskinesia gene contribution in Tunisia: Identification of a major Mediterranean allele.
Mani R, Belkacem S, Soua Z, Chantot S, Montantin G, Tissier S, Copin B, Bouguila J, Rive Le Gouard N, Boughamoura L, Ben Ameur S, Hachicha M, Boussoffara R, Boussetta K, Hammouda S, Bedoui A, Besbes H, Meddeb S, Chraeit K, Khlifa M, Escudier E, Amselem S, Mabrouk I, Legendre M. Mani R, et al. Among authors: boughamoura l. Hum Mutat. 2020 Jan;41(1):115-121. doi: 10.1002/humu.23905. Epub 2019 Sep 15. Hum Mutat. 2020. PMID: 31469207
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: boughamoura l. 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
Infant acute myocarditis mimicking acute myocardial infarction.
Jedidi M, Tilouche S, Masmoudi T, Sahnoun M, Chkirbène Y, Mestiri S, Boughamoura L, Ben Dhiab M, Souguir MK. Jedidi M, et al. Among authors: boughamoura l. Autops Case Rep. 2016 Dec 30;6(4):15-19. doi: 10.4322/acr.2016.052. eCollection 2016 Oct-Dec. Autops Case Rep. 2016. PMID: 28210569 Free PMC article.
[Pseudohypoparathyroidism revealed by Fahr syndrome].
Kahloul N, Chaari W, Boughamoura L, Charfeddine L, Khammeri S, Amri F. Kahloul N, et al. Among authors: boughamoura l. Arch Pediatr. 2009 May;16(5):444-8. doi: 10.1016/j.arcped.2009.02.017. Epub 2009 Apr 1. Arch Pediatr. 2009. PMID: 19339164 French.
Moderate phenotypic expression of familial hypercholesterolemia in Tunisia.
Jelassi A, Slimani A, Jguirim I, Najah M, Abid A, Boughamoura L, Mzid J, Fkih M, Maatouk F, Rouis M, Varret M, Slimane MN. Jelassi A, et al. Among authors: boughamoura l. Clin Chim Acta. 2010 May 2;411(9-10):735-8. doi: 10.1016/j.cca.2010.02.008. Epub 2010 Feb 6. Clin Chim Acta. 2010. PMID: 20144596
Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria.
Jellouli NK, Hadj Salem I, Ellouz E, Kamoun Z, kamoun F, tlili A, Kaabachi N, Triki C, Fakhfakh F; Tunisian Network on Mental Retardation study. Jellouli NK, et al. J Hum Genet. 2014 Apr;59(4):216-22. doi: 10.1038/jhg.2014.4. Epub 2014 Feb 27. J Hum Genet. 2014. PMID: 24573090
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: boughamoura l. Afr Health Sci. 2020 Mar;20(1):444-452. doi: 10.4314/ahs.v20i1.51. Afr Health Sci. 2020. PMID: 33402933 Free PMC article.
31 results