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Page 1
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: ben ameur s. Hum Mutat. 2020 Jan;41(1):115-121. doi: 10.1002/humu.23905. Epub 2019 Sep 15. Hum Mutat. 2020. PMID: 31469207
[Bardet - Biedl syndrome in the child. A study of 11 cases].
Aloulou H, Cheikhrouhou H, Belguith N, Ben Ameur S, Ben Mansour L, Chabchoub I, Kammoun T, Hachicha M. Aloulou H, et al. Among authors: ben ameur s, ben mansour l. Tunis Med. 2011 Jan;89(1):31-6. Tunis Med. 2011. PMID: 21267825 Free article. French.
Familial haemophagocytosis lymphohisticytosis type 3: A case report.
Kamoun F, Hsairi M, Grandin V, Ben Ameur S, De Saint Basile G, Hachicha M. Kamoun F, et al. Among authors: ben ameur s. Arch Pediatr. 2017 Jan;24(1):33-35. doi: 10.1016/j.arcped.2016.10.021. Epub 2016 Nov 30. Arch Pediatr. 2017. PMID: 27914778
[Granulomatous lymphadenitis revealing a deficiency in receptor IL12].
Kamoun F, Sfaihi L, Ben Mustapha I, Ben Ameur S, Barbouche MR, Hachicha M. Kamoun F, et al. Among authors: ben ameur s, ben mustapha i. Presse Med. 2017 Mar;46(3):346-348. doi: 10.1016/j.lpm.2016.11.017. Epub 2016 Dec 26. Presse Med. 2017. PMID: 28034490 French. No abstract available.
Frequent Infections, Hypotonia, and Anemia in a Breastfed Infant.
Kamoun F, Guirat R, Megdich F, Ben Ameur S, Kallel C, Hachicha M. Kamoun F, et al. Among authors: ben ameur s. J Pediatr Hematol Oncol. 2017 Mar;39(2):141-142. doi: 10.1097/MPH.0000000000000725. J Pediatr Hematol Oncol. 2017. PMID: 28060111
34 results