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Year Number of Results
2002 1
2008 1
2009 1
2010 3
2011 4
2012 5
2013 4
2014 7
2015 5
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2020 1
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47 results

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Page 1
Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988-2012).
Mellouli F, Mustapha IB, Khaled MB, Besbes H, Ouederni M, Mekki N, Ali MB, Larguèche B, Hachicha M, Sfar T, Gueddiche N, Barsaoui S, Sammoud A, Boussetta K, Becher SB, Meherzi A, Guandoura N, Boughammoura L, Harbi A, Amri F, Bayoudh F, Jaballah NB, Tebib N, Bouaziz A, Mahfoudh A, Aloulou H, Mansour LB, Chabchoub I, Boussoffara R, Chemli J, Bouguila J, Hassayoun S, Hammami S, Habboul Z, Hamzaoui A, Ammar J, Barbouche MR, Bejaoui M. Mellouli F, et al. Among authors: aloulou h. J Clin Immunol. 2015 Nov;35(8):745-53. doi: 10.1007/s10875-015-0206-9. Epub 2015 Oct 13. J Clin Immunol. 2015. PMID: 26464197 Review.
Factor XIII deficiency in south of Tunisia.
Maaloul I, Medhaffer M, Louhichi N, Krichen I, Alibi S, Kmiha S, Aloulou H, Fakhfakh F, Elloumi M, Kallel C, Hachicha M. Maaloul I, et al. Among authors: aloulou h. Blood Coagul Fibrinolysis. 2017 Sep;28(6):485-489. doi: 10.1097/MBC.0000000000000649. Blood Coagul Fibrinolysis. 2017. PMID: 28704210
Hypoparathyroidism in children: a study of eight cases.
Maaloul I, Aloulou H, Kmiha S, Belfitouri Y, Kamoun H, Fakhfakh F, Chabchoub I, Kammoun T, Hachicha M. Maaloul I, et al. Among authors: aloulou h. Tunis Med. 2018 Aug-Sep;96(8-9):472-476. Tunis Med. 2018. PMID: 30430523
[Primary immunodeficiency disorders in 51 cases].
Lamia S, Aloulou H, Kamoun T, Chabchoub I, Ben Moustapha I, Barbouch R, Mongia H. Lamia S, et al. Among authors: aloulou h. Tunis Med. 2013 Jan;91(1):38-43. Tunis Med. 2013. PMID: 23404596 French.
[Rheumatic cardiopathies and its risk factors: about 50 cases].
Maaloul I, Bouzidi N, Kolsi R, Ameur SB, Abid L, Aloulou H, Kamoun T. Maaloul I, et al. Among authors: aloulou h. Ann Cardiol Angeiol (Paris). 2024 Feb;73(1):101676. doi: 10.1016/j.ancard.2023.101676. Epub 2023 Nov 20. Ann Cardiol Angeiol (Paris). 2024. PMID: 37988890 French.
Van Wyk-Grumbach syndrome: A rare cause of precocious puberty.
Hachicha M, Maaloul I, Aissa K, Kamoun T, Aloulou H. Hachicha M, et al. Among authors: aloulou h. Presse Med. 2018 May;47(5):483-486. doi: 10.1016/j.lpm.2018.02.012. Epub 2018 Mar 17. Presse Med. 2018. PMID: 29555166 No abstract available.
47 results