Mellouli F - Search Results

1

Diagnostic challenge in a series of eleven patients with hyper IgE syndromes.

Yaakoubi R, Mekki N, Ben-Mustapha I, Ben-Khemis L, Bouaziz A, Ben Fraj I, Ammar J, Hamzaoui A, Turki H, Boussofara L, Denguezli M, Haddad S, Ouederni M, Bejaoui M, Chan KW, Lau YL, Mellouli F, Barbouche MR, Ben-Ali M. Yaakoubi R, et al. Among authors: mellouli f. Front Immunol. 2023 Jan 10;13:1057679. doi: 10.3389/fimmu.2022.1057679. eCollection 2022. Front Immunol. 2023. PMID: 36703986 Free PMC article.

2

[The hyper-IgM syndrome: 13 observations].

Bejaoui M, Mellouli F, Chouanine R, Dellagi K, Barbouche MR. Bejaoui M, et al. Among authors: mellouli f. Presse Med. 2003 Mar 29;32(12):544-9. Presse Med. 2003. PMID: 12714921 French.

3

Contribution to the description of the beta-thalassemia spectrum in Tunisia and the origin of mutation diversity.

Chouk I, Daoud BB, Mellouli F, Bejaoui M, Gérard N, Dellagi K, Abbes S. Chouk I, et al. Among authors: mellouli f. Hemoglobin. 2004 Aug;28(3):189-95. doi: 10.1081/hem-120040305. Hemoglobin. 2004. PMID: 15481885

4

Successful treatment of Fusarium solani ecthyma gangrenosum in a patient affected by leukocyte adhesion deficiency type 1 with granulocytes transfusions.

Mellouli F, Ksouri H, Barbouche R, Maamer M, Hamed LB, Hmida S, Hassen AB, Béjaoui M. Mellouli F, et al. BMC Dermatol. 2010 Oct 7;10:10. doi: 10.1186/1471-5945-10-10. BMC Dermatol. 2010. PMID: 20929531 Free PMC article.

5

Hypocalcaemia due to hypoparathyroidism in β-thalassemia major. A study of a new case.

Dhouib N, Turki Z, Mellouli F, Ouederni M, Yahiaoui S, Nagi S, Kouki R, Ben Slama C, Bejaoui M. Dhouib N, et al. Among authors: mellouli f. Tunis Med. 2011 Mar;89(3):302-4. Tunis Med. 2011. PMID: 21387240

6

Primary immunodeficiencies in highly consanguineous North African populations.

Barbouche MR, Galal N, Ben-Mustapha I, Jeddane L, Mellouli F, Ailal F, Bejaoui M, Boutros J, Marsafy A, Bousfiha AA. Barbouche MR, et al. Among authors: mellouli f. Ann N Y Acad Sci. 2011 Nov;1238:42-52. doi: 10.1111/j.1749-6632.2011.06260.x. Ann N Y Acad Sci. 2011. PMID: 22129052

7

Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome).

Guirat-Dhouib N, Baccar Y, Mustapha IB, Ouederni M, Chouaibi S, El Fekih N, Barbouche MR, Fezaa B, Kouki R, Hmida S, Mellouli F, Bejaoui M. Guirat-Dhouib N, et al. Among authors: mellouli f. Clin Mol Allergy. 2012 Apr 23;10(1):6. doi: 10.1186/1476-7961-10-6. Clin Mol Allergy. 2012. PMID: 22524894 Free PMC article.

8

High susceptibility for enterovirus infection and virus excretion features in Tunisian patients with primary immunodeficiencies.

Driss N, Ben-Mustapha I, Mellouli F, Ben Yahia A, Touzi H, Bejaoui M, Ben Ghorbel M, Triki H, Barbouche MR. Driss N, et al. Among authors: mellouli f. Clin Vaccine Immunol. 2012 Oct;19(10):1684-9. doi: 10.1128/CVI.00293-12. Epub 2012 Aug 22. Clin Vaccine Immunol. 2012. PMID: 22914367 Free PMC article.

9

Clinical, immunological and genetic findings of a large tunisian series of major histocompatibility complex class II deficiency patients.

Ben-Mustapha I, Ben-Farhat K, Guirat-Dhouib N, Dhemaied E, Larguèche B, Ben-Ali M, Chemli J, Bouguila J, Ben-Mansour L, Mellouli F, Khemiri M, Béjaoui M, Barbouche MR. Ben-Mustapha I, et al. Among authors: mellouli f. J Clin Immunol. 2013 May;33(4):865-70. doi: 10.1007/s10875-013-9863-8. Epub 2013 Jan 13. J Clin Immunol. 2013. PMID: 23314770

10

Cytogenetic assessment of Fanconi anemia in children with aplastic anemia in Tunisia.

Talmoudi F, Kammoun L, Benhalim N, Torjemane L, Ouederni M, Aissaoui L, Lakhal A, Mellouli F, Othmen TB, Bejaoui M, Abdelhak S, Meddeb M, Dellagi K, Hdiji S, Amouri A; Tunisian Fanconi Anemia Study Group. Talmoudi F, et al. Among authors: mellouli f. J Pediatr Hematol Oncol. 2013 Oct;35(7):547-50. doi: 10.1097/MPH.0b013e31827e56cb. J Pediatr Hematol Oncol. 2013. PMID: 23337544

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