Recherche · Publications scientifiques
Les publications.
178 références scientifiques du Pr. Hatem Masmoudi.
Articles originaux et études · 2017
Role of FOXP3 gene polymorphism in the susceptibility to Tunisian endemic pemphigus foliaceus
Ben Jmaa M, Abida O, Bahloul E, Toumi A, Khlif S, Fakhfakh R, Elloumi N, Sellami K, Masmoudi A, Turki H, Masmoudi H. Role of FOXP3 gene polymorphism in the susceptibility to Tunisian endemic pemphigus foliaceus. Immunol Lett. 2017;184:105-111. https://doi.org/10.1016/j.imlet.2017.02.005
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The increased expression of toll-like receptor 4 in renal and skin lesions in lupus erythematosus
Elloumi N, Fakhfakh R, Ayadi L, Sellami K, Abida O, Ben Jmaa M, Sellami T, Kammoun K, Masmoudi H. The increased expression of toll-like receptor 4 in renal and skin lesions in lupus erythematosus. J Histochem Cytochem. 2017;65(7):389-398. https://doi.org/10.1369/0022155417709234
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Genetic association and phenotypic correlation of TLR4 but not NOD2 variants with Tunisian inflammatory bowel disease
Feki S, Bouzid D, Abida O, Chtourou L, Elloumi N, Toumi A, Hachicha H, Amouri A, Tahri N, Masmoudi H. Genetic association and phenotypic correlation of TLR4 but not NOD2 variants with Tunisian inflammatory bowel disease. J Dig Dis. 2017;18(11):625-633. https://doi.org/10.1111/1751-2980.12552
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Relevant genetic polymorphisms and kidney expression of toll-like receptor (TLR)-5 and TLR-9 in lupus nephritis
Elloumi N, Fakhfakh R, Abida O, Ayadi L, Marzouk S, Hachicha H, Fourati M, Bahloul Z, Mhiri MN, Kammoun K, Masmoudi H. Relevant genetic polymorphisms and kidney expression of toll-like receptor (TLR)-5 and TLR-9 in lupus nephritis. Clin Exp Immunol. 2017;190(3):328-339. https://doi.org/10.1111/cei.13022
Lire le PDF ↗ Articles originaux et études · 2016
Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients
Ouadani H, Ben-Mustapha I, Ben-ali M, Ben-khemis L, Larguèche B, Boussoffara R, Maalej S, Fetni I, Hassayoun S, Mahfoudh A, Mellouli F, Yalaoui S, Masmoudi H, Bejaoui M, Barbouche MR. Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients. Immunogenetics. 2016;68(1):19-28. https://doi.org/10.1007/s00251-015-0878-6
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Elevated prolactin levels in patients with pemphigus foliaceus
Toumi A, Chaabouni K, Abida O, Hachicha H, Ben Ayed M, Masmoudi A, Turki H, Ayedi F, Masmoudi H. Elevated prolactin levels in patients with pemphigus foliaceus. Clinical Dermatology & Therapy. 2016;3(1):1-6. https://doi.org/10.24966/cdt-8771/100017
Lire le PDF ↗ Articles originaux et études · 2016
Association between the IL2RA polymorphism and type 1 diabetes risk: family based association study
Zouidi F, Bouzid D, Fourati H, Fakhfakh R, Kammoun T, Hachicha M, Penha-Gonçalves C, Masmoudi H. Association between the IL2RA polymorphism and type 1 diabetes risk: family based association study. Meta Gene. 2016;10:118-122. https://doi.org/10.1016/j.mgene.2016.08.006
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Autoantibodies diabetes and micronutriments in type 1 diabetics and siblings of Abidjan district, Ivory Coast
Yapo-Crezoit CCA, Trébissou AFJ, Yapo FA, Khlif S, Lahyani A, Agbo-Soumahoro K, Makni Ayedi F, Masmoudi H, Djaman JA, Dosso M. Autoantibodies diabetes and micronutriments in type 1 diabetics and siblings of Abidjan district, Ivory Coast. European Journal of Pharmaceutical and Medical Research. 2016;3(11):637-643.