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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Articles originaux et études · 2017

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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Articles originaux et études · 2017

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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Articles originaux et études · 2017

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

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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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Articles originaux et études · 2016

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

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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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Articles originaux et études · 2016

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.