Hasil Pencarian - Imen Ben Mustapha

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  1. 1
    Lessons from Genetic Studies of Primary Immunodeficiencies in a Highly Consanguineous Population

    Lessons from Genetic Studies of Primary Immunodeficiencies in a Highly Consanguineous Population oleh Mohamed-Ridha Barbouche, Mohamed-Ridha Barbouche, Najla Mekki, Najla Mekki, Meriem Ben-Ali, Imen Ben-Mustapha, Imen Ben-Mustapha

    Diterbitkan 2017-06-01
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  2. 2
    Case Report: FOXP3 Mutation in a Patient Presenting With ALPS

    Case Report: FOXP3 Mutation in a Patient Presenting With ALPS oleh Afef Rais, Afef Rais, Afef Rais, Najla Mekki, Najla Mekki, Najla Mekki, Faten Fedhila, Faten Fedhila, Faten Fedhila, Mohammed Faraj Alosaimi, Monia Ben Khaled, Monia Ben Khaled, Monia Ben Khaled, Amal Zameli, Amal Zameli, Nourhen Agrebi, Nourhen Agrebi, Maryam Kallel Sellami, Maryam Kallel Sellami, Maryam Kallel Sellami, Raif Geha, Imen Ben-Mustapha, Imen Ben-Mustapha, Imen Ben-Mustapha, Mohamed-Ridha Barbouche, Mohamed-Ridha Barbouche, Mohamed-Ridha Barbouche

    Diterbitkan 2021-08-01
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  3. 3
    In silico comparative study of SARS-CoV-2 proteins and antigenic proteins in BCG, OPV, MMR and other vaccines: evidence of a possible putative protective effect

    In silico comparative study of SARS-CoV-2 proteins and antigenic proteins in BCG, OPV, MMR and other vaccines: evidence of a possible putative protective effect oleh Sondes Haddad-Boubaker, Houcemeddine Othman, Rabeb Touati, Kaouther Ayouni, Marwa Lakhal, Imen Ben Mustapha, Kais Ghedira, Maher Kharrat, Henda Triki

    Diterbitkan 2021-03-01
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  4. 4
    CUTANEOUS MANIFESTATIONS OF PRIMARY IMMUNODEFICIENCY DISEASES IN TUNISIAN CHILDREN

    CUTANEOUS MANIFESTATIONS OF PRIMARY IMMUNODEFICIENCY DISEASES IN TUNISIAN CHILDREN oleh Naouel GUIRAT, Monia Ben Khaled, Monia Ouederni, Imen Ben-Mustapha, Ridha Kouki, Habib Besbes, Mohamed Ridha Barbouche, Fethi Mellouli, mohamed bejaoui

    Diterbitkan 2018-10-01
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  5. 5
    Diagnostic challenge in a series of eleven patients with hyper IgE syndromes

    Diagnostic challenge in a series of eleven patients with hyper IgE syndromes oleh Roukaya Yaakoubi, Roukaya Yaakoubi, Najla Mekki, Najla Mekki, Imen Ben-Mustapha, Imen Ben-Mustapha, Leila Ben-Khemis, Asma Bouaziz, Ilhem Ben Fraj, Jamel Ammar, Agnès Hamzaoui, Hamida Turki, Lobna Boussofara, Mohamed Denguezli, Samir Haddad, Monia Ouederni, Mohamed Bejaoui, Koon Wing Chan, Yu Lung Lau, Fethi Mellouli, Mohamed-Ridha Barbouche, Mohamed-Ridha Barbouche, Meriem Ben-Ali

    Diterbitkan 2023-01-01
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