Search Results - Kahloul, Najoua

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  1. 1
    Disseminated BCG infection revealing a severe combined immunodeficiency: A case report

    Disseminated BCG infection revealing a severe combined immunodeficiency: A case report by Ben Belgacem, Hajer, Bouguila, Jihene, Tej, Amel, Tilouche, Samia, Kebaili, Raoudha, Kahloul, Najoua, Barbouche, Mohamed Ridha, Soyah, Nejla, Boughammoura, Lamia

    Published in Tunisie Medicale
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  2. 2
    ATP6V0A2‐related cutis laxa in 10 novel patients: Focus on clinical variability and expansion of the phenotype

    ATP6V0A2‐related cutis laxa in 10 novel patients: Focus on clinical variability and expansion of the phenotype by Beyens, Aude, Moreno‐Artero, Ester, Bodemer, Christine, Cox, Helen, Gezdirici, Alper, Yilmaz Gulec, Elif, Kahloul, Najoua, Khau Van Kien, Philippe, Ogur, Gonul, Harroche, Annie, Vasse, Marc, Salhi, Aïcha, Symoens, Sofie, Hadj‐Rabia, Smail, Callewaert, Bert

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  3. 3
    ATP 6V0A2 ‐related cutis laxa in 10 novel patients: Focus on clinical variability and expansion of the phenotype

    ATP 6V0A2 ‐related cutis laxa in 10 novel patients: Focus on clinical variability and expansion of the phenotype by Beyens, Aude, Moreno‐Artero, Ester, Bodemer, Christine, Cox, Helen, Gezdirici, Alper, Yilmaz Gulec, Elif, Kahloul, Najoua, Khau Van Kien, Philippe, Ogur, Gonul, Harroche, Annie, Vasse, Marc, Salhi, Aïcha, Symoens, Sofie, Hadj‐Rabia, Smail, Callewaert, Bert

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  4. 4
    Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family

    Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family by Ben Charfeddine, Ilhem, Riepe, Felix G, Kahloul, Najoua, Kulle, Alexandra E, Adala, Labiba, Mamaï, Ons, Amara, Abdelbasset, Mili, Amira, Amri, Fathi, Saad, Ali, Holterhus, Paul-Martin, Gribaa, Moez

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  5. 5
    Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: Characterization of three novel polymorphisms

    Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: Characterization of three novel polymorphisms by Ben Charfeddine, Ilhem, Riepe, Felix G., Clauser, Eric, Ayedi, Abdelkarim, Makni, Saloua, Sfar, Mohamed Tahar, Sboui, Hassen, Kahloul, Najoua, Ben Hamouda, Hechmi, Chouchane, Slaheddine, Trimech, Sihem, Zouari, Noura, M'Rabet, Samir, Amri, Fathi, Saad, Ali, Holterhus, Paul-Martin, Gribaa, Moez

    Published in Gene
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  6. 6
    Les complications coronaires de la maladie de Kawasaki et ses facteurs de risque : à propos de 65 cas d'enfants tunisien

    Les complications coronaires de la maladie de Kawasaki et ses facteurs de risque : à propos de 65 cas d'enfants tunisien by Ajmi, Houda, Ghorbel, Sameh, Ezzi, Olfa, Mabrouk, Sameh, Mansour, Kais, Kahloul, Najoua, Chemli, Jalel, Zouari, Noura, Mejaouel, Houssin, Boughammoura, Lamia, Abroug, Saoussen

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