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A 9month-old-boy with atypical hemophagocytic lymphohistiocytosis by Monia Ouederni, MONIA BEN KHALED, Samia Rekaya, Ilhem Ben Fraj, Fethi Mellouli, Mohamed Bejaoui
Published 2017-10-01
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Case Report: FOXP3 Mutation in a Patient Presenting With ALPS by 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
Published 2021-08-01
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Consanguineous unions and endogamy in families of beta-thalassaemia patients from two Mediterranean populations: Tunisia and Italy by Ramla Weslati, Monia Ouederni, Giovanbattista Ruffo, Monia Ben Khaled, Ridha Kouki, Caterine Di Girgenti, Zelia Borsellino, Irene Sammartano, Mohamed El Gazzah, Safia El- Bok, Mohamed Bejaoui
Published 2019-11-01
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