Hurler disease (mucopolysaccharidosis type IH): clinical features and consanguinity in Tunisian population by Chkioua Latifa, Khedhiri Souhir, Ben Turkia Hadhami, Chahed Henda, Ferchichi Salima, Ben Dridi Marie, Laradi Sandrine, Miled Abdelhedi

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Molecular analysis of mucopolysaccharidosis type I in Tunisia: identification of novel mutation and eight Novel polymorphisms by Froissart Roseline, Ferchichi Salima, Bibi Amina, Kassab Asma, Khedhiri Souhir, Chkioua Latifa, Vianey-Saban Christine, Laradi Sandrine, Miled Abdelhedi

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Brain MRI and biological diagnosis in five Tunisians MLD patients by Barboura Ilhem, Hadded Samir, Chebel Saber, Mansour Rachida, Chahed Hinda, Gueddiche Mohamed-Néji, Frih-Ayed Mahbouba, Ferchichi Salima, Miled Abdelhédi

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Hsp70-2 gene polymorphism: susceptibility implication in Tunisian patients with coronary artery disease by Hrira Mohamed Yahia, Chkioua Latifa, Slimani Afef, Chahed Henda, Mosbah Habib, Khaldoun Hamda Ben, Ferchichi Salima, Addad Faouzi, Miled Abdelhedi

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Mucopolysaccharidosis type I: molecular characteristics of two novel alpha-L-iduronidase mutations in Tunisian patients by Chahed Henda, Froissart Roseline, Tcheng Rémy, Turkia Hadhami, Khedhiri Souhir, Chkioua Latifa, Ferchichi Salima, Ben Dridi Marie, Vianey-Saban Christine, Laradi Sandrine, Miled Abdelhedi

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