Ferchichi Salima

Savoirs

Polymorphisms in Tunisian patients with N-acetylgalactosamine-6-sulfate sulfatase gene deficiency: Implication in Morquio A disease

Khedhiri Souhir, Chkioua Latifa, Ferchichi Salima, Miled Abdelhedi, Laradi, Laradi Sandrine

Savoirs

Molecular analysis of mucopolysaccharidosis type I in Tunisia: identification of novel mutation and eight Novel polymorphisms

Chkioua Latifa, Khedhiri Souhir, Kassab Asma, Bibi Amina, Ferchichi Salima, Froissart Roseline, Vianey-Saban Christine, Laradi Sandrine, Miled, Miled Abdelhedi

Savoirs

Hurler disease (mucopolysaccharidosis type IH): clinical features and consanguinity in Tunisian population

Ben, Chkioua Latifa, Khedhiri Souhir, Chahed Henda, Ferchichi Salima, Laradi Sandrine, Miled, Miled Abdelhedi

Savoirs

Brain MRI and biological diagnosis in five Tunisians MLD patients

Barboura Ilhem, Hadded Samir, Chebel Saber, Mansour Rachida, Chahed Hinda, Gueddiche Mohamed-Néji, Frih-Ayed Mahbouba, Ferchichi Salima, Miled, Miled Abdelhedi

Savoirs

Mucopolysaccharidosis type I: molecular characteristics of two novel alpha-L-iduronidase mutations in Tunisian patients

Chkioua Latifa, Khedhiri Souhir, Turkia Hadhami, Tcheng Rémy, Froissart Roseline, Chahed Henda, Ferchichi Salima, Vianey-Saban Christine, Laradi Sandrine, Miled Abdelhedi, Ben