Resultados de búsqueda - Khedhiri Souhir

Polymorphisms in Tunisian patients with N-acetylgalactosamine-6-sulfate sulfatase gene deficiency: Implication in Morquio A disease por Chkioua Latifa, Khedhiri Souhir, Ferchichi Salima, Miled Abdelhedi, Laradi Sandrine

Connect to this object online.

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

Connect to this object online.

Molecular analysis of iduronate -2- sulfatase gene in Tunisian patients with mucopolysaccharidosis type II por Chkioua Latifa, Khedhiri Souhir, Ferchichi Salima, Tcheng Rémy, Chahed Henda, Froissart Roseline, Vianey-Saban Christine, Laradi Sandrine, Miled Abdelhedi

Connect to this object online.

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

Connect to this object online.

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

Connect to this object online.