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

por Khedhiri, Souhir, Chkioua, Latifa, Ferchichi, Salima, Miled, Abdelhedi, Laradi, Sandrine
Publicado 2011

Low erythrocyte catalase enzyme activity is correlated with high serum total homocysteine levels in tunisian patients with acute myocardial infarction

por Noichri, Yosri, Chalghoum, Abdelkader, Chkioua, Latifa, Baudin, Bruno, Ernez, Samia, Ferchichi, Salima, Miled, Abdelhédi
Publicado 2013

Novel splice site IDUA gene mutation in Tunisian pedigrees with hurler syndrome

por Chkioua, Latifa, Boudabous, Hela, Jaballi, Ibtissem, Grissa, Oussama, Turkia, Hadhami Ben, Tebib, Neji, Laradi, Sandrine
Publicado 2018

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

por Chkioua, Latifa, Khedhiri, Souhir, Kassab, Asma, Bibi, Amina, Ferchichi, Salima, Froissart, Roseline, Vianey-Saban, Christine, Laradi, Sandrine, Miled, Abdelhedi
Publicado 2011

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
Publicado 2011

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 Françoise, Laradi, Sandrine, Miled, Abdelhedi
Publicado 2011

Molecular analysis in a GALNS study cohort of 15 Tunisian patients: description of a novel mutation

por Chkioua, Latifa, Khedhiri, Souhir, Hafsi, Hind, Grissa, Oussama, Ben Turkia, Hadhami, Miled, Abdelhedi, Laradi, Sandrine, Froissart, Roseline, Alif, Najat
Publicado 2016

Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme

por Chkioua, Latifa, Amri, Yessine, Saheli, Chayma, Fenni, Ferdawes, Boudabous, Hela, Ben Turkia, Hadhami, Messaoud, Taieb, Tebib, Neji, Laradi, Sandrine
Publicado 2021

Correction to: Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme

por Chkioua, Latifa, Amri, Yessine, Chaima, Sahli, Fenni, Ferdawes, Boudabous, Hela, Ben Turkia, Hadhami, Messaoud, Taieb, Tebib, Neji, Laradi, Sandrine
Publicado 2021

Hsp70-2 gene polymorphism: susceptibility implication in Tunisian patients with coronary artery disease

por Hrira, Mohamed Yahia, Chkioua, Latifa, Slimani, Afef, Chahed, Henda, Mosbah, Habib, Khaldoun, Hamda Ben, Ferchichi, Salima, Addad, Faouzi, Miled, Abdelhedi
Publicado 2012

Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b

por Chkioua, Latifa, Amri, Yessine, Sahli, Chayma, Rhouma, Ferdawes Ben, Chehida, Amel Ben, Tebib, Neji, Messaoud, Taieb, Abdennebi, Hassen Ben, Laradi, Sandrine
Publicado 2023

Genetic basis of cystinosis in Tunisian patients: Identification of novel mutation in CTNS gene

por Chkioua, Latifa, Khedhiri, Souhir, Grissa, Oussama, Aloui, Chaker, Turkia, Hadhami Ben, Ferchichi, Salima, Miled, Abdelhedi, Froissart, Roseline, Acquaviva, Cecile, Laradi, Sandrine
Publicado 2015

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

por Chkioua, Latifa, Khedhiri, Souhir, Turkia, Hadhami Ben, Tcheng, Rémy, Froissart, Roseline, Chahed, Henda, Ferchichi, Salima, Ben Dridi, Marie Françoise, Vianey-Saban, Christine, Laradi, Sandrine, Miled, Abdelhedi
Publicado 2011

Molecular characterization of CTNS mutations in Tunisian patients with ocular cystinosis

por Chkioua, Latifa, Amri, Yessine, Saheli, Chaima, Mili, Wassila, Mabrouk, Sameh, Chabchoub, Imen, Boudabous, Hela, Azzouz, Wissem Ben, Turkia, Hadhami Ben, Ferchichi, Salima, Tebib, Neji, Massoud, Taieb, Ghorbel, Mohamed, Laradi, Sandrine
Publicado 2022