Biochemical and clinical profiles of 52 Tunisian patients affected by Zellweger syndrome by Fahmi Nasrallah, Wiem Zidi, Moncef Feki, Samia Kacem, Neji Tebib, Naziha Kaabachi

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Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme by Latifa Chkioua, Yessine Amri, Chayma Saheli, Ferdawes Fenni, Hela Boudabous, Hadhami Ben Turkia, Taieb Messaoud, Neji Tebib, Sandrine Laradi

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Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b by Latifa Chkioua, Yessine Amri, Chayma Sahli, Ferdawes Ben Rhouma, Amel Ben Chehida, Neji Tebib, Taieb Messaoud, Hassen Ben Abdennebi, Sandrine Laradi

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Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study by Rim Ben Abdelaziz, Habiba Hafsi, Hela Hajji, Hela Boudabous, Amel Ben Chehida, Ali Mrabet, Khadija Boussetta, Sihem Barsaoui, Azza Sammoud, Mourad Hamzaoui, Hatem Azzouz, Néji Tebib

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Molecular characterization of CTNS mutations in Tunisian patients with ocular cystinosis by Latifa Chkioua, Yessine Amri, Chaima Saheli, Wassila Mili, Sameh Mabrouk, Imen Chabchoub, Hela Boudabous, Wissem Ben Azzouz, Hadhami Ben Turkia, Salima Ferchichi, Neji Tebib, Taieb Massoud, Mohamed Ghorbel, Sandrine Laradi

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Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment. by Rahma Mkaouar, Zied Riahi, Cherine Charfeddine, Imen Chelly, Hela Boudabbous, Hamza Dallali, Crystel Bonnet, Meriem Hechmi, Soumeya Bekri, Nadia Zitouna, Lotfi Zekri, Amel Tounsi, Rym Kefi, Jihene Marrakchi, Olfa Messaoud, Ichraf Kraoua, Sonia Maalej, Ilhem Turki Ben Youssef, Ahlem Ben Hmid, Fabrice Giraudet, Sami Bouchoucha, Neji Tebib, Ghazi Besbes, Christine Petit, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi

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