日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Crush syndrome after the Marrakesh earthquake: a case report and review of the literature

马拉喀什地震后挤压综合征:病例报告及文献综述

Zidouh, Ali; Tebib, Tarek; Salmi, Othmane; Mourouth, Hanane; Ziadi, Amra

Comparison of methods to normalize urine output in critically ill patients: a multicenter cohort study

比较不同方法治疗危重患者尿量正常化的效果:一项多中心队列研究

Monard, Céline; Tebib, Nicolas; Trächsel, Bastien; Kelevina, Tatiana; Schneider, Antoine Guillaume

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

鉴定导致突尼斯1b型糖原贮积症患者葡萄糖-6-磷酸转运蛋白缺陷的突变

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

Prevalence and risk factors of Strongyloides stercoralis in haemodialysis in Cochabamba, Bolivia: a cross-sectional study

玻利维亚科恰班巴血液透析患者粪类圆线虫感染的流行情况及危险因素:一项横断面研究

Tebib, Nicolas; Tebib, Nathalie; Paredes, Mauricio; Castro, Rosario; Baggio, Stéphanie; Torrico, Mario Villarroel; Leon, Amilcar Alejandro Flores; Zamorano, Maya Herbas; Chappuis, Francois; Getaz, Laurent

Molecular characterization of CTNS mutations in Tunisian patients with ocular cystinosis

突尼斯眼胱氨酸病患者CTNS基因突变的分子特征分析

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

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

更正:突尼斯患者的岩藻糖苷贮积症:FUCA1酶的突变分析和基于同源性的建模

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

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

突尼斯患者的岩藻糖苷酶缺乏症:FUCA1酶的突变分析和基于同源性的建模

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

The mutational spectrum of hunter syndrome reveals correlation between biochemical and clinical profiles in Tunisian patients

亨特综合征的突变谱揭示了突尼斯患者的生化特征与临床特征之间的相关性

Chkioua, L; Grissa, O; Leban, N; Gribaa, M; Boudabous, H; Turkia, H Ben; Ferchichi, S; Tebib, N; Laradi, S

Preliminary national report on cystic fibrosis epidemiology in Tunisia: the actual state of affairs

突尼斯囊性纤维化流行病学初步全国报告:现状

Hamouda, Samia; Fredj, Sondess Hadj; Hilioui, Sonia; Khalsi, Fatma; Ameur, Salma Ben; Bouguila, Jihene; Boussoffara, Raoudha; Besbes, Habib; Ajmi, Houda; Mattoussi, Nadia; Messaoud, Taieb; Mehrezi, Ahmed; Hachicha, Mongia; Boughamoura, Lamia; Sfar, Mohamed Taher; Gueddiche, Neji; Abroug, Saoussen; Becheur, Saida Ben; Barsaoui, Sihem; Tebib, Neji; Samoud, Azza; Gandoura, Najoua; Tinsa, Faten; Boussetta, Khadija

A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation

全球第二例携带 RAF1 S259Y 新突变的努南综合征患者表现出严重的临床表型,伴有新生儿肥厚型心肌病。

Jaouadi, Hager; Chehida, Amel Ben; Kraoua, Lilia; Etchevers, Heather C; Argiro, Laurent; Kasdallah, Nadia; Blibech, Sonia; Delague, Valérie; Lévy, Nicolas; Tebib, Néji; Mrad, Ridha; Abdelhak, Sonia; Benkhalifa, Rym; Zaffran, Stéphane