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

Vitamin D deficiency in sickle cell disease: a neglected comorbidity in Tunisia

镰状细胞病合并维生素D缺乏症:突尼斯一种被忽视的合并症

Othmani, Mariem; Amri, Yessine; Jouini, Yosr; Ouali, Faida; Chelbi, Siwar; Hadj Fredj, Sondess; Dabboubi, Rym; Messaoud, Taieb

Cardiovascular disease in North African women: insights from the Middle East African Women CardioVascular Disease (MEA-WCVD) registry

北非女性心血管疾病:来自中东非洲女性心血管疾病(MEA-WCVD)登记研究的启示

Charfeddine, Salma; Abid, Leila; Chenik, Sarra; Ben Krayen, Iheb; Haddar, Oussama; Ghrab, Aymen; Boudiche, Selim; Touati, Haithem; Ayedi, Oumaima; Ammar, Mohamed Amine; Ben Halima, Manel; Ben Ayed, Houssem; Brahim, Asma; ElAyech, Faten; Allouche, Emna; Thabet, Houssem; Mahfoudhi, Houaida; Jabloun, Taha Yessine; Ayadi, Yasmine; Ayadi, Alaeddine; Romdhani, Ghassen; Gargouri, Hassen; Zidi, Oumayma; Guedri, Mohamed Ali; Tlili, Rami; Trabelsi, Bechir; Hammami, Selim; Othmen, Rim; Antit, Saoussen; Saidane, Syrine; Dardour, Sirine; Iddir, Skander; Kharrat, Elmahdi; Cheikhrouhou, Anis; Derwich, Mohamed; Mrabet, Amal; Lassoued, Taha; Rekik, Emna; Gmiha, Sahar; Laribi, Niez; Lamine, Hakim; Triki, Zied; Ayari, Samir; Boujelbene, Fatma; Boughzela, Essia; Rekik, Hajer; Ben Ameur, Ines; Abid, Syrine; Oueghlani, Khalil; Haggui, Abddayem; Ben Halima, Afef; Ouechtati, Wejdene; Bennour, Emna; Hammami, Rania; Jabeur, Mariem; Zairi, Ihsen; Drissa, Mariem; Addad, Faouzi; Milouchi, Sami; Mourali, Mohamed Sami; Ben Slima, Hedi; Bezdah, Leila; Neffati, Elyes; Ben Ameur, Youssef; Kraiem, Sondos; Kachboura, Salem; Kammoun, Ikram; Zakhama, Lilia; Lbn Hadj Amor, Hassen; Ben Hamda, Khaldoun; Messoudi, Yosra; Ben Hlima, Nejah; Dahmani, Rana; Gamra, Habib; Ibn Elhadj, Zied; Denguir, Hichem; Ghorbel, Chayma; Mechri, Nizar; Ernez Hajri, Samia; Mebazaa, Alexandre; Ben Dhaou, Fedi; Trigui, Maroua; Fehri, Wafa; Abdessalem, Salem

Revealing silent alpha-thalassemia: characterization of novel HBA1 deletion and missense mutation in Tunisian families

揭示隐性α地中海贫血:突尼斯家族中新型HBA1缺失和错义突变的特征分析

Amri, Yessine; Fredj, Sondess Hadj; Dabboubi, Rym; Othmani, Rym; Sahli, Chaima; Baccouche, Imen; Ouali, Faida; Messaoud, Taieb

Comprehensive analysis of a novel LYST mutation in a Tunisian patient with Chediak-Higashi syndrome

对一名患有切迪亚克-希加西综合征的突尼斯患者体内发现的新型LYST基因突变进行全面分析。

Amri, Yessine; Chouchene, Saoussen; Foddha, Hajer; Abderahmene, Amani; Kooli, Ikbel; Toumi, Adnen; Hadj Khalifa, Kawthar; Mezrigui, Rihem; Messaoud, Taieb; Hassine, Mohsen; Dabboubi, Rym

Left ventricular untwist determines intradialytic hemodynamics and outcomes in mildly reduced and preserved ejection fraction patients

左心室扭转程度决定了轻度射血分数降低和射血分数保留患者的透析中血流动力学和预后。

Bouchahda, Nidhal; Scheipl, Fabian; Rouetbi, Wissal; Hafi, Kouloud; Kallela, Mohamed Yessine; Najjar, Aymen; Ben Mahmoud, Nouha; Ben Salem, Meriam; Hadj Ibrahim, Maissa; Habib, Sallemi; Mani, Hajer; Aloui, Sabra; Ben Messaoud, Mejdi; Skhiri, Habib

Genetic variations in the IDUA gene in Tunisian MPS I families: Identification of a novel microdeletion disrupting substrate binding and structural insights

突尼斯MPS I家族中IDUA基因的遗传变异:鉴定出一种破坏底物结合的新型微缺失及其结构解析

Rebai, Mariem; Amri, Yessine; Sahli, Chaima; Foddha, Hajer; Messaoud, Taieb; Boudabous, Hela; Ben Abdennebi, Hassen; Ferchichi, Salima; Chkioua, Latifa

Bilateral papillary cystadenoma of the broad ligament: a manifestation of Von Hippel-Lindau disease: a case report

双侧阔韧带乳头状囊腺瘤:冯·希佩尔-林道病的一种表现:病例报告

Bergaoui, Haifa; Ghaddab, Imen; Dhouib, Wafa; Njima, Manel; Belghaib, Ichrak; Farhat, Imen Ben; Gharbi, Nedra; Taher, Yessine Bel Haj; Zoukar, Olfa; Toumi, Dhekra; Faleh, Raja

Mucopolysaccharidosis type I: founder effect of the p.P533R mutation in North Africa

I型粘多糖贮积症:p.P533R突变在北非的创始人效应

Chkioua, Latifa; El Fissi, Houda; Amri, Yessine; Sahli, Chayma; Bouzid, Fadoua; Boudabous, Hela; Tbib, Neji; Ferchichi, Salima; Massoud, Taieb; Alif, Najat; Laradi, Sandrine; Ben Abdennebi, Hassen

Respiratory Chain Complex I Deficiency in Leber Hereditary Optic Neuropathy: Insights from Ophthalmologic and Molecular Investigations in Tunisia

莱伯遗传性视神经病变中的呼吸链复合物I缺陷:来自突尼斯眼科和分子研究的启示

Chkioua, Latifa; Amri, Yessine; Sahli, Chayma; Nasri, Tawfik; Miladi, Mohamed Omar; Massoud, Taieb; Laradi, Sandrine; Ghorbel, Mohamed; Ben Abdennebi, Hassen

Contribution of HLA class I (A, B, C) and HLA class II (DRB1, DQA1, DQB1) alleles and haplotypes in exploring ethnic origin of central Tunisians

HLA I类(A、B、C)和HLA II类(DRB1、DQA1、DQB1)等位基因和单倍型在探索突尼斯中部民族起源中的作用

Ben Bnina, Amène; Yessine, Amri; El Bahri, Yasmine; Chouchene, Saoussen; Ben Lazrek, Nada; Mimouna, Mariem; Mlika, Zeineb; Messoudi, Aziza; Zellama, Dorsaf; Sahtout, Wissal; Bouatay, Amina