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

New design of a high-efficiency rectenna for wireless power transfer in 5G applications

一种用于5G应用中无线电力传输的高效整流天线的新型设计

Hamadi, Hamza Ben; Ghnimi, Said; Karoui, Mohamed Salah; Ghayoula, Ridha; Boulejfen, Noureddine; Gharsallah, Ali; Al-Rasheed, Amal; Bayisenge, Lotta

Fulminant Idiopathic Intracranial Hypertension-Clinical Characteristics and Continuous Drainage as a Novel Treatment Approach

暴发性特发性颅内高压——临床特征及持续引流作为一种新型治疗方法

Schwartzmann, Yoel; Moscovici, Samuel; Ekstein, Dana; Jubran, Hamza; Ben-Hur, Tamir; Kruger, Joshua M

Tessier type 3 facial clefts: A case report and literature review

Tessier 3型面裂:病例报告及文献综述

Bensaghir, Hamza; Ben Driss, Chaimae; Fejjal, Nawfal

Unmasking the Deception: A Pediatric Surgery Team's Role in Diagnosing Factitious Disorder Imposed on Another

揭露骗局:儿科外科团队在诊断他人被强加的虚构性障碍中的作用

Bensaghir, Hamza; Ben Driss, Chaimae; Benomar, Ismail; Akhssas, Zakaria; Mai, Oussama; Lahrech, Ali; Fejjal, Nawfal

Bioavailability and health risk of pollutants around a controlled landfill in Morocco: Synergistic effects of landfilling and intensive agriculture

摩洛哥一处受控垃圾填埋场周围污染物的生物有效性和健康风险:垃圾填埋和集约化农业的协同效应

El Fadili, Hamza; Ben Ali, Mohammed; Rahman, Md Naimur; El Mahi, Mohammed; Lotfi, El Mostapha; Louki, Sami

From Thesis to Publication: Unveiling the Predictive Factors for Cardiology Research at a North African Faculty of Medicine (Tunisia)

从论文到发表:揭示北非某医学院(突尼斯)心脏病学研究的预测因素

Yahia, Faten; Gazzeh, Hamza; Ben Mansour, Fares; Zanina, Youssef; Neffati, Elyes; Ben Abdelaziz, Ahmed

Phenotypic intrafamilial variability including H syndrome and Rosai-Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene

表型家族内变异,包括与SLC29A3基因中相同的c.1088G>A突变相关的H综合征和Rosai-Dorfman病。

Chouk, Hamza; Ben Rejeb, Mohamed; Boussofara, Lobna; Elmabrouk, Haїfa; Ghariani, Najet; Sriha, Badreddine; Saad, Ali; H'Mida, Dorra; Denguezli, Mohamed

Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins

鉴定新的致病性MSH2突变和新的DNA修复基因变异:对一个突尼斯林奇综合征家族中不一致双胞胎的研究

Jaballah-Gabteni, Amira; Tounsi, Haifa; Kabbage, Maria; Hamdi, Yosr; Elouej, Sahar; Ben Ayed, Ines; Medhioub, Mouna; Mahmoudi, Moufida; Dallali, Hamza; Yaiche, Hamza; Ben Jemii, Nadia; Maaloul, Afifa; Mezghani, Najla; Abdelhak, Sonia; Hamzaoui, Lamine; Azzouz, Mousaddak; Boubaker, Samir

Polymorphisms of the thiopurine S-methyltransferase gene among the Libyan population

利比亚人群中硫嘌呤S-甲基转移酶基因的多态性

Zeglam, Hamza Ben; Benhamer, Abdrazak; Aboud, Adel; Rtemi, Haitem; Mattardi, Meftah; Saleh, Saleh Suleiman; Bashein, Abdullah; Enattah, Nabil

Association between vitamin D receptor gene polymorphisms and chronic periodontitis among Libyans

利比亚人维生素D受体基因多态性与慢性牙周炎的关联

El Jilani, Mouna M; Mohamed, Abdenaser A; Zeglam, Hamza Ben; Alhudiri, Inas M; Ramadan, Ahmad M; Saleh, Saleh S; Elkabir, Mohamed; Amer, Ibrahim Ben; Ashammakhi, Nureddin; Enattah, Nabil S