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

Idiopathic Pulmonary Fibrosis: A Comprehensive Review of Risk Factors, Genetics, Diagnosis, and Therapeutic Approaches

特发性肺纤维化:风险因素、遗传学、诊断和治疗方法的全面综述

Senhaji, Lamiyae; Senhaji, Nadia; Abbassi, Meriame; Karhate, Mariem; Serraj, Mounia; El Biaze, Mohammed; Benjelloun, Mohamed Chakib; Ouldim, Karim; Bouguenouch, Laila; Amara, Bouchra

X-ray microscopy and talbot imaging with the matter in extreme conditions X-ray imager at LCLS

利用LCLS的X射线成像仪,在极端条件下对物质进行X射线显微镜和塔尔博特成像。

Galtier, Eric; Lee, Hae Ja; Khaghani, Dimitri; Boiadjieva, Nina; McGehee, Peregrine; Arnott, Ariel; Arnold, Brice; Berboucha, Meriame; Cunningham, Eric; Czapla, Nick; Dyer, Gilliss; Ettelbrick, Robert; Hart, Philip; Heimann, Philip; Welch, Marc; Makita, Mikako; Gleason, Arianna E; Pandolfi, Silvia; Sakdinawat, Anne; Liu, Yanwei; Wojcik, Michael J; Hodge, Daniel; Sandberg, Richard; Valdivia, Maria Pia; Bouffetier, Victorien; Pérez-Callejo, Gabriel; Seiboth, Frank; Nagler, Bob

MUC5B Polymorphism and Susceptibility to Idiopathic Pulmonary Fibrosis in Morocco

摩洛哥人群中MUC5B多态性与特发性肺纤维化易感性的关系

Senhaji, Lamiyae; Abbassi, Meriame; Senhaji, Nadia; Benmaamar, Soumaya; Dani, Lamyae; El Rhazi, Karima; Karhate, Meryem; Serraj, Mounia; El Biaze, Mohamed; Benjelloun, Mohammed Chakib; Ouldim, Karim; Bouguenouch, Laila; Amara, Bouchra

Impact of Deletion on Angelman Syndrome Phenotype Variability: Phenotype-Genotype Correlation in 97 Patients with Motor Developmental Delay

基因缺失对安格曼综合征表型变异的影响:97例运动发育迟缓患者的表型-基因型相关性研究

Belghiti, Hanae Daha; Abbassi, Meriame; Sayel, Hanane; Ahakoud, Mohamed; El Makhzen, Badr Eddine; Lee, Norman; Russo, Silvia; Chaouki, Sana; Bouguenouch, Laila

Influence of CYP450 Enzymes and ABCB1 Polymorphisms on Clopidogrel Response in Moroccan Patients with Acute Coronary Syndromes

CYP450酶和ABCB1多态性对摩洛哥急性冠脉综合征患者氯吡格雷反应的影响

Mouhrach, Ismail; Bouguenouch, Laila; Kamal, Adil; Meriame, Abbassi; El Khorb, Nada; El Azami El Idrissi, Mohammed; Akoudad, Hafid; Bekkari, Hicham

Autosomal Dominant Intellectual Development Disorder-6 (MRD6) Without Seizures Linked to a De Novo Mutation in the grin2b Gene Revealed by Exome Sequencing: A Case Report of a Moroccan Child

通过外显子组测序发现,摩洛哥一名儿童患有与 grin2b 基因新发突变相关的常染色体显性遗传智力发育障碍-6 (MRD6),且无癫痫发作。

El Mouhi, Hinde; Abbassi, Meriame; Sayel, Hanane; Trhanint, Said; Natiq, Abdelhafid; El Hejjioui, Brahim; Jalte, Merym; Ahmadi, Youssef; Chaouki, Sana

Acellular bioactivity and drug delivery of new strontium doped bioactive glasses prepared through a hydrothermal process

通过水热法制备的新型锶掺杂生物活性玻璃的非细胞生物活性和药物递送

El Baakili, Salwa; El Mabrouk, Khalil; Bricha, Meriame

Case report of an angiosarcoma of the abdominal wall during liraglutide injections: A coincidence?

利拉鲁肽注射期间发生腹壁血管肉瘤的病例报告:纯属巧合吗?

Bergeron, Eric; Dami, Meriame; Do, Xuan Vien; Vallee, Chantal; Noujaim, Jonathan

Mesoporous bioactive glass nanoparticles doped with magnesium: drug delivery and acellular in vitro bioactivity

镁掺杂介孔生物活性玻璃纳米粒子:药物递送和非细胞体外生物活性

Tabia, Zakaria; El Mabrouk, Khalil; Bricha, Meriame; Nouneh, Khalid

[Lynch syndrome: case report and review of the literature]

[林奇综合征:病例报告及文献综述]

Bouguenouch, Laila; Samri, Imane; Belhassan, Khadija; Sayel, Hanane; Abbassi, Meriame; Bennis, Sanae; Benajah, Dafr Allah; Ibrahimi, Adil; Amarti, Afaf; Ouldim, Karim