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

Case Report: IL2RA (CD25) deficiency: first reported cases in Morocco

病例报告:IL2RA(CD25)缺乏症:摩洛哥首例报告病例

Elamine, Ahamada; Benhsaien, Ibtihal; Errami, Abderrahmane; Bellarhrib, Yousra; Aadam, Zahra; Fahi, Mohammed; Bousfiha, Ahmed Aziz; El Bakkouri, Jalila; Ailal, Fatima

A delayed presentation of a giant traumatic pseudocyst of the pancreas

胰腺巨大创伤性假性囊肿的延迟就诊

Yassine, Yasmina; Sbihi, Siham; Haij, Khaoula; Aouroud, Hala; Nacir, Oussama; Lairani, Fatima Ezzahra; Errami, Adil Ait; Oubaha, Sofia; Samlani, Zouhour; Krati, Khadija

Loss of the aryl hydrocarbon receptor promotes cancer cell resistance to BRAFV600E targeted therapies

芳烃受体的缺失会促进癌细胞对BRAFV600E靶向治疗产生耐药性

Zerfaoui, Mourad; Patel, Dharmeshkumar; Zhang, Yueqi; Schinazi, Raymond F; Errami, Youssef

BRAFV600E-PROTAC versus inhibitors in melanoma cells: Deep transcriptomic characterisation

BRAFV600E-PROTAC 与黑色素瘤细胞中的抑制剂:深度转录组表征

Solomon O Alhassan, Zakaria Y Abd Elmageed, Youssef Errami, Guangdi Wang, Joe A Abi-Rached, Emad Kandil, Mourad Zerfaoui

Case Report: A novel CIITA mutation causing MHC class II deficiency: first reported case in Morocco

病例报告:一种导致MHC II类缺陷的新型CIITA突变:摩洛哥首例报告病例

Kattra, Aziza Bachir; Ailal, Fatima; Benhsaien, Ibtihal; Fahi, Mohammed; Drissi Bourhanbour, Asmaa; Elamine, Ahamada; Aadam, Zahra; Errami, Abderrahmane; Bousfiha, Ahmed Aziz; El Bakkouri, Jalila

Integrated optical and radar remote sensing for litho-structural mapping of the Kerdous and Ait Abdellah inliers, western Anti-Atlas, Morocco

利用光学和雷达遥感技术对摩洛哥西部阿特拉斯山脉的克尔杜斯和艾特阿卜杜拉内陆地区进行岩性构造测绘

Aadaj, Jaouad; Tabit, Abdelhalim; Algouti, Ahmed; Aydda, Ali; Moujane, Said; Agli, Saloua; Farah, Abdelouahed; Errami, Maryam; Shebl, Ali

Autoimmune manifestations in children with inborn errors of immunity in Morocco: A study from the national registry

摩洛哥先天性免疫缺陷患儿的自身免疫表现:一项基于国家登记处的研究

Elamine, Ahamada; Benhsaien, Ibtihal; Ailal, Fatima; Errami, Abderrahmane; Kasmi, Zakaria; Aadam, Zahra; Bourhanbour, Asmaa Drissi; Bousfiha, Ahmed Aziz; El Bakkouri, Jalila

Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case report

糖原贮积症Ib型合并高钙血症及TBX1基因突变:病例报告

Kasmi, Zakaria; Ain El Hayat, Imane; Aadam, Zahra; Errami, Abderrahmane; Benhsaien, Ibtihal; El Bakkouri, Jalila; Ben Sabbahia, Dalal; Atrassi, Meryem; Bousfiha, Ahmed Aziz; Ailal, Fatima

Correction: Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case report

更正:Ib型糖原贮积症合并高钙血症和TBX1基因突变:病例报告

Kasmi, Zakaria; Ain El Hayat, Imane; Aadam, Zahra; Errami, Abderrahmane; Benhsaien, Ibtihal; El Bakkouri, Jalila; Ben Sabbahia, Dalal; Atrassi, Meryem; Bousfiha, Ahmed Aziz; Ailal, Fatima

Major Histocompatibility Complex Class II Deficiency Beyond Infancy

婴儿期后主要组织相容性复合体 II 类缺乏症

Kattra, Aziza Bachir; Benhsaien, Ibtihal; Drissi Bourhanbour, Asmaa; Aadam, Zahra; Errami, Abderrahmane; Ailal, Fatima; Bousfiha, Ahmed Aziz; El Bakkouri, Jalila