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

Monitoring Cross-Border Dissemination of Antimicrobial Resistance (AMR) via Air Travel to Saudi Arabia: Formulation of Monitoring Strategies to Mitigate AMR Concerns

监测通过航空旅行跨境传播至沙特阿拉伯的抗菌素耐药性(AMR):制定监测策略以减轻抗菌素耐药性问题

Wang, Changzhi; Narayanasamy, Shaman; Shaabad, Manal; Dallol, Ashraf; Hala, Sharif; Hong, Pei-Ying

Clinical relevance of the somatic mutational landscaping in predicting outcome of bladder cancer patients

体细胞突变图谱在预测膀胱癌患者预后中的临床意义

Nedjadi, Taoufik; Ansari, Hifzur; Khan, Muhammad A; Sannan, Naif; Al-Mansour, Mubarak; Al-Maghrabi, Jaudah; Dallol, Ashraf

The Diagnostic Value of Pan-Trk Expression to Detect Neurotrophic Tyrosine Receptor Kinase (NTRK) Gene Fusion in CNS Tumours: A Study Using Next-Generation Sequencing Platform

Pan-Trk 表达对中枢神经系统肿瘤中神经营养酪氨酸受体激酶 (NTRK) 基因融合的诊断价值:一项使用下一代测序平台的研究

Fawaz Mohamed, Maher Kurdi, Saleh Baeesa, Abdulrahman Jafar Sabbagh, Sahar Hakamy, Yazid Maghrabi, Mohammed Alshedokhi, Ashraf Dallol, Taher F Halawa, Ahmed A Najjar, Imad Fdl-Elmula

A paediatric dysembryoplastic neuroepithelial tumour (DNET) with deregulated stem cell markers: a case report

一例患有干细胞标志物失调的儿童胚胎发育不良性神经上皮肿瘤 (DNET) 的病例报告

Deema Hussein #, Alazouf Alhowity #, Rinad Algehani, Abdulla Ahmed A Salwati, Ashraf Dallol, Hans-Juergen Schulten, Saleh Baeesa, Mohammed Bangash, Fahad Alghamdi, Mohamad Saka, Adeel Chaudhary, Adel Abuzenadah

A novel DOK7 mutation causing congenital myasthenic syndrome with limb-girdle weakness: case series of three family members

一种新的DOK7基因突变导致先天性肌无力综合征伴肢带型无力:三名家族成员的病例系列研究

Alsallum, Mohammed S; Alshareef, Aysha; Abuzinadah, Ahmad R; Bamaga, Ahmed K; Dallol, Ashraf

Prognostic value of TP53 expression and MGMT methylation in glioblastoma patients treated with temozolomide combined with other chemotherapies

TP53表达和MGMT甲基化在接受替莫唑胺联合其他化疗治疗的胶质母细胞瘤患者中的预后价值

Kurdi, Maher; Butt, Nadeem Shafique; Baeesa, Saleh; Alghamdi, Badrah; Maghrabi, Yazid; Bardeesi, Anas; Saeedi, Rothaina; Dallol, Ashraf; Mohamed, Fawaz; Bari, Mohammed O; Samkari, Alaa; Lary, Ahmed I; Alkhayyat, Shadi

Klotho promoter methylation status and its prognostic value in ovarian cancer

Klotho启动子甲基化状态及其在卵巢癌中的预后价值

Al-Zahrani, Maryam H; Yahya, Fatimah M; Assidi, Mourad; Dallol, Ashraf; Buhmeida, Abdelbaset

Leptin Protein Expression and Promoter Methylation in Ovarian Cancer: A Strong Prognostic Value with Theranostic Promises

卵巢癌中瘦素蛋白的表达和启动子甲基化:具有治疗诊断前景的强大预后价值

Mourad Assidi, Fatimah M Yahya, Maryam H Al-Zahrani, Razan Elkhatib, Ali Zari, Aisha Elaimi, Jaudah Al-Maghrabi, Ashraf Dallol, Abdelbaset Buhmeida, Muhammad Abu-Elmagd

Polycystic ovary syndrome is linked with the fat mass obesity (FTO) gene variants rs17817449 and rs1421085 in western Saudi Arabia

在沙特阿拉伯西部,多囊卵巢综合征与脂肪量肥胖(FTO)基因变异rs17817449和rs1421085有关。

Bakhashab, Sherin; Batarfi, Asma A; Filimban, Najlaa; Bajouh, Osama S; Dallol, Ashraf; Alqahtani, Mohammed H

Overlapping variants in the blood, tissues and cell lines for patients with intracranial meningiomas are predominant in stem cell-related genes

颅内脑膜瘤患者血液、组织和细胞系中的重叠变异主要集中在干细胞相关基因中。

Hussein, Deema; Dallol, Ashraf; Quintas, Rita; Schulten, Hans-Juergen; Alomari, Mona; Baeesa, Saleh; Bangash, Mohammed; Alghamdi, Fahad; Khan, Ishaq; ElAssouli, M-Zaki Mustafa; Saka, Mohamad; Carracedo, Angel; Chaudhary, Adeel; Abuzenadah, Adel