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

Implications of occult hepatitis B infection for blood donor management: a five-year evaluation from Western Saudi Arabia

隐匿性乙型肝炎感染对献血者管理的影响:来自沙特阿拉伯西部的一项五年评估

Tounsi, Wajnat A; Noorsaeed, Somaya; Almars, Amany I; Almramhi, Mona M; Basri, Ahmed M; Basabrain, Ammar A; Rokan, Ahmed; Almansouri, Taghreed S; Mokhtar, Sara H; Hakami, Nora Y

Prevalence and Risk Factors of Cardiovascular Disease in Chronic Kidney Disease Patients at King Abdulaziz University Hospital (KAUH)

阿卜杜勒阿齐兹国王大学医院(KAUH)慢性肾脏病患者心血管疾病的患病率和危险因素

Nabalawi, Rana A; Bamuflih, Mohammed Abdullah; Farid, Abdullah Alaa; Almramhi, Khalid Ghali; Dawood, Muhannad Salem; Ahmed, Mohammad Salah; Alfawaz, Khaled S; Adnan, Abdulaziz Mustafa

Exploring the Role of Plasma Lipids and Statin Interventions on Multiple Sclerosis Risk and Severity: A Mendelian Randomization Study

探讨血浆脂质和他汀类药物干预对多发性硬化症风险和严重程度的影响:一项孟德尔随机化研究

Almramhi, Mona M; Finan, Chris; Storm, Catherine S; Schmidt, Amand F; Kia, Demis A; Coneys, Rachel; Chopade, Sandesh; Hingorani, Aroon D; Wood, Nick W

Prevalence and Risk Factors for Acute Kidney Injury Among Adults Undergoing Cardiac Interventions in King Abdulaziz University Hospital: A Retrospective Review

阿卜杜勒阿齐兹国王大学医院接受心脏介入治疗的成年患者急性肾损伤的患病率和危险因素:一项回顾性研究

Almramhi, Khalid G; Alkhateeb, Moussa A; Alsulami, Omar A; Alhudaifi, Saeed A; Alamoudi, Hamza; Nabalawi, Rana A

Finding genetically-supported drug targets for Parkinson's disease using Mendelian randomization of the druggable genome

利用孟德尔随机化方法筛选帕金森病药物靶点

Storm, Catherine S; Kia, Demis A; Almramhi, Mona M; Bandres-Ciga, Sara; Finan, Chris; Hingorani, Aroon D; Wood, Nicholas W

Using Mendelian randomization to understand and develop treatments for neurodegenerative disease

利用孟德尔随机化来理解和开发神经退行性疾病的治疗方法

Storm, Catherine S; Kia, Demis A; Almramhi, Mona; Wood, Nicholas W

A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features

TRAPPC6A 的错义突变导致患有神经发育综合征和畸形特征的患者体内蛋白质积聚

Hussein Sheikh Mohamoud, Saleem Ahmed, Musharraf Jelani, Nuha Alrayes, Kay Childs, Nirmal Vadgama, Mona Mohammad Almramhi, Jumana Yousuf Al-Aama, Steve Goodbourn, Jamal Nasir

Whole-exome sequencing reveals a recurrent mutation in the cathepsin C gene that causes Papillon-Lefevre syndrome in a Saudi family

全外显子组测序揭示了沙特阿拉伯一个家族中导致帕皮隆-勒费弗尔综合征的组织蛋白酶C基因复发性突变

Alkhiary, Yaser Mohammad; Jelani, Musharraf; Almramhi, Mona Mohammad; Mohamoud, Hussein Sheikh Ali; Al-Rehaili, Rayan; Al-Zahrani, Hams Saeed; Serafi, Rehab; Yang, Huanming; Al-Aama, Jumana Yousuf