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

Perceptions of pediatric neurologists on the ideal candidate: a nationwide survey

全国范围内对儿科神经科医生理想候选人的看法调查

期刊:BMC Medical Education
影响因子:3.2
doi:10.1186/s12909-026-08938-w
Bamaga, Ahmed; Qashqari, Hebah; Alyazidi, Anas; Babiker, Mohamed O E; Madani, Jihan; Almudhry, Montaha; Almobarak, Sulaiman; Ismail, Fatima
发表日期：2026
文献求助 收藏

Outcome of two siblings with late-onset Krabbe disease following allogeneic hematopoietic stem cell transplantation: And review of literature

两名患有晚发型克拉伯病的兄弟姐妹接受异基因造血干细胞移植后的预后：及文献综述

期刊:Molecular Genetics and Metabolism Reports
影响因子:1.9
doi:10.1016/j.ymgmr.2025.101242
Almudhry, Montaha; Prasad, Chitra; Tay, Keng Yow; Rupar, C Anthony; Atkins, Harold; Prasad, Asuri N
细胞生物学
发育与干细胞
干细胞
发表日期：2025
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Long-term follow-up of an attenuated presentation of NAXE-related disease, a potentially actionable neurometabolic disease: a case report

对一例NAXE相关疾病（一种潜在可干预的神经代谢疾病）症状较轻的病例进行长期随访：病例报告

期刊:Frontiers in Neurology
影响因子:2.8
doi:10.3389/fneur.2024.1204848
Almudhry, Montaha; Prasad, Chitra; Rupar, C Anthony; Tay, Keng Yeow; Prasad, Asuri N
代谢
发表日期：2024
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Short term effectiveness of ustekinumab versus vedolizumab in Crohn's disease after failure of anti-TNF agents: An observational comparative study design with a Bayesian analysis

乌司奴单抗与维多珠单抗在抗TNF药物治疗失败后治疗克罗恩病短期疗效的比较：一项采用贝叶斯分析的观察性比较研究

期刊:Saudi Journal of Gastroenterology
影响因子:2
doi:10.4103/sjg.sjg_101_24
Alamer, Ahmad; Al Lehaibi, Lina H; Alomar, Mukhtar; Aldhuwayan, Fahad; Alshouish, Saleh; Al-Ali, Anfal Y; Almudhry, Zakia; Almulhim, Abdulaziz; Althagafi, Abdulhamid; Aldosari, Saad; AlAmeel, Turki
克罗恩病
发表日期：2024
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Brain Volumes in Opsoclonus-Myoclonus Ataxia Syndrome: A Longitudinal Study

眼阵挛-肌阵挛共济失调综合征患者的脑容量：一项纵向研究

期刊:Journal of Child Neurology
影响因子:1.6
doi:10.1177/08830738241240181
Almudhry, Montaha; Wagner, Matthias W; Longoni, Giulia; Yea, Carmen; Vidarsson, Logi; Ertl-Wagner, Birgit; Yeh, E Ann
神经科学
发表日期：2024
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A milder form of molybdenum cofactor deficiency type A presenting as Leigh's syndrome-like phenotype highlighting the secondary mitochondrial dysfunction: a case report

一种表现为类似莱氏综合征表型的轻型A型钼辅因子缺乏症，突出了继发性线粒体功能障碍：病例报告

期刊:Frontiers in Neurology
影响因子:2.8
doi:10.3389/fneur.2023.1214137
Almudhry, Montaha; Prasad, Asuri N; Rupar, C Anthony; Tay, Keng Yeow; Ratko, Suzanne; Jenkins, Mary E; Prasad, Chitra
线粒体
发表日期：2023
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Methylmalonic aciduria as a biochemical marker for mitochondrial DNA depletion syndrome in patients with developmental delay and movement disorders: a case series

甲基丙二酸尿症作为发育迟缓和运动障碍患者线粒体DNA耗竭综合征的生化标志物：病例系列研究

期刊:Frontiers in Neurology
影响因子:2.8
doi:10.3389/fneur.2023.1265115
Almudhry, Montaha; Saini, Arushi Gahlot; Al-Omari, Mohammed A; Sharma, Yashu; Nouri, Maryam Nabavi; Rupar, C Anthony; Prasad, Chitra; Yu, Andrea C; Attri, Savita Verma; Prasad, Asuri Narayan
发育与干细胞
线粒体
发表日期：2023
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Prevalence of the HLA-B*5701 Allele and Abacavir Hypersensitivity in Saudi HIV Patients: A Multicenter Study

沙特阿拉伯HIV患者中HLA-B*5701等位基因和阿巴卡韦超敏反应的患病率：一项多中心研究

期刊:Cureus Journal of Medical Science
影响因子:1.3
doi:10.7759/cureus.48229
Alsaeed, Ali; Alkhadrawi, Zahra; Alsadah, Batool; Almudhry, Zakia; AlBayat, Hawra; Alhadad, Fadel; Dahlawi, Albaraa; Abu Ali, Batool; Al Muhainy, Badr; Alhaddad, Taher A; Alhaddad, Mousa J
HIV
微生物学
发表日期：2023
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