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

Identification of novel and recurrent mutations in nicotinamide nucleotide transhydrogenase (NNT) underlying familial glucocorticoid deficiency-type 4 in multiple Saudi families

在多个沙特阿拉伯家族中鉴定出导致家族性糖皮质激素缺乏症4型的烟酰胺核苷酸转氢酶（NNT）基因的新型和复发性突变

期刊:Journal of Clinical and Translational Endocrinology
影响因子:3.3
doi:10.1016/j.jcte.2026.100433
Alwan, Ibrahim Al; Ali, Raja Hussain; Umair, Muhammad; Khan, Imran Ali; Alotaibi, Nada; Aloyouni, Essra; Alwadaani, Deemah; Alayyar, Latifah; Haddad, Shahad; Alawaji, Shahad; Althenayyan, Saleh; Alfaidi, Ahmed; Algattan, Manal; Alquraishi, Ali S; Alzaben, Abdullah; Alfaraidi, Haifa; Almulhem, Beshaier; Almannai, Mohammed; Alfadhel, Majid
免疫/内分泌
发表日期：2026
文献求助 收藏

The effect of probiotic supplementation on perceived stress and bowel function in healthy young adults: evidence from a randomized controlled trial in Makkah

益生菌补充剂对健康年轻成人感知压力和肠道功能的影响：来自麦加一项随机对照试验的证据

期刊:Frontiers in Nutrition
影响因子:5.1
doi:10.3389/fnut.2025.1717047
Noorwali, Essra A; Aljaadi, Abeer M; Abusudah, Wafaa F; Bakhdar, Fatmah A; Bin-Ali, Dania H; Alshinawi, Amani; Bawazir, Asma; Mutlaq, Raghad A; Maimany, Heba A; Barnawi, Layan A; Murshed, Bshayer; Aljared, Bayan; Azzeh, Firas S
发表日期：2025
文献求助 收藏

Clinical and Demographic Characteristics of Oral Sarcoidosis: A Systematic Review of Case Reports and Case Series

口腔结节病的临床和人口统计学特征：病例报告和病例系列的系统评价

期刊:Journal of Clinical Medicine
影响因子:2.9
doi:10.3390/jcm14197006
Jaber, Mohamed; Abouseif, Nadin; Abdelmagied, Mawada; El-Ameen, Essra Mohamed
发表日期：2025
文献求助 收藏

Truncated SPAG9 as a novel candidate gene for a new syndrome: Coarse facial features, albinism, cataract and developmental delay (CACD syndrome)

截短的 SPAG9 作为一种新综合征的新候选基因：粗糙面部特征、白化病、白内障和发育迟缓（CACD 综合征）

期刊:Genetics and Molecular Biology
影响因子:1.7
doi:10.1590/1678-4685-GMB-2024-0094
Majid Alfadhel, Bashayr S Alhubayshi, Muhammad Umair, Ahmed Alfaidi, Deemah Alwadaani, Essra Aloyouni, Safdar Abbas, Abdulkareem Al Abdulrahman, Mohammed Aldrees, Abeer Al Tuwaijri, Ruaa S Alharithy, Abdulaziz Alajlan, Abdulrahman Alswaid, Saad Almohrij, Sultan Al-Khenaizan
发育与干细胞
发表日期：2025
文献求助 收藏

Diagnostic Performance of Neural Network-Based Artificial Intelligence in the Detection and Classification of Pediatric Astrocytoma: A Systematic Review

基于神经网络的人工智能在儿童星形细胞瘤检测和分类中的诊断性能：系统评价

期刊:Cureus Journal of Medical Science
影响因子:1.3
doi:10.7759/cureus.83543
Elbakry Abdelmahdy, Nermin Ezat; Abd Alnour Suliman, Essra Tajelsir; Osman Mohmed, Fatima Mahmoud; Ali Elamin, Nazik Siddig; Hamza Yousif, Belgees Altigani; Ahmmed, Nazik Abbas Mohammed
细胞生物学
发表日期：2025
文献求助 收藏

The Impact of Neonatal Sepsis on Long-Term Neurodevelopment: A Systematic Review of Cognitive and Sensory Outcomes

新生儿败血症对长期神经发育的影响：认知和感觉结果的系统评价

期刊:Cureus Journal of Medical Science
影响因子:1.3
doi:10.7759/cureus.90176
Mohamed Ahmed Hamid, Sara Mohamedosman; Ibrahim Shaban, Kamal Shaban; Abdulhamid Abdulaziz, Solafa Babeker; Ahmed Mohamed, Sanaa Yosif Mohamed; Abdo Osman, Safwa Khatme; Abd Alnour Suliman, Essra Tajelsir
发育与干细胞
败血症
神经科学
发表日期：2025
文献求助 收藏

Clinical Audit of Acute Oxygen Therapy: Enhancing Patient Care at Atbara Teaching Hospital

急性氧疗临床审核：提升阿特巴拉教学医院的患者护理水平

期刊:Cureus Journal of Medical Science
影响因子:1.3
doi:10.7759/cureus.91472
Muhammed, Abubakr; Awad, Mustafa; Abbas, Alaa; Alradi, Essra Hassan Adam; Taha, Rawan Salah Mohamed; Mohamed, Wishah Busati Saad; Mohammed, Reham Abdelgadir Abdelhafeez; Baket, Hashim Faiez Khader; Salih Mohamed Salih, Tayseer; Osman Ahmed Osman, Mohammed; Mohamed, Doaa Mahmoud Akasha; Mohamed, Ahmed Nabil; Musa Mohamed, Abeer Hussien; Ibrahim, Samir Khedir Bahageil; Ali Mohamed, Mawada M; Abakar, Saad Adam Abdallah; Wedatalla, Mohamed Abdalla Elawad; Alneama, Musab Alhadi Bushra; Alzain Adam, Mohammad
发表日期：2025
文献求助 收藏

Azolla pinnata as a phytoremediator: improves germination, growth and yield of maize irrigated with Ni-polluted water

满江红作为植物修复剂：可改善用镍污染水灌溉的玉米的发芽率、生长和产量。

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-024-72651-1
Zeid, Ibrahim; Ghaly, Essra Khaled; Shedeed, Zeinab Ashour
发表日期：2024
文献求助 收藏

Biallelic HMGXB4 loss-of-function variant causes intellectual disability, developmental delay, and dysmorphic features

HMGXB4基因双等位基因功能缺失变异会导致智力障碍、发育迟缓和畸形特征。

期刊:Heliyon
影响因子:3.6
doi:10.1016/j.heliyon.2024.e35361
Al Mutairi, Fuad; Joueidi, Faisal; Alshalan, Maha; Aloyouni, Essra; Ballow, Mariam; Aldrees, Mohammed; Al Abdulrahman, Abdulkareem; Al Tuwaijri, Abeer; Abbas, Safdar; Umair, Muhammad; Alfadhel, Majid
发育与干细胞
发表日期：2024
文献求助 收藏

First Report from Saudi Arabia of Trimethylaminuria Caused by a Premature Stop Codon Mutation in the FMO3 Gene

沙特阿拉伯首次报道由FMO3基因提前终止密码子突变引起的三甲胺尿症

期刊:Application of Clinical Genetics
影响因子:2.8
doi:10.2147/TACG.S497959
Alghanem, Bandar; Alamri, Hassan S; Barhoumi, Tlili; Ali Khan, Imran; Almuhalhil, Khawlah; Aloyouni, Essra; Shaibah, Hayat; Mashhour, Abdullah; Algheribe, Shatha; Islam, Imadul; Boudjelal, Mohamed; Alfadhel, Majid
发表日期：2024
文献求助 收藏