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

A novel homozygous CA5A gene deletion in carbonic anhydrase VA deficiency presenting as developmental delay without metabolic crisis

一种新型的碳酸酐酶VA缺乏症纯合CA5A基因缺失,表现为发育迟缓,但无代谢危机。

Bin Hadyan, Maryam F; Saleh, Mohammed A; Aldalaqan, Saad; Mushiba, Aziza M; Alasmari, Ali M; Faqeih, Eissa A; Peer-Zada, Abdul A

The association of artificial sweeteners intake and risk of cancer: an umbrella meta-analysis

人工甜味剂摄入与癌症风险的关联:一项综合性荟萃分析

Abu-Zaid, Ahmed; Kutbi, Emad; Alshammari, Nawal; AlJurayyan, Abdullah Nasser; Adly, Heba M; Saleh, Saleh A K; Baradwan, Saeed; Jamal, Madiha; Peer-Zada, Feham; Mohamed, Shaimaa; Syed, Huda; Ahmed, Rania Salah; Abuzaid, Mohammed; Alomar, Osama

Clinical and molecular characterization of hepatic glycogen storage disease in Saudi Arabia

沙特阿拉伯肝糖原贮积症的临床和分子特征

Al-Hussaini, Abdulrahman; AlMannai, Mohammed; Alruwaithi, Muhannad; Faqeih, Eissa; Alasmari, Ali; Alfadhel, Majid; Al Mutairi, Fuad; Saleh, Mohammed; AlZaben, Abdullah; Alobailan, Yaser; Alharbi, Moodhi; AlAfqi, Manal; Alayed, Alaa; Peer-Zada, Abdul Ali; Alrusayni, Yasir

Knowledge, attitude, and practice of medical students toward Mpox in Saudi Arabia: a cross-sectional study

沙特阿拉伯医学生对痘病毒的认知、态度和实践:一项横断面研究

Peer-Zada, Feham; Mahmoud, Hadil; Rahman, Heba; Abdulmowla, Ola Muwafak; Mohamed, Shaimaa; Raziq, Tehreemah; Sajjad, Maryam; Arai, Momo; Dahman, Huda; Naimi, Hamna Waseem; Shibl, Atef; Dirar, Qais

Aggressive Disease and Poor Clinical Outcome in CEBPα-Mutated Acute Myeloid Leukemia Patient

CEBPα突变型急性髓系白血病患者的侵袭性疾病和不良临床结局

Alshammari, Abdullah Attullah; AlSabbagh, Mohammed O; Alshehri, Hasan M; AlSwayyed, Azizah F; Alseraye, Faisal M; Peer-Zada, Abdul Ali

Incidence of Inborn Errors of Metabolism and Endocrine Disorders Among 40965 Newborn Infants at Riyadh Second Health Cluster of the Ministry of Health Saudi Arabia

沙特阿拉伯卫生部利雅得第二卫生集群40965名新生儿先天性代谢缺陷和内分泌疾病的发生率

Alshehri, Abdullah S; Peer-Zada, Abdul A; Algadhi, Abeer A; Aldehaimi, Abdulwahed; Saleh, Mohammed A; Mushiba, Aziza M; Faqeih, Eissa A; AlAsmari, Ali M

Novel de novo heterozygous CACNA1A gene variant in generalised dystonia: a case report

一例全身性肌张力障碍患者发现新的从头杂合CACNA1A基因变异:病例报告

Alshareet, Mohammed; Alakkas, Aljoharah; Alsinaidi, Omar A; Bawazeer, Shahad; Peer-Zada, Abdul Ali

A rare presentation of BCR-ABL1 and RUNX1-MECOM rearrangement in a pediatric patient with acute myeloid leukemia

儿童急性髓系白血病患者中罕见的 BCR-ABL1 和 RUNX1-MECOM 重排表现

Alamri, Ragdah M; Alanazi, Maryam; AlRajeh, Rajeh K; Tashkandi, Suha A; Alswayyed, Azizah F; Samman, Manar A; Peer-Zada, Abdul Ali

Novel TLR7 hemizygous variant in post-COVID-19 neurological deterioration: a case report with literature review

新冠肺炎后神经功能恶化中一种新型TLR7半合子变异:病例报告及文献综述

Noor Eddin, Ahmed; Al-Rimawi, Mohammed; Peer-Zada, Feham; Hundallah, Khalid; Alhashem, Amal

Favorable outcome of PML-RARα short isoform and FLT3-ITD mutation in a patient with several adverse prognostic markers: A case report

PML-RARα短亚型和FLT3-ITD突变在具有多个不良预后指标的患者中取得良好预后:病例报告

Bafail, Mohammed A; AlTahan, Rahaf; Samman, Manar A; Tashkandi, Suha A; Motabi, Ibraheem H; Peer-Zada, Abdul Ali