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

Pycnodysostosis: a case series of eight Saudi patients with cathepsin K gene mutation and a literature review

骨硬化症:8例沙特阿拉伯组织蛋白酶K基因突变患者的病例系列及文献综述

Alsagheir, Afaf; Alhuthil, Raghad; Alissa, Ahmad T; Joueidi, Faisal; Sayed, Ahmed G; Al-Amoudi, Waleed; Alabdulhadi, Alanoud S; Bin-Abbas, Bassam

Pregnancy Outcomes in Women with Low and Ultra-Low Ejection Fraction: A Retrospective Study in a Tertiary Care Center

低射血分数和超低射血分数女性的妊娠结局:三级医疗中心的回顾性研究

Saeed, Bashayer; ALbalawi, Amani; Bintalib, Marwah; Alturki, Amjad; De Vol, Edward B; ALzayed, Balqees; Mohty, Dania; Veldtman, Gruschen; AlMugbel, Maisoon; Latta, Nayef; Joueidi, Faisal; Kurdi, Wesam

Evaluation of the effectiveness of contrast-enhanced ultrasound in the diagnosis of early hepatocellular carcinoma: a systematic review

对比增强超声在早期肝细胞癌诊断中的有效性评价:一项系统性综述

AlTaweel, Abdulaziz; Joueidi, Faisal; Joueidi, Ahmad; AlDhubaiki, Ahmed; Qabha, Hamad Mohammed; AlZaid, Homoud Abdulaziz

First case of primary CNS lymphoma in a patient with severe combined immunodeficiency carrying a novel ZAP70 mutation: a case report

首例携带新型ZAP70突变的重症联合免疫缺陷患者发生原发性中枢神经系统淋巴瘤:病例报告

Albitar, Mohammed Hady; Sayed, Ahmed Gamal; Joueidi, Faisal; Mariyam, Nida; AlDamouni, Maeen Bassam; Albalawi, Waad Ahmed; Arnaout, Rand

Balloon dilatation for failed pyeloplasty is it a valid alternate option in pediatric age group: A comparative retrospective study

对于肾盂成形术失败的儿童患者,球囊扩张术是否是一种有效的替代方案:一项比较性回顾性研究

Alqarni, Naif; Alyami, Fahad; Alrumaih, Abdullah; Joueidi, Faisal; Alshayie, Mohammad; Alrefaei, Mohammad A; Alsarari, Abdulrahman A; Latta, Nayef; Enabi, Hamza M Kossai; Alfattani, Areej; Alsuwaida, Areej

Homozygous α-Spectrin (SPTA1) Variant Causing Persistent Hereditary Pyropoikilocytosis in a Newborn: A Case Report and Literature Review

纯合α-血影蛋白(SPTA1)变异导致新生儿持续性遗传性红细胞热异形症:病例报告及文献综述

Sayed, Jamal; Alabdulhadi, Alanoud Sulaiman; Alzahrani, Waheed Abdullah; Joueidi, Faisal; Alzahrani, Ghaida Ali; Sayed, Ahmed Gamal; Ebid, Gamal T

Clinical characteristics and long-term management for patients with vitamin D-dependent rickets type II: a retrospective study at a single center in Saudi Arabia

维生素D依赖性佝偻病II型患者的临床特征和长期管理:沙特阿拉伯单中心回顾性研究

Alsagheir, Afaf; Al-Ashwal, Abdullah; Binladen, Amal; Alhuthil, Raghad; Joueidi, Faisal; Ramzan, Khushnooda; Imtiaz, Faiqa

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。

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

Transjugular Intrahepatic Portosystemic Shunt for Budd-Chiari Syndrome: A Single-Centre Experience

经颈静脉肝内门体分流术治疗布加氏综合征:单中心经验

Joueidi, Faisal; Alhanaee, Amnah; Alsuhaibani, Hamad; Albenmousa, Ali; Joueidi, Ahmad; Elhassan, Ahmed; Nasir, Abdallah Nabeel; Marquez, Kris Ann Hervera; Alghamdi, Saad; Al Hamoudi, Waleed; Abualganam, Saad; Broering, Dieter; Bzeizi, Khalid Ibrahim

Bell's palsy characteristics, clinical manifestations, complications, and prognosis in a primary care setting, a single center study: A retrospective cohort study

贝尔氏麻痹症的特征、临床表现、并发症和预后:一项单中心回顾性队列研究

Alamodi, Mohammed; Joueidi, Faisal; Sayed, Ahmed Gamal; Alsarari, Abdulrahman; Alaswad, Hani; Alhamdan, Wejdan; Alendijani, Yaser; Almufrij, Sarah; Alkhenizan, Abdullah