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

Assessing Community Readiness to Use Social Platforms for Stroke Survivors' Recovery and Caregiver Support in Saudi Arabia

评估沙特阿拉伯社区利用社交平台帮助中风幸存者康复和为照护者提供支持的准备情况

Babkair, Lisa A; Al-Sahabi, Mohammed; Al-Ghamedi, Husam; Al-Shehri, Abdulmajeed S; Al-Zeer, Ahmed; Shibily, Faygah; Alyafee, Rwan M

Parental measurement and correlation of empathy among families attending pediatric neurology clinics

儿科神经科门诊就诊家庭中父母同理心的测量和相关性

Bamaga, Ahmed K; Alyazidi, Anas S; Hamad, Alaa; Alageel, Dalal F; Arabi, Tarek; Alotibi, Taif K; Bakheet, Hadeel A; Aljefri, Yara F; Alyafee, Areej M; Alayed, Rasil S

Non-invasive prenatal testing for autosomal recessive disorders: A new promising approach

常染色体隐性遗传病的无创产前检测:一种有前途的新方法

Yusra Alyafee, Abeer Al Tuwaijri, Muhammad Umair, Mashael Alharbi, Shahad Haddad, Maryam Ballow, Latifah Alayyar, Qamre Alam, Saleh Althenayyan, Nadia Al Ghilan, Aziza Al Khaldi, Majid S Faden, Hamad Al Sufyan, Majid Alfadhel

Novel homozygous pathogenic mitochondrial DNAJC19 variant in a patient with dilated cardiomyopathy and global developmental delay

扩张型心肌病和全身发育迟缓患者出现新型纯合致病线粒体 DNAJC19 变异

Abeer Al Tuwaijri, Yusra Alyafee, Mashael Alharbi, Maryam Ballow, Mohammed Aldrees, Qamre Alam, Rola A Sleiman, Muhammad Umair, Majid Alfadhel

Mutated VWA8 Is Associated With Developmental Delay, Microcephaly, and Scoliosis and Plays a Novel Role in Early Development and Skeletal Morphogenesis in Zebrafish

突变的VWA8基因与斑马鱼发育迟缓、小头畸形和脊柱侧弯相关,并在斑马鱼早期发育和骨骼形态发生中发挥新的作用。

Umair, Muhammad; Farooq Khan, Muhammad; Aldrees, Mohammed; Nashabat, Marwan; Alhamoudi, Kheloud M; Bilal, Muhammad; Alyafee, Yusra; Al Tuwaijri, Abeer; Aldarwish, Manar; Al-Rumayyan, Ahmed; Alkhalaf, Hamad; Wadaan, Mohammad A M; Alfadhel, Majid

The Journey of Saudi Male Nurses Studying within the Nursing Profession: A Qualitative Study

沙特阿拉伯男护士在护理专业学习历程:一项定性研究

Banakhar, Maram; Bamohrez, Maha; Alhaddad, Raghad; Youldash, Reema; Alyafee, Rwan; Sabr, Sufanah; Sharif, Loujain; Mahsoon, Alaa; Alasmee, Nofaa

Identification of the TTC26 Splice Variant in a Novel Complex Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations

在一种具有胆道、肾脏、神经和骨骼表现的新型复杂纤毛病综合征中鉴定出TTC26剪接变异体

Alfadhel, Majid; Umair, Muhammad; Almuzzaini, Bader; Asiri, Abdulaziz; Al Tuwaijri, Abeer; Alhamoudi, Khaloud; Alyafee, Yusra; Al-Owain, Mohammed

Next-Generation Sequencing-Based Pre-Implantation Genetic Testing for Aneuploidy (PGT-A): First Report from Saudi Arabia

基于下一代测序的非整倍体植入前基因检测 (PGT-A):来自沙特阿拉伯的第一份报告

Yusra Alyafee, Qamre Alam, Abeer Al Tuwaijri, Muhammad Umair, Shahad Haddad, Meshael Alharbi, Hayat Alrabiah, Maha Al-Ghuraibi, Sahar Al-Showaier, Majid Alfadhel

Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay

RAP1GDS1基因突变会导致一种新的综合征,其特征为面部畸形、智力障碍和语言发育迟缓。

Asiri, Abdulaziz; Aloyouni, Essra; Umair, Muhammad; Alyafee, Yusra; Al Tuwaijri, Abeer; Alhamoudi, Kheloud M; Almuzzaini, Bader; Al Baz, Abeer; Alwadaani, Deemah; Nashabat, Marwan; Alfadhel, Majid

Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report

NEK10 纯合截断突变与原发性纤毛运动障碍相关:病例报告

Al Mutairi, Fuad; Alkhalaf, Randa; Alkhorayyef, Abdullah; Alroqi, Fayhan; Yusra, Alyafee; Umair, Muhammad; Nouf, Fetaini; Khan, Amjad; Meshael, Alharbi; Hamad, Aleidi; Monira, Alaujan; Asiri, Abdulaziz; Alhamoudi, Kheloud M; Alfadhel, Majid