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

Ectrodactyly, Cleft Lip/Palate, and Urinary Anomalies With a Tumor Protein p63 (TP63) Mutation: A Case Report and Literature Review

伴有肿瘤蛋白p63 (TP63) 突变的缺指、唇腭裂和泌尿系统畸形：病例报告及文献综述

期刊:Cureus Journal of Medical Science
影响因子:1.3
doi:10.7759/cureus.92888
Mohamed, Rayan H; Khalifa, Haydy M; Hassan, Hisham Y; Shajira, Eman; Al-Qashar, Fahad A
肿瘤
肿瘤免疫
发表日期：2025
文献求助 收藏

Aldosterone Synthase Deficiency Type I in a Neonate: Diagnostic, Genetic, and Therapeutic Insights From a Novel CYP11B2 Variant

新生儿醛固酮合成酶缺乏症 I 型：来自新型 CYP11B2 变异体的诊断、遗传和治疗见解

期刊:Cureus Journal of Medical Science
影响因子:1.3
doi:10.7759/cureus.97170
Khalifa, Haydy M; Mohamed, Rayan H; Hassan, Hisham Y; Al-Qashar, Fahad A; Alkhayyat, Haya
发表日期：2025
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Validity and reliability of the WHOQOL-BREF in the measurement of the quality of life of Sickle disease patients in Bahrain

WHOQOL-BREF 在巴林测量镰状细胞病患者生活质量方面的有效性和可靠性

期刊:Frontiers in Psychology
影响因子:2.9
doi:10.3389/fpsyg.2023.1219576
Almarabheh, Amer; Salah, Afif Ben; Alghamdi, Manal; Al Saleh, Aseel; Elbarbary, Abdulla; Al Qashar, Ahmed; Alserdieh, Faisal; Alahmed, Fatema; Alhaddar, Hasan; Alsada, Lulwa; Yosri, Mohamed; Omran, Mahmood; Khudhair, Mina; Salih, Motasem; Fuad, Noora; Chlif, Sadok
细胞生物学
发表日期：2023
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Case report: Homozygous variants of NEB and KLHL40 in two Arab patients with nemaline myopathy

病例报告：两例阿拉伯线状肌病患者携带NEB和KLHL40纯合变异

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2023.1098102
Skrypnyk, Cristina; Husain, Aseel Ahmed; Hassan, Hisham Y; Ahmed, Jameel; Darwish, Abdulla; Almusalam, Latifa; Ben Khalaf, Noureddine; Al Qashar, Fahad
发表日期：2023
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