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

Congenital Anemia Due to Erythropoietin Gene Mutation Presenting With Diamond-Blackfan Anemia-like features

由促红细胞生成素基因突变引起的先天性贫血,表现为类似Diamond-Blackfan贫血的特征

AboGhayyada, Ibrahim; Zeidan, Mohammad; Abusnaina, Dalya; Abouodeh, Saja; Ghnimat, Mosab; Najajreh, Mohammad

Mitochondrial HMG-CoA Synthase Deficiency Presenting as Pediatric Metabolic Stroke: A Case Report of a Novel Homozygous HMGCS2 (p.Ile56Asn) Variant

线粒体HMG-CoA合成酶缺乏症表现为儿童代谢性卒中:一例新型纯合HMGCS2(p.Ile56Asn)变异病例报告

Alshami, Yasmeen; Hroub, Osama; Hroub, Mohammad; Abouodeh, Saja; Makhamre, Zahra; Hammouri, Ahmad G; Alzatari, Ibrahim; Atawneh, Osama

Extremely Rare Neonatal Case With Pyloric Atresia, Heart Defects, Hypotonia, Jaundice, and Acidosis

极其罕见的先天性幽门闭锁、心脏缺陷、肌张力低下、黄疸和酸中毒新生儿病例

Abouodeh, Saja; Alshami, Yasmeen; Hroub, Osama; Hroub, Mohammad; Hammouri, Ahmad G; Shaltaf, Ahmad; Shihadeh, Wafa; Dawod, Nimatee