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

Unprecedented coexistence of Dent's disease type 1 and Wilson's disease in a two-year-old Chinese boy: implications for precision medicine

一名两岁中国男童罕见地同时患有1型登特氏病和威尔逊氏病:对精准医疗的启示

Mao, Qingxian; Cheung, Wai W; Che, Ruochen; Zhao, Fei; Cheng, Xueqin; Ding, Guixia

Phenotype and genotype analyses of 21 Chinese patients with Dent disease.

对 21 名中国 Dent 病患者进行表型和基因型分析

Che Ruochen, Cai Yuwen, Zhou Wei, Zhao Sanlong, Huang Songming

Monogenic Causes Identified in 23.68% of Children with Steroid-Resistant Nephrotic Syndrome: A Single-Centre Study

单中心研究发现,23.68%的类固醇抵抗性肾病综合征患儿存在单基因病因。

Zhang, Luyan; Zhao, Fei; Ding, Guixia; Chen, Ying; Zhao, Sanlong; Chen, Qiuxia; Sha, Yugen; Che, Ruochen; Huang, Songming; Zheng, Bixia; Zhang, Aihua

A Potential Therapy Using Antisense Oligonucleotides to Treat Autosomal Recessive Polycystic Kidney Disease

利用反义寡核苷酸治疗常染色体隐性多囊肾病的潜在疗法

Li, Huixia; Wang, Chunli; Che, Ruochen; Zheng, Bixia; Zhou, Wei; Huang, Songming; Jia, Zhanjun; Zhang, Aihua; Zhao, Fei; Ding, Guixia

Hemoperfusion and intravenous immunoglobulins for refractory gastrointestinal involvement in pediatric Henoch-Schönlein purpura: a single-center retrospective cohort study

血液灌流和静脉注射免疫球蛋白治疗儿童亨诺赫-舍恩莱因紫癜难治性胃肠道受累:一项单中心回顾性队列研究

Zhang, Xiaolu; Che, Ruochen; Xu, Haisheng; Ding, Guixia; Zhao, Fei; Huang, Songming; Zhang, Aihua

A rare case of pediatric recurrent rhabdomyolysis with compound heterogenous variants in the LPIN1

一例罕见的儿童复发性横纹肌溶解症,伴有LPIN1基因的复合异质性变异

Che, Ruochen; Wang, Chunli; Zheng, Bixia; Zhang, Xuejuan; Ding, Guixia; Zhao, Fei; Jia, Zhanjun; Zhang, Aihua; Huang, Songming; Feng, Quancheng

Huaier Cream Protects against Adriamycin-Induced Nephropathy by Restoring Mitochondrial Function via PGC-1α Upregulation

华伊尔乳膏通过上调PGC-1α恢复线粒体功能,从而保护肾脏免受阿霉素诱导的肾病侵害。

Che, Ruochen; Zhu, Chunhua; Ding, Guixia; Zhao, Min; Bai, Mi; Jia, Zhanjun; Zhang, Aihua; Huang, Songming