| Issue Date |
Title |
Author(s) |
| 2015 |
Anticancer drug nanomicelles formed by self-assembling amphiphilic dendrimer to combat cancer drug resistance |
Wei, Tuo;Chen, Chao;Liu, Juan;Liu, Cheng;Posocco, Paola;Liu, Xiaoxuan;Cheng, Qiang;Huo, Shuaidong;Liang, Zicai;Fermeglia, Maurizio;Pricl, Sabrina;Liang, Xing-Jie;Rocchi, Palma;Peng, Ling |
| 24-Aug-2022 |
Case report: A variant of the FIG4 gene with rapidly progressive amyotrophic lateral sclerosis |
Yilihamu, Mubalake;Liu, Xiaolu;Liu, Xiaoxuan;Chen, Yong;Fan, Dongsheng |
| 12-Feb-2021 |
Characteristics of Clinical and Electrophysiological Pattern in a Large Cohort of Chinese Patients With Charcot-Marie-Tooth 4C |
Duan, Xiaohui;Ma, Yan;Fan, Dongsheng;Liu, Xiaoxuan |
| 31-May-2021 |
Characterization of genotype-phenotype correlation with MORC2 mutated Axonal Charcot-Marie-Tooth disease in a cohort of Chinese patients |
Duan, Xiaohui;Liu, Xiaoxuan;Wang, Guochun;Gu, Weihong;Xu, Min;Hao, Ying;Dong, Mingrui;Sun, Qing;Sun, Shaojie;Chen, Yuanyuan;Wang, Wei;Li, Jing;Zhang, Yuting;Cao, Zhenhua;Fan, Dongsheng;Wang, Renbin;Da, Yuwei |
| 3-Jul-2020 |
Clinical and Genetic Diversity of PMP22 Mutations in a Large Cohort of Chinese Patients With Charcot-Marie-Tooth Disease |
Liu, Xiaoxuan;Duan, Xiaohui;Zhang, Yingshuang;Fan, Dongsheng |
| 8-Nov-2021 |
Clinical and Genetic Features of Biallelic Mutations in SORD in a Series of Chinese Patients With Charcot-Marie-Tooth and Distal Hereditary Motor Neuropathy |
Liu, Xiaoxuan;He, Ji;Yilihamu, Mubalake;Duan, Xiaohui;Fan, Dongsheng |
| 27-Feb-2023 |
Clinical features and genetic spectrum of Chinese patients with hereditary spastic paraplegia: A 14-year study |
Yu, Weiyi;He, Ji;Liu, Xiangyi;Wu, Jieying;Cai, Xiying;Zhang, Yingshuang;Liu, Xiaoxuan;Fan, Dongsheng |
| Dec-2020 |
Corneal whorl-like nerve plexus: A biomarker for early and follow-up evaluation in FAP |
Zhang, Yixuan;Liu, Xiaoxuan;Zhang, Yuanjin;Zhang, Shuo;Liu, Ziyuan;Fan, Dongsheng |
| 31-Jul-2020 |
Cross-Sectional Study in a Large Cohort of Chinese Patients WithGJB1Gene Mutations |
Liu, Xiaoxuan;Duan, Xiaohui;Zhang, Yingshuang;Sun, Aping;Fan, Dongsheng |
| Aug-2022 |
A de novo c.113 T > C: p.L38R mutation of SPTLC1: case report of a girl with sporadic juvenile amyotrophic lateral sclerosis |
Liu, Xiaoxuan;He, Ji;Yu, Weiyi;Fan, Dongsheng |
| Apr-2022 |
Eye Movement Abnormalities in Amyotrophic Lateral Sclerosis |
Guo, Xintong;Liu, Xiaoxuan;Ye, Shan;Liu, Xiangyi;Yang, Xu;Fan, Dongsheng |
| 13-Oct-2021 |
The Genotype and Phenotype Features in a Large Chinese MFN2 Mutation Cohort |
Ma, Yan;Sun, Aping;Zhang, Yingshuang;Fan, Dongsheng;Liu, Xiaoxuan |
| 2016 |
Mastering Dendrimer Self-Assembly for Efficient siRNA Delivery: From Conceptual Design to In Vivo Efficient Gene Silencing |
Chen, Chao;Posocco, Paola;Liu, Xiaoxuan;Cheng, Qiang;Laurini, Erik;Zhou, Jiehua;Liu, Cheng;Wang, Yang;Tang, Jingjie;Dal Col, Valentina;Yu, Tianzhu;Giorgio, Suzanne;Fermeglia, Maurizio;Qu, Fanqi;Liang, Zicai;Rossi, John J.;Liu, Minghua;Rocchi, Palma;Pricl, Sabrina;Peng, Ling |
| 2012 |
Micro focusing of fast electrons with opened cone targets |
Liu, Feng;Liu, Xiaoxuan;Liu, Bicheng;Ding, Wenjun;Du, Fei;Li, Yutong;Ma, Jinglong;Liu, Xiaolong;Sheng, Zhengming;Chen, Liming;Lu, Xin;Dong, Quanli;Wang, Weimin;Wang, Zhaohua;Wei, Zhiyi;Zhang, Jie |
| 23-Jun-2020 |
Screening for REEP1 Mutations in 31 Chinese Hereditary Spastic Paraplegia Families |
Ma, Xinran;He, Ji;Liu, Xiaoxuan;Fan, Dongsheng |
| 2009 |
STRATIFYING DISEASE STAGES WITH DIFFERENT PROGRESSION RATES DETERMINED BY ELECTROPHYSIOLOGICAL TESTS IN PATIENTS WITH AMYOTROPHIC LATERAL SCLEROSIS (REPLY) |
Liu, Xiaoxuan;Fan, Dongsheng |
| 2011 |
Systemic Administration of Combinatorial dsiRNAs via Nanoparticles Efficiently Suppresses HIV-1 Infection in Humanized Mice |
Zhou, Jiehua;Neff, C. Preston;Liu, Xiaoxuan;Zhang, Jane;Li, Haitang;Smith, David D.;Swiderski, Piotr;Aboellail, Tawfik;Huang, Yuanyu;Du, Quan;Liang, Zicai;Peng, Ling;Akkina, Ramesh;Rossi, John J. |
| 2019 |
Vestibular evoked myogenic potentials and their clinical utility in patients with amyotrophic lateral sclerosis |
Liu, Xiaoxuan;Zhang, Shuo;Huang, Xiao;Zhang, Yingshuang;Fan, Dongsheng |
| Mar-2020 |
Whole-exome sequencing identified novel KIF5A mutations in Chinese patients with amyotrophic lateral sclerosis and Charcot-Marie-Tooth type 2 |
He, Jing;Liu, Xiaoxuan;Tang, Lu;Zhao, Chen;He, Ji;Fan, Dongsheng |
