Shi Xiaoliu相关文献与解析，生知库 | 链接生命科学的每一步

Clinical and radiological characteristics of adult-onset X-linked adrenoleukodystrophy: a Chinese cohort study and review of the literature

成人发病型X连锁肾上腺脑白质营养不良的临床和放射学特征：一项中国队列研究及文献综述

Xiao, Han; Huang, Hui; Chen, Ying; Luo, Yingying; Tang, Zhenchu; Tan, Xuling; Shi, Xiaoliu; Wang, Chunyu; Zhang, Hainan; Fang, Jia; Tang, Jianguang

神经科学

免疫/内分泌

发表日期：2025

文献求助收藏

The influence of Nav1.9 channels on intestinal hyperpathia and dysmotility

Nav1.9通道对肠道高功能性和运动障碍的影响

期刊:Channels

影响因子:3.2

doi:10.1080/19336950.2023.2212350

Zhao, Chenyu; Zhou, Xi; Shi, Xiaoliu

发表日期：2023

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Clinical and genetic diagnosis for 26 paitents with hereditary spherocytosis

对26例遗传性球形红细胞症患者进行临床和基因诊断

期刊:Journal of Central South University (Medical Sciences)

影响因子:

doi:10.11817/j.issn.1672-7347.2023.220390

Bai, Lihong; Zheng, Liping; Li, Binyuan; Huang, Hui; Shi, Xiaoliu; Yi, Yan

Omalizumab for STAT3 Hyper-IgE Syndromes in Adulthood: A Case Report and Literature Review

奥马珠单抗治疗成人STAT3高IgE综合征：病例报告及文献综述

期刊:Frontiers in Medicine

影响因子:3

doi:10.3389/fmed.2022.835257

Lan, Jun; Zhang, Yi; Song, Min; Cai, Shan; Luo, Hong; OuYang, Ruoyun; Yang, Pan; Shi, Xiaoliu; Long, Yingjiao; Chen, Yan

Case Report: Three novel pathogenic ABCC2 mutations identified in two patients with Dubin-Johnson syndrome

病例报告：在两名杜宾-约翰逊综合征患者中发现三种新的致病性ABCC2突变

期刊:Frontiers in Genetics

影响因子:2.8

doi:10.3389/fgene.2022.895247

Zhao, Chenyu; Shi, Xiaoliu; Zhang, Yonghong; Huang, Hui

发表日期：2022

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The Gain-of-Function R222S Variant in Scn11a Contributes to Visceral Hyperalgesia and Intestinal Dysmotility in Scn11a (R222S/R222S) Mice.

Scn11a 中的 R222S 功能获得性变异导致 Scn11a (R222S/R222S) 小鼠出现内脏痛觉过敏和肠道运动障碍

期刊:Frontiers in Neurology

影响因子:2.8

doi:10.3389/fneur.2022.856459

Zhao Chenyu, Jin Jishuo, Hu Haoye, Zhou Xi, Shi Xiaoliu

Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report

重症肌无力合并HINT1相关运动轴索性神经病（无神经肌强直）：病例报告

期刊:BMC Neurology

影响因子:2.2

doi:10.1186/s12883-022-02690-6

Fang, Jia; Huang, Hui; Lei, Qiang; Luo, Yingying; Tang, Zhengchu; Shi, Xiaoliu; Tang, Jian Guang

Clinical Presentations and Genetic Characteristics of Late-Onset MADD Due to ETFDH Mutations in Five Patients: A Case Series

五例由ETFDH基因突变引起的晚发性MADD患者的临床表现和遗传特征：病例系列研究

期刊:Frontiers in Neurology

影响因子:2.8

doi:10.3389/fneur.2021.747360

Tang, Zhenchu; Gao, Shan; He, Miao; Chen, Qihua; Fang, Jia; Luo, Yingying; Yan, Weiqian; Shi, Xiaoliu; Huang, Hui; Tang, Jianguang

发表日期：2021

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Adipose tissue-derived PRXL2A suppresses hepatic lipogenesis in a study with male mice.

一项针对雄性小鼠的研究表明，脂肪组织来源的 PRXL2A 可抑制肝脏脂肪生成

Immune profiling of premalignant lesions in patients with Peutz-Jeghers syndrome.

对患有Peutz-Jeghers综合征的患者进行癌前病变的免疫分析

Clinical and radiological characteristics of adult-onset X-linked adrenoleukodystrophy: a Chinese cohort study and review of the literature

成人发病型X连锁肾上腺脑白质营养不良的临床和放射学特征：一项中国队列研究及文献综述

The influence of Nav1.9 channels on intestinal hyperpathia and dysmotility

Nav1.9通道对肠道高功能性和运动障碍的影响

Clinical and genetic diagnosis for 26 paitents with hereditary spherocytosis

对26例遗传性球形红细胞症患者进行临床和基因诊断

Omalizumab for STAT3 Hyper-IgE Syndromes in Adulthood: A Case Report and Literature Review

奥马珠单抗治疗成人STAT3高IgE综合征：病例报告及文献综述

Case Report: Three novel pathogenic ABCC2 mutations identified in two patients with Dubin-Johnson syndrome

病例报告：在两名杜宾-约翰逊综合征患者中发现三种新的致病性ABCC2突变

The Gain-of-Function R222S Variant in Scn11a Contributes to Visceral Hyperalgesia and Intestinal Dysmotility in Scn11a (R222S/R222S) Mice.

Scn11a 中的 R222S 功能获得性变异导致 Scn11a (R222S/R222S) 小鼠出现内脏痛觉过敏和肠道运动障碍

Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report

重症肌无力合并HINT1相关运动轴索性神经病（无神经肌强直）：病例报告

Clinical Presentations and Genetic Characteristics of Late-Onset MADD Due to ETFDH Mutations in Five Patients: A Case Series

五例由ETFDH基因突变引起的晚发性MADD患者的临床表现和遗传特征：病例系列研究