Distribution characteristics of ABO and RhD blood groups among the voluntary blood donors in Chongqing: A retrospective study

por Liao, Hongmei, Li, Jun
Publicado 2020

Application of Thermosonication in Red Pitaya Juice Processing: Impacts on Native Microbiota and Quality Properties during Storage

por Zhu, Wenxian, Ai, Yana, Fang, Fang, Liao, Hongmei
Publicado 2021

ARHGEF9 gene variant leads to developmental and epileptic encephalopathy: Genotypic phenotype analysis and treatment exploration

por Yang, Haiyan, Liao, Hongmei, Gan, Siyi, Xiao, Ting, Wu, Liwen
Publicado 2022

Case Report: ISPD Gene Mutation Leads to Dystroglycanopathies: Genotypic Phenotype Analysis and Treatment Exploration

por Yang, Haiyan, Cai, Fang, Liao, Hongmei, Gan, Siyi, Xiao, Ting, Wu, Liwen
Publicado 2021

MORC2 gene de novo mutation leads to Charcot–Marie–Tooth disease type 2Z: A pediatric case report and literature review

por Yang, Haiyan, Yang, Sai, Kang, Qingyun, Yang, Liming, Liao, Hongmei, Wu, Liwen
Publicado 2021

Clinical Characteristics and Short-Term Prognosis of Children With Antibody-Mediated Autoimmune Encephalitis: A Single-Center Cohort Study

por Kang, Qingyun, Liao, Hongmei, Yang, Liming, Fang, Hongjun, Hu, Wenjing, Wu, Liwen
Publicado 2022

Clinical Characteristics and Prognostic Factors of Children With Anti-N-Methyl-D-Aspartate Receptor Encephalitis

por Yang, Sai, Yang, Liming, Liao, Hongmei, Chen, Mei, Feng, Mei, Liu, Shulei, Tan, Lihong
Publicado 2021

Sclerotinia sclerotiorum Thioredoxin1 (SsTrx1) is required for pathogenicity and oxidative stress tolerance

por Rana, Kusum, Ding, Yijuan, Banga, Surinder S., Liao, Hongmei, Zhao, Siqi, Yu, Yang, Qian, Wei
Publicado 2021

Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy in Children: A Retrospective Analysis of 35 Cases

por Fang, Hongjun, Hu, Wenjing, Jiang, Zhi, Yang, Haiyan, Liao, Hongmei, Yang, Liming, Wu, Liwen
Publicado 2021

Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study

por Kang, Qingyun, Liao, Hongmei, Yang, Liming, Fang, Hongjun, Ning, Zeshu, Liao, Caishi, Gan, Siyi, Wu, Liwen
Publicado 2023

A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case report

por Kang, Qingyun, Yang, Liming, Liao, Hongmei, Yang, Sai, Kuang, Xiaojun, Ning, Zeshu, Liao, Caishi, Chen, Bo
Publicado 2021

Host-Induced Gene Silencing of a Multifunction Gene Sscnd1 Enhances Plant Resistance Against Sclerotinia sclerotiorum

por Ding, Yijuan, Chen, Yangui, Yan, Baoqin, Liao, Hongmei, Dong, Mengquan, Meng, Xinran, Wan, Huafang, Qian, Wei
Publicado 2021

Case Report: Compound Heterozygous Variants of SLC13A3 Identified in a Chinese Patient With Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation

por Kang, Qingyun, Yang, Liming, Liao, Hongmei, Yang, Sai, Yang, Haiyang, Ning, Zeshu, Liao, Caishi, Wu, Liwen
Publicado 2021

Clinical and Genetic Study on a Chinese Patient with Infantile Onset Epileptic Encephalopathy carrying a PPP3CA Null Variant: a case report

por Yang, Sai, Shen, Xiang, Kang, Qingyun, Kuang, Xiaojun, Ning, Zeshu, Liu, Shulei, Liao, Hongmei, Cao, Zhenhua, Yang, Liming
Publicado 2020

CNKSR2 gene mutation leads to Houge type of X-linked syndromic mental retardation: A case report and review of literature

por Kang, Qingyun, Yang, Liming, Liao, Hongmei, Wu, Liwen, Chen, Bo, Yang, Sai, Kuang, Xiaojun, Yang, Haiyang, Liao, Caishi
Publicado 2021

Clinical spectrum of contactin-associated protein 2 autoimmune encephalitis in children

por Hu, Wenjing, Wang, Enhui, Fang, Hongjun, Li, Li, Yi, Jurong, Liu, Qingqing, Qing, Wei, Guo, Danni, Tan, Qianqian, Liao, Hongmei
Publicado 2023

Mutant BCL11B in a Patient With a Neurodevelopmental Disorder and T-Cell Abnormalities

por Yang, Sai, Kang, Qingyun, Hou, Yanqi, Wang, Lili, Li, Liping, Liu, Shulei, Liao, Hongmei, Cao, Zhenhua, Yang, Liming, Xiao, Zhenghui
Publicado 2020

Nabais Sa‐de Vries syndrome in a Chinese infant associated with a novel SPOP mutation: A clinical study and genetic report

por Hu, Wenjing, Fang, Hongjun, Peng, Yu, Li, Li, Liu, Shulei, Liao, Hongmei, Tang, Jingwen, Yi, Jurong, Liu, Qingqing, Xu, Li, Wu, Liwen
Publicado 2022

Association between blood eosinophil count and Duchenne muscular dystrophy severity and prognosis: a retrospective cohort study

por Jiang, Zhi, Liao, Hongmei, Wu, Liwen, Hu, Wenjing, Yang, Liming, Chen, Bo, Ning, Zeshu, Tang, Jingwen, Xu, Rong, Chen, Mei, Guo, Feng, Liu, Shulei
Publicado 2023