The Mechanical Properties and Degradation Behavior of 3D-Printed Cellulose Nanofiber/Polylactic Acid Composites

por Zhang, Zhongsen, Cao, Bingyan, Jiang, Ning
Publicado 2023

Twice-daily injections and multiple daily injections of insulin in toddlers with type 1 diabetes: a retrospective cohort study

por Wang, Qiao, Feng, Guoshuang, Cao, Bingyan, Gong, Chunxiu
Publicado 2023

Glucose fluctuations in association with oxidative stress among children with type 1 diabetes mellitus: comparison of different phases

por Meng, Xi, Gong, Chunxiu, Cao, Bingyan, Peng, Xiaoxia
Publicado 2015

Chronic oral mucocutaneous candidiasis, recurrent respiratory infection, hepatosplenomegaly, and autoimmune diabetes mellitus: A case report of a gain-of-function mutation of STAT1...

por Cao, Bingyan, Liu, Meijuan, Zhao, Yun, Gong, Chunxiu
Publicado 2022

Associations between body mass index and pubertal development based on the outcomes of girls with early breast development

por Zhao, Manman, Liu, Meijuan, Cao, Bingyan, Gong, Chunxiu
Publicado 2022

The clinical and molecular genetic study of 20 Silver Russell Syndrome cases

por Gong, Chunxiu, Zhu, Ming-Qiang, Wu, Di, Cao, Bingyan
Publicado 2013

Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases

por LI, WENJING, GONG, CHUNXIU, QI, ZHAN, WU, DI, CAO, BINGYAN
Publicado 2015

Kabuki syndrome: novel pathogenic variants, new phenotypes and review of literature

por Shangguan, Huakun, Su, Chang, Ouyang, Qian, Cao, Bingyan, Wang, Jian, Gong, Chunxiu, Chen, Ruimin
Publicado 2019

Mechanism of Electroacupuncture Regulating IRS-1 Phosphorylation in Skeletal Muscle to Improve Insulin Sensitivity

por Song, Shanshan, Li, Rui, Cao, Bingyan, Zhang, Jingyi, Kim, Youngcho, Kim, Bonggyu, Yu, Xue
Publicado 2021

Use of magnoflorine-phospholipid complex to permeate blood-brain barrier and treat depression in the CUMS animal model

por Li, Bingjie, Han, Linmeng, Cao, Bingyan, Yang, Xiaoying, Zhu, Xuehui, Yang, Bing, Zhao, Haodong, Qiao, Wei
Publicado 2019

One hundred twelve cases of 46, XY DSD patients after initial gender assignment: a short-term survey of gender role and gender dysphoria

por Hou, Liping, Zhao, Ming, Fan, Lijun, Cao, Bingyan, Chen, Jiajia, Cui, Yonghua, Polak, Michel, Gong, Chunxiu
Publicado 2021

Hormonal changes throughout puberty in boys: an observational study on the treatment outcome of congenital hypogonadotropic hypogonadism

por Ren, Xiaoya, Tian, Yuanyuan, Feng, Guoshuang, Wang, Yi, Zhang, Beibei, Cao, Bingyan, Chen, Jiajia, Gong, Chunxiu
Publicado 2022

Clinical, Biochemical, Molecular, and Outcome Features of Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency in 10 Chinese Patients

por Wu, Shengnan, Shen, Linghua, Chen, Qiong, Gong, Chunxiu, Yang, Yanling, Wei, Haiyan, Cao, Bingyan, Chen, Yongxing
Publicado 2022

Correction to: One hundred twelve cases of 46, XY DSD patients after initial gender assignment: a short-term survey of gender role and gender dysphoria

por Hou, Liping, Zhao, Ming, Fan, Lijun, Cao, Bingyan, Chen, Jiajia, Cui, Yonghua, Polak, Michel, Gong, Chunxiu
Publicado 2022

Analysis of the Incidence and Risk Factors of Precocious Puberty in Girls during the COVID-19 Pandemic

por Fu, Dongxia, Li, Tao, Zhang, Yingxian, Wang, Huizhen, Wu, Xue, Chen, Yongxing, Cao, Bingyan, Wei, Haiyan
Publicado 2022

Efficacy and safety of octreotide treatment for diazoxide‐unresponsive congenital hyperinsulinism in China

por Cao, Bingyan, Di, Wu, Su, Chang, Chen, Jiajia, Liang, Xuejun, Liu, Min, Li, Wenjing, Li, Xiaoqiao, Gong, Chunxiu
Publicado 2020

Clinical and genetic characteristics of hypophosphatasia in Chinese children

por Liu, Meijuan, Liu, Min, Liang, Xuejun, Wu, Di, Li, Wenjing, Su, Chang, Cao, Bingyan, Chen, Jiajia, Gong, Chunxiu
Publicado 2021

High Prevalence of Obesity but Low Physical Activity in Children Aged 9–11 Years in Beijing

por Liu, Meijuan, Cao, Bingyan, Liu, Min, Liang, Xuejun, Wu, Di, Li, Wenjing, Su, Chang, Chen, Jiajia, Gong, Chunxiu
Publicado 2021

Genetic and Phenotypic Spectrum of KBG Syndrome: A Report of 13 New Chinese Cases and a Review of the Literature

por Gao, Fenqi, Zhao, Xiu, Cao, Bingyan, Fan, Xin, Li, Xiaoqiao, Li, Lele, Sui, Shengbin, Su, Zhe, Gong, Chunxiu
Publicado 2022

DNA Hypermethylation and a Specific Methylation Spectrum on the X Chromosome in Turner Syndrome as Determined by Nanopore Sequencing

por Fan, Xin, Zhang, Beibei, Fan, Lijun, Chen, Jiajia, Su, Chang, Cao, Bingyan, Wei, Liya, Qin, Miao, Gong, Chunxiu
Publicado 2022