Study on the Relationship between AAD and Clinical Features in Emergency Ward Patients and the Application Effect of Probiotics

por Qiu, Wenjuan, Bai, Fangfang
Publicado 2022

Myxedema coma: A case report of pediatric emergency care

por Zhu, Yueniu, Qiu, Wenjuan, Deng, Mengyan, Zhu, Xiaodong
Publicado 2017

Dynamic functional connectivity analysis of Taichong (LR3) acupuncture effects in various brain regions★

por Qiu, Wenjuan, Yan, Bin, He, Hongjian, Tong, Li, Li, Jianxin
Publicado 2012

The Predictive Value of Genetic Analyses in the Diagnosis of Tetrahydrobiopterin (BH4)-Responsiveness in Chinese Phenylalanine Hydroxylase Deficiency Patients

por Zhu, Tianwen, Ye, Jun, Han, Lianshu, Qiu, Wenjuan, Zhang, Huiwen, Liang, Lili, Gu, Xuefan
Publicado 2017

Genetic analysis and clinical assessment of four patients with Glycogen Storage Disease Type IIIa in China

por Zhang, Yu, Xu, Mingming, Chen, Xiaoxia, Yan, Aijuan, Zhang, Guoyong, Liu, Zhenguo, Qiu, Wenjuan
Publicado 2018

A nursing protocol targeting risk factors for reducing postoperative delirium in patients following coronary artery bypass grafting: Results of a prospective before-after study

por Zhang, Weiying, Sun, Yan, Liu, Yang, Qiu, Wenjuan, Ye, Xiaofei, Zhang, Guihong, Zhang, Lingjuan
Publicado 2017

Uniparental isodisomy caused autosomal recessive diseases: NGS‐based analysis allows the concurrent detection of homogenous variants and copy‐neutral loss of heterozygosity

por Xiao, Bing, Wang, Lili, Liu, Huili, Fan, Yanjie, Xu, Yan, Sun, Yu, Qiu, Wenjuan
Publicado 2019

Novel PYGL mutations in Chinese children leading to glycogen storage disease type VI: two case reports

por Luo, Xiaomei, Hu, Jiacheng, Gao, Xueren, Fan, Yanjie, Sun, Yu, Gu, Xuefan, Qiu, Wenjuan
Publicado 2020

Identification of a distinct mutation spectrum in the SMPD1 gene of Chinese patients with acid sphingomyelinase-deficient Niemann-Pick disease

por Zhang, Huiwen, Wang, Yu, Gong, Zhuwen, Li, Xiaoyan, Qiu, Wenjuan, Han, Lianshu, Ye, Jun, Gu, Xuefan
Publicado 2013

Diagnosis of Niemann-Pick disease type C with 7-ketocholesterol screening followed by NPC1/NPC2 gene mutation confirmation in Chinese patients

por Zhang, Huiwen, Wang, Yu, Lin, Na, Yang, Rui, Qiu, Wenjuan, Han, Lianshu, Ye, Jun, Gu, Xuefan
Publicado 2014

Haplotype-based Noninvasive Prenatal Diagnosis of Hyperphenylalaninemia through Targeted Sequencing of Maternal Plasma

por Ye, Jun, Chen, Chao, Yuan, Yuan, Han, Lianshu, Wang, Yaoshen, Qiu, Wenjuan, Zhang, Huiwen, Asan, Gu, Xuefan
Publicado 2018

Analysis of the IDS Gene in 38 Patients with Hunter Syndrome: The c.879G>A (p.Gln293Gln) Synonymous Variation in a Female Create Exonic Splicing

por Zhang, Huiwen, Li, Jing, Zhang, Xinshun, Wang, Yu, Qiu, Wenjuan, Ye, Jun, Han, Lianshu, Gao, Xiaolan, Gu, Xuefan
Publicado 2011

Evaluation of the Clinical, Biochemical, Neurological, and Genetic Presentations of Glutaric Aciduria Type 1 in Patients From China

por E., Huishu, Liang, Lili, Zhang, Huiwen, Qiu, Wenjuan, Ye, Jun, Xu, Feng, Gong, Zhuwen, Gu, Xuefan, Han, Lianshu
Publicado 2021

Late-onset cblC defect: clinical, biochemical and molecular analysis

por Ding, Si, Ling, Shiying, Liang, Lili, Qiu, Wenjuan, Zhang, Huiwen, Chen, Ting, Zhan, Xia, Xu, Feng, Gu, Xuefan, Han, Lianshu
Publicado 2023

Clinical, Biochemical, and Molecular Analyses of Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Chinese Patients

por Gong, Zhuwen, Liang, Lili, Qiu, Wenjuan, Zhang, Huiwen, Ye, Jun, Wang, Yu, Ji, Wenjun, Chen, Ting, Gu, Xuefan, Han, Lianshu
Publicado 2021

Clinical, biochemical, and genetic analysis of 28 Chinese patients with holocarboxylase synthetase deficiency

por Ling, Shiying, Qiu, Wenjuan, Zhang, Huiwen, Liang, Lili, Lu, Deyun, Chen, Ting, Zhan, Xia, Wang, Yu, Gu, Xuefan, Han, Lianshu
Publicado 2023

Clinical and molecular characteristics of 69 Chinese patients with ornithine transcarbamylase deficiency

por Lu, Deyun, Han, Feng, Qiu, Wenjuan, Zhang, Huiwen, Ye, Jun, Liang, Lili, Wang, Yu, Ji, Wenjun, Zhan, Xia, Gu, Xuefan, Han, Lianshu
Publicado 2020

Examining the blood amino acid status in pretherapeutic patients with  hyperphenylalaninemia

por Liang, Lili, Ye, Jun, Han, Lianshu, Qiu, Wenjuan, Zhang, Huiwen, Yu, Yongguo, Zhu, Tianwen, Xu, Feng, Zhan, Xia, Bao, Peizhong, Ji, Wenjun, Gu, Xuefan
Publicado 2019

Value of amniotic fluid homocysteine assay in prenatal diagnosis of combined methylmalonic acidemia and homocystinuria, cobalamin C type

por Chen, Ting, Liang, Lili, Zhang, Huiwen, Ye, Jun, Qiu, Wenjuan, Xiao, Bing, Zhu, Hong, Wang, Lei, Xu, Feng, Gong, Zhuwen, Gu, Xuefan, Han, Lianshu
Publicado 2021

Prenatal Diagnosis of Isovaleric Acidemia From Amniotic Fluid Using Genetic and Biochemical Approaches

por Ding, Si, Liang, Lili, Qiu, Wenjuan, Zhang, Huiwen, Xiao, Bing, Dong, Liping, Ji, Wenjun, Xu, Feng, Gong, Zhuwen, Gu, Xuefan, Wang, Lei, Han, Lianshu
Publicado 2022