Search

Your search keyword '"Zhao, Qianqian"' showing total 1,850 results
Start Over Author "Zhao, Qianqian"
1,850 results on '"Zhao, Qianqian"'

154. Mutation and clinical analysis of the CLCC1 gene in amyotrophic lateral sclerosis patients from Central South China

Author

Tang, Linxin, primary, Tang, Xuxiong, additional, Zhao, Qianqian, additional, Li, Yongchao, additional, Bu, Yue, additional, Liu, Zhen, additional, Li, Jinchen, additional, Guo, Jifeng, additional, Shen, Lu, additional, Jiang, Hong, additional, Tang, Beisha, additional, Xu, Renshi, additional, Cao, Wenfeng, additional, Yuan, Yanchun, additional, and Wang, Junling, additional

Published
2023
Full Text
View/download PDF

155. Ru-RuO2 nano-heterostructures stabilized by the sacrificing oxidation strategy of Mn3O4 substrate for boosting acidic oxygen evolution reaction

Author

Long, Xin, primary, Zhao, Bin, additional, Zhao, Qianqian, additional, Wu, Xuexian, additional, Zhu, Meng-Nan, additional, Feng, Renfei, additional, Shakouri, Mohsen, additional, Zhang, Yu, additional, Xiao, Xinxin, additional, Zhang, Jiujun, additional, Fu, Xian-Zhu, additional, and Luo, Jing-Li, additional

Published
2023
Full Text
View/download PDF

164. Single-Port Robot–Assisted Radical Prostatectomy with the Novel Shurui Single-Port Robotic Surgical System

Author

Jing, Taile, primary, Peng, Ding, additional, Yao, Xiaolin, additional, Ye, Sunyi, additional, Zhao, Qianqian, additional, Ni, Meng, additional, Shao, Jing, additional, Xu, Xin, additional, He, Anbang, additional, Liang, Zhen, additional, Lai, Chong, additional, Qi, Honggang, additional, Meng, Hongzhou, additional, Wang, Ping, additional, Wang, Shuo, additional, and Xia, Dan, additional

Published
2023
Full Text
View/download PDF

181. SSRW: A Scalable Algorithm for Estimating Graphlet Statistics Based on Random Walk

Author

Yang, Chen, Lyu, Min, Li, Yongkun, Zhao, Qianqian, Xu, Yinlong, Hutchison, David, Editorial Board Member, Kanade, Takeo, Editorial Board Member, Kittler, Josef, Editorial Board Member, Kleinberg, Jon M., Editorial Board Member, Mattern, Friedemann, Editorial Board Member, Mitchell, John C., Editorial Board Member, Naor, Moni, Editorial Board Member, Pandu Rangan, C., Editorial Board Member, Steffen, Bernhard, Editorial Board Member, Terzopoulos, Demetri, Editorial Board Member, Tygar, Doug, Editorial Board Member, Weikum, Gerhard, Series Editor, Goos, Gerhard, Founding Editor, Hartmanis, Juris, Founding Editor, Bertino, Elisa, Editorial Board Member, Gao, Wen, Editorial Board Member, Woeginger, Gerhard, Editorial Board Member, Yung, Moti, Editorial Board Member, Pei, Jian, editor, Manolopoulos, Yannis, editor, Sadiq, Shazia, editor, and Li, Jianxin, editor

Published
2018
Full Text
View/download PDF

187. Ambulatory quality, special health care needs, and emergency department or hospital use for US children

Author

Coller, Ryan J., Kelly, Michelle M., Sklansky, Daniel J., Shadman, Kristin A., Ehlenbach, Mary L., Barreda, Christina B., Chung, Paul J., Zhao, Qianqian, and Edmonson, Marshall Bruce

Subjects
Hospital emergency services -- User statistics, Ambulatory care facilities -- Quality management, Child health services -- Quality management, Medical care needs assessment -- Demographic aspects, Business, Health care industry
Abstract

Objective: This study examined family-reported ambulatory care quality and its association with emergency department and hospital utilization, and how these relationships differed across levels of medical complexity. Data sources: The 2006-2013 Medical Expenditure Panel Survey (MEPS). Study Design: Secondary analysis of MEPS data. Variables fitting the National Quality Measures Clearinghouse clinical quality measures domain framework were selected. Exploratory factor analysis grouped ambulatory quality into 12 access, experience, or process measures. Weighted negative binomial regression stratified by health status identified associations between ambulatory quality and ED visits or hospitalizations. Data Collection: 41,497 children [less than or equal to]18 years were included. The 5-item special health care needs (SHCN) screener categorized health status as complex, less complex, or noSHCN. Principal Findings: Weighted SHCN proportions were 1.6 Percent complex, 18.2 Percent less complex, and 80.0 Percent no SHCN. Mean ED visits were 130 and 335 visits/1000 children/year for no/ complex SHCN, respectively. Mean hospitalizations were 20 and 175 hospitalizations/1000 children/year for no/complex SHCN, respectively. ED visits were associated with 8 of 12 quality measures for no/less complex SHCN. For example, usually/always receiving needed care right away was associated with 22 Percent lower ED visit rate (95% CI 0.64-0.96). Hospitalizations were associated with 4 of 12 quality measures for less complex SHCN. In complex SHCN, associations between ambulatory quality and ED/hospital use were weak and inconsistent. Conclusions: Ambulatory quality may best predict ED and hospital use for children with no or less complex SHCN. Whether and how ambulatory care predicts emergency and hospital care in complex SHCN remains an important question. KEYWORDS ambulatory care, emergency service, hospitalization, quality of health care, 1 | INTRODUCTION Over $20B are spent annually on non-neonatal and nonmaternal hospitalizations for US children. (1) Hospital and emergency department (ED) visits are measures of health and chronic disease [...]

Published
2020
Full Text
View/download PDF

190. Letrozole combined with rhGH treatment increases the adult height of short pubertal boys.

Author

He, Mingming, Zhang, Yanhong, Zhao, Qianqian, He, Dongye, Li, Yanying, Zhang, Mei, and Ban, Bo

Abstract

This study was performed to investigate the effectiveness of the combination of letrozole and recombinant human growth hormone (rhGH) to improve the predicted adult height (PAH) and final adult height (FAH) of Chinese short pubertal boys. In total, 171 Chinese short pubertal boys were recruited for this study. 96 of them received letrozole (2.5 mg/d) combined with rhGH (33.3–66.6 μg/kg.d), and the others received rhGH alone. Follow-up visits were conducted at 1, 3, 6, 9, and 12 months or regularly after the first treatment. During each visit, plasma samples were collected for clinical tests and biomedical analyses, all of which were performed according to standard protocols. This study was registered at www.chictr.org.cn under ID number ChiCTR1900026142. After receiving treatment for at least 3 months, 68 boys (91 %) in the rhGH therapy group and 90 (94 %) in the letrozole combined with rhGH (letrozole+rhGH) therapy group achieved an increase in PAH, with the latter treatment leading to a more effective slowing of bone age (BA) advancement. Moreover, the increased PAH showed a significant positive correlation with treatment time in both groups, and letrozole+rhGH increased the PAH to a greater degree than rhGH alone (p=0.0023). And letrozole+rhGH not only slowed the increase in BA more efficiently than rhGH therapy alone (p=0.0025), but also achieved a higher FAH (p=0.0078). Letrozole combined with rhGH treatment is a promising therapy to increase the PAH and FAH of Chinese short pubertal boys. [ABSTRACT FROM AUTHOR]

Published
2024
Full Text
View/download PDF

191. Mutation and clinical analysis of the CLCC1 gene in amyotrophic lateral sclerosis patients from Central South China.

Author

Tang, Linxin, Tang, Xuxiong, Zhao, Qianqian, Li, Yongchao, Bu, Yue, Liu, Zhen, Li, Jinchen, Guo, Jifeng, Shen, Lu, Jiang, Hong, Tang, Beisha, Xu, Renshi, Cao, Wenfeng, Yuan, Yanchun, and Wang, Junling

Subjects
AMYOTROPHIC lateral sclerosis, GENETIC variation, CHLORIDE channels, FISHER exact test, MISSENSE mutation
Abstract

Introduction: Recently, chloride channel CLIC‐like 1 (CLCC1) was reported to be a novel ALS‐related gene. We aimed to screen CLCC1 variants in our ALS cohort and further explore the genotype–phenotype correlation of CLCC1‐related ALS. Methods: We screened rare damaging variants in CLCC1 from our cohorts of 1005 ALS patients and 1224 healthy controls with whole‐exome sequencing in Central South China. Fisher's exact test was conducted for association analysis at the entire gene level and single variant level. Results: In total, four heterozygous missense variants in CLCC1 were identified from four unrelated sporadic ALS patients and predicted to be putative pathogenic by in silico tools and protein model prediction, accounting for 0.40% of all patients (4/1005). The four variants were c.A275C (p.Q92P), c.G1139A (p.R380K), c.C1244T (p.T415M), and c.G1328A (p.R443Q), respectively, which had not been reported in ALS patients previously. Three of four variants were located in exon 10. Patients harboring CLCC1 variants seemed to share a group of similar clinical features, including earlier age at onset, rapid progression, spinal onset, and vulnerable cognitive status. Statistically, we did not find CLCC1 to be associated with the risk of ALS at the entire gene level or single variant level. Conclusion: Our findings further expanded the genetic and clinical spectrum of CLCC1‐related ALS and provided more genetic evidence for anion channel involvement in the pathogenesis of ALS, but further investigations are needed to verify our findings. [ABSTRACT FROM AUTHOR]

Published
2024
Full Text
View/download PDF

199. Study on Value Extraction and exchange and sharing Mode of historical Retained information

Author

Wen Quan, Zhao Qianqian, Xiao Lei, and Zheng Kouquan

Subjects
Social Sciences
Abstract

Among the many retained historical information, The CPC’s archives show their unique value because of their original and authentic nature. The CPC’s history archives are used to tell the red story, spread the red culture and highlight the unique advantages of retained historical information. In the one hundred birthday of CPC, test training base in the camp salute an archives exhibition tributing to CPC centennial. The archives exhibition expands the scope of publicity, restores historical information, and highlights the role of archives in education, communication and sharing.

Published
2022
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results