Search Results - "Shi, WeiZhe"

To Angulate or Not to Angulate the Ulna during the Progressive Distraction Period Performed with a Monolateral External Fixator in Paediatric Patients with a Chronic Monteggia Fracture? by Liu, Yanhan, Zhao, Hai, Xu, Hongwen, Shi, Weizhe, Li, Jingchun, Li, Yiqiang, Canavese, Federico

“…Background and Objectives: The purpose of this study was to compare the clinical and radiographic evolution of chronic Monteggia fractures (CMFs) treated by…”
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Expression and significance of related genes in the early stage of post-traumatic heterotopic ossification in a rat model of Achilles tenotomy by Yu, Du, Ju, Jinyong, Xue, Feng, Zhao, Yong, Shi, Weizhe, Xiao, Haijun

“…This study aims to determine expression profiles of relevant genes in the early stages of post-traumatic heterotopic ossification (HO) in a rat model of…”
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The mucolipidosis III-causing mutation in GNPTAB, c.1760G>C, disrupts the development of somites in rats by Nong, Tianying, Li, Jiangui, Li, Xia, Li, Yiqiang, Li, Zhaohui, Shi, Weizhe, Zhou, Qiuchan, Xu, Hongwen, Zhu, Mingwei, Tang, Ya-Ping

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Novel de novo TRPV4 mutation identified in a Chinese family with metatropic dysplasia inhibits chondrogenic differentiation by Wei, Ping, Shi, Weizhe, Nong, Tianying, Xian, Caixia, Li, Xia, Li, Zhaohui, Li, Xin, Wu, Jianping, Shang, Liyuan, Xu, Fulong, Xu, Yibo, Xu, Hongwen, Zhu, Mingwei

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A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate by Xian, Caixia, Zhu, Mingwei, Nong, Tianying, Li, Yiqiang, Xie, Xingmei, Li, Xia, Li, Jiangui, Li, Jingchun, Wu, Jianping, Shi, Weizhe, Wei, Ping, Xu, Hongwen, Tang, Ya-ping

“…Hereditary multiple exostoses (HME) is a rare skeletal disorder characterized by the formation of multiple benign cartilage-capped tumors, usually in the…”
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Identification of a novel TBX5 mutation in a Chinese family with rare symptoms of Holt–Oram syndrome by Li, Xia, Shi, Weizhe, Ding, Xuejiao, Li, Jingchun, Li, Yiqiang, Wu, Jianping, Yuan, Zhe, Nong, Tianying, Xu, Hongwen, Zhu, Mingwei

“…Holt–Oram syndrome (HOS) is a rare autosomal dominant disorder characterized by skeletal abnormalities of the upper limbs and often cardiac malformations. We…”
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A novel compound heterozygous variation in the FKBP10 gene causes Bruck syndrome without congenital contractures: A case report by Shang, Liyuan, Shi, Weizhe, Xu, Yibo, Nong, Tianying, Li, Xia, Li, Zhaohui, Liu, Yanhan, Li, Jingchun, Tang, Ya-Ping, Zhu, Mingwei, Xu, Hongwen

“…Bruck syndrome (BS) is an extremely rare autosomal-recessive connective tissue disorder mainly characterized by bone fragility, congenital joint contracture,…”
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Radiographic features of congenital thumb duplication type C2 of Wu et al. classification: new subtypes and surgical strategies by Wu, JianPing, Shi, WeiZhe, Zhao, Hai, Li, JingChun, Li, YiQiang, Hong, Kai, Yuan, Zhe, Zhu, MingWei, Liu, YuanZhong, Canavese, Federico, Xu, HongWen

“…This study aimed (i) to evaluate the radiographic characteristics of patients with congenital thumb duplication (CTD) type C2 according to the classification…”
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Epidemiological characteristics and distribution of congenital thumb duplication in south China: An analysis of 2,300 thumbs in 2,108 children by Wu, JianPing, Shi, WeiZhe, Lin, XueMei, Li, JingChun, Yuan, Zhe, Zhu, Mingwei, Liu, YuanZhong, Li, YiQiang, Canavese, Federico, Xu, HongWen

“…ObjectiveThe objective of this study was to evaluate epidemiological and anatomical characteristics of children with congenital thumb duplication (CTD)…”
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Closed reduction and percutaneous pinning versus open reduction and internal fixation for Jakob type 3 lateral condyle fractures in children by Liu, Yanhan, Shi, Weizhe, Zhao, Hai, Li, Yiqiang, Li, Jingchun, Xun, Fuxin, Canavese, Federico, Xu, Hongwen

“…Purpose The management of type 3 lateral condyle fractures (LCFs) remains controversial. The main goal of this study was to evaluate the feasibility of closed…”
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Ulnar osteotomy and monolateral external fixator for the treatment of chronic Monteggia fractures in children: comparison between gradual and acute radial head reduction by Liu, Yanhan, Shi, Weizhe, Li, Yiqiang, Hong, Kai, Li, Jingchun, Xun, Fuxin, Canavese, Federico, Xu, Hongwen

“…This study evaluated the outcomes of chronic Monteggia fractures (CMFs) treated by ulnar osteotomy and monolateral external fixator (MEF), and compare the…”
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Carpaine alleviates tendinopathy in mice by promoting the ubiquitin-proteasomal degradation of p65 via targeting the E3 ubiquitin ligase LRSAM1 by Lin, Xuemei, Tian, Xinggui, Jiang, Huaji, Li, Wenjun, Wang, Chaomin, Wu, Jianping, Chen, Weidong, Shi, Weizhe, Tian, Qinyu, Gong, Xiaoqian, Zhou, Qinghe, Xu, Hongwen, Zwingenberger, Stefan

“…Currently, there are no specific drugs or targets available for the treatment of tendinopathy. However, inflammation has recently been found to play a pivotal…”
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Modified Radiographic Classification System for Congenital Thumb Duplication: An Analysis of 2,300 Thumbs in 2,108 Children by Wu, JianPing, Shi, WeiZhe, Lin, XueMei, Li, JingChun, Hong, Kai, Liu, YuanZhong, Li, YiQiang, Canavese, Federico, Xu, HongWen

“…The objectives of this study were to (1) evaluate the radiographic characteristics of children with congenital thumb duplication (CTD) seen in our institution…”
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Effects of posterior hemivertebra resection and short segment fusion on the evolution of sagittal balance in children with congenital scoliosis by Xu, Fulong, Canavese, Federico, Liang, Feng, Li, Yiqiang, Xun, Fuxing, Shi, Weizhe, Xu, Hongwen

“…There is a paucity of data describing sagittal alignment changes in children with congenital scoliosis (CS) treated by hemivertebra (HV) resection. This study…”
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Effects of posterior hemivertebra resection and short segment fusion on the evolution of sagittal balance in children with congenital scoliosis by Xu, Fulong, Canavese, Federico, Liang, Feng, Li, Yiqiang, Xun, Fuxing, Shi, Weizhe, Xu, Hongwen

“…There is a paucity of data describing sagittal alignment changes in children with congenital scoliosis (CS) treated by hemivertebra (HV) resection. This study…”
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MYH7, c.2011C>T, is responsible for congenital scoliosis in a Chinese family by Wei, Ping, Xu, Fulong, Xian, Caixia, Liu, Yanhan, Xu, Yibo, Zhang, Ting, Shi, Weizhe, Huang, Sihong, Zhou, Xiang, Zhu, Mingwei, Xu, Hongwen

“…Neuromuscular scoliosis can be caused by muscular or nervous system dysfunction resulting from genetic variants. Variation in MYH7 may cause hypertrophic or…”
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Novel denovo TRPV4 mutation identified in a Chinese family with metatropic dysplasia inhibits chondrogenic differentiation by Wei, Ping, Shi, Weizhe, Nong, Tianying, Xian, Caixia, Li, Xia, Li, Zhaohui, Li, Xin, Wu, Jianping, Shang, Liyuan, Xu, Fulong, Xu, Yibo, Xu, Hongwen, Zhu, Mingwei

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Low-loss LTCC-based gap waveguide feeding network for W-band application by Baolin Cao, Dan Li, Hao Wang, Weizhe Shi, Yong Huang

“…In this paper, a novel low-loss gap waveguide (GWG) transmission line with Low Temperature Co-Fired Ceramic (LTCC) technology for W-band is presented. To…”
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A Ka-band axial ratio bandwidth enhanced circularly polarized LTCC patch antenna with truncated artificial magnetic conductor by Baolin Cao, Jing Dai, Dan Li, Hao Wang, Weizhe Shi, Yong Huang

“…In this paper, a novel method to enhance axial ratio bandwidth of circularly polarized (CP) patch antenna using artificial magnetic conductor (AMC) structures…”
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Analysis of a case of Multiple pterygium syndrome due to a novel variant of CHRNG gene by Chen, Yiru, Nong, Tianying, Shi, Weizhe, Li, Jiangui, Ding, Xuejiao, Li, Yue, Zhu, Mingwei, Xu, Hongwen

“…To explore the clinical characteristics and genetic etiology of a child with multiple pterygium syndrome (MPS). A child with MPS who was treated at the…”
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