CRANIOSYNOSTOSIS

作品数：13被引量：27H指数：2
导出分析报告
相关领域：医药卫生更多>>
相关作者：王刚更多>>
相关机构：南京医科大学第二附属医院更多>>
相关期刊：《Genes & Diseases》《World Journal of Radiology》《World Journal of Clinical Cases》《Open Journal of Modern Neurosurgery》更多>>
-
在结果中检索

检索结果分析

结果分析中...
共 条 记 录，以下是1-10
全选清除导出
参考文献引证文献引用追踪
视图：
排序：
Maternal hyperthyroidism increases the synthesis activity and the osteogenic markers expression of calvarial osteoblasts from offspring in a murine model
《BIOCELL》2023年第2期423-430,共8页FABIANA ROCHA ARAÚJO BRUNO MACHADO BERTASSOLI ISABELLA CRISTINA SOUZA FÉLIX DOUGLAS MARINHO ABREU NATÁLIA MELO OCARINO AMANDA MARIA SENA REIS JUNEO FREITAS SILVA ROGÉRIA SERAKIDES 
supported by grants from the Conselho Nacional de Desenvolvimento Científico e Tecnológico(CNPq);Fundação de Amparo a Pesquisa de Minas Gerais(Fapemig);Coordenação de Aperfeiçoamento de Pessoal de Nível Superior(Capes).
To evaluate the characteristics and synthesis activity of osteoblasts extracted from the calvaria of offspring of rats exposed to maternal hyperthyroidism.Twelve adult Wistar rats were divided into two groups,one cont...
关键词：CRANIOSYNOSTOSIS Intramembranous growth OSSIFICATION Rat Thyroid dysfunction 
Early Rehabilitation After Craniosynostosis Surgery被引量：1
《Computers, Materials & Continua》2022年第8期3899-3912,共14页Dan Wang Lanzheng Bian Xiaoyan Hao Yiming Liu Jinyue Xia Jing Hu 
This work is supported by science and technology development fund of Nanjing Medical University(Grand No.NMUB2018095).
Craniosynostosis is a common congenital craniofacial deformity caused by premature ossification and closure of one or more cranial sutures.Craniosynostosis will not only affect the normal development of the skull,but ...
关键词：CRANIOSYNOSTOSIS early rehabilitation desirability function 
Crouzon syndrome in a fraternal twin:A case report and review of the literature
《World Journal of Clinical Cases》2022年第16期5317-5323,共7页Xiao-Jing Li Ji-Mei Su Xiao-Wei Ye 
BACKGROUND Crouzon syndrome(CS;OMIM 123500)is an autosomal dominant inherited craniofacial disorder caused by mutations in the fibroblast growth factor receptor 2(FGFR2)gene.CS is characterized by craniofacial dysosto...
关键词：Crouzon syndrome CRANIOSYNOSTOSIS Fibroblast growth factor receptor 2 MUTATION Fraternal twin Case report 
Patient Blood Management in Craniosynostosis Surgery被引量：2
《Open Journal of Modern Neurosurgery》2021年第4期211-222,共12页Claudine Kumba 
Background: Craniosynostosis surgery is one of the most hemorrhagic interventions, where transfusion rates vary from 20
关键词：CRANIOSYNOSTOSIS Children TRANSFUSION OUTCOME Point of Care Viscoelastic Assays Rotational Thromboelastometry 
Notch signaling:Its essential roles in bone and craniofacial development被引量：5
《Genes & Diseases》2021年第1期8-24,共17页Mikhail Pakvasa Pranav Haravu Michael Boachie-Mensah Alonzo Jones Elam Coalson Junyi Liao Zongyue Zeng Di Wu Kevin Qin Xiaoxing Wu Huaxiu Luo Jing Zhang Meng Zhang Fang He Yukun Mao Yongtao Zhang Changchun Niu Meng Wu Xia Zhao Hao Wang Linjuan Huang Deyao Shi Qing Liu Na Ni Kai Fu Michael J.Lee Jennifer Moriatis Wolf Aravind Athiviraham Sherwin S.Ho Tong-Chuan He Kelly Hynes Jason Strelzow Mostafa El Dafrawy Russell R.Reid 
the National Institutes of Health(CA226303to TCH);the U.S.Department of Defense(OR130096 to JMW);the Scoliosis Research Society(TCH and MJL);the Pritzker-Northshore Fellowship at The University of Chicago;the Medical Scientist Training Program of the National Institutes of Health(T32 GM007281);The University of Chicago Cancer Center Support Grant(P30CA014599);the National Center for Advancing Translational Sciences of the National Institutes of Health through Grant Number UL1 TR000430;the Mabel Green Myers Research Endowment Fund and The University of Chicago Orthopaedics Alumni Fund。
Notch is a cellecell signaling pathway that is involved in a host of activities including development,oncogenesis,skeletal homeostasis,and much more.More specifically,recent research has demonstrated the importance of...
关键词：Alagille syndrome BONE Craniofacial development CRANIOSYNOSTOSIS NOTCH ONCOGENESIS OSTEOGENESIS Spondylocostal dysosotosis 
A custom-designed panel sequencing study in 201 Chinese patients with craniosynostosis revealed novel variants and distinct mutation spectra
《Journal of Genetics and Genomics》2021年第2期167-171,共5页Yingzhi Wu Meifang Peng Jieyi Chen Jinlong Suo Sihai Zou Yanqing Xu Andrew O.M.Wilkie Weiguo Zou Xiongzheng Mu Sijia Wang 
supported by the foundation of Shanghai municipal commission of Health and Family Planning(20174Y0088);the Shanghai Municipal Science and Technology Major Project(2017SHZDZX01);the CAS Interdisciplinary Innovation Team Project;the NIHR Oxford Biomedical Research Centre Programme。
Craniosynostosis is a rare disease in which one or more of the cranial sutures in an infant skull prematurely fuses by turning into bone,with a prevalence of 1 in 2,000—2,500 individuals from reports in Western count...
关键词：patients TURNING 
Three dimensional finite element biomechanical analysis of unilateral coronal synostosis and reconstructive operation
《Chinese Journal of Plastic and Reconstructive Surgery》2019年第1期24-30,共7页Li-dan CHEN Bin YANG 
Objective To establish finite element models of skull, fronto-orbital advancement and fronto-orbital distraction osteogenesis of craniosynostosis, to analyze the mechanical characteristics of skull base and fronto-orb...
关键词：CRANIOSYNOSTOSIS finite element ANALYSIS biomechanical ANALYSIS 
Apert’s syndrome:Study by whole exome sequencing被引量：1
《Genes & Diseases》2018年第2期119-122,共4页Anjana Munshi Preeti Khetarpal Satrupa Das Venkateshwar Rao Monica Valecha Manita Bansal Roshan Kumar 
In the present study we attempted a parente-child trio,whole exome sequencing(WES)approach to study Apert’s syndrome.Clinical characteristics of the child were noted down and WES was carried out using Ion Torrent Sys...
关键词：Apert syndrome CRANIOSYNOSTOSIS Exome sequencing FGFR2 gene Parente-child trio study 
Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12-19p13.2
《Genes & Diseases》2015年第4期347-352,共6页Sarah M.Lyon Darrel Waggoner Sara Halbach Erik C.Thorland Leila Khorasani Russell R.Reid 
Craniosynostosis,a condition in which the cranial sutures prematurely fuse,can lead to elevated intracranial pressure and craniofacial abnormalities in young children.Currently surgical intervention is the only therap...
关键词：Chromosome 19 Craniofacial syndrome CRANIOSYNOSTOSIS MICROARRAY MICRODELETION 
Signaling pathways in osteogenesis and osteoclastogenesis:Lessons from cranial sutures and applications to regenerative medicine被引量：2
《Genes & Diseases》2015年第1期57-68,共12页Justin B.Maxhimer James P.Bradley Justine C.Lee 
supported by the Jean Perkins Foundation(JCL)and the Plastic Surgery Foundation(JCL)(234813).
One of the simplest models for examining the interplay between bone formation and resorption is the junction between the cranial bones.Although only roughly a quarter of patients diagnosed with craniosynostosis have b...
关键词：CRANIOSYNOSTOSIS OPG OSTEOCLAST RANK RANKL Tissue engineering OSTEOGENESIS Signaling 
全选清除导出
共2页<12>
检索报告 对象比较 聚类工具 使用帮助 返回顶部