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科研机构
复旦大学上海医学院 [25]
内容类型
期刊论文 [25]
发表日期
2019 [6]
2018 [8]
2017 [3]
2016 [1]
2013 [2]
2012 [4]
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Interleukin-1 Receptor Associated Kinase 1 Mediates the Maintenance of Neuropathic Pain after Chronic Constriction Injury in Rats
期刊论文
NEUROCHEMICAL RESEARCH, 2019, 卷号: 44, 期号: 5
作者:
Wang, Binbin
;
Zhu, Shunxing
;
Fan, Bingbing
;
Xu, Zhongling
;
Yin, Dekun
收藏
  |  
浏览/下载:24/0
  |  
提交时间:2019/12/05
Neuropathic pain (NP)
IRAK1
P-NF-B
Chronic constriction injury (CCI)
Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants
期刊论文
BMC MEDICAL GENETICS, 2019, 卷号: 20
作者:
Chen, Xiang
;
Yan, Kai
;
Gao, Yanyan
;
Wang, Huijun
;
Chen, Guoqiang
收藏
  |  
浏览/下载:24/0
  |  
提交时间:2019/12/05
CHARGE syndrome
CHD7 gene
Variant
Feeding difficulty
Newborn
Chemokine CXCL10/CXCR3 signaling contributes to neuropathic pain in spinal cord and dorsal root ganglia after chronic constriction injury in rats
期刊论文
NEUROSCIENCE LETTERS, 2019, 卷号: 694
作者:
Chen, Yonglin
;
Yin, Dekun
;
Fan, Bingbing
;
Zhu, Xiang
;
Chen, Qiuping
收藏
  |  
浏览/下载:17/0
  |  
提交时间:2019/12/05
Neuropathic pain
CXCL1O
CXCR3
p-ERK
Chronic constriction injury (CCI)
The molecular epidemiology of hyperphenylalaninemia in Uygur population: incidence from newborn screening and mutational spectra
期刊论文
ANNALS OF TRANSLATIONAL MEDICINE, 2019, 卷号: 7, 期号: 12
作者:
Xian, A.
;
Qian, Yanyan
;
Li, Mingzhu
;
Lu, Yulan
;
Ren, Yan
收藏
  |  
浏览/下载:21/0
  |  
提交时间:2019/12/05
Phenylalanine hydroxylase (PAH)
Uygur
neonatal screening
gene mutation
genotyping
Early onset developmental delay and epilepsy in pediatric patients with WDR45 variants
期刊论文
EUROPEAN JOURNAL OF MEDICAL GENETICS, 2019, 卷号: 62, 期号: 2
作者:
Chen, Hongbo
;
Qian, Yanyan
;
Yu, Sha
;
Xiao, Deyong
;
Guo, Xiao
收藏
  |  
浏览/下载:20/0
  |  
提交时间:2019/12/05
WDR45
Early onset
Developmental delay
Epilepsy
Pediatric
Clinical and genetic spectrum of a large cohort of children with epilepsy in China
期刊论文
GENETICS IN MEDICINE, 2019, 卷号: 21, 期号: 3
作者:
Yang, Lin
;
Kong, Yanting
;
Dong, Xinran
;
Hu, Liyuan
;
Lin, Yifeng
收藏
  |  
浏览/下载:28/0
  |  
提交时间:2019/12/05
Seizures
Epilepsy
Children
Genetics
Pathogenic variant spectrum
Population based hospitalization burden of laboratory-confirmed hand, foot and mouth disease caused by multiple enterovirus serotypes in Southern China
期刊论文
PLOS ONE, 2018, 卷号: 13, 期号: 12
作者:
Yu, Shuanbao
;
Liao, Qiaohong
;
Zhou, Yonghong
;
Hu, Shixiong
;
Chen, Qi
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2019/12/05
One Novel 2.43Kb Deletion and One Single Nucleotide Mutation of the INSR Gene in a Chinese Neonate with Rabson-Mendenhall Syndrome
期刊论文
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, 2018, 卷号: 10, 期号: 2
作者:
Chen, Xiang
;
Wang, Huijun
;
Wu, Bingbing
;
Dong, Xinran
;
Liu, Bo
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
Insulin receptor gene
Rabson-Mendenhall syndrome
neonate
mutation
next generation sequencing
Spectrum of Enterovirus Serotypes Causing Uncomplicated Hand, Foot, and Mouth Disease and Enteroviral Diagnostic Yield of Different Clinical Samples
期刊论文
CLINICAL INFECTIOUS DISEASES, 2018, 卷号: 67, 期号: 11
作者:
Gao, Lidong
;
Zou, Gang
;
Liao, Qiaohong
;
Zhou, Yonghong
;
Liu, Fengfeng
收藏
  |  
浏览/下载:19/0
  |  
提交时间:2019/12/05
HFMD
enterovirus
diagnostic yield
virological surveillance
Evaluation of serum ferritin and thyroid function in the second trimester of pregnancy
期刊论文
ENDOCRINE JOURNAL, 2018, 卷号: 65, 期号: 1
作者:
He, Leqi
;
Shen, Chunmei
;
Zhang, Yanan
;
Chen, Zaoping
;
Ding, Heyuan
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2019/12/05
Serum ferritin
Thyroid function
Thyroid stimulating hormone
Pregnancy
The second trimester
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