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科研机构
复旦大学上海医学院 [10]
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期刊论文 [10]
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2018 [1]
2017 [1]
2015 [1]
2014 [2]
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Palpebral portion of the orbicularis oculi muscle to repetitive nerve stimulation testing: A potential assessment indicator in patients with generalized myasthenia gravis
期刊论文
JOURNAL OF CLINICAL NEUROSCIENCE, 2018, 卷号: 48
作者:
Yan, Chong
;
Song, Jie
;
Pang, Song
;
Yi, Fangfang
;
Xi, Jianying
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
Generalized myasthenia gravis
Repetitive nerve stimulation
Orbicularis oculi
Quantitative myasthenia gravis
Manual muscle testing
Activities of daily living
Novel SEA and LG2 Agrin mutations causing congenital Myasthenic syndrome
期刊论文
ORPHANET JOURNAL OF RARE DISEASES, 2017, 卷号: 12
作者:
Zhao, Chongbo
;
Xi, Jianying
;
Yan, Chong
;
Liu, Wei-Wei
;
Qiao, Kai
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2019/12/05
Congenital Myasthenic syndrome
Agrin
Distal myopathy
Neuromuscular junction
Salbutamol
Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types
期刊论文
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2015, 卷号: 107, 期号: 12
作者:
Sampson, Joshua N.
;
Wheeler, William A.
;
Yeager, Meredith
;
Panagiotou, Orestis
;
Wang, Zhaoming
收藏
  |  
浏览/下载:47/0
  |  
提交时间:2019/12/19
Novel LAMP2 mutations in Chinese patients with Danon disease cause varying degrees of clinical severity
期刊论文
CLINICAL NEUROPATHOLOGY, 2014, 卷号: 33, 期号: 4
作者:
Luo, Su-shan
;
Xi, Jian-ying
;
Cai, Shuang
;
Zhao, Chong-bo
;
Lu, Jia-hong
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2019/12/19
Danon disease
LAMP2
synonymous mutation
exon skipping
muscle biopsy
Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33
期刊论文
HUMAN MOLECULAR GENETICS, 2014, 卷号: 23, 期号: 24
作者:
Wang, Zhaoming
;
Zhu, Bin
;
Zhang, Mingfeng
;
Parikh, Hemang
;
Jia, Jinping
收藏
  |  
浏览/下载:34/0
  |  
提交时间:2019/12/19
Genetic variability and clinical spectrum of Chinese patients with limb-girdle muscular dystrophy type 2A
期刊论文
MUSCLE & NERVE, 2012, 卷号: 46, 期号: 5
作者:
Luo, Su-Shan
;
Xi, Jian-Ying
;
Zhu, Wen-Hua
;
Zhao, Chong-Bo
;
Lu, Jia-Hong
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/19
CAPN3
genotype
LGMD2A
novel mutation
phenotype
HLA-DQA1*03:02/DQB1*03:03:02 is strongly associated with susceptibility to childhood-onset ocular myasthenia gravis in Southern Han Chinese
期刊论文
JOURNAL OF NEUROIMMUNOLOGY, 2012, 卷号: 247, 期号: 1-2
作者:
Zhu, Wen-Hua
;
Lu, Jia-Hong
;
Lin, Jie
;
Xi, Jian-Ying
;
Lu, Jun
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/19
Myasthenia gravis with childhood-onset
Ocular myasthenia gravis
HLA-DQA1
HLA-DQB1
High prevalence of plasmid-mediated 16S rRNA methylase gene rmtB among Escherichia coli clinical isolates from a Chinese teaching hospital
期刊论文
BMC INFECTIOUS DISEASES, 2010, 卷号: 10
作者:
Yu, Fang-you
;
Yao, Dan
;
Pan, Jing-ye
;
Chen, Chong
;
Qin, Zhi-qiang
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/19
Measurements of hc(P11) in ψ
′
Decays
期刊论文
Physical Review Letters, 2010, 卷号: 104, 期号: 13
作者:
Ablikim, Medina N./35226931500[0]
;
Achasov, M. N./7003450501[1]
;
An, L./56179951100[2]
;
AN, Qi/35780471800[3]
;
An, Zhenghua/55437476000[4]
收藏
  |  
浏览/下载:38/0
  |  
提交时间:2019/12/19
Report on the first Chinese family with Gerstmann-Straussler-Scheinker disease manifesting the codon 102 mutation in the prion protein gene
期刊论文
NEUROPATHOLOGY, 2006, 卷号: 26, 期号: 5
作者:
Wang, Yin
;
Qiao, Xiang-Yang
;
Zhao, Chong-Bo
;
Gao, Xiang
;
Yao, Zhen-Wei
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/27
amyloid plaque
cerebellar ataxia
Gerstmann-Straussler-Scheinker disease
prion protein
PrP gene
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