Shaojuan Gu
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Explore the profile of Shaojuan Gu including associated specialties, affiliations and a list of published articles.
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8
Citations
39
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Recent Articles
1.
Li H, Xiao G, Tan X, Liu G, Xu Y, Gu S
Exp Brain Res
. 2023 May;
241(6):1585-1598.
PMID: 37142782
Cerebral infarction is one of the most prevalent cerebrovascular disorders. Microglia and infiltrating macrophages play a key role in regulating the inflammatory response after ischemic stroke. Regulation of microglia/macrophages polarization...
2.
Xiao H, Deng S, Deng X, Gu S, Yang Z, Yin H, et al.
Digestion
. 2018 Nov;
99(4):319-326.
PMID: 30384382
Background: Wilson's disease (WD) is an autosomal recessive disease, which is characterized by an excessive copper accumulation in the liver and brain, leading to subsequent hepatic and/or neurological disorders. The...
3.
Wu Y, Yuan L, Guo Y, Lu A, Zheng W, Xu H, et al.
J Cell Mol Med
. 2018 Aug;
22(11):5533-5538.
PMID: 30160005
GNE myopathy is a rare, recessively inherited, early adult-onset myopathy, characterized by distal and proximal muscle degeneration which often spares the quadriceps. It is caused by mutations in the UDP-N-acetylglucosamine...
4.
Liu Y, Yang H, Song Z, Gu S
Turk J Gastroenterol
. 2015 Apr;
25 Suppl 1:116-21.
PMID: 25910288
Background/aims: Copper is an essential trace element that serves as an important catalytic cofactor for cuproenzymes, carrying out major biological functions in growth and development. Although Wilson's disease (WD) is...
5.
Gu S, Song Z, Fan X, Chen R, Zheng W, Yan W
Zhong Nan Da Xue Xue Bao Yi Xue Ban
. 2013 Dec;
38(11):1172-6.
PMID: 24316936
Objective: To determine the effect of Parkinson's disease-weight bearing exercise for better balance (PD-WEBB) exercise on balance impairment and falls in people with Parkinson's disease (PD). Methods: A single-blind, randomized...
6.
Gu S, Yang H, Qi Y, Deng X, Zhang L, Guo Y, et al.
PLoS One
. 2013 Jul;
8(7):e66526.
PMID: 23843956
Wilson's disease (WD) is an autosomal recessive inherited disorder caused by mutations in the ATPase Cu(2+) transporting beta polypeptide gene (ATP7B). The detailed metabolism of copper-induced pathology in WD is...
7.
Yuan L, Song Z, Xu H, Gu S, Zhu A, Gong L, et al.
Neurosci Lett
. 2013 Apr;
543:69-71.
PMID: 23562511
Growing evidences show that genetic abnormalities play an important role in the etiopathogenesis of Parkinson disease (PD). At least 18 genetic loci and 13 disease-related genes for parkinsonism have been...
8.
Gu S, Liu Y, Song Z, Zi X, Deng H
J Clin Neurol
. 2013 Jan;
9(1):61-4.
PMID: 23346163
Background: Vogt-Koyanagi-Harada (VKH) disease is characterized by bilateral granulomatous uveitis with neurologic, auditory, and dermatologic manifestations. However, acute myelitis complicating VKH disease has rarely been reported. Case Report: A 50-year-old...